Ting Zhou
Allie Lee
Amy Cheuk Yin Lo- Department of Ophthalmology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong SAR, China
Diabetes mellitus (DM) is a major global public health problem that can cause complications such as diabetic retinopathy, diabetic neuropathy, and diabetic nephropathy. Besides the reporting of reduction in corneal nerve density and decrease in corneal sensitivity in diabetic patients, there may be a subsequent result in delayed corneal wound healing and increased corneal infections. Despite being a potential cause of blindness, these corneal nerve changes have not gained enough attention. It has been proposed that corneal nerve changes may be an indicator for diabetic neuropathy, which can provide a window for early diagnosis and treatment. In this review, the authors aimed to give an overview of the relationship between corneal nerves and diabetic neuropathy as well as the underlying pathophysiological mechanisms of corneal nerve fiber changes caused by DM for improved prediction and prevention of diabetic neuropathy. In addition, the authors summarized current and novel therapeutic methods for delayed corneal wound healing, nerve protection and regeneration in the diabetic cornea.
Introduction
Diabetes mellitus (DM) is a chronic metabolic disorder characterized by abnormally increased blood glucose level, which over time leads to severe systemic damage such as diabetic foot ulcers, nephropathy and neuropathy. According to World Health Organization (WHO), about 422 million people worldwide suffer from DM, and 1.6 million deaths are directly attributed to DM each year (WHO, 2021). Over the past few decades, the number of cases and prevalence of DM have been increasing steadily. Thus, the huge public health challenge and economic burden that many countries are about to face emphasize the importance of effective treatment and prevention for various complications associated with DM.
The complications of DM include cardiovascular disease, nephropathy, retinopathy and neuropathy (Markoulli et al., 2018). Among them, diabetic retinopathy has been well-recognized. Besides, it was reported that more than half of the patients were presented with alternation of anterior segment (such as cornea, conjunctiva, lacrimal gland and lens) during DM progression (Vieira-Potter et al., 2016; Barsegian et al., 2018); but these symptoms are sometimes overlooked. Indeed, DM patients have shown a progressive loss in corneal nerve fiber and a decrease in corneal sensitivity (Dogru et al., 2001; Pritchard et al., 2015), which subsequently led to delayed nerve regeneration and wound healing after injury, dry eye, persistent epithelial defects, and neurotrophic ulcers (Kaiserman et al., 2005; Pritchard et al., 2011). These complications may cause severe vision loss or even blindness, reminding us that it is vital to understand the effects of DM on corneal nerves (Bikbova et al., 2018; Han et al., 2018).
In this review, the authors outlined the association between DM and corneal nerves and summarized the current knowledge regarding the underlying pathophysiologic mechanisms of corneal nerve fiber changes caused by DM. Also, the authors explored current and the most recent therapeutic approaches for nerve protection and regeneration in the diabetic cornea.
Diabetic Corneal Neuropathy
Clinical Perspectives of Corneal Neuropathy in Diabetes Mellitus
The cornea is one of the most important parts of optical system. Its transparent and avascular physiological characteristics ensure clear vision (Al-Aqaba et al., 2019). The cornea is innervated by the trigeminal nerve; it indeed is the most densely innervated structure in the entire human body. The cornea is also one of the most sensitive body parts to pain as the number of free epithelial nerve endings are 300–600 times that of the skin. Cornea contains a large number of small nerve fibers like myelinated A-δ fibers and unmyelinated C fibers. The physiological function of A-δ fibers is cold sensation and nociception, while C fibers are mainly responsible for warm, cold, thermal perception (Körei et al., 2016). These sensory nerves also control reflex function and tear secretion. In addition, the corneal nerves play a crucial neurotrophic role through releasing neurotrophic factors to maintain integral and healthy structure and function of the ocular surface, and are the major determinant in maintaining ocular surface homeostasis, corneal sensitivity, epithelial health, and wound healing (Byun et al., 2015; Labetoulle et al., 2019).
It was reported that neuropathy of the cornea occurred in the early stage of DM (Zhao et al., 2019). The clinical symptoms in diabetic patients with corneal neuropathy are photophobia, eye irritation or pain (Bikbova et al., 2018). Some patients have no symptoms, but subclinical changes in the cornea may exist (Rehany et al., 2000; Scheler et al., 2012). Chronic hyperglycemia in diabetic patients can cause damage to the trigeminal nerve, leading to a reduction or loss of corneal nerves, most of which are damages to A-δ and C nerve fibers. Damage or loss of corneal innervation can in turn lead to reduced corneal nerve fiber density, attenuated corneal sensitivity, dry eyes, delayed wound healing, subsequently developing into corneal ulcers, perforations, and even blindness (Shaheen et al., 2014).
In vivo corneal confocal microscopy (CCM) is an essential method to investigate the fine structure of corneal nerves in detail. It provides real-time visualization of corneal nerve fibers in a non-invasive way, allowing long-term longitudinal studies in both patients and animal models (Leckelt et al., 2016). The acquired corneal images can be analyzed by appropriate software for the identification of quantitative indicators (Schaldemose et al., 2020). Using CCM, several published studies reported corneal nerve fiber changes in diabetic patients. Whether it is type 1 diabetes (TID) or type 2 diabetes (T2D), the nerve fiber length, nerve fiber density and nerve branch density in these patients were significantly reduced (Chen et al., 2018; Li et al., 2019; Lewis et al., 2020). Lagali et al. revealed that as type 2 diabetes continued, the sub-basal nerve plexus showed a progressive degeneration (Lagali et al., 2017). They found a reduction of the main nerve branches, an apparent loss of the secondary nerve fiber branches as well as a loss of the connection with the primary nerve. In addition, one study examined the correlation between corneal nerve parameters and glucose variability. It explored whether short-term measures of blood glucose control were related to structural and functional alternations of corneal nerve in TID patients and found that significant loss of corneal nerve length in the inferior whorl occurred in patients with increased glucose variability and time above range (Issar et al., 2020). Moreover, the decrease in corneal keratocyte density was associated with damage in the sub-basal nerve plexus in diabetic patients (Kalteniece et al., 2018a). Other studies found that the density of the sub-basal nerve plexus in diabetic patients was attenuated while the density of Langerhans cells was increased (Qu et al., 2018; Ferdousi et al., 2019). These changes (lower corneal keratocyte density and higher Langerhans cells density) were related to delayed corneal epithelial healing (Qu et al., 2018). These data can help clinicians to better understand when and how diabetic corneal neuropathy develops and monitor cornea alternation and its progression.
Many clinical studies also explored the association between diabetic corneal nerve damage and complications of DM with CCM. Several studies demonstrated that changes in corneal nerve fibers were related to the development of diabetic retinopathy (DR). One study reported that in T2D patients, corneal nerve damage preceded the development of DR (Bitirgen et al., 2014). In TID patients with a four-year development of DM with/without DR, it was found that their corneal nerve fiber length was one of the predictors for worsening of DR (Srinivasan et al., 2018). The authors also reported that neuronal degeneration of both cornea and retina may occur in early stage of DR, so examination of corneal nerve was necessary especially when clinical signs of DR was absent (Srinivasan et al., 2017; Srinivasan et al., 2018). Meanwhile, reduction of corneal nerve fiber density, corneal nerve fiber length and nerve fractal dimension occurred in T2D patients with diabetic nephropathy. These corneal alternations were related to the decline of kidney function (Tummanapalli et al., 2020a). There were more clinical studies that focused on the damage of corneal nerve in diabetic neuropathy (DN). Edwards et al. demonstrated that the length and density of corneal nerve fibers in diabetic patients with mild DN were significantly reduced (compared to the control group and diabetic patients without DN) (Edwards et al., 2012). Similarly, other studies have reached consistent conclusions. They stated that the parameters of corneal nerve fibers could predict the development of DN and are a potential clinical biomarker for evaluating DN (Deák et al., 2019). Compared with controls, the corneal parameters of T1D and T2D patients, such as nerve fiber density, branch density, and nerve fiber length, were significantly reduced, and these indicators progressively worsened when the severity of DN increased (Kalteniece et al., 2020). The corneal nerve fibers in the inferior whorl region of diabetic patients were shown to be more sensitive to the damage than those in the central cornea, suggesting that the reduction of corneal nerve fibers is more significant in the inferior region (Kalteniece et al., 2018b; Ferdousi et al., 2020). Moreover, corneal nerve fiber damage was more severe in patients with painful neuropathy when compared with painless neuropathy (Kalteniece et al., 2018b). The results obtained from all these studies indicated an important association of corneal nerve with DM while corneal nerve fibers may be a reproducible biomarker for detection and assessment of early nerve damage in diabetes.
Of note, current diagnosis tests for DN patients without obvious symptoms include filament test, quantitative sensory test, nerve conduction test, muscle response test (electromyography), and autonomic test. All of these are tests designed for assessing large nerve fiber function (Selvarajah et al., 2019). However, impairment of small nerve fibers (type C and A-δ nerve fiber) is considered the earliest alteration in the course of DN, which progresses to large nerve fiber (Körei et al., 2016). Since the gold standard test for small fiber neuropathy is skin biopsy with intraepidermal nerve fiber density analysis, this invasive procedure makes it hard to implement in routine clinical practice (Basantsova et al., 2019). By the time when DN is detected with the aforementioned tests for large nerve fibers, it is very often well established already; but the neuropathic process can no longer be reversed. In conclusion, the detection of corneal nerve fiber with CCM may provide an open window for diagnosis of DN. It may potentially be a biomarker for the progression, or even treatment efficacy of DN. This emphasizes the importance of understanding the pathogenic mechanisms of corneal neuropathy in diabetes.
Pathogenesis
Many pathological changes were involved in diabetic corneal neuropathy, which interplayed and complemented each other, leading to abnormalities in cornea, including severe damage to corneal nerves (Roszkowska et al., 2021). The mechanism is summarized in Figure 1.
FIGURE 1. Pathogenesis of corneal neuropathy in diabetes mellitus. The Solid line represents increase and promotion, and the dashed line represents decrease and inhibition.
Hyperglycemia
Advanced Glycation End Products
Advanced glycation end products (AGEs) are reactive metabolites produced by the glycation of proteins or lipids that are exposed to sugar molecules and form non-enzymatic covalent bonds with each other (Babizhayev et al., 2015). The structural and functional proteins of peripheral nerves were reported to be glycosylated and they underwent cross-linking over time in diabetic patients and diabetic animal models. This resulted in an elevation of AGE level and in turn led to segmental demyelination, impaired axon transport and impaired regenerative activity (Sugimoto et al., 2008). In addition, AGEs may cause cross-linking of collagen fibris (Sady et al., 1995). Kaji et al. reported that glycosylated laminin and fibronectin reduced cell adhesion of corneal endothelial cells, thus leading to abnormalities of the diabetic cornea (Kaji et al., 2001). Moreover, AGEs were shown to change the structure and function of corneal epithelium, stroma and basement membrane (Bejarano and Taylor, 2019).
The Polyol Pathway
The polyol pathway is also known as the sorbitol-aldose reductase pathway. Chronic hyperglycemia leads to excessive glucose in nerve cells, resulting in saturation of the normal glycolytic pathway. Excess glucose is then shunted to the polyol pathway; it is first converted to sorbitol and then fructose by intracellular enzymes reductase and sorbitol dehydrogenase, respectively (Stavniichuk et al., 2012). These two sugar molecules (sorbitol and fructose) tend to accumulate within nerve cells because nerve cell membrane is impermeable to them, thus increasing the osmotic stress of nerve cells (Oates, 2008). At the same time, during the reduction process, aldose reductase consumes the cofactor nicotinamide adenine dinucleotide phosphate (NADPH) and leads to a decrease of reduced glutathione production, tissue antioxidant capacity and free radical scavenging, thereby causing tissue damage (Lyu et al., 2019). In addition, excessive amounts of sorbitol and fructose results in the decrease of free nerve myoinositol, which is sugar alcohol required for normal nerve conduction velocity (Greene et al., 1992). A decrease in its level can lead to a reduction in membrane sodium potassium adenosine triphosphatase (Na+/K+ ATPase) activity, resulting in electrolyte imbalance, reducing nerve conduction velocity, and destroying the structure of nerve fibers (Zhu et al., 2019).
Protein Kinase C Activation Pathway
Protein kinase C (PKC) is also an important pathogenic mechanism. In DM, increased intracellular glucose level plays a role in the synthesis of PKC activator diacylglycerol. The activation of PKC inhibits Na+/K+ ATPase activity, thereby affecting nerve conduction and nerve regeneration (Geraldes and King, 2010). A study found that the use of the PKC inhibitor ruboxistaurin mesylate improved microvascular blood flow and nerve conduction, thereby alleviating the symptoms of DN and improving the life quality of diabetic patients (Casellini et al., 2007).
Neurotrophic Factors
Results of several in vitro studies indicated that there is a mutual trophic support between the corneal nerve plexus and the corneal epithelium. The corneal nerve plexus secretes neuropeptides to maintain epithelial homeostasis and enhance wound healing. The corneal epithelium releases neurotrophic factors, such as nerve growth factor (NGF) and glial cell line-derived neurotrophic factor (GDNF), which can accelerate epithelial wound healing and stimulate neurite survival (Bikbova et al., 2016; Barsegian et al., 2018). Brain-derived neurotrophic factor (BDNF) is found in both corneal epithelial cells and corneal neurons (Byun et al., 2015). Therefore, the corneal nerve is closely related to the corneal epithelium. Neuropeptides released by sensory nerves could support epithelial cells and dendritic cells in the cornea to maintain its homeostasis. Chronic hyperglycemia may affect the neuropeptide secretion from the corneal nerves, thereby affecting the proliferation of cells in cornea (Markoulli et al., 2017; Zhang J. et al., 2020). In the denervated cornea of rats, the rate of mitosis of corneal epithelial cells was changed (Ferrari et al., 2011). Gao et al. discovered that the number of dendritic cells, the main source of ciliary neurotrophic factor (CNTF), in the diabetic cornea was reduced. They demonstrated that the neural communication of dendritic cells was affected, resulting in impaired innervation and regeneration of sensory nerves (Gao et al., 2016). Zhou et al. found that in diabetic mice, a reduction of ciliary neurotrophic factor (CNTF) caused impaired corneal epithelial wounds, while CNTF supplementation could improve this pathology (Zhou et al., 2015). These articles demonstrated that diabetes could affect the corneal nerves through the secretion of neurotrophic factors, and at the same time affect the function of the corneal epithelium.
Oxidative Stress
Oxidative stress refers to the phenomenon that cells and tissues contain excessively high levels of reactive oxygen species (ROS), and the biological system has limited ability to reduce these active products to non-toxic substances (Pizzino et al., 2017). During hyperglycemia, there is an excessive influx of glucose into the mitochondria accelerating the oxidative metabolism of glucose in the mitochondria and the production of superoxide ions, thereby promoting the production of ROS (Babizhayev et al., 2015). Mitochondrial fission has been reported to occur in the neurites in response to hyperglycemia, generating oxidative stress and activating caspase 3. This was an indication of hyperglycemia-induced neurite damage (Vincent et al., 2010). In T2D patients, the length and density of corneal nerve fiber were decreased together with expanded beads in corneal nerve fiber. The bead is a novel parameter for a composite of accumulated mitochondria, glycogen particles and vesicles, which might be a predictor of slow sensory nerve conduction velocity in DM (Ishibashi et al., 2016). Mitochondrial abnormalities might be initiated by interrupted axonal transport, causing mitochondria to aggregate or cluster. As swollen mitochondria were difficult to be transported compared to smaller mitochondria, this eventually led to axonal demyelination and conduction dysfunction (Hamid et al., 2014). Mitochondrial damage is also related to the reduction of neurotrophic factors such as NGF and neurotrophin-3 (NT-3) (Zherebitskaya et al., 2009). One study found that increased 8-hydroxydeoxyguanosine (a marker of oxidative stress) was detected in the cornea of diabetic rats when compared with the control group (Kim et al., 2011a). This indicated a potential role of oxidative stress in the apoptosis of diabetic corneal cells.
Neuro-Immune Interactions
Neuro-immune interactions may also play a role in diabetic corneal neuropathy. In diabetic mouse models, high concentrations of Langerhans cells and dendritic cells, the main antigen-presenting cells, were found in the cornea and they aggregated around corneal nerve fibers (Leppin et al., 2014). When compared with the control group, the number of dendritic cells and Langerhans cells of diabetic patients elevated significantly, which negatively correlated with the length and density of corneal nerve fibers (Tavakoli et al., 2011). Another clinical study reported that early immune activation and corneal nerve degeneration occurred in adolescents with T1D (Ferdousi et al., 2019). In addition, it was reported that DNase I could promote corneal nerve regeneration and corneal sensitivity through decreasing the neutrophils extracellular traps caused by neutrophil aggregation (Zhang J. et al., 2020). However, this view is controversial (Ljubimov, 2017), and no concrete conclusion has been reached yet. It is not clear whether the infiltration of immune cells in the cornea precedes the induction of hyperglycemia.
Lipids
In addition to the effects of long-term hyperglycemia, dyslipidemia may also be a key factor in neuropathy, especially in T2D. Firstly, dyslipidemia can lead to an excessive increase in the level of free fatty acid (FFA), which can cause an elevation in nitric oxide, thereby leading to cell apoptosis (Stickings and Cunningham, 2002). Secondly, FFA enters the mitochondria and is catabolized by ß-oxidation to generate acetyl CoA. Excessive accumulation of acetyl CoA after dyslipidemia facilitates its conversion into toxic acylcarnitine substances, leading to nerve injury. Also, ß-oxidation activates inflammatory cells to release cytokines and induces the production of ROS, resulting in the production of peroxides. The oxidation of low-density lipoprotein inversely induces the generation of ROS, inhibits the electron transfer in the respiratory chain and aggravates nerve injury, which in turn forms a vicious circle (Roselló-Busquets et al., 2019; Rumora et al., 2019). Also, it is reported that decreased corneal nerve fiber length has an inverse correlation with low-density lipoprotein cholesterol (LDL-C) in T1D patients (Ferdousi et al., 2021). Moreover, when excessive FFA exhausts the oxidizing capacity of tissues, they are markedly deposited in non-fat tissues in the form of triglycerides, causing damage to these tissues. This phenomenon is called lipotoxicity. It is worth noting that the ability of neuronal mitochondria to metabolize and consume fatty acids is very limited (Schönfeld and Reiser, 2013). High levels of active oxygen can easily induce fatty acid peroxidation. If neuronal cells cannot clear up these peroxidized fatty acids in time, pathological changes will occur in the neurons, leading to neuropathy (Sultana et al., 2013).
Alternation of Gene Expression
Recently, several studies focused on the difference of gene expression between normal and diabetic trigeminal ganglion tissues. It was reported that in the trigeminal nerve tissue of T1D mice, abnormal expression of miR-34c could decrease sensory neuron growth of trigeminal nerve and the repair of corneal nerve endings by regulating the autophagy-related proteins Atg4B and LC3-II, thereby causing corneal neuropathy (Hu et al., 2019). Another study showed that some miRNA-mRNA pairs, such as miR-350-5p/Mup20, miR-592-5p/Angptl7 and miR-351-5p/Elovl6, are related to diabetic corneal neuropathy. And they reported that dysregulated genes could affect cell proliferation and death, glucose metabolism, and synaptic transmission (Zhang et al., 2020a). Recently, they further identified the miR-223-5p/Hpgds axis after screening by RNA sequencing. They reported that Hpgds is the direct target gene of miR-223-5p, and downregulation of miR-223-5p could promote corneal nerve regeneration by ameliorating inflammation (Zhang et al., 2021).
These studies provided new investigations on the pathogenesis of corneal neuropathy in DM and suggested that these alternations may be targets for gene therapy on diabetic corneal neuropathy.
Treatment
Strict glycemic control is a vital prerequisite for the treatment in diabetic complications. So far, treatment of diabetic corneal diseases is still symptomatic. Here, we summarized and discussed current and innovative treatments for diabetes-related corneal pathologies. The advantages and limitations of various treatments are summarized in Table 1.
TABLE 1. Clinical and experimental therapeutic strategies for anterior segment disorders associated with diabetes.
Glycemic Control
Since chronic hyperglycemia can cause nerve damage through a variety of pathological mechanisms, strict glycemic control is believed to be an essential means to treat diabetes and reduce the progression of its related complications (Ponirakis et al., 2021a). Many drugs have been used to control blood glucose; they include oral drugs such as metformin, glucagon-like peptide-1 (GLP-1) receptor agonist or sodium–glucose cotransporter type 2 inhibitor, as well as injection drugs such as insulin.
Through analyzing the data of 1172 T1D patients, a prospective study of European Diabetes identified that the incidence of neuropathy was associated with potential risk factors like the duration of diabetes, total cholesterol and LDL-C and triglycerides, body mass index, hypertension and smoking (Tesfaye et al., 2005). Studies demonstrated that in TID and T2D patients, DN might be prevented or delayed by the improvement in glycemic control (Ishibashi and Tavakoli, 2018; Mahelková et al., 2018). A clinical trial found that after application of insulin eye drops in 14 diabetic patients, the rate of corneal epithelial regeneration and the healing rate of epithelial defects increased (Bastion and Ling, 2013). In two animal studies, the authors reported that insulin eye drops could prevent corneal sub-basal nerve or sub-epithelial nerve loss in streptozotocin (STZ)-induced diabetic mice (T1D) (Chen et al., 2013; Yorek et al., 2014). In addition, Song et al. found that early insulin treatment was beneficial to normalise the circadian rhythm of the cornea in mice with T1D (Song et al., 2016). Moreover, in T1D rats, metformin treatment showed a protective function in hyperglycemia-induced ocular deteriorations like corneal epithelial defects and damaged Bowman’s membrane through ameliorating oxygenated free radicals in the endothelial cells by inhibiting protein kinase C, reducing mitochondrial respiratory chain pathways (Nahar et al., 2021). These data indicated that insulin might be used for the treatment of diabetic corneal defects. However, in T2D, the role of glycemic control in complications is controversial. One clinical trial found that in T2D subjects, treatment with exenatide plus pioglitazone or basic bolus insulin therapy for more than 12 months could significantly improve corneal nerve morphology, which was manifested by increased corneal nerve length and branch density, indicating the promotion of corneal nerve regeneration (Ponirakis et al., 2020). Nonetheless, another clinical trial demonstrated that treatment with exenatide combined with pioglitazone or insulin had a limited effect on nerve regeneration in T2D subjects with high insulin resistance (Ponirakis et al., 2021b). However, it should be noted that in non-diabetic cornea of rats, topical insulin had no effect on wound healing (Zagon et al., 2007). Also, insulin treatment may up-regulate insulin-like growth factor-1 (IGF-1), activate vascular endothelial growth factor production, increase the susceptibility to T2D and DR, and exacerbate retinopathy (Smith et al., 1999; Khan et al., 2020). Therefore, before insulin is considered as the treatment for diabetic corneal disorder, it is necessary to monitor the changes in retina.
Restoring insulin secretion is another means to treat diabetes and its complications. Pancreatic transplantation may be an effective way to restore normal glycemic (Tavakoli and Liong, 2012). A recent study demonstrated that in T1D patients, improvement in corneal nerve fiber regeneration was found after simultaneous transplantation of pancreas and kidney (Azmi et al., 2019). Nevertheless, suitable organs are limited, and surgery also brings huge risks and unpredictable postoperative complications. Hence, an alternative method, pancreatic islet cell transplantation has been considered to restore endogenous insulin production. Islet cell transplantation is a procedure to infuse purified islet cells from a deceased donor into the recipient’s liver. Therefore, it requires the use of immunosuppressive agents for life-long treatment (Senior et al., 2018). Overall, studies indicated that pancreatic islet cell transplantation may improve glycemic stability and may reduce the occurrence of diabetic complications (retinopathy and neuropathy) (Foster et al., 2018; Vantyghem et al., 2019). However, pancreatic islet cell transplantation can cause surgical complications such as infection, and the lifetime effectiveness is uncertain. An economic evaluation compared the cost of islet cell transplantation to insulin treatment and found that islet cell transplantation was not cost-effective (Wallner et al., 2016).
It was reported that worsening of DR occurred when diabetic patients changed from poor glycemic control to tight glycemic control (Bain et al., 2019), which emphasized the importance of monitoring blood glucose level. Recently, greater glucose variability was shown to be related to poor ocular nerve function, which was mentioned in Clinical perspectives of corneal neuropathy in diabetes mellitus Section (Issar et al., 2020). Therefore, more studies about treatments with less glucose variability in the prevention of neuropathy are needed.
Pharmacological Intervention
Lipid-Lowering Drugs
Lipids include fatty acids, glycerolipids, sphingolipids and sterols (Fahy et al., 2005). In Lipids Section, we have concluded that dyslipidemia plays an essential role in DN. Moreover, a recent study revealed that T2D patients with metabolic syndrome manifested poorer peripheral nerve structure and function when compared with T2D patients alone (Issar et al., 2021), which again stressed the importance of lowering the level of harmful lipids.
Statins are the most used lipid-lowering drugs. According to published reports, statin treatment can improve neuropathic indicators by anti-inflammation in vincristine sulphate-induced DN in rats (Bhalla et al., 2015). A clinical trial revealed that simvastatin/ezetimibe and rosuvastatin could significantly reduce lipid peroxidation in patients with DN (Villegas-Rivera et al., 2015). However, other studies did not find significant association between statins and DN (Miao Wang et al., 2021). Fibrates are also used to lower triglyceride and increase high-density lipoprotein. Moreover, peroxisome proliferator-activated receptor (PPAR) played vital roles in modulating inflammation and metabolism. A drug in one of the fibrate classes, fenofibrate, is a PPARα agonist used to treat abnormal blood lipid levels. Knockout of PPARα in T1D mice and rats aggravated the reduction in corneal nerve fiber density and lowering in corneal sensitivity, which could be prevented by fenofibrate (Matlock et al., 2020).
Nevertheless, in T2D patients with/without DN, low levels of LDL-C could decrease nerve conduction velocity and amplitude and increase nerve lesions, despite being an effective treatment for dyslipidemia in T2D patients (Jende et al., 2019). A case report revealed that when PCSK9 inhibitor-alirocumab (Praluent) was used to treat patients with pre-diabetes and dyslipidemia, their level of LDL-C was reduced (Franco et al., 2019). The effects of triglyceride-lowering drugs on diabetic corneal neuropathy are largely unclear, and more well-designed experiments are warranted.
Supplements of Fatty Acids and Its Metabolites
Menhaden oil is a source of omega-3 fatty acids and is enriched in docosahexaenoic acid (DHA). It can be used as a dietary supplement for human (Shevalye et al., 2015). In both T1D and T2D rat models, the number of their corneal nerves was significantly reduced, indicating that the nerve fibers were excessively damaged. After treatment with a diet rich in menhaden oil, loss of corneal nerve was reversed, indicating that omega-3 fatty acids are a beneficial treatment (Coppey et al., 2020; Lewis et al., 2021). Another study found that in a T2D mouse model, the use of menhaden oil or resolvin D1 can reverse the attenuation in corneal innervation and motor and sensory nerve conduction velocity. In addition, through in vitro experiments, the author found that resolvin D1 stimulated neurite outgrowth in the dorsal root ganglion (Shevalye et al., 2015). Resolvin D1 is the metabolite of DHA and has anti-inflammatory and neuroprotective effects (Lee et al., 2015). DHA is involved in neuroprotection, synaptic function, and brain and retina development. DHA is the precursor of neuroprotectin D1 (NPD1), which could resist oxidative stress induced by cell injury (Serhan et al., 2015). One study reported that in injured rabbit cornea, treatment with NPD1 could attenuate inflammatory response, increase corneal sensitivity and stimulate neurite outgrowth (Cortina et al., 2013). In fact, corneas treated with DHA and pigment epithelium-derived factors exhibited increased NPD1 synthesis (Cortina et al., 2013).
Moreover, one article compared the effects of menhaden oil, resolvin D1 and salsalate on DN (Yorek et al., 2016). The authors found that in T1D mice, monotherapy could improve both motor and sensory nerve conduction velocities and increase the density of nerves in corneal epithelium, with no difference among the three drugs. Salsalate, a prodrug of salicylate, is used to treat pain and inflammation associated with rheumatic diseases in humans. Salsalate could reduce circulating triglycerides (Davidson et al., 2018), block vascular insulin resistance mediated by free fatty acid and reduce inflammation (Yorek et al., 2016) by reducing NF-κB and increasing nitric oxide to prevent ischemic nerve damage (McCarty, 2010). The authors found that the combined use of menhaden oil and salsalate could increase the level of plasma resolvin D1 when compared with that observed in monotherapy (Yorek et al., 2016). The authors put forward the hypothesis that under the same curative effect, the effective concentration of menhaden oil could be reduced to reach the highest standard of human dietary dose in order to increase its clinical feasibility.
Meanwhile, the combined use of enalapril, a-lipoic acid and menhaden oil in T2D rats could help the recovery of corneal sub-basal nerve fiber length and corneal sensitivity (Davidson et al., 2017). Alpha-lipoic acid is a free radical scavenger that can alleviate oxidative stress. Previous studies have shown that alpha-lipoic acid administration led to clinically significant improvement and prevention of neurological damage progression (Ziegler et al., 2011). Additionally, when combined with aldose reductase inhibitors, it could further enhance the improvement effect (Yorek et al., 2014). Enalapril is an angiotensin converting enzyme inhibitor that is widely used to treat hypertension and diabetic nephropathy. The authors hypothesized that the mechanism of this combination therapy might be a reduction of oxidative stress and inflammation and an increase omega-3 polyunsaturated fatty acids.
Therefore, the aforementioned fatty acids and its metabolites provide other options for potential new treatments for diseases involving corneal nerve injury.
Aldose Reductase Inhibitors
Aldose reductase is the rate-limiting enzyme in the polyol pathway, whose activation by hyperglycemia can cause corneal nerve injury. It is also a key promoter of inflammation and cytotoxic conditions. Therefore, in theory, aldose reductase inhibitor (ARI) can reduce corneal nerve injury and promote corneal epithelial regeneration via attenuating the activation of polyol pathway (Markoulli et al., 2018). Takamura et al. found that rats fed with galactose have corneal abnormalities like those in diabetic animals. Treatment with ARI (ranirestat) has been found to facilitate corneal wound healing in rats by reducing the expression of matrix metalloproteinase (MMP)-10 (Takamura et al., 2013).
However, the therapeutic effect of another ARI (CT-112) is controversial. One study reported that the topical application of CT-112 to 39 diabetic patients could reverse the abnormal morphology of corneal epithelial cells and reduce corneal sensitivity (Hosotani et al., 1995). Interestingly, a randomized double-masked clinical trial using CT-112 found that after 4 and 8 weeks of treatment, the healing of corneal epithelial wounds was accelerated, but no changes in corneal sensitivity were found (Nakahara et al., 2005).
Another double-masked clinical trial (Fujishima and Tsubota, 2002) found an effective improvement of corneal epithelial injury and recovery of corneal sensitivity with treatment of oral ARI (ONO-2235).
Hence, different ARIs may have different effects in diabetic patients, and more studies need to be conducted to determine the efficacy of individual drug. The effectiveness of combinational administration should be tested as well.
Trophic Factor Supplements
Insulin-like Growth Factor-1
IGF-1 is a peptide with multiple functions in central and peripheral nervous system. In both human and animal models of TID and T2D, the level of serum IGF-1 was significantly reduced (Aghanoori et al., 2019). The density of corneal sub-basal nerves in type 2 diabetic mice was reported to be reduced, and retrobulbar injections of IGF-I could increase nerve density and prevent corneal damage (Ueno et al., 2014). Using STZ-induced diabetic rats, one study revealed that IGF-1 enhanced mitochondrial function and drove axon growth through AMP-activated protein kinase, which prevented the death of distal fibers in DN (Aghanoori et al., 2019).
Nerve Growth Factor
NGF is a protein involved in the growth, differentiation, and survival of neurons. NGF, NT-3, NT-4, BDNF and GDNF are present in the cornea (You et al., 2000). Many studies have reported the association between NGF and ocular surface health. One study demonstrated (Lambiase et al., 2000) that NGF could facilitate the proliferation of corneal epithelial cells and accelerate epithelial wound healing in rabbits. During corneal wound healing, a variety of cytokines such as interleukin 1, were released to regulate the synthesis of NGF (Wilson et al., 1996). In mice with moderate to severe neurotrophic keratitis, topical NGF eye drops enhanced corneal epithelial healing, and improved corneal sensitivity and visual function (Bonini et al., 2000). Besides, damaged nerve repair and nutritional function abnormalities occurred in mice with vascular endothelial growth factor (VEGF)-B deficiency, which could be recovered with the administration of VEGF-B (Guaiquil et al., 2014). Indeed, SA treatment upregulated the expression of VEGF in cornea nerve after injury, thereby enhancing the repair ability of corneal nerve (Di et al., 2017). In another study, it was reported that exogenous VEGF-B could activate the PI-3K/Akt-GSK3β-mTOR signaling pathway. As a result, regeneration of diabetic corneal nerve fiber was promoted, with improved corneal sensitivity and a higher level of corneal pigment epithelial-derived factor (Li et al., 2017).
These findings indicated that neurotrophins were involved in the regulation of physiological and pathological processes on the ocular surface. It is therefore believed that NGF may become a potential therapeutic agent for ocular disorders. Numerous studies have investigated the use of recombinant human nerve growth factor (rhNGF). Yet, the role of rhNGF remained to be discussed. Several phase II or III clinical trials showed conflicting results on its early efficacy due to limited dosage testing (high dosage may cause severe side effects) and investigations in different populations (Apfel, 2002). Increasing the dose and at the same time reducing the adverse effects have become an urgent problem to be solved. One study reported that their laboratory could produce large amounts of rhNGF, whose pharmacological effects performed well without apparent side effects (Colangelo et al., 2005). This certainly provided supportive evidence for further clinical trials.
Neuropeptides
Neuropeptides co-exist with neurotransmitters in nerve cells, acting as both transmitters and trophic factors.
Substance P (SP) is a neuropeptide that acts as a neurotransmitter and neuromodulator and is mainly released by sensory nerve fibers. SP is present in the normal cornea in physiologically relevant concentrations (Nishida et al., 1996). The concentration of substance P in tears is thought to reflect the level of neuropeptides in ocular tissues (Suvas 2017). Compared with diabetic patients without DN, the SP concentration in tears of T1D patients with DN is significantly lower, and it was related to corneal nerve fiber density (Tummanapalli et al., 2019). Yet, there was no difference in substance P concentration in T2D patients with DN (Tummanapalli et al., 2020b). An article found that in T1D rats, reduction in hyporesponsiveness of C nerve fiber was found, which was related to the significantly decreased levels of substance P and calcitonin gene-related peptide (Rocha-Neto et al., 2019). One study revealed that in T1D mice, exogenous SP could accelerate skin wound healing, possibly because SP treatment induced an acute inflammatory response, which promoted cell proliferation and activated M2 macrophages (Leal et al., 2015). Thus, exogenous SP may be an effective treatment for neuropathy in diabetes. However, SP administration in rabbits had no significant effect on the healing of corneal epithelial wounds. But studies have found that topical co-treatment of SP and IGF-1 could facilitate the proliferation and migration of corneal epithelial cells in diabetic corneal neuropathy (Abdelkader et al., 2011).
C-peptide is a neuropeptide. During insulin biosynthesis, proinsulin is cleaved into insulin and C-peptide (Steiner et al., 1967). Due to the short biological half-life of C-peptide, Peg-C-peptide (a long-acting form of C-peptide) has been developed to increase patient compliance and facilitate translation into clinical applications. Jolivalt et al. found that T1D mice treated with C-peptide or Peg-C-peptide showed a significant increase in the corneal sub-basal nerve, but its specific mechanism was still unclear (Jolivalt et al., 2015).
Studies revealed that the synthesis of SP was regulated by NGF and exogenous NGF treatment in diabetic rats could restore nerve SP levels (Lindsay and Harmar, 1989). Meanwhile, C peptide could promote both NGF and SP levels (Kamiya et al., 2006). These results suggested that factors may interact with each other, whether the combination treatment can produce a synergistic effect deserves more research.
Another neuropeptide, GLP-1, has a role in inhibiting glucagon secretion and stimulating insulin secretion. It has been reported that GLP-1 receptor agonists had neuroprotective effects. In T1D mice, exendin-4 (a GLP-1 receptor agonist) could increase sensory and motor nerve conduction velocity and intraepidermal nerve fiber density as well as significantly promote neurite outgrowth from dorsal root ganglions (Himeno et al., 2011). However, in T2D mice, although exendin-4 improved motor nerve conduction velocity, it had no effect on sensory nerves (Kan et al., 2012). There is still a lack of research on the effect of GFP-1 on diabetic corneal nerves.
Vasoactive intestinal peptide (VIP) is an immunosuppressive neuropeptide that belongs to the glucagon superfamily. Recently, Zhang et al. found that the exogenous use of neuropeptides such as calcitonin gene-related peptide, SP and VIP could partially restore damaged corneal epithelial wounds and inhibit the overexpression of pro-inflammatory factors in T1D mice corneas. In addition, the authors further discovered that VIP up-regulated the expression of NGF, CNTF, anti-inflammatory cytokines and improved corneal epithelial wound healing and nerve regeneration through VIP/VIP type 1 receptor/Sonic Hedgehog pathway (Zhang et al., 2020b).
ARA 290 is a non-hematopoietic peptide designed based on the structure of erythropoietin. In one phase II clinical trial, treatment with ARA 290 in T2D patients markedly increased the mean corneal nerve fiber density when compared with the placebo group (Brines et al., 2015).
These studies showed that neurotrophic factors interact with neuropeptides. When the cornea is injured, their expression and function may form a positive feedback loop: NGF from the healed corneal epithelial cells and CNTF from the dendritic cells can induce regeneration of sensory nerve, which in turn cause the release of more neuropeptides to nourish and maintain the proliferation and migration of corneal epithelial cells and dendritic cells. DM disrupts this interaction, leading to corneal injury. Based on the published data, we hypothesized that combination treatment with both neurotrophic factors and neuropeptides might be a promising approach for diabetic corneal damage.
Antioxidants or Anti-inflammatory Drugs
Naltrexone
The endogenous opioid system affects the proliferation of many cells like neurons and glial cells. Opioid growth factor (OGF) has been detected in bovine and rabbit corneal epithelium and was found to have an inhibitory effect on the proliferation and growth of corneal epithelial cells (McLaughlin et al., 2010).
Naltrexone is a long-acting and potent opioid antagonist that can block the interaction of OGF and its receptor OGFr. In both in vitro and in vivo studies, treatment with naltrexone could significantly facilitate DNA synthesis, cell division, cell migration, corneal epithelial wound healing, and corneal epithelium proliferation and growth (Sassani et al., 2016). Interestingly, the combined topical use of naltrexone and insulin has no additive or synergistic effect on corneal epithelial regeneration in T1D rats (Klocek et al., 2009).
Although a lot of evidence demonstrated the effectiveness of naltrexone aqueous solution, there are very few reports on its ocular delivery system and therefore more research is needed for its use in clinical treatment of diabetic corneal damage.
Other Antioxidants
Antioxidants such as ß-carotene (Abdul-Hamid and Moustafa, 2014) and carnosine (Shevalye et al., 2015) have also been shown to have effects on diabetic corneal repair and can be used to combat the consequences of AGEs on the ocular surface. One recent study found that an antioxidant mitoquinone reduced the oxidative stress produced by mitochondria in nerves (Fink et al., 2020). Adding mitoquinone to the diet of diabetic rats accelerated nerve conduction velocity, increased corneal and intraepidermal nerve fiber density and restored corneal sensitivity.
Other drugs have also been investigated. 1,5-isoquinolinediol, an inhibitor of poly(ADP-ribose) polymerase, partially reversed the epithelial innervation loss, corneal sensitivity reduction and epithelial wound healing delay (Byun et al., 2015). Meanwhile, administration of KIOM-79 (a mixture of 80% ethanol extracts of parched Puerariae radix, gingered Magnoliae cortex, Glycyrrhizae radix and Euphorbiae radix) protected keratocyte from cell death, lessened oxidative stress in corneas via suppression of the AGEs/NF-κB signal pathway (Kim et al., 2011b).
Other Drugs
Vitamin B
One recent study reported that topical vitamin B12 and citicoline treatment could ameliorate the morphology and function of corneal nerves in diabetic patients, indicating a neuroprotective effect (Fogagnolo et al., 2020). Despite these promising results, more clinical trials need to be conducted to provide more evidence for the use of vitamin B in patients with diabetic corneal neuropathy.
Vitamin D
In recent years, several studies have focused on the relationship between vitamin D and DN. A clinical study involving nearly 10,000 subjects demonstrated that 50% of T2D patients had low serum vitamin D levels (Herrmann et al., 2015). Furthermore, a systematic review (involving 1,484 T2D patients) reported a marked association between vitamin D deficiency and the development of DN (Lv et al., 2015). Other studies revealed that the vitamin D level of painful DN patients was significantly lower than that of painless DN patients (Alam et al., 2021), and the corneal nerve fiber density decreased more significantly in patients with low vitamin D level (Almurdhi et al., 2017). The possible mechanism behind vitamin D’s effects is unclear. But previous animal studies have found that treating diabetic rats with a vitamin D analog promoted NGF production in their sciatic nerves (Riaz et al., 1999). Similarly, it has been found that Tacalcitol, an active vitamin D3, could up-regulate NGF level in human epidermal keratinocytes (Fukuoka et al., 2001). The involvement of growth factors is indicated, and further investigations are essential.
Bariatric Surgery
Interestingly, two recent studies found an association between obesity and corneal nerve fibers. One study showed that in patients with severe obesity, early corneal nerve fiber and keratocyte density were attenuated (Iqbal et al., 2021). After bariatric surgery, corneal nerve regeneration was observed. Another study showed that in obese T2D patients, corneal nerve fiber length, corneal nerve fiber density and nerve branch density were significantly improved after bariatric surgery (Adam et al., 2021). These protection function may be related to an improvement in inflammation (Adam et al., 2021; Iqbal et al., 2021).
Gene Therapy
Gene therapy has obvious potential in the treatment of corneal diseases because the cornea carries many advantages suitable for genetic research. One advantage is that the cornea has immune privilege, which means that it can tolerate antigens without evoking inflammatory immune responses. Another advantage is that the cornea can be cultured in vitro and maintained for several weeks, making it possible to optimize gene transfer to improve the effectiveness and safety of gene therapy. Nonetheless, due to the lack of information on the genetic causes of corneal diseases and the goals of gene therapy, clinical transformation is still slow. It has been reported that epigenetics may play a role in diabetic complications including corneal changes (Kowluru et al., 2015). DM may cause specific changes in gene expression levels and patterns, which may be corrected by gene therapy.
Viral gene therapy is an effective delivery tool for delivering specific genes to the cornea (Ljubimov and Saghizadeh, 2015). Nevertheless, traditional viruses may induce inflammation, immune responses, and uncontrolled virus integration. New recombinant adenovirus, adeno-associated virus and lentivirus are main types of viral vectors commonly used in cornea transfection, which will not evoke serious immune response and can transfect non-dividing cells. Studies have shown that both adenovirus and adeno-associated virus can deliver target genes into the human cornea successfully. However, compared with adeno-associated virus transduction, the transgene expression level with adenovirus transduction was much higher, which made it a good choice as a gene therapy vehicle (Liu et al., 2008).
In studies of gene therapy, the authors mentioned that in diabetic cornea, c-met is down-regulated and protease is up-regulated (Saghizadeh et al., 2014; Kramerov et al., 2016). Therefore, adenovirus gene therapy implemented with upregulation of c-met by gene overexpression as well as silencing of MMP-10 and cathepsin F by short hairpin RNA technology could improve the wound healing rate of diabetic cornea and restore the expression of some stem cell markers in the limbus. Combination therapy using these three adenoviruses had the best effect, and the EGFR-Akt and p38 pathways were found to be involved.
In addition, there are other gene therapy targets such as microRNAs to effectively normalize the pathologies in the diabetic cornea. Studies have found that miR-146a inhibitor (antagomir) promoted the wound healing of the cultured diabetic cornea by activating EGFR, and restored some stem cell expression markers (Winkler et al., 2014). Inspired by miRNA research, a study found that inhibition of miR-34c expression in T1D mice increased the expression of autophagy-related protein Atg4B in the trigeminal ganglion, and markedly promoted the growth of trigeminal sensory neurons and the regeneration of corneal nerve fibers (Hu et al., 2019). Interestingly, another study obtained the same experimental effect. It reported that subconjunctival injection of miR-181a antagomir in diabetic mice resulted in corneal nerve fiber regeneration and trigeminal sensory neuron growth through ATG5-mediated autophagy activation and BCL-2 mediated apoptosis inhibition (Hu et al., 2020). Although research related to microRNAs has made some progress, it should be noted that when compared with other targeted therapies that only affect specific genes or pathways, most miRNAs act on multiple targets and can simultaneously regulate many different genes in multiple pathways. This property may generate unpredictable side effects. Therefore, miRNAs treatment should be used cautiously and the delivery route and its biodistribution need to be repeatedly verified.
Nanotechnology also has potential applications in gene delivery. Viral vector has better transduction efficiency than nanocarriers like nanoparticles. Yet, many advantages, such as ease of synthesis and operation, low production cost, accommodation in large-size vectors, less inflammatory response, no risk for genomic insertion and mutation, made nanotechnology an attractive target (Han et al., 2012). Numerous studies on nanotechnology for corneal injury have emerged. It has been reported that dipotassium glycyrrhizinate-micelle formulation encapsulating active agents (Hou et al., 2021), nanoparticle-encapsulated Fidgetin-like 2 siRNA (Jessi Wang et al., 2021), and high-density lipoprotein nanoparticles with a gold nanoparticle core (Lavker et al., 2021) showed promising results in accelerating corneal re-epithelialization and anti-inflammation. In addition, poly (lactic-co-glycolic acid) nanoparticles could be a drug release system of Lingzhi to reduce oxidative damage in corneal epithelium cells (Tsai et al., 2021). In conclusion, nanotechnology is a potential therapeutic approach for gene transfer and drug delivery in diabetic corneal neuropathy.
In addition, using plasmid with PGC-1α promoter, using gene silencing and nanotechnology to knockdown CaMKKβ, the authors revealed that muscarinic toxin 7 augmented elevated mitochondrial function, neurite outgrowth in dorsal root ganglia neurons, and increased corneal nerve density through Ca2+/Calmodulin-Dependent Protein kinase ß (Saleh et al., 2020).
Overall, gene therapy may be a promising way to restore abnormalities of diabetic corneal but there is an urgent need for further studies in its clinical use.
Summary
Diabetic corneal defects could be a biomarker for evaluating DN. Since studies (see Clinical Perspectives of Corneal Neuropathy in Diabetes Mellitus Section) showed that in diabetic patients, corneal defects commenced and showed a progressive degeneration as DM continued. Moreover, there was also reported a greater loss of corneal nerve fiber in DN patients when compared with diabetic subjects without DN. In addition, parameters of corneal nerve fibers worsened with increasing severity of DN. Therefore, it is essential to recognize and treat diabetic corneal neuropathy timely.
Firstly, since the complications of diabetes are caused by chronic hyperglycemia through a variety of pathological mechanisms, strict glycemic control is an important way to treat and reduce the progression of diabetic complications. Secondly, there have been many lipid-related clinical trials. Although the effects of triglyceride-lowering drugs such as statins and fibrates on diabetic corneal nerves are largely unknown, the fatty acids and their metabolites such as menhaden oil, resolvein D1, or their combined administration with free radical scavengers have provided alternative options for potential new therapies in diseases involving corneal nerve damage. Therefore, more elaborate and well-planned experimental and clinical studies are needed. Moreover, various ARI drugs have been shown to have different efficacy in diabetic patients, indicating the need for more clinical trials to determine what medication plan would yield better therapeutic effects. Growth factors such as IGF-1 and NGF have shown initial promising results in animal experiments. However, the reported serious side effects caused by high doses need to be addressed, since low doses have not achieved great efficacy in clinical trials. There were also many animal studies on neuropeptides such as SP and C-peptide, which reported that the combined therapy of neurotrophic factors and neuropeptides might be a promising therapeutic agent for ocular disorders. Meanwhile, vitamin B, vitamin D and naltrexone initially showed promising results. Yet, more clinical trials should be conducted to identify an effective ocular delivery system and provide evidence of their effects on diabetic corneal neuropathy. In addition, some progress has been made in microRNAs research. Due to the possibility of unpredictable side effects, miRNAs therapy should be used with caution, and their delivery methods and biodistribution need to be verified. Also, nanotechnology has become a promising therapeutic method for gene transfer and drug delivery. In general, gene therapy may be a potential method to restore diabetic corneal abnormalities, but again further clinical trials are needed.
Conclusion
Diabetes mellitus has adverse effects on corneal nerve fibers, corneal sensitivity and corneal epithelial regeneration. Corneal nerve damage in diabetic patients usually precedes neuropathy in other tissues and is associated with the severity of DN, making it a potential early indicator of DN. Corneal confocal microscopy is an examination method that quantitatively evaluates the morphology of the corneal nerve, facilitating the use of corneal nerve plexus as an early biomarker to access DN. It is essential to increase the awareness of damage on diabetic ocular surface and take actions to timely detect diabetic corneal neuropathy and monitor its subclinical progress.
At the current stage, the prevention of corneal nerve damage and the promotion of corneal nerve regeneration have achieved positive preliminary results, but most of the published work involved animal models and some preliminary clinical studies. Further investigations on the mechanism of diabetic corneal neuropathy, potential biomarkers, and pathogen-oriented therapy need to be conducted.
Author Contributions
TZ conceived and wrote the manuscript. TZ, ALe, JK, and ALo critically revised the manuscript. All authors read and approved the final version.
Funding
This research was supported by The University of Hong Kong Seed Funding Programme for Basic Research (202011159124).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Abbreviations
AGEs, advanced glycation end products; ARI, aldose reductase inhibitor; BDNF, brain-derived neurotrophic factor; CCM, corneal confocal microscopy; CNTF, ciliary neurotrophic factor; DHA, docosahexaenoic acid; DM, diabetes mellitus; DN, diabetic neuropathy; DR, diabetic retinopathy; FFA, free fatty acid; GDNF, glial cell line-derived neurotrophic factor; GLP-1, glucagon-like peptide 1; IGF-1, insulin-like growth factor-1; LDL-C, low-density lipoprotein cholesterol; NADPH, nicotinamide adenine dinucleotide phosphate; NGF, nerve growth factor; NPD1, neuroprotectin D1; NT-3, neurotrophin-3; OGF, opioid growth factor; PKC, protein kinase C; PPAR, proliferator-activated receptor; rhNGF, recombinant human nerve growth factor; ROS, reactive oxygen species; SP, Substance P; STZ, streptozotocin; TID, type 1 diabetes; T2D, type 2 diabetes; VEGF, vascular endothelial growth factor; VIP, vasoactive intestinal peptide; WHO, World Health Organization.
References
Abdelkader, H., Patel, D. V., McGhee, C. Nj., and Alany, R. G. (2011). New Therapeutic Approaches in the Treatment of Diabetic Keratopathy: a Review. Clin. Exp. Ophthalmol. 39 (3), 259–270. doi:10.1111/j.1442-9071.2010.02435.x
Abdul-Hamid, M., and Moustafa, N. (2014). Amelioration of Alloxan-Induced Diabetic Keratopathy by Beta-Carotene. Exp. Toxicol. Pathol. 66 (1), 49–59. doi:10.1016/j.etp.2013.08.003
Adam, S., Azmi, S., Ho, J. H., Liu, Y., Ferdousi, M., Siahmansur, T., et al. (2021). Improvements in Diabetic Neuropathy and Nephropathy after Bariatric Surgery: a Prospective Cohort Study. Obes. Surg. 31 (2), 554–563. doi:10.1007/s11695-020-05052-8
Aghanoori, M. R., Smith, D. R., Shariati-Ievari, S., Ajisebutu, A., Nguyen, A., Desmond, F., et al. (2019). Insulin-like Growth Factor-1 Activates AMPK to Augment Mitochondrial Function and Correct Neuronal Metabolism in Sensory Neurons in Type 1 Diabetes. Mol. Metab. 20, 149–165. doi:10.1016/j.molmet.2018.11.008
Al-Aqaba, M. A., Dhillon, V. K., Mohammed, I., Said, D. G., and Dua, H. S. (2019). Corneal Nerves in Health and Disease. Prog. Retin. Eye Res. 73, 100762. doi:10.1016/j.preteyeres.2019.05.003
Alam, U., Petropoulos, I. N., Ponirakis, G., Ferdousi, M., Asghar, O., Jeziorska, M., et al. (2021). Vitamin D Deficiency Is Associated with Painful Diabetic Neuropathy. Diabetes Metab. Res. Rev. 37 (1), e3361. doi:10.1002/dmrr.3361
Almurdhi, M. M., Reeves, N. D., Bowling, F. L., Boulton, A. J., Jeziorska, M., and Malik, R. A. (2017). Distal Lower Limb Strength Is Reduced in Subjects with Impaired Glucose Tolerance and Is Related to Elevated Intramuscular Fat Level and Vitamin D Deficiency. Diabet Med. 34 (3), 356–363. doi:10.1111/dme.13163
Apfel, S. C. (2002). Nerve Growth Factor for the Treatment of Diabetic Neuropathy: what Went Wrong, what Went Right, and what Does the Future Hold. Int. Rev. Neurobiol. 50, 393–413. doi:10.1016/s0074-7742(02)50083-0
Azmi, S., Jeziorska, M., Ferdousi, M., Petropoulos, I. N., Ponirakis, G., Marshall, A., et al. (2019). Early Nerve Fibre Regeneration in Individuals with Type 1 Diabetes after Simultaneous Pancreas and Kidney Transplantation. Diabetologia 62 (8), 1478–1487. doi:10.1007/s00125-019-4897-y
Babizhayev, M. A., Strokov, I. A., Nosikov, V. V., Savel'yeva, E. L., Sitnikov, V. F., Yegorov, Y. E., et al. (2015). The Role of Oxidative Stress in Diabetic Neuropathy: Generation of Free Radical Species in the Glycation Reaction and Gene Polymorphisms Encoding Antioxidant Enzymes to Genetic Susceptibility to Diabetic Neuropathy in Population of Type I Diabetic Patients. Cell Biochem Biophys 71 (3), 1425–1443. doi:10.1007/s12013-014-0365-y
Bain, S. C., Klufas, M. A., Ho, A., and Matthews, D. R. (2019). Worsening of Diabetic Retinopathy with Rapid Improvement in Systemic Glucose Control: A Review. Diabetes Obes. Metab. 21 (3), 454–466. doi:10.1111/dom.13538
Barsegian, A., Lee, J., Salifu, M. O., and McFarlane, S. I. (2018). Corneal Neuropathy: An Underrated Manifestation of Diabetes Mellitus. J. Clin. Endocrinol. Diabetes 2 (1), 111
Basantsova, N. Y., Starshinova, A. A., Dori, A., Zinchenko, Y. S., Yablonskiy, P. K., and Shoenfeld, Y. (2019). Small-fiber Neuropathy Definition, Diagnosis, and Treatment. Neurol. Sci. 40 (7), 1343–1350. doi:10.1007/s10072-019-03871-x
Bastion, M. L., and Ling, K. P. (2013). Topical Insulin for Healing of Diabetic Epithelial Defects?: A Retrospective Review of Corneal Debridement during Vitreoretinal Surgery in Malaysian Patients. Med. J. Malaysia 68 (3), 208–216.
Bejarano, E., and Taylor, A. (2019). Too Sweet: Problems of Protein Glycation in the Eye. Exp. Eye Res. 178, 255–262. doi:10.1016/j.exer.2018.08.017
Bhalla, S., Singh, N., and Jaggi, A. S. (2015). Dose-related Neuropathic and Anti-neuropathic Effects of Simvastatin in Vincristine-Induced Neuropathic Pain in Rats. Food Chem. Toxicol. 80, 32–40. doi:10.1016/j.fct.2015.02.016
Bikbova, G., Oshitari, T., Baba, T., Bikbov, M., and Yamamoto, S. (2018). Diabetic Corneal Neuropathy: Clinical Perspectives. Clin. Ophthalmol. 12, 981–987. doi:10.2147/OPTH.S145266
Bikbova, G., Oshitari, T., Baba, T., and Yamamoto, S. (2016). Neuronal Changes in the Diabetic Cornea: Perspectives for Neuroprotection. Biomed. Res. Int. 2016, 5140823. doi:10.1155/2016/5140823
Bitirgen, G., Ozkagnici, A., Malik, R. A., and Kerimoglu, H. (2014). Corneal Nerve Fibre Damage Precedes Diabetic Retinopathy in Patients with Type 2 Diabetes Mellitus. Diabet Med. 31 (4), 431–438. doi:10.1111/dme.12324
Bonini, S., Lambiase, A., Rama, P., Caprioglio, G., and Aloe, L. (2000). Topical Treatment with Nerve Growth Factor for Neurotrophic Keratitis. Ophthalmology 107 (7), 1347–1351. doi:10.1016/s0161-6420(00)00163-9
Brines, M., Dunne, A. N., van Velzen, M., Proto, P. L., Ostenson, C. G., Kirk, R. I., et al. (2015). ARA 290, a Nonerythropoietic Peptide Engineered from Erythropoietin, Improves Metabolic Control and Neuropathic Symptoms in Patients with Type 2 Diabetes. Mol. Med. 20 (1), 658–666. doi:10.2119/molmed.2014.00215
Byun, Y. S., Kang, B., Yoo, Y. S., and Joo, C. K. (2015). Poly(ADP-Ribose) Polymerase Inhibition Improves Corneal Epithelial Innervation and Wound Healing in Diabetic Rats. Invest. Ophthalmol. Vis. Sci. 56 (3), 1948–1955. doi:10.1167/iovs.14-16259
Casellini, C. M., Barlow, P. M., Rice, A. L., Casey, M., Simmons, K., Pittenger, G., et al. (2007). A 6-month, Randomized, Double-Masked, Placebo-Controlled Study Evaluating the Effects of the Protein Kinase C-Beta Inhibitor Ruboxistaurin on Skin Microvascular Blood Flow and Other Measures of Diabetic Peripheral Neuropathy. Diabetes care 30 (4), 896–902. doi:10.2337/dc06-1699
Chen, D. K., Frizzi, K. E., Guernsey, L. S., Ladt, K., Mizisin, A. P., and Calcutt, N. A. (2013). Repeated Monitoring of Corneal Nerves by Confocal Microscopy as an index of Peripheral Neuropathy in Type-1 Diabetic Rodents and the Effects of Topical Insulin. J. Peripher. Nerv Syst. 18 (4), 306–315. doi:10.1111/jns5.12044
Chen, X., Graham, J., Petropoulos, I. N., Ponirakis, G., Asghar, O., Alam, U., et al. (2018). Corneal Nerve Fractal Dimension: A Novel Corneal Nerve Metric for the Diagnosis of Diabetic Sensorimotor Polyneuropathy. Invest. Ophthalmol. Vis. Sci. 59 (2), 1113–1118. doi:10.1167/iovs.17-23342
Colangelo, A. M., Finotti, N., Ceriani, M., Alberghina, L., Martegani, E., Aloe, L., et al. (2005). Recombinant Human Nerve Growth Factor with a Marked Activity In Vitro and In Vivo. Proc. Natl. Acad. Sci. U S A. 102 (51), 18658–18663. doi:10.1073/pnas.0508734102
Coppey, L., Davidson, E., Shevalye, H., Obrosov, A., Torres, M., and Yorek, M. A. (2020). Progressive Loss of Corneal Nerve Fibers and Sensitivity in Rats Modeling Obesity and Type 2 Diabetes Is Reversible with Omega-3 Fatty Acid Intervention: Supporting Cornea Analyses as a Marker for Peripheral Neuropathy and Treatment. Diabetes Metab. Syndr. Obes. 13, 1367–1384. doi:10.2147/DMSO.S247571
Cortina, M. S., He, J., Russ, T., Bazan, N. G., and Bazan, H. E. (2013). Neuroprotectin D1 Restores Corneal Nerve Integrity and Function after Damage from Experimental Surgery. Invest. Ophthalmol. Vis. Sci. 54 (6), 4109–4116. doi:10.1167/iovs.13-12075
Davidson, E. P., Coppey, L. J., Shevalye, H., Obrosov, A., Kardon, R. H., and Yorek, M. A. (2017). Impaired Corneal Sensation and Nerve Loss in a Type 2 Rat Model of Chronic Diabetes Is Reversible with Combination Therapy of Menhaden Oil, α-Lipoic Acid, and Enalapril. Cornea 36 (6), 725–731. doi:10.1097/ICO.0000000000001182
Davidson, E. P., Coppey, L. J., Shevalye, H., Obrosov, A., and Yorek, M. A. (2018). Effect of Dietary Content of Menhaden Oil with or without Salsalate on Neuropathic Endpoints in High-Fat-Fed/Low-Dose Streptozotocin-Treated Sprague Dawley Rats. J. Diabetes Res. 2018, 2967127. doi:10.1155/2018/2967127
Deák, E. A., Szalai, E., Tóth, N., Malik, R. A., Berta, A., Csutak, A., et al. (2019). Longitudinal Changes in Corneal Cell and Nerve Fiber Morphology in Young Patients with Type 1 Diabetes with and without Diabetic Retinopathy: A 2-Year Follow-up Study. Investig. Ophthalmol. Vis. Sci. 60 (2), 830–837. doi:10.1167/iovs.18-24516
Di, G., Zhao, X., Qi, X., Zhang, S., Feng, L., Shi, W., et al. (2017). VEGF-B Promotes Recovery of Corneal Innervations and Trophic Functions in Diabetic Mice. Sci. Rep. 7, 40582. doi:10.1038/srep40582
Dogru, M., Katakami, C., and Inoue, M. (2001). Tear Function and Ocular Surface Changes in Noninsulin-dependent Diabetes Mellitus. Ophthalmology 108 (3), 586–592. doi:10.1016/s0161-6420(00)00599-6
Edwards, K., Pritchard, N., Vagenas, D., Russell, A., Malik, R. A., and Efron, N. (2012). Utility of Corneal Confocal Microscopy for Assessing Mild Diabetic Neuropathy: Baseline Findings of the LANDMark Study. Clin. Exp. Optom. 95 (3), 348–354. doi:10.1111/j.1444-0938.2012.00740.x
Fahy, E., Subramaniam, S., Brown, H. A., Glass, C. K., Merrill, A. H., Murphy, R. C., et al. (2005). A Comprehensive Classification System for Lipids. J. Lipid Res. 46 (5), 839–861. doi:10.1194/jlr.E400004-JLR200
Ferdousi, M., Kalteniece, A., Azmi, S., Petropoulos, I. N., Ponirakis, G., Alam, U., et al. (2021). Diagnosis of Neuropathy and Risk Factors for Corneal Nerve Loss in Type 1 and Type 2 Diabetes: A Corneal Confocal Microscopy Study. Diabetes care 44 (1), 150–156. doi:10.2337/dc20-1482
Ferdousi, M., Kalteniece, A., Petropoulos, I., Azmi, S., Dhage, S., Marshall, A., et al. (2020). Diabetic Neuropathy Is Characterized by Progressive Corneal Nerve Fiber Loss in the Central and Inferior Whorl Regions. Invest. Ophthalmol. Vis. Sci. 61 (3), 48. doi:10.1167/iovs.61.3.48
Ferdousi, M., Romanchuk, K., Mah, J. K., Virtanen, H., Millar, C., Malik, R. A., et al. (2019). Early Corneal Nerve Fibre Damage and Increased Langerhans Cell Density in Children with Type 1 Diabetes Mellitus. Sci. Rep. 9 (1), 8758. doi:10.1038/s41598-019-45116-z
Ferrari, G., Chauhan, S. K., Ueno, H., Nallasamy, N., Gandolfi, S., Borges, L., et al. (2011). A Novel Mouse Model for Neurotrophic Keratopathy: Trigeminal Nerve Stereotactic Electrolysis through the Brain. Invest. Ophthalmol. Vis. Sci. 52 (5), 2532–2539. doi:10.1167/iovs.10-5688
Fink, B., Coppey, L., Davidson, E., Shevalye, H., Obrosov, A., Chheda, P. R., et al. (2020). Effect of Mitoquinone (Mito-Q) on Neuropathic Endpoints in an Obese and Type 2 Diabetic Rat Model. Free Radic. Res. 54 (5), 311–318. doi:10.1080/10715762.2020.1754409
Fogagnolo, P., Melardi, E., Tranchina, L., and Rossetti, L. (2020). Topical Citicoline and Vitamin B12 versus Placebo in the Treatment of Diabetes-Related Corneal Nerve Damage: a Randomized Double-Blind Controlled Trial. BMC Ophthalmol. 20 (1), 315. doi:10.1186/s12886-020-01584-w
Foster, E. D., Bridges, N. D., Feurer, I. D., Eggerman, T. L., Hunsicker, L. G., and Alejandro, R. (2018). Improved Health-Related Quality of Life in a Phase 3 Islet Transplantation Trial in Type 1 Diabetes Complicated by Severe Hypoglycemia. Diabetes care 41 (5), 1001–1008. doi:10.2337/dc17-1779
Franco, D. C., Neupane, N., Riaz, M., Mohammadzadeh, S., and Sachmechi, I. (2019). Chronic Inflammatory Demyelinating Polyradiculoneuropathy Association with Low Cholesterol Levels: A Case Report in a Patient Taking PCSK9 Inhibitor. J. Neurol. Res. 9 (4-5), 72–74. doi:10.14740/jnr552
Fujishima, H., and Tsubota, K. (2002). Improvement of Corneal Fluorescein Staining in post Cataract Surgery of Diabetic Patients by an Oral Aldose Reductase Inhibitor, ONO-2235. Br. J. Ophthalmol. 86 (8), 860–863. doi:10.1136/bjo.86.8.860
Fukuoka, M., Sakurai, K., Ohta, T., Kiyoki, M., and Katayama, I. (2001). Tacalcitol, an Active Vitamin D3, Induces Nerve Growth Factor Production in Human Epidermal Keratinocytes. Skin Pharmacol. Appl. Skin Physiol. 14 (4), 226–233. doi:10.1159/000056351
Gao, N., Yan, C., Lee, P., Sun, H., and Yu, F. S. (2016). Dendritic Cell Dysfunction and Diabetic Sensory Neuropathy in the Cornea. J. Clin. Invest. 126 (5), 1998–2011. doi:10.1172/JCI85097
Geraldes, P., and King, G. L. (2010). Activation of Protein Kinase C Isoforms and its Impact on Diabetic Complications. Circ. Res. 106 (8), 1319–1331. doi:10.1161/CIRCRESAHA.110.217117
Greene, D. A., Sima, A. A., Stevens, M. J., Feldman, E. L., and Lattimer, S. A. (1992). Complications: Neuropathy, Pathogenetic Considerations. Diabetes Care 15 (12), 1902–1925. doi:10.2337/diacare.15.12.1902
Guaiquil, V. H., Pan, Z., Karagianni, N., Fukuoka, S., Alegre, G., and Rosenblatt, M. I. (2014). VEGF-B Selectively Regenerates Injured Peripheral Neurons and Restores Sensory and Trophic Functions. Proc. Natl. Acad. Sci. U S A. 111 (48), 17272–17277. doi:10.1073/pnas.1407227111
Hamid, H. S., Mervak, C. M., Münch, A. E., Robell, N. J., Hayes, J. M., Porzio, M. T., et al. (2014). Hyperglycemia- and Neuropathy-Induced Changes in Mitochondria within Sensory Nerves. Ann. Clin. Transl Neurol. 1 (10), 799–812. doi:10.1002/acn3.119
Han, S. B., Yang, H. K., and Hyon, J. Y. (2018). Influence of Diabetes Mellitus on Anterior Segment of the Eye. Clin. Interv. Aging 14, 53–63. doi:10.2147/CIA.S190713
Han, Z., Conley, S. M., Makkia, R., Guo, J., Cooper, M. J., and Naash, M. I. (2012). Comparative Analysis of DNA Nanoparticles and AAVs for Ocular Gene Delivery. PloS one 7 (12), e52189. doi:10.1371/journal.pone.0052189
Herrmann, M., Sullivan, D. R., Veillard, A. S., McCorquodale, T., Straub, I. R., Scott, R., et al. FIELD Study Investigators (2015). Serum 25-hydroxyvitamin D: a Predictor of Macrovascular and Microvascular Complications in Patients with Type 2 Diabetes. Diabetes care 38 (3), 521–528. doi:10.2337/dc14-0180
Himeno, T., Kamiya, H., Naruse, K., Harada, N., Ozaki, N., Seino, Y., et al. (2011). Beneficial Effects of Exendin-4 on Experimental Polyneuropathy in Diabetic Mice. Diabetes 60 (9), 2397–2406. doi:10.2337/db10-1462
Hosotani, H., Ohashi, Y., Yamada, M., and Tsubota, K. (1995). Reversal of Abnormal Corneal Epithelial Cell Morphologic Characteristics and Reduced Corneal Sensitivity in Diabetic Patients by Aldose Reductase Inhibitor, CT-112. Am. J. Ophthalmol. 119 (3), 288–294. doi:10.1016/s0002-9394(14)71169-9
Hou, Y., Xin, M., Li, Q., and Wu, X. (2021). Glycyrrhizin Micelle as a Genistein Nanocarrier: Synergistically Promoting Corneal Epithelial Wound Healing through Blockage of the HMGB1 Signaling Pathway in Diabetic Mice. Exp. Eye Res. 204, 108454. doi:10.1016/j.exer.2021.108454
Hu, J., Hu, X., and Kan, T. (2019). MiR-34c Participates in Diabetic Corneal Neuropathy via Regulation of Autophagy. Invest. Ophthalmol. Vis. Sci. 60 (1), 16–25. doi:10.1167/iovs.18-24968
Hu, J., Huang, Y., Lin, Y., and Lin, J. (2020). Protective Effect Inhibiting the Expression of miR-181a on the Diabetic Corneal Nerve in a Mouse Model. Exp. Eye Res. 192, 107925. doi:10.1016/j.exer.2020.107925
Iqbal, Z., Kalteniece, A., Ferdousi, M., Adam, S., D'Onofrio, L., Ho, J. H., et al. (2021). Corneal Keratocyte Density and Corneal Nerves Are Reduced in Patients with Severe Obesity and Improve after Bariatric Surgery. Invest. Ophthalmol. Vis. Sci. 62 (1), 20. doi:10.1167/iovs.62.1.20
Ishibashi, F., Kojima, R., Taniguchi, M., Kosaka, A., Uetake, H., and Tavakoli, M. (2016). The Expanded Bead Size of Corneal C-Nerve Fibers Visualized by Corneal Confocal Microscopy Is Associated with Slow Conduction Velocity of the Peripheral Nerves in Patients with Type 2 Diabetes Mellitus. J. Diabetes Res. 2016, 3653459. doi:10.1155/2016/3653459
Ishibashi, F., and Tavakoli, M. (2018). Impact of Normoglycemia in Reducing Microvascular Complications in Patients with Type 2 Diabetes: A Follow-Up Study. Front. Endocrinol. (Lausanne) 9, 52. doi:10.3389/fendo.2018.00052
Issar, T., Tummanapalli, S. S., Borire, A. A., Kwai, N. C. G., Poynten, A. M., Arnold, R., et al. (2021). Impact of the Metabolic Syndrome on Peripheral Nerve Structure and Function in Type 2 Diabetes. Eur. J. Neurol. 28 (6), 2074–2082. doi:10.1111/ene.14805
Issar, T., Tummanapalli, S. S., Kwai, N. C. G., Chiang, J. C. B., Arnold, R., Poynten, A. M., et al. (2020). Associations between Acute Glucose Control and Peripheral Nerve Structure and Function in Type 1 Diabetes. Diabet Med. 37 (9), 1553–1560. doi:10.1111/dme.14306
Jende, J. M. E., Groener, J. B., Rother, C., Kender, Z., Hahn, A., Hilgenfeld, T., et al. (2019). Association of Serum Cholesterol Levels with Peripheral Nerve Damage in Patients with Type 2 Diabetes. JAMA Netw. Open 2 (5), e194798. doi:10.1001/jamanetworkopen.2019.4798
Jolivalt, C. G., Rodriguez, M., Wahren, J., and Calcutt, N. A. (2015). Efficacy of a Long-Acting C-Peptide Analogue against Peripheral Neuropathy in Streptozotocin-Diabetic Mice. Diabetes Obes. Metab. 17 (8), 781–788. doi:10.1111/dom.12477
Kaiserman, I., Kaiserman, N., Nakar, S., and Vinker, S. (2005). Dry Eye in Diabetic Patients. Am. J. Ophthalmol. 139 (3), 498–503. doi:10.1016/j.ajo.2004.10.022
Kaji, Y., Amano, S., Usui, T., Suzuki, K., Tanaka, S., Oshika, T., et al. (2001). Advanced Glycation End Products in Descemet's Membrane and Their Effect on Corneal Endothelial Cell. Curr. Eye Res. 23 (6), 469–477. doi:10.1076/ceyr.23.6.469.6968
Kalteniece, A., Ferdousi, M., Azmi, S., Marshall, A., Soran, H., and Malik, R. A. (2018a). Keratocyte Density Is Reduced and Related to Corneal Nerve Damage in Diabetic Neuropathy. Invest. Ophthalmol. Vis. Sci. 59 (8), 3584–3590. doi:10.1167/iovs.18-23889
Kalteniece, A., Ferdousi, M., Azmi, S., Mubita, W. M., Marshall, A., Lauria, G., et al. (2020). Corneal Confocal Microscopy Detects Small Nerve Fibre Damage in Patients with Painful Diabetic Neuropathy. Sci. Rep. 10 (1), 3371. doi:10.1038/s41598-020-60422-7
Kalteniece, A., Ferdousi, M., Petropoulos, I., Azmi, S., Adam, S., Fadavi, H., et al. (2018b). Greater Corneal Nerve Loss at the Inferior Whorl Is Related to the Presence of Diabetic Neuropathy and Painful Diabetic Neuropathy. Sci. Rep. 8 (1), 3283. doi:10.1038/s41598-018-21643-z
Kamiya, H., Zhang, W., Ekberg, K., Wahren, J., and Sima, A. A. (2006). C-peptide Reverses Nociceptive Neuropathy in Type 1 Diabetes. Diabetes 55 (12), 3581–3587. doi:10.2337/db06-0396
Kan, M., Guo, G., Singh, B., Singh, V., and Zochodne, D. W. (2012). Glucagon-like Peptide 1, Insulin, Sensory Neurons, and Diabetic Neuropathy. J. Neuropathol. Exp. Neurol. 71 (6), 494–510. doi:10.1097/NEN.0b013e3182580673
Khan, N., Paterson, A. D., Roshandel, D., Raza, A., Ajmal, M., Waheed, N. K., et al. (2020). Association of IGF1 and VEGFA Polymorphisms with Diabetic Retinopathy in Pakistani Population. Acta Diabetol. 57 (2), 237–245. doi:10.1007/s00592-019-01407-5
Kim, J., Kim, C. S., Kim, H., Jeong, I. H., Sohn, E., and Kim, J. S. (2011b). Protection against Advanced Glycation End Products and Oxidative Stress during the Development of Diabetic Keratopathy by KIOM-79. J. Pharm. Pharmacol. 63 (4), 524–530. doi:10.1111/j.2042-7158.2010.01206.x
Kim, J., Kim, C. S., Sohn, E., Jeong, I. H., Kim, H., and Kim, J. S. (2011a). Involvement of Advanced Glycation End Products, Oxidative Stress and Nuclear Factor-kappaB in the Development of Diabetic Keratopathy. Graefes Arch. Clin. Exp. Ophthalmol. 249 (4), 529–536. doi:10.1007/s00417-010-1573-9
Klocek, M. S., Sassani, J. W., McLaughlin, P. J., and Zagon, I. S. (2009). Naltrexone and Insulin Are Independently Effective but Not Additive in Accelerating Corneal Epithelial Healing in Type I Diabetic Rats. Exp. Eye Res. 89 (5), 686–692. doi:10.1016/j.exer.2009.06.010
Körei, A. E., Istenes, I., Papanas, N., and Kempler, P. (2016). Small-Fiber Neuropathy: A Diabetic Microvascular Complication of Special Clinical, Diagnostic, and Prognostic Importance. Angiology 67 (1), 49–57. doi:10.1177/0003319715583595
Kowluru, R. A., Kowluru, A., Mishra, M., and Kumar, B. (2015). Oxidative Stress and Epigenetic Modifications in the Pathogenesis of Diabetic Retinopathy. Prog. Retin. Eye Res. 48, 40–61. doi:10.1016/j.preteyeres.2015.05.001
Kramerov, A. A., Saghizadeh, M., and Ljubimov, A. V. (2016). Adenoviral Gene Therapy for Diabetic Keratopathy: Effects on Wound Healing and Stem Cell Marker Expression in Human Organ-Cultured Corneas and Limbal Epithelial Cells. J. Vis. Exp. (110), e54058. doi:10.3791/54058
Labetoulle, M., Baudouin, C., Calonge, M., Merayo-Lloves, J., Boboridis, K. G., Akova, Y. A., et al. (2019). Role of Corneal Nerves in Ocular Surface Homeostasis and Disease. Acta Ophthalmol. 97 (2), 137–145. doi:10.1111/aos.13844
Lagali, N. S., Allgeier, S., Guimarães, P., Badian, R. A., Ruggeri, A., Köhler, B., et al. (2017). Reduced Corneal Nerve Fiber Density in Type 2 Diabetes by Wide-Area Mosaic Analysis. Invest. Ophthalmol. Vis. Sci. 58 (14), 6318–6327. doi:10.1167/iovs.17-22257
Lambiase, A., Manni, L., Bonini, S., Rama, P., Micera, A., and Aloe, L. (2000). Nerve Growth Factor Promotes Corneal Healing: Structural, Biochemical, and Molecular Analyses of Rat and Human Corneas. Invest. Ophthalmol. Vis. Sci. 41 (5), 1063–1069.
Lavker, R. M., Kaplan, N., McMahon, K. M., Calvert, A. E., Henrich, S. E., Onay, U. V., et al. (2021). Synthetic High-Density Lipoprotein Nanoparticles: Good Things in Small Packages. Ocul. Surf. 21, 19–26. doi:10.1016/j.jtos.2021.03.001
Leal, E. C., Carvalho, E., Tellechea, A., Kafanas, A., Tecilazich, F., Kearney, C., et al. (2015). Substance P Promotes Wound Healing in Diabetes by Modulating Inflammation and Macrophage Phenotype. Am. J. Pathol. 185 (6), 1638–1648. doi:10.1016/j.ajpath.2015.02.011
Leckelt, J., Guimarães, P., Kott, A., Ruggeri, A., Stachs, O., and Baltrusch, S. (2016). Early Detection of Diabetic Neuropathy by Investigating CNFL and IENFD in Thy1-YFP Mice. J. Endocrinol. 231 (2), 147–157. doi:10.1530/JOE-16-0284
Lee, J. E., Sun, Y., Gjorstrup, P., and Pearlman, E. (2015). Inhibition of Corneal Inflammation by the Resolvin E1. Invest. Ophthalmol. Vis. Sci. 56 (4), 2728–2736. doi:10.1167/iovs.14-15982
Leppin, K., Behrendt, A. K., Reichard, M., Stachs, O., Guthoff, R. F., Baltrusch, S., et al. (2014). Diabetes Mellitus Leads to Accumulation of Dendritic Cells and Nerve Fiber Damage of the Subbasal Nerve Plexus in the Cornea. Invest. Ophthalmol. Vis. Sci. 55 (6), 3603–3615. doi:10.1167/iovs.14-14307
Lewis, E. J. H., Lovblom, L. E., Cisbani, G., Chen, D. K., Bazinet, R. P., Wolever, T. M. S., et al. (2021). Baseline omega-3 Level Is Associated with Nerve Regeneration Following 12-months of omega-3 Nutrition Therapy in Patients with Type 1 Diabetes. J. Diabetes Complications 35 (3), 107798. doi:10.1016/j.jdiacomp.2020.107798
Lewis, E. J. H., Lovblom, L. E., Ferdousi, M., Halpern, E. M., Jeziorska, M., Pacaud, D., et al. (2020). Rapid Corneal Nerve Fiber Loss: A Marker of Diabetic Neuropathy Onset and Progression. Diabetes care 43 (8), 1829–1835. doi:10.2337/dc19-0951
Li, D., Chen, Y. G., Zhang, C. J., Tian, J., and Li, X. (2017). Safflower Extract and Aceglutamide Injection Promoting Recovery of Peripheral Innervations via Vascular Endothelial Growth Factor-B Signaling in Diabetic Mice. Chin. Med. J. (Engl) 130 (23), 2829–2835. doi:10.4103/0366-6999.219143
Li, Q., Zhong, Y., Zhang, T., Zhang, R., Zhang, Q., Zheng, H., et al. (2019). Quantitative Analysis of Corneal Nerve Fibers in Type 2 Diabetics with and without Diabetic Peripheral Neuropathy: Comparison of Manual and Automated Assessments. Diabetes Res. Clin. Pract. 151, 33–38. doi:10.1016/j.diabres.2019.03.039
Lindsay, R. M., and Harmar, A. J. (1989). Nerve Growth Factor Regulates Expression of Neuropeptide Genes in Adult Sensory Neurons. Nature 337 (6205), 362–364. doi:10.1038/337362a0
Liu, J., Saghizadeh, M., Tuli, S. S., Kramerov, A. A., Lewin, A. S., Bloom, D. C., et al. (2008). Different Tropism of Adenoviruses and Adeno-Associated Viruses to Corneal Cells: Implications for Corneal Gene Therapy. Mol. Vis. 14, 2087–2096.
Ljubimov, A. V. (2017). Diabetic Complications in the Cornea. Vis. Res 139, 138–152. doi:10.1016/j.visres.2017.03.002
Ljubimov, A. V., and Saghizadeh, M. (2015). Progress in Corneal Wound Healing. Prog. Retin. Eye Res. 49, 17–45. doi:10.1016/j.preteyeres.2015.07.002
Lv, W. S., Zhao, W. J., Gong, S. L., Fang, D. D., Wang, B., Fu, Z. J., et al. (2015). Serum 25-hydroxyvitamin D Levels and Peripheral Neuropathy in Patients with Type 2 Diabetes: a Systematic Review and Meta-Analysis. J. Endocrinol. Invest. 38 (5), 513–518. doi:10.1007/s40618-014-0210-6
Lyu, Y., Zeng, X., Li, F., and Zhao, S. (2019). The Effect of the Duration of Diabetes on Dry Eye and Corneal Nerves. Cont Lens Anterior Eye 42 (4), 380–385. doi:10.1016/j.clae.2019.02.011
Mahelková, G., Burdová, M. C., Malá, Š., Hoskovcová, L., Dotrelová, D., and Štechová, K. (2018). Higher Total Insulin Dose Has Positive Effect on Corneal Nerve Fibers in DM1 Patients. Invest. Ophthalmol. Vis. Sci. 59 (10), 3800–3807. doi:10.1167/iovs.18-24265
Markoulli, M., Flanagan, J., Tummanapalli, S. S., Wu, J., and Willcox, M. (2018). The Impact of Diabetes on Corneal Nerve Morphology and Ocular Surface Integrity. Ocul. Surf. 16 (1), 45–57. doi:10.1016/j.jtos.2017.10.006
Markoulli, M., You, J., Kim, J., Duong, C. L., Tolentino, J. B., Karras, J., et al. (2017). Corneal Nerve Morphology and Tear Film Substance P in Diabetes. Optom. Vis. Sci. 94 (7), 726–731. doi:10.1097/OPX.0000000000001096
Matlock, H. G., Qiu, F., Malechka, V., Zhou, K., Cheng, R., Benyajati, S., et al. (2020). Pathogenic Role of PPARα Downregulation in Corneal Nerve Degeneration and Impaired Corneal Sensitivity in Diabetes. Diabetes 69 (6), 1279–1291. doi:10.2337/db19-0898
McCarty, M. F. (2010). Salsalate May Have Broad Utility in the Prevention and Treatment of Vascular Disorders and the Metabolic Syndrome. Med. Hypotheses 75 (3), 276–281. doi:10.1016/j.mehy.2009.12.027
McLaughlin, P. J., Sassani, J. W., Klocek, M. S., and Zagon, I. S. (2010). Diabetic Keratopathy and Treatment by Modulation of the Opioid Growth Factor (OGF)-OGF Receptor (OGFr) axis with Naltrexone: a Review. Brain Res. Bull. 81 (2-3), 236–247. doi:10.1016/j.brainresbull.2009.08.008
Nahar, N., Mohamed, S., Mustapha, N. M., Lau, S., Ishak, N. I. M., and Umran, N. S. (2021). Metformin Attenuated Histopathological Ocular Deteriorations in a Streptozotocin-Induced Hyperglycemic Rat Model. Naunyn Schmiedebergs Arch. Pharmacol. 394 (3), 457–467. doi:10.1007/s00210-020-01989-w
Nakahara, M., Miyata, K., Otani, S., Miyai, T., Nejima, R., Yamagami, S., et al. (2005). A Randomised, Placebo Controlled Clinical Trial of the Aldose Reductase Inhibitor CT-112 as Management of Corneal Epithelial Disorders in Diabetic Patients. Br. J. Ophthalmol. 89 (3), 266–268. doi:10.1136/bjo.2004.049841
Nishida, T., Nakamura, M., Ofuji, K., Reid, T. W., Mannis, M. J., and Murphy, C. J. (1996). Synergistic Effects of Substance P with Insulin-like Growth Factor-1 on Epithelial Migration of the Cornea. J. Cel Physiol 169 (1), 159–166. doi:10.1002/(SICI)1097-4652(199610)169:1<159:AID-JCP16>3.0.CO;2-8
Oates, P. J. (2008). Aldose Reductase, Still a Compelling Target for Diabetic Neuropathy. Curr. Drug Targets 9 (1), 14–36. doi:10.2174/138945008783431781
Pizzino, G., Irrera, N., Cucinotta, M., Pallio, G., Mannino, F., Arcoraci, V., et al. (2017). Oxidative Stress: Harms and Benefits for Human Health. Oxidative Med. Cell. longevity 2017, 1–13. doi:10.1155/2017/8416763
Ponirakis, G., Abdul-Ghani, M. A., Jayyousi, A., Almuhannadi, H., Petropoulos, I. N., Khan, A., et al. (2020). Effect of Treatment with Exenatide and Pioglitazone or Basal-Bolus Insulin on Diabetic Neuropathy: a Substudy of the Qatar Study. BMJ Open Diabetes Res. Care 8 (1), e001420. doi:10.1136/bmjdrc-2020-001420
Ponirakis, G., Abdul-Ghani, M. A., Jayyousi, A., Zirie, M. A., Qazi, M., Almuhannadi, H., et al. (2021a). Painful Diabetic Neuropathy Is Associated with Increased Nerve Regeneration in Patients with Type 2 Diabetes Undergoing Intensive Glycemic Control. J. Diabetes Investig. 12 (9), 1642–1650. doi:10.1111/jdi.13544
Ponirakis, G., Abdul‐Ghani, M. A., Jayyousi, A., Zirie, M. A., Al‐Mohannadi, S., Almuhannadi, H., et al. (2021b). Insulin Resistance Limits Corneal Nerve Regeneration in Patients with Type 2 Diabetes Undergoing Intensive Glycemic Control. J. Diabetes Investig. 12, 2002–2009. doi:10.1111/jdi.13582
Pritchard, N., Edwards, K., Russell, A. W., Perkins, B. A., Malik, R. A., and Efron, N. (2015). Corneal Confocal Microscopy Predicts 4-year Incident Peripheral Neuropathy in Type 1 Diabetes. Diabetes care 38 (4), 671–675. doi:10.2337/dc14-2114
Pritchard, N., Edwards, K., Shahidi, A. M., Sampson, G. P., Russell, A. W., Malik, R. A., et al. (2011). Corneal Markers of Diabetic Neuropathy. Ocul. Surf. 9 (1), 17–28. doi:10.1016/s1542-0124(11)70006-4
Qu, J. H., Li, L., Tian, L., Zhang, X. Y., Thomas, R., and Sun, X. G. (2018). Epithelial Changes with Corneal Punctate Epitheliopathy in Type 2 Diabetes Mellitus and Their Correlation with Time to Healing. BMC Ophthalmol. 18 (1), 1. doi:10.1186/s12886-017-0645-6
Rehany, U., Ishii, Y., Lahav, M., and Rumelt, S. (2000). Ultrastructural Changes in Corneas of Diabetic Patients: an Electron-Microscopy Study. Cornea 19 (4), 534–538. doi:10.1097/00003226-200007000-00026
Riaz, S., Malcangio, M., Miller, M., and Tomlinson, D. R. (1999). A Vitamin D(3) Derivative (CB1093) Induces Nerve Growth Factor and Prevents Neurotrophic Deficits in Streptozotocin-Diabetic Rats. Diabetologia 42 (11), 1308–1313. doi:10.1007/s001250051443
Rocha-Neto, L. M., Gamarra-Suárez, J. R., Freitas, F. F., Muzilli, A., Abdalla, H. B., Macedo, C. G., et al. (2019). Early Phase of Type 1 Diabetes Decreases the Responsiveness of C-Fiber Nociceptors in the Temporomandibular Joint of Rats. Neuroscience 416, 229–238. doi:10.1016/j.neuroscience.2019.08.011
Roselló-Busquets, C., de la Oliva, N., Martínez-Mármol, R., Hernaiz-Llorens, M., Pascual, M., Muhaisen, A., et al. (2019). Cholesterol Depletion Regulates Axonal Growth and Enhances Central and Peripheral Nerve Regeneration. Front. Cel. Neurosci. 13, 40. doi:10.3389/fncel.2019.00040
Roszkowska, A. M., Licitra, C., Tumminello, G., Postorino, E. I., Colonna, M. R., and Aragona, P. (2021). Corneal Nerves in Diabetes-The Role of the In Vivo Corneal Confocal Microscopy of the Subbasal Nerve Plexus in the Assessment of Peripheral Small Fiber Neuropathy. Surv. Ophthalmol. 66 (3), 493–513. doi:10.1016/j.survophthal.2020.09.003
Rumora, A. E., LoGrasso, G., Hayes, J. M., Mendelson, F. E., Tabbey, M. A., Haidar, J. A., et al. (2019). The Divergent Roles of Dietary Saturated and Monounsaturated Fatty Acids on Nerve Function in Murine Models of Obesity. J. Neurosci. 39 (19), 3770–3781. doi:10.1523/JNEUROSCI.3173-18.2019
Sady, C., Khosrof, S., and Nagaraj, R. (1995). Advanced Maillard Reaction and Crosslinking of Corneal Collagen in Diabetes. Biochem. Biophys. Res. Commun. 214 (3), 793–797. doi:10.1006/bbrc.1995.2356
Saghizadeh, M., Dib, C. M., Brunken, W. J., and Ljubimov, A. V. (2014). Normalization of Wound Healing and Stem Cell Marker Patterns in Organ-Cultured Human Diabetic Corneas by Gene Therapy of Limbal Cells. Exp. Eye Res. 129, 66–73. doi:10.1016/j.exer.2014.10.022
Saleh, A., Sabbir, M. G., Aghanoori, M. R., Smith, D. R., Roy Chowdhury, S. K., Tessler, L., et al. (2020). Muscarinic Toxin 7 Signals via Ca2+/Calmodulin-dependent Protein Kinase Kinase β to Augment Mitochondrial Function and Prevent Neurodegeneration. Mol. Neurobiol. 57 (6), 2521–2538. doi:10.1007/s12035-020-01900-x
Sassani, J. W., Mc Laughlin, P. J., and Zagon, I. S. (2016). The Yin and Yang of the Opioid Growth Regulatory System: Focus on Diabetes-The Lorenz E. Zimmerman Tribute Lecture. J. Diabetes Res. 2016, 9703729. doi:10.1155/2016/9703729
Schaldemose, E. L., Hammer, R. E., Ferdousi, M., Malik, R. A., Nyengaard, J. R., and Karlsson, P. (2020). An Unbiased Stereological Method for Corneal Confocal Microscopy in Patients with Diabetic Polyneuropathy. Sci. Rep. 10 (1), 12550. doi:10.1038/s41598-020-69314-2
Scheler, A., Spoerl, E., and Boehm, A. G. (2012). Effect of Diabetes Mellitus on Corneal Biomechanics and Measurement of Intraocular Pressure. Acta Ophthalmol. 90 (6), e447–51. doi:10.1111/j.1755-3768.2012.02437.x
Schönfeld, P., and Reiser, G. (2013). Why Does Brain Metabolism Not Favor Burning of Fatty Acids to Provide Energy? - Reflections on Disadvantages of the Use of Free Fatty Acids as Fuel for Brain. J. Cereb. Blood Flow Metab. 33 (10), 1493–1499. doi:10.1038/jcbfm.2013.128
Selvarajah, D., Kar, D., Khunti, K., Davies, M. J., Scott, A. R., Walker, J., et al. (2019). Diabetic Peripheral Neuropathy: Advances in Diagnosis and Strategies for Screening and Early Intervention. Lancet Diabetes Endocrinol. 7 (12), 938–948. doi:10.1016/S2213-8587(19)30081-6
Senior, P. A., Senior, P. A., AlMehthel, M., Miller, A., and Paty, B. W. (2018). Diabetes and Transplantation. Can. J. Diabetes 42 Suppl 1 (Suppl. 1), S145–S149. doi:10.1016/j.jcjd.2017.10.017
Serhan, C. N., Dalli, J., Colas, R. A., Winkler, J. W., and Chiang, N. (2015). Protectins and Maresins: New Pro-resolving Families of Mediators in Acute Inflammation and Resolution Bioactive Metabolome. Biochim. Biophys. Acta 1851 (4), 397–413. doi:10.1016/j.bbalip.2014.08.006
Shaheen, B. S., Bakir, M., and Jain, S. (2014). Corneal Nerves in Health and Disease. Surv. Ophthalmol. 59 (3), 263–285. doi:10.1016/j.survophthal.2013.09.002
Shevalye, H., Yorek, M. S., Coppey, L. J., Holmes, A., Harper, M. M., Kardon, R. H., et al. (2015). Effect of Enriching the Diet with Menhaden Oil or Daily Treatment with Resolvin D1 on Neuropathy in a Mouse Model of Type 2 Diabetes. J. Neurophysiol. 114 (1), 199–208. doi:10.1152/jn.00224.2015
Smith, L. E., Shen, W., Perruzzi, C., Soker, S., Kinose, F., Xu, X., et al. (1999). Regulation of Vascular Endothelial Growth Factor-dependent Retinal Neovascularization by Insulin-like Growth Factor-1 Receptor. Nat. Med. 5 (12), 1390–1395. doi:10.1038/70963
Song, F., Xue, Y., Dong, D., Liu, J., Fu, T., Xiao, C., et al. (2016). Insulin Restores an Altered Corneal Epithelium Circadian Rhythm in Mice with Streptozotocin-Induced Type 1 Diabetes. Sci. Rep. 6, 32871. doi:10.1038/srep32871
Srinivasan, S., Dehghani, C., Pritchard, N., Edwards, K., Russell, A. W., Malik, R. A., et al. (2017). Corneal and Retinal Neuronal Degeneration in Early Stages of Diabetic Retinopathy. Invest. Ophthalmol. Vis. Sci. 58 (14), 6365–6373. doi:10.1167/iovs.17-22736
Srinivasan, S., Dehghani, C., Pritchard, N., Edwards, K., Russell, A. W., Malik, R. A., et al. (2018). Ophthalmic and Clinical Factors that Predict Four-Year Development and Worsening of Diabetic Retinopathy in Type 1 Diabetes. J. Diabetes Complications 32 (1), 67–74. doi:10.1016/j.jdiacomp.2017.09.002
Stavniichuk, R., Shevalye, H., Hirooka, H., Nadler, J. L., and Obrosova, I. G. (2012). Interplay of Sorbitol Pathway of Glucose Metabolism, 12/15-lipoxygenase, and Mitogen-Activated Protein Kinases in the Pathogenesis of Diabetic Peripheral Neuropathy. Biochem. Pharmacol. 83 (7), 932–940. doi:10.1016/j.bcp.2012.01.015
Steiner, D. F., Cunningham, D., Spigelman, L., and Aten, B. (1967). Insulin Biosynthesis: Evidence for a Precursor. Science 157 (3789), 697–700. doi:10.1126/science.157.3789.697
Stickings, P., and Cunningham, J. M. (2002). Interleukin-1beta-induced Nitric Oxide Production and Inhibition of Insulin Secretion in Rat Islets of Langerhans Is Dependent upon the Nitric Oxide Synthase Cofactor Tetrahidrobiopterin. Cytokine 18 (2), 81–85. doi:10.1006/cyto.2002.0881
Sugimoto, K., Yasujima, M., and Yagihashi, S. (2008). Role of Advanced Glycation End Products in Diabetic Neuropathy. Curr. Pharm. Des. 14 (10), 953–961. doi:10.2174/138161208784139774
Sultana, R., Perluigi, M., and Butterfield, D. A. (2013). Lipid Peroxidation Triggers Neurodegeneration: a Redox Proteomics View into the Alzheimer Disease Brain. Free Radic. Biol. Med. 62, 157–169. doi:10.1016/j.freeradbiomed.2012.09.027
Suvas, S. (2017). Role of Substance P Neuropeptide in Inflammation, Wound Healing, and Tissue Homeostasis. J. Immunol. 199 (5), 1543–1552. doi:10.4049/jimmunol.1601751
Takamura, Y., Matsumoto, T., Tomomatsu, T., Matsumura, T., Takihara, Y., and Inatani, M. (2013). Aldose Reductase Inhibitor Counteracts the Enhanced Expression of Matrix Metalloproteinase-10 and Improves Corneal Wound Healing in Galactose-Fed Rats. Mol. Vis. 19, 2477–2486.
Tavakoli, A., and Liong, S. (2012). Pancreatic Transplant in Diabetes. Adv. Exp. Med. Biol. 771, 420–437. doi:10.1007/978-1-4614-5441-0_30
Tavakoli, M., Boulton, A. J., Efron, N., and Malik, R. A. (2011). Increased Langerhan Cell Density and Corneal Nerve Damage in Diabetic Patients: Role of Immune Mechanisms in Human Diabetic Neuropathy. Cont Lens Anterior Eye 34 (1), 7–11. doi:10.1016/j.clae.2010.08.007
Tesfaye, S., Chaturvedi, N., Eaton, S. E., Ward, J. D., Manes, C., Ionescu-Tirgoviste, C., et al. EURODIAB Prospective Complications Study Group (2005). Vascular Risk Factors and Diabetic Neuropathy. N. Engl. J. Med. 352 (4), 341–350. doi:10.1056/NEJMoa032782
Tsai, I. L., Tsai, C. Y., Kuo, L. L., Woung, L. C., Ku, R. Y., and Cheng, Y. H. (2021). PLGA Nanoparticles Containing Lingzhi Extracts rescue Corneal Epithelial Cells from Oxidative Damage. Exp. Eye Res. 206, 108539. doi:10.1016/j.exer.2021.108539
Tummanapalli, S. S., Issar, T., Kwai, N., Pisarcikova, J., Poynten, A. M., Krishnan, A. V., et al. (2020b). A Comparative Study on the Diagnostic Utility of Corneal Confocal Microscopy and Tear Neuromediator Levels in Diabetic Peripheral Neuropathy. Curr. Eye Res. 45 (8), 921–930. doi:10.1080/02713683.2019.1705984
Tummanapalli, S. S., Issar, T., Yan, A., Kwai, N., Poynten, A. M., Krishnan, A. V., et al. (2020a). Corneal Nerve Fiber Loss in Diabetes with Chronic Kidney Disease. Ocul. Surf. 18 (1), 178–185. doi:10.1016/j.jtos.2019.11.010
Tummanapalli, S. S., Willcox, M. D. P., Issar, T., Yan, A., Pisarcikova, J., Kwai, N., et al. (2019). Tear Film Substance P: A Potential Biomarker for Diabetic Peripheral Neuropathy. Ocul. Surf. 17 (4), 690–698. doi:10.1016/j.jtos.2019.08.010
Ueno, H., Hattori, T., Kumagai, Y., Suzuki, N., Ueno, S., and Takagi, H. (2014). Alterations in the Corneal Nerve and Stem/progenitor Cells in Diabetes: Preventive Effects of Insulin-like Growth Factor-1 Treatment. Int. J. Endocrinol. 2014, 312401. doi:10.1155/2014/312401
Vantyghem, M.-C., Chetboun, M., Gmyr, V., Jannin, A., Espiard, S., Le Mapihan, K., et al. (2019). & Members of the Spanish Back Pain Research Network Task Force for the Improvement of Inter-disciplinary Management of Spinal MetastasisTen-Year Outcome of Islet Alone or Islet after Kidney Transplantation in Type 1 Diabetes: A Prospective Parallel-Arm Cohort Study. Diabetes care 42 (11), 2042–2049. doi:10.2337/dc19-0401
Vieira-Potter, V. J., Karamichos, D., and Lee, D. J. (2016). Ocular Complications of Diabetes and Therapeutic Approaches. Biomed. Res. Int. 2016, 3801570. doi:10.1155/2016/3801570
Villegas-Rivera, G., Román-Pintos, L. M., Cardona-Muñoz, E. G., Arias-Carvajal, O., Rodríguez-Carrizalez, A. D., Troyo-Sanromán, R., et al. (2015). Effects of Ezetimibe/Simvastatin and Rosuvastatin on Oxidative Stress in Diabetic Neuropathy: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial. Oxid Med. Cel Longev 2015, 756294. doi:10.1155/2015/756294
Vincent, A. M., Edwards, J. L., McLean, L. L., Hong, Y., Cerri, F., Lopez, I., et al. (2010). Mitochondrial Biogenesis and Fission in Axons in Cell Culture and Animal Models of Diabetic Neuropathy. Acta Neuropathol. 120 (4), 477–489. doi:10.1007/s00401-010-0697-7
Wallner, K., Shapiro, A. M., Senior, P. A., and McCabe, C. (2016). Cost Effectiveness and Value of Information Analyses of Islet Cell Transplantation in the Management of 'unstable' Type 1 Diabetes Mellitus. BMC Endocr. Disord. 16, 17. doi:10.1186/s12902-016-0097-7
Wang, J., Dey, A., Kramer, A. H., Miao, Y., Liu, J., Baker, L., et al. (2021). A Novel Therapeutic Approach to Corneal Alkaline Burn Model by Targeting Fidgetin-like 2, a Microtubule Regulator. Trans. Vis. Sci. Tech. 10 (1), 17. doi:10.1167/tvst.10.1.17
Wang, M., Li, M., and Xie, Y. (2021). The Association between Statins Exposure and Peripheral Neuropathy Risk: A Meta-Analysis. J. Clin. Pharm. Ther. 46 (4), 1046–1054. doi:10.1111/jcpt.13393
Wilson, S. E., He, Y. G., Weng, J., Li, Q., McDowall, A. W., Vital, M., et al. (1996). Epithelial Injury Induces Keratocyte Apoptosis: Hypothesized Role for the Interleukin-1 System in the Modulation of Corneal Tissue Organization and Wound Healing. Exp. Eye Res. 62 (4), 325–327. doi:10.1006/exer.1996.0038
Winkler, M. A., Dib, C., Ljubimov, A. V., and Saghizadeh, M. (2014). Targeting miR-146a to Treat Delayed Wound Healing in Human Diabetic Organ-Cultured Corneas. PloS one 9 (12), e114692. doi:10.1371/journal.pone.0114692
World Health Organization (2021). Effect of Fidarestat Andα-Lipoic Acid on Diabetes-Induced Epineurial Arteriole Vascular Dysfunction. Available at: https://www.who.int/health-topics/diabetes (Accessed Oct 15, 2021).
Yorek, M. S., Coppey, L. J., Shevalye, H., Obrosov, A., Kardon, R. H., and Yorek, M. A. (2016). Effect of Treatment with Salsalate, Menhaden Oil, Combination of Salsalate and Menhaden Oil, or Resolvin D1 of C57Bl/6J Type 1 Diabetic Mouse on Neuropathic Endpoints. J. Nutr. Metab. 2016, 5905891. doi:10.1155/2016/5905891
Yorek, M. S., Obrosov, A., Shevalye, H., Lupachyk, S., Harper, M. M., Kardon, R. H., et al. (2014). Effect of Glycemic Control on Corneal Nerves and Peripheral Neuropathy in Streptozotocin-Induced Diabetic C57Bl/6J Mice. J. Peripher. Nerv Syst. 19 (3), 205–217. doi:10.1111/jns.12086
You, L., Kruse, F. E., and Völcker, H. E. (2000). Neurotrophic Factors in the Human Cornea. Invest. Ophthalmol. Vis. Sci. 41 (3), 692–702.
Zagon, I. S., Klocek, M. S., Sassani, J. W., and McLaughlin, P. J. (2007). Use of Topical Insulin to Normalize Corneal Epithelial Healing in Diabetes Mellitus. Arch. Ophthalmol. 125 (8), 1082–1088. doi:10.1001/archopht.125.8.1082
Zhang, J., Dai, Y., Wei, C., Zhao, X., Zhou, Q., and Xie, L. (2020). DNase I Improves Corneal Epithelial and Nerve Regeneration in Diabetic Mice. J. Cel Mol Med 24 (8), 4547–4556. doi:10.1111/jcmm.15112
Zhang, Y., Dou, S., Qi, X., Zhang, Z., Qiao, Y., Wang, Y., et al. (2021). Transcriptional Network Analysis Reveals the Role of miR-223-5p during Diabetic Corneal Epithelial Regeneration. Front. Mol. Biosci. 8, 737472. doi:10.3389/fmolb.2021.737472
Zhang, Y., Gao, N., Wu, L., Lee, P. S. Y., Me, R., Dai, C., et al. (2020b). Role of VIP and Sonic Hedgehog Signaling Pathways in Mediating Epithelial Wound Healing, Sensory Nerve Regeneration, and Their Defects in Diabetic Corneas. Diabetes 69 (7), 1549–1561. doi:10.2337/db19-0870
Zhang, Y., Jiang, H., Dou, S., Zhang, B., Qi, X., Li, J., et al. (2020a). Comprehensive Analysis of Differentially Expressed microRNAs and mRNAs Involved in Diabetic Corneal Neuropathy. Life Sci. 261, 118456. doi:10.1016/j.lfs.2020.118456
Zhao, H., He, Y., Ren, Y. R., and Chen, B. H. (2019). Corneal Alteration and Pathogenesis in Diabetes Mellitus. Int. J. Ophthalmol. 12 (12), 1939–1950. doi:10.18240/ijo.2019.12.17
Zherebitskaya, E., Akude, E., Smith, D. R., and Fernyhough, P. (2009). Development of Selective Axonopathy in Adult Sensory Neurons Isolated from Diabetic Rats: Role of Glucose-Induced Oxidative Stress. Diabetes 58 (6), 1356–1364. doi:10.2337/db09-0034
Zhou, Q., Chen, P., Di, G., Zhang, Y., Wang, Y., Qi, X., et al. (2015). Ciliary Neurotrophic Factor Promotes the Activation of Corneal Epithelial Stem/progenitor Cells and Accelerates Corneal Epithelial Wound Healing. Stem Cells 33 (5), 1566–1576. doi:10.1002/stem.1942
Zhu, L., Titone, R., and Robertson, D. M. (2019). The Impact of Hyperglycemia on the Corneal Epithelium: Molecular Mechanisms and Insight. Ocul. Surf. 17 (4), 644–654. doi:10.1016/j.jtos.2019.06.007
Keywords: corneal nerve damage, corneal confocal microscopy, diabetic complications, dry eye, nerve regeneration, ocular disease, ocular surface
Citation: Zhou T, Lee A, Lo ACY and Kwok JSWJ (2022) Diabetic Corneal Neuropathy: Pathogenic Mechanisms and Therapeutic Strategies. Front. Pharmacol. 13:816062. doi: 10.3389/fphar.2022.816062
Received: 16 November 2021; Accepted: 27 January 2022;
Published: 23 February 2022.
Edited by:
Kyriaki Thermos, University of Crete, GreeceReviewed by:
Simone Baltrusch, University Hospital Rostock, GermanyGuei-Sheung Liu, Centre for Eye Research Australia, Australia
Copyright © 2022 Zhou, Lee, Lo and Kwok. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Amy Cheuk Yin Lo, amylo@hku.hk