Miriam Longo1
Giuseppe Bellastella1*
Maria Ida Maiorino1Juris J. Meier2Katherine Esposito3Dario Giugliano1- 1Unit of Endocrinology and Metabolic Diseases, Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy
- 2Diabetes Division, St Josef Hospital, Ruhr-University Bochum, Bochum, Germany
- 3Diabetes Unit, Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy
Diabetes is becoming one of the most widespread health burning problems in the elderly. Worldwide prevalence of diabetes among subjects over 65 years was 123 million in 2017, a number that is expected to double in 2045. Old patients with diabetes have a higher risk of common geriatric syndromes, including frailty, cognitive impairment and dementia, urinary incontinence, traumatic falls and fractures, disability, side effects of polypharmacy, which have an important impact on quality of life and may interfere with anti-diabetic treatment. Because of all these factors, clinical management of type 2 diabetes in elderly patients currently represents a real challenge for the physician. Actually, the optimal glycemic target to achieve for elderly diabetic patients is still a matter of debate. The American Diabetes Association suggests a HbA1c goal <7.5% for older adults with intact cognitive and functional status, whereas, the American Association of Clinical Endocrinologists (AACE) recommends HbA1c levels of 6.5% or lower as long as it can be achieved safely, with a less stringent target (>6.5%) for patients with concurrent serious illness and at high risk of hypoglycemia. By contrast, the American College of Physicians (ACP) suggests more conservative goals (HbA1c levels between 7 and 8%) for most older patients, and a less intense pharmacotherapy, when HbA1C levels are ≤6.5%. Management of glycemic goals and antihyperglycemic treatment has to be individualized in accordance to medical history and comorbidities, giving preference to drugs that are associated with low risk of hypoglycemia. Antihyperglycemic agents considered safe and effective for type 2 diabetic older patients include: metformin (the first-line agent), pioglitazone, dipeptidyl peptidase 4 inhibitors, glucagon-like peptide 1 receptor agonists. Insulin secretagogue agents have to be used with caution because of their significant hypoglycemic risk; if used, short-acting sulfonylureas, as gliclazide, or glinides as repaglinide, should be preferred. When using complex insulin regimen in old people with diabetes, attention should be paid for the risk of hypoglycemia. In this paper we aim to review and discuss the best glycemic targets as well as the best treatment choices for older people with type 2 diabetes based on current international guidelines.
Introduction
Life expectancy is defined as the average number of years that a newborn is expected to live assuming that current mortality rates remain the same throughout its life. Global average life expectancy has increased by 5.5 years between 2000 and 2016, with the fastest increase since the 1960s, as a consequence of declining number of deaths from infectious causes (1). Latest estimates of life expectancy at birth were of 80.9 years across the 28 European member states (2) and 78.9 years in United States of America (USA) (3). The progressive decline of age-standardized rates of death from non-communicable chronic diseases (NCDs, cardiovascular and respiratory diseases, cancer, and diabetes) registered globally between 2006 and 2016 (4), together with the rising number of people older than 65 years, especially in westernized countries, has led to an increased prevalence of NCDs among elderly, resulting in more years of life spent with morbidity and disability (5).
Diabetes is recognized as an important cause of premature death and disability. In the past three decades the age-standardized prevalence of diabetes has risen substantially in countries at all income levels; 40% of this increase is estimated to result from population growth and aging (6). Therefore, diabetes is one of the most widespread health burning problems in the elderly, which represent a heterogeneous and complex population as it include both newly diagnosed older diabetic patients and patients with long-standing diabetes with onset in middle or early age (7). Consequently, management of diabetes in elderly subjects is particularly complex and challenging for clinicians, due to difficulty in individualizing glycemic targets, treatment strategies, coexisting comorbidities, polypharmacy, and hypoglycemic risk. The aim of this review is to discuss the best glycemic targets as well as the best treatment choices for old people with type 2 diabetes based on current shared international guidelines.
Epidemiology
Type 2 diabetes represents the most common metabolic disease in older adults. According to the latest estimates of the International Diabetes Federation (IDF), diabetes shows a high prevalence in people older than 65 years (8). In 2017, the number of diabetic people aged 65–99 was estimated to be 122.8 million (around 18% of prevalence rate), of whom 98 million had <80 years (65–79 years); these numbers are expected to easily exceed 200 million in 2045 (8). China, United States of America and India are the countries with highest numbers of people older than 65 with diabetes. Similar prevalence rates of diabetes were found in the European Region, reaching values ranging between 14.9 and 25.0% (8). The main reasons imputable to this spreading may be found in the longer life expectancy, the global diffusion of both unhealthy lifestyle habits and environmental pollution (9).
The number of deaths caused by diabetes in the age range of 60–99 years in 2017 was 3,200,000, which represents ~60% of deaths due to diabetes among the age group between 18 and 99 (8). Moreover, elderly diabetic patients are exposed to a higher risk of cardiovascular complications, including peripheral vascular disease, heart disease, and stroke (10), and many geriatric syndromes (from cognitive impairment to urinary incontinence) (11).
Pathophysiology of Diabetes in Elderly
Several factors participate in the pathophysiology of diabetes in older age. Chronological age per sè represents a risk factor for many chronic diseases (12). Advanced age leads to the exacerbation of systemic chronic inflammation, oxidative stress, DNA damage, decline of mitochondrial function, cellular senescence, and tissue dysfunction, all conditions which contribute to generate metabolic disorders (13). Indeed, aging is associated with raised levels of pro-inflammatory molecules, including interleukin (IL) 1, IL-6, IL-8, IL-13, IL-18, C-reactive protein, interferons α and β, transforming growth factor β (TGF-β), tumor necrosis factor α (TNF-α), and serum amyloid (14). Furthermore, the age-related variation of body composition leads to an increase in fat mass, especially visceral adiposity, and an equal decrease in lean and skeletal mass (15). With aging, there is a decline in preadipocyte replication and an expansion of senescent cells in adipose tissue which enhance lipotoxicity and favor the generation of a pro-inflammatory status (16). Moreover, some studies have showed that aging (1) impairs insulin secretion from β-cells in response to endogenous incretins (GIP), (2) is associated with reduced insulin sensitivity, and (3) promotes β-cell death by inducing mitochondrial dysfunction (14). In older subjects, abnormalities in both insulin sensitivity and insulin secretion lead gradually to impaired glucose tolerance and consequently to clinically manifest diabetes. Postprandial hyperglycemia is a characteristic feature of type 2 diabetes in older patients. Therefore, an oral glucose tolerance test should be performed in older subjects with impaired fasting glucose to early detect diabetes, which otherwise could be undiagnosed using fasting plasma glucose alone (7).
Diabetes and Geriatric Syndromes
Diabetes onset in elderly usually manifest with vague and not specific symptoms, such as dehydration, dry mouth, confusion, fatigue, lethargy, weight loss, and an increased tendency toward genitourinary infections (17). It has been estimated that 60% of older patients with type 2 diabetes has at least one other comorbid disease, and 40% of these patients has actually no <4 concurrent illnesses (18). Most common type 2 diabetes comorbidities, including cognitive impairment, disability, depression, apathy, urinary incontinence, polypharmacy, hearing, and visual impairment, falls and fractures, fall under geriatric syndromes (19) (Figure 1). With advanced age, malnutrition, physical inactivity, and unwanted weight loss become more frequent. Moreover, elderly diabetic patients are more likely to experience severe or unaware hyper/hypoglycemic episodes and major adverse cardiovascular events (MACE), due to peripheral and autonomic neuropathy. Therefore, a comprehensive geriatric assessment including screening for microvascular complications, cardiovascular risk factors, and geriatric syndromes should be performed at initial diagnosis of diabetes in elderly patients (20).
Figure 1. Most common clinical conditions associated with aging.
Cognitive Dysfunction and Depression
There is evidence that type 2 diabetes is associated with cognitive dysfunctions. Older diabetic patients have higher risk to develop mild cognitive impairment (MCI), all-cause dementia and Alzheimer's disease (21). Specific mechanisms underlying this association are still unclear; however, main factors involved are vascular dysfunction, high blood pressure, hyperglycemia, hypoglycemic events, insulin resistance, and neuroinflammation (22). Furthermore, depressive and apathic symptoms frequently co-exist with diabetes (23), and some studies have found that combination of diabetes and depression may express a toxic effect on the brain, increasing the risk for dementia (24). In light of this, the American Diabetes Association (ADA) recommends for subjects over 65 years old (with a level of evidence B) a neuro-psychological screening at the initial visit and annually to early detect mild cognitive impairment and depression, by using some specific test (Mini-Mental State Examination, Montreal Cognitive Assessment and Geriatric Depression Scale), and minimizing hypoglycemic events to reduce the risk of MCI (25).
Disability, Fractures and Urinary Incontinence
Type 2 diabetes in elderly is a powerful risk factor for functional limitations, frailty, loss of independence, and disability (26). Moreover, there is evidence that type 2 diabetes increases the risk of fracture risk and secondary hypogonadism, which also contribute to enhance risk of osteoporosis and muscle weakness in men (27, 28). With aging there is a progressive loss of strength and toughness of skeletal and muscle mass which leads to a status of osteo- and sarcopenia. Changes in skeletal muscle protein turnover could accelerate these alterations in type 2 diabetic patients (29), resulting in a greater risk of falling and bone fractures (30). As testosterone decline with advancing age, the assessment of its concentrations may be useful in case of signs and symptoms of overt hypogonadism to better evaluate the risk of fracture in this selected population (31, 32). Indeed, there is evidence that older patients with type 2 diabetes have an increased risk of hip fractures, particularly in insulin-treated patients, and non-skeletal fall injuries (33). A moderate but regular physical activity and a high adherence to Mediterranean dietary pattern showed some benefits in reducing the risk of falls and physical impairments in patients older than 75 years (34, 35). The American Geriatrics Society suggests to interrogate older patients about falls at least every 12 months, examine potentially reversible causes of falls (medications, environmental factors, limiting factors) and perform a complete basic evaluation when an injurious fall occurs (level of evidence III, strength B) (36).
Urinary incontinence is a frequent comorbidity of diabetes, although it is usually not-reported by patients (37). Therefore, according to the American Geriatrics Society, physicians should always perform an annual screening for urinary incontinence which may be an important cause of social isolation, depression, falls, and fractures (level of evidence III, strength A) (36).
Overtreatment and Polypharmacy
Both overtreatment and polypharmacy are very common among frail older diabetic subjects. The prevalence of polypharmacy regimen, defined as the use of more than 5 medications, increases with age. Results from a Dutch study revealed that 64 persons (20%) out of 319 type 2 diabetic patients aged ≥70 years were overtreated and frail (38). Furthermore, one-quarter of US older diabetic adults are on potential overtreatment for tight glycemic control using glucose-lowering medications at high risk of hypoglycemia (39). In a cohort of 8,932 adults with diabetes, 78% of patients had polypharmacy, which was more likely associated with age ≥60 years, female sex, and coexisting chronic diseases (40). Polypharmacy in older diabetic patients may produce detrimental effects mainly due to increased risk of drug-drug interactions and adverse side effects (41). However, a deintensification rather than intensification of pharmacological therapy should be advisable in diabetic patients in older age, in consideration of both benefits and risks associated with complex therapeutic regimens. Moreover, older adults with diabetes should annually update the list of used medications for their own clinicians (level of evidence II, strength A) (36).
Glycemic Control
Older patients represent a very heterogeneous and challenging population concerning diabetes care and treatment. While treating diabetes in elderly, clinicians should be always aware of maintaining a good quality of life. Patient-centered glycemic targets are needed in order to achieve the glycemic control avoiding dangerous or extreme glucose excursions. Elderly patients are highly vulnerable to hypoglycemic events, as a consequence of progressive age-related decrease in β-adrenergic receptor function. Indeed, hypoglycemia in older age has been associated with an increased risk to develop cognitive impairment, dementia, all-cause hospitalization, and all cause mortality (42–44). Use of insulin or insulin secretagogues, polypharmacy, coexisting comorbidities, renal insufficiency, dehydration, impairment of counter-regulatory responses represent the main predisposing risk factors for hypoglycemic episodes (45). Assessment of potential risk factors for hypoglycemia is an important part of the clinical management of older diabetic subjects. Moreover, both patients and caregivers have to be trained and well-educated on the prevention, detection, and treatment of hypoglycemic events (11). On the other hand, both untreated or undertreated hyperglycemic events should be avoided in old people, given the higher risk of dehydration, dizziness, falls, and long-term mortality (46).
The paucity of randomized controlled trials (RCTs) for diabetes treatment in older adults does not allow to clearly establish the most appropriate therapeutic goals in the elderly. Three major high-profile trials (ACCORD, VADT, and ADVANCE trials) (47–49) conducted on type 2 diabetic people aged around 60 years old showed that achieving tight glycemic control (HbA1c < 6% or < 6.5%) was not associated with improvements in cardiovascular outcomes, and one of them (47) has been stopped earlier because of increased mortality in the intensive glucose control arm (number of death in intensive vs. standard therapy, 257 vs. 203, HR 1.22; P = 0.04) and increased hypoglycemic events (538 vs. 179, P < 0.001). On the other hand, a large observational study reported that an HbA1c level > 8% was associated with increased risk of all-cause, cardiovascular, and cancer mortality in older adults with diabetes (50). Actually, the best glycemic target to achieve for elderly diabetic patients is still a matter of debate (51). However, there is agreement on tailoring glycemic goals in function of patient's life expectancy, diabetes duration, functional status, existing comorbidities, and pursuing moderate (HbA1c between 7 and 8%) rather than tight control (52) in old diabetic patients.
What Do Current International Guidelines Say on Glycemic Goals?
Table 1 summarizes the glycemic goals for elderly affected by diabetes according different international guidelines. The current Standards of Medical Care in Diabetes 2019 released by American Diabetes Association (ADA) indicate an HbA1c goal < 7.5% for healthy older adults with intact cognitive and functional status and a fasting or pre-prandial glucose between 90 and 130 mg/dL, whereas less stringent targets (HbA1c < 8.0–8.5%) may be advisable for frail older adults with limited life expectancy, with fasting glucose level between 100 and 180 mg/dL (25). These therapeutic objectives are in line with those for adults older than 65 years indicated by American Geriatrics Society (HbA1c ranging between 7.5 and 8%), which suggest to determine HbA1c at least every 6 months, or more frequently if needed (36). Beyond tailored glycemic goals, ADA highlights the importance of controlling any other cardiovascular risk factor with an appropriate lipid-lowering, anti-platelet, and anti-hypertensive therapy.
Table 1. Glycemic targets in elderly patients according to the current international guidelines.
Differing from ADA, the American Association of Clinical Endocrinologists (AACE) advises an HbA1c goal of 6.5% or lower for most patients without history of cardiovascular diseases (CVD) as it can be safely achieved, whereas, a broader HbA1c target (>6.5%) is suggested for older patients with concurrent serious illness, high risk of hypoglycemia, and limited life expectancy, as the patient does not experience characteristic hyperglycemic symptoms (polydipsia, polyuria, polyphagia) (53).
On the other hand, the American College of Physicians (ACP) suggests more conservative goals (HbA1c levels between 7 and 8%) for most older patients, and a less intense pharmacotherapy when HbA1c ≤ 6.5% (54). Moreover, for patients over 80 years old and with important serious chronic diseases (dementia, cancer, end-stage kidney disease, respiratory, and heart disease) clinicians should focus on minimizing symptoms related to hyperglycemia and avoiding an HbA1c target in patients with a life expectancy <10 years (54). Despite discrepancies in international guidelines (55), the mantra that every physician should follow could be resumed in “treat the patient, not the HbA1c level” (56).
Diabetes Treatments
Studies comparing the effectiveness of anti-diabetes drugs in elderly are lacking, due to the exclusion of older diabetic adults from RCTs, given the high number of comorbidity and their enhanced cardiovascular risk. Every therapeutic strategy should be chosen considering age, health status, self-manageability, cognitive and nutritional status, and comorbidities (Table 2). Generally, in older adults at higher risk to experience hypoglycemic events, medications with low risk of hypoglycemia should be preferred. Furthermore, it is advisable to simplify poly-pharmacological regimens in order to reduce adverse effects and achieve most appropriate glycemic goals. The latest consensus on the management of hyperglycemia in type 2 diabetes of the ADA and the European Association for the Study of Diabetes (EASD) (57) recommends to use drugs with proven cardiovascular benefit in patients with established clinical cardiovascular disease. Anti-hyperglycemic agents considered safe and effective for type 2 diabetic older patients can be divided in oral and injectable drugs (Table 3).
Table 2. Most frequent clinical phenotypes in elderly with suggested HbA1c target and glucose-lowering treatment.
Table 3. Glucose-lowering medications available in Europe with specific characteristics to drive the treatment choice for old people with type 2 diabetes.
Oral Anti-hyperglycemic Drugs
Metformin is the first-line medication recommended in the management of type 2 diabetes. It reduces both insulin-resistance and hepatic gluconeogenesis, lowering glucose concentrations without increasing hypoglycemic risk. The starting dose is of 500 mg once or twice a day to be assumed with meals up to 2,500 mg/day at the maximum dose. Moreover, a once daily extended-release formulation of metformin is now available, which is associated with a better gastrointestinal tolerability profile and patients' compliance. As it is excreted by the urine, a good glomerular filtration rate is needed (58). Therefore, a dose reduction has to be considered if glomerular filtration rate (GFR) is between 30 and 45 mL/min/1.73 m2, while discontinuation is recommended if GFR < 30 mL/min/1.73 m2 (59). The main adverse effects described are commonly gastrointestinal symptoms and very rarely lactic acidosis. It is a safe and effective anti-hyperglycemic drug, with low cost, and minimal risk of hypoglycemia. Nevertheless, it should be carefully used under conditions of congestive heart failure and hepatic dysfunction, which could increase the risk of lactic acidosis (25).
Thiazolidinediones also act as insulin sensing agent influencing transcriptional processes by activation of peroxisome proliferator-activated receptor-γ (PPAR-γ). Pioglitazone is the only one remaining drug of this class, as it has proven to be safe in the presence of cardiovascular disease (60). It is characterized by good efficacy, low cost, and no risk of hypoglycemia when used in monotherapy. It can be used even in case of low GFR value (61) starting from the lowest dose of 15 mg to the maximum dose of 45 mg with meals. Pioglitazone is associated with weight gain and fluid retention, so that it is contraindicated in case of congestive heart failure (NYHA class III, IV). Furthermore, it is not advisable to use the drug in older person at risk for falls because it has proven to increase risk of non-osteoporotic bone fractures (62). Finally, it is contraindicated in patients with or at high risk for bladder cancer (63).
Sulfonylureas are an insulin secretagogue class, which act by favoring β-cells membrane depolarization and consequently insulin secretion. They are characterized by high glucose lowering efficacy and low cost, but they should be used with extreme caution because of the high risk of hypoglycemia and weigh gain. Short acting ones with lowest hypoglycemic risk, such as gliclazide, should be preferred in older diabetic patients, when initial therapy with metformin is contraindicated or not tolerated (64). By contrast, long acting sulfonylureas, as glibenclamide, are considered inappropriate in elderly diabetes management.
Metiglinides are short-acting insulin secretagogue agents, that enhance early phase of insulin secretion at meals, lowering postprandial glucose levels. They present lower risk of hypoglycemia than sulfonylureas, since their activity is dependent on the presence of glucose (20). Repaglinide is the most effective agent of this class, with a moderate effect on weight gain. Use of repaglinide may be indicated for elderly patients with type 2 diabetes because of the low risk of hypoglycemia, high efficacy on postprandial hyperglycemia, and safe use in renal impairment (65).
Dipeptidyl peptidase 4 (DPP-4) inhibitors belong to the class of incretin enhancer agents. They inhibit the DPP-4 enzyme, thereby extending the life-time of GLP-1 and increasing insulin secretion in a glucose dependent manner. Drugs in this class are generally well-tolerated in older people, with neutral effect on body weight and very low risk of hypoglycemia (66, 67). DPP-4 inhibitors have proven to be effective in reducing baseline HbA1c levels and fasting plasma glucose (68). Moreover, a study of 80 elderly diabetic patients treated with oral glucose-lowering drug (DPP4-inhibitors or sulfonylureas) for at least 24 months showed that patients using DPP-4 inhibitors had better sarcopenic parameters (fat-free mass, skeletal muscle mass, and related indices, muscle strength, and gait speed) as compared with those receiving sulfonylureas (69). The cardiovascular safety of this class of agents has been confirmed by several randomized controlled trials (70–74). Alogliptin, saxagliptin, sitagliptin, and linagliptin (70–74) have proven to neither increase nor decrease risk of the combined major adverse cardiovascular events (MACE) in type 2 diabetic patients with established cardiovascular disease. However, in the SAVOR-TIMI 53 study (72), saxagliptin, showed a 27% increased risk of hospitalization for heart failure (HF) among patients with elevated levels of natriuretic peptides, previous heart failure, or chronic kidney disease, as compared with placebo (75). In the EXAMINE trial, patients with type 2 diabetes and recent acute coronary syndromes assigned to alogliptin had an increased, although non-statistically significant, rate of HF hospitalization when compared to the placebo group (76). Recently, in the TECOS trial, sitagliptin showed neutral effects on cardiovascular risk without any significant risk of HF hospitalization when compared with placebo in patients aged ≥75 years with well-controlled type 2 diabetes and cardiovascular disease (77). Moreover, data from the TECOS trial report that sitagliptin is not associated with a higher fracture risk, major osteoporotic fractures, or hip fractures (78). Therefore, DPP-4 inhibitors may be considered as an effective and safely treatment option for older patients with type 2 diabetes (79).
Sodium-glucose cotransporter 2 (SGLT-2) inhibitors are the latest marketed oral anti-hyperglycemic agents in diabetes management. These molecules act with an innovative and different mechanism of action: they inhibit Na/glucose renal cotransporter on kidney proximal convoluted tubule, increasing urinary glucose concentration, and favoring osmotic diuresis (diuretic effect). Beyond glucose lowering efficacy, SGLT-2 inhibitors have also beneficial effects in reducing body weight and blood pressure. Their use is permitted until GFR ≥ 30 mL/min/1.73 m2, due to safety concerns and lack of dedicated study in diabetic population with severe chronic renal disease. If SGLT-2 inhibitors are used in combination with diuretics, lowering the dose of diuretics is needed to minimize the risks of hypotension and dehydration (79). SGLT2-inhibitors are generally well-tolerated in older adults, except for increased risk of mycotic genital infections in both sexes. There is evidence from cardiovascular outcome trials (80, 81) that this class has beneficial effects in reducing the composite endpoint of cardiovascular deaths, non-fatal myocardial infarction and non-fatal stroke as compared with placebo in patients with type 2 diabetes and high cardiovascular risk. Similarly, in the multinational, observational CVD-REAL study, new users of empaglifozin, canaglifozin, and dapaglifozin reported lower risk of cardiovascular mortality, MACE and hospitalization for heart failure as compared with new users of other glucose-lowering drugs (82). Moreover, a subgroup analysis of the EMPA-REG OUTCOME study showed a significant reduction in the risk of MACE especially in patients older than 65 years treated with empaglifozin (80). Based on these results, ADA and EASD recommend their use in patients with established or at high risk of cardiovascular disease (57). In the respective RCTs designed to test the efficacy and safety of SGLT-2 inhibitors on renal outcomes (83, 84), both empagliflozin and canagliflozin use was associated with reduced risk of sustained loss of kidney function, attenuated GFR decline, and a reduction in albuminuria, which supports a possible renoprotective effect of this drugs in people with type 2 diabetes. More recently, treatment with dapagliflozin, compared with placebo, produced a significant 24% risk reduction in renal composite events, namely ≥40% decrease in eGFR below 60 ml/min/1.73 m2 of body-surface area, new end-stage renal disease, or death from renal or cardiovascular causes (85). Conversely, on May 2015 the Food and Drug Administration released a warning relative to an increased risk of diabetic ketoacidosis (DKA) associated with use of SGLT-2 inhibitors (86), on the basis of a comparative evaluation with DPP-4 inhibitors on a cohort of more than 140,000 type 2 diabetic patients (87). The increased incidence of DKA related to SGLT2-inhibitors may be probably related to the non-insulin-dependent glucose clearance, hyperglucagonemia, and volume depletion (88). Therefore, although this class has many beneficial effects on cardiovascular and renal outcomes, caution is needed using SGLT2 inhibitors in elderly because of increased risk of genital infections, dehydration, orthostatic hypotension, lower extremities amputations, and bone fracture (89, 90).
Injectable Anti-hyperglycemic Drugs
Glucagon-like peptide 1 receptor agonists (GLP-1RAs) are innovative and pleiotropic drugs that act by promoting insulin secretion and reducing glucagon secretion in a glucose dependent manner and favoring weight loss. As they use the injectable way of administration, they require neuro-psychological and physical integrity. GLP-1RAs are highly effective in lowering glucose levels, with minimal risk of hypoglycemia (91, 92). Recently, a phase III RCT showed the superiority of lixisenatide as compared with placebo in reducing HbA1c levels and postprandial hyperglycemia in patients ≥70 years uncontrolled on their current antidiabetic treatment (93). The main adverse effects associated with GLP-1RAs use consist of nausea, vomiting, diarrhea, and an increase in heart rate (94). Furthermore, there is strong evidence from RCTs (95–97) that these drugs can reduce the risk of MACE in type 2 diabetic patients with high cardiovascular risk. Results from preclinical studies showed also favorable effects of GLP-1RAs on neuronal protection and cognitive performances (98, 99). Randomized controlled trials assessing effects of incretin therapy on cognitive function and Alzheimer's disease in humans are currently ongoing. If these benefits will be confirmed, use of GLP-1RA may be a helpful option even in patients with mild cognitive impairment.
Free and fixed-ratio combinations of GLP-1RAs and basal insulin formulations have been approved by regulatory agencies to potentiate antihyperglycemic effects and glycemic control in type 2 diabetic patients (57, 100). At the moment, two fixed-ratio combinations, insulin glargine plus lixisenatide (IGlarLixi) and insulin degludec plus liraglutide (IDegLira), have been approved for treatment of type 2 diabetes (101). A recent analysis compared effectiveness of fixed-ratio combination iGlarlixi vs. sequential administration of iGlar + Lixi in glucose control in type 2 diabetic patients (102). IGlarLixi was associated with significantly higher HbA1c reductions, weight loss and number of patients reaching HbA1c target despite lower insulin doses, with similar rates oh hypoglycemic events and lower rates of gastrointestinal adverse events. A meta-analysis of 26 RCTs have shown a mean reduction of 0.47% in HbA1c level associated with a mean weight loss of 2.5 Kg favoring the insulin/GLP-1RA combination as compared with other injectable anti-diabetes treatments, with no increased risk of hypoglycaemia (103). Moreover, when compared with intensive insulin therapy, either free or fixed combination of GLP-1RA and basal insulin led to a greater mean decrease of 0.53% in HbA1c level, a higher proportion of patients at HbA1c target of < 7% and reduction in body weight (104). Based on this evidence, combination strategies, either free or fixed, represent a good option for intensifying basal insulin therapy in patients with type 2 diabetes who need amelioration of glycemic control, without increasing the risk of hypoglycemia and weight gain (104).
Insulin remains the most effective drug for type 2 diabetes (105). The main limitations of insulin therapy are the risk of hypoglycemia and weight gain, although it can be administered at any GFR value. Insulin therapy requires patients' autonomy, intact visual, motor, and cognitive ability in diabetes management (25). Since its discovery in 1921, several and innovative insulin formulations have been developed. Insulin glargine (U100 or U300), degludec (U100 or U200), and detemir represent long acting insulin analogs which provide daily basal insulin profiles (106). A recent meta-analysis reported that insulin glargine U300 was as effective as glargine U100 in type 2 diabetic patients aged >65 years, with a reduced risk of nocturnal hypoglycemia (107). Compared with human insulin neutral protamine Hagedorn (NPH), long-acting insulin analogs have a longer duration of action and a fatter pharmacokinetic profile, with a reduced risk of hypoglycemia (106). Therefore, the newer basal insulins should be preferentially used in diabetic elderly, where they may be indicated as starting insulin therapy. Prandial rapid (aspart, lispro, glulisine) and ultra-rapid acting (faster aspart) insulin analogs used at mealtime can be combined with basal insulin to sooner improve and intensify glycemic control (108). However, both basal and prandial insulin require frequent titration to achieve the best anti-hyperglycemic effects. Patients on enteral or parenteral nutrition may require frequent glucose monitoring (intervals of 4–6 h) to better titrate the insulin dose and to avoid hypo- and hyperglycemic events (64). Caution is needed in insulin titration because a simple error can easily precipitate major hypoglycemic episodes, leading to falls, and bone fractures (109). Alternatively, premixed insulin regimen, eliminating the challenge of mixing insulin, may have a role in elderly patients who have regular eating habits, with similar efficacy as compared with basal bolus therapy (110). Therefore, use of insulin therapy in elderly patients often requires the assistance of a caregiver if patients' abilities are limited.
Conclusions
Older adults with type 2 diabetes represent a complex and heterogenous age group. Managing diabetes in older age remains an important clinical challenge for all physicians, either primary care providers or specialists. As older diabetic patients present frequently frailty and/or multiple comorbidities, an individualized patient-centered glycemic target is needed in order to achieve a glycemic control avoiding dangerous hypo- and hyperglycemic events. A comprehensive geriatric assessment should be performed at diagnosis of diabetes to better understand cognitive, visual and motor abilities, and coexisting comorbidities. In the choice of anti-hyperglycemic strategies, drugs with proven tolerability, safety, and minimal hypoglycemic risk should be preferred. Anti-diabetes treatment regimens in elderly must be simple, sustainable, and safe to best mirror patients' preferences, wishes, and needs.
Author Contributions
GB, MIM, KE, and DG conceived the manuscript. ML, GB, and MIM drafted the manuscript. JM, KE, and DG reviewed and edited the manuscript. All authors gave the approval to the final version of the manuscript.
Conflict of Interest Statement
MIM received a consultancy fee from MSD and has held lectures for Sanofi, Astrazeneca, and Novo Nordisk. JM has held lectures for Astra Zeneca, Boehringer-Ingelheim, Eli Lilly, MSD, Novo Nordisk, Sanofi, and Servier and received research support from Boehringer-Ingelheim, MSD, Novo Nordisk, Sanofi. KE received a consultancy fee from Eli Lilly and has held lectures for Eli Lilly, Sanofi, and Novo Nordisk. DG received a consultancy fee from Eli Lilly and has held lectures for Eli Lilly and Sanofi.
The remaining 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.
References
1. WHO. Life Expectancy. Available online at: http://www.who.int/gho/mortality_burden_disease/life_tables/situation_trends_text/en/ (Accessed November 10, 2018).
2. OECD/EU. Health at a Glance: Europe 2016 – State of Health in the EU Cycle. Paris: OECD Publishing. doi: 10.1787/9789264265592-en (Accessed November 10, 2018).
3. Centers for Disease Control and Prevention. Life Expectancy by Age, Race, and Sex, 1900–2014. Available online at: https://www.cdc.gov/nchs/data/nvsr/nvsr66/nvsr66_04.pdf (Accessed November 10, 2018).
4. GBD 2016 causes of death collaborators. global, regional, and national age-sex specific mortality for 264 causes of death, 1980–2016: a systematic analysis for the global burden of disease study 2016. Lancet (2017) 390:1151–210. doi: 10.1016/S0140-6736(17)32152-9
5. World Health Statistics 2018: Monitoring Health for the SDGs SUSTAINABLE Development Goals. Geneva: World Health Organization (2018).
7. Kalyani RR, Golden SH, Cefalu WT. Diabetes and aging: unique considerations and goals of care. Diabetes Care (2017) 40:440–43. doi: 10.2337/dci17-0005
9. Yang Y, Guo Y, Qian ZM, Ruan Z, Zheng Y, Woodward A, et al. Ambient fine particulate pollution associated with diabetes mellitus among the elderly aged 50 years and older in China. Environ Pollut. (2018) 243:815–23. doi: 10.1016/j.envpol.2018.09.056
10. Halter JB, Musi N, McFarland Horne F, Crandall JP, Goldberg A, Harkless L, et al. Diabetes and cardiovascular disease in older adults: current status and future directions. Diabetes (2014) 63:2578–89. doi: 10.2337/db14-0020
11. Kirkman MS, Briscoe VJ, Clark N, Florez H, Haas LB, Halter JB, et al. Consensus development conference on diabetes and older adults. Diabetes in older adults: a consensus report. J Am Geriatr Soc. (2012) 60:2342–56. doi: 10.1111/jgs.12035
12. Barzilai N, Cuervo AM, Austad S. Aging as a biological target for prevention and therapy. JAMA (2018) 320:1321–2. doi: 10.1001/jama.2018.9562
13. Tchkonia T, Kirkland JL. Aging, cell senescence, and chronic disease: emerging therapeutic strategies. JAMA (2018) 320:1319–20. doi: 10.1001/jama.2018.12440
14. Chia CW, Egan JM, Ferrucci L. Age-related changes in glucose metabolism, hyperglycemia, and cardiovascular risk. Circ Res. (2018) 123:886–904. doi: 10.1161/CIRCRESAHA.118.312806
15. St-Onge MP, Gallagher D. Body composition changes with aging:the cause or the result of alterations in metabolic rate andmacronutrient oxidation? Nutrition (2010) 26:152–5. doi: 10.1016/j.nut.2009.07.004
16. Tchkonia T, Morbeck DE, Von Zglinicki T, Van Deursen J, Lustgarten J, Scrable H, et al. Fat tissue, aging, and cellular senescence. Aging Cell (2010) 9:667–84. doi: 10.1111/j.1474-9726.2010.00608.x
17. Mooradian AD. Evidence-based management of diabetes in older adults. Drugs Aging (2018) 35:1065–78. doi: 10.1007/s40266-018-0598-3
18. Huang ES. Management of diabetes mellitus in older people with comorbidities. BMJ (2016) 353:i2200. doi: 10.1136/bmj.i2200
19. Kotsani M, Chatziadamidou T, Economides D, Benetos A. Higher prevalence and earlier appearance of geriatric phenotypes in old adults with type 2 diabetes mellitus. Diabetes Res Clin Pract. (2018) 135:206–17. doi: 10.1016/j.diabres.2017.10.026
20. Abdelhafiz AH, Sinclair AJ. Management of type 2 diabetes in older people. Diabetes Ther. (2013) 4:13–26. doi: 10.1007/s13300-013-0020-4
21. Xu WL, von Strauss E, Qiu CX, Winblad B, Fratiglioni L. Uncontrolled diabetes increases the risk of Alzheimer's disease: a population-based cohort study. Diabetologia (2009) 52:1031–9. doi: 10.1007/s00125-009-1323-x
22. Umegaki H. Type 2 diabetes as a risk factor for cognitive impairment: current insights. Clin Interv Aging (2014) 9:1011–9. doi: 10.2147/CIA.S48926
23. Bruce DG, Nelson ME, Mace JL, Davis WA, Davis TM, Starkstein SE. Apathy in older patients with type 2 diabetes. Am J Geriatr Psychiatry (2015) 23:615–21. doi: 10.1016/j.jagp.2014.09.010
24. Park M, Reynolds CF. Depression among older adults with diabetes mellitus. Clin Geriatr Med. (2015) 31:117–37. doi: 10.1016/j.cger.2014.08.022
25. American Diabetes Association. 12. Older adults: standards of medical care in diabetes-2019. Diabetes Care (2019) 42:S139–47. doi: 10.2337/dc19-S012
26. Bianchi L, Volpato S. Muscle dysfunction in type 2 diabetes: a major threat to patient's mobility and independence. Acta Diabetol. (2016) 53:879–89. doi: 10.1007/s00592-016-0880-y
27. Paschou SA, Dede AD, Anagnostis PG, Vryonidou A, Morganstein D, Goulis DG. Type 2 diabetes and osteoporosis: a guide to optimal management. J Clin Endocrinol Metab. (2017) 102:3621–34. doi: 10.1210/jc.2017-00042
28. Dhindsa S, Ghanim H, Batra M, Dandona P. Hypogonadotropic hypogonadism in men with diabesity. Diabetes Care (2018) 41:1516–25. doi: 10.2337/dc17-2510
29. Pereira S, Marliss EB, Morais JA, Chevalier S, Gougeon R. Insulin resistance of protein metabolism in type 2 diabetes. Diabetes (2008) 57:56–63. doi: 10.2337/db07-0887
30. Lipscombe LL, Jamal SA, Booth GL, Hawker GA. The risk of hip fractures in older individuals with diabetes: a population-based study. Diabetes Care (2007) 30:835–41. doi: 10.2337/dc06-1851
31. Rochira V, Antonio L, Vanderschueren D. EAA clinical guideline on management of bone health in the andrological outpatient clinic. Andrology (2018) 6:272–85. doi: 10.1111/andr.12470
32. Bhasin S, Brito JP, Cunningham GR, Hayes FJ, Hodis HN, Matsumoto AM, et al. Testosterone therapy in men with hypogonadism: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. (2018) 103:1715–44. doi: 10.1210/jc.2018-00229
33. Wallander M, Axelsson KF, Nilsson AG, Lundh D, Lorentzon M. Type 2 diabetes and risk of hip fractures and non-skeletal fall injuries in the elderly: a study from the fractures and fall injuries in the elderly cohort (FRAILCO). J Bone Miner Res. (2017) 32:449–60. doi: 10.1002/jbmr.3002
34. Vogel T, Brechat PH, Leprêtre PM, Kaltenbach G, Berthel M, Lonsdorfer J. Health benefits of physical activity in older patients: a review. Int J Clin Pract (2009) 63:303–20. doi: 10.1111/j.1742-1241.2008.01957.x
35. Tepper S, Alter Sivashensky A, Rivkah Shahar D, Geva D, Cukierman-Yaffe T. The association between mediterranean diet and the risk of falls and physical function indices in older type 2 diabetic people varies by age. Nutrients (2018) 14:10. doi: 10.3390/nu10060767
36. American Geriatrics Society Expert Panel on Care of Older Adults with Diabetes Mellitus, Moreno G, Mangione CM, Kimbro L, Vaisberg E. Guidelines abstracted from the American geriatrics society guidelines for improving the care of older adults with diabetes mellitus: 2013 update. J Am Geriatr Soc. (2013) 61:2020–6. doi: 10.1111/jgs.12514
37. Hsu A, Conell-Price J, Stijacic Cenzer I, Eng C, Huang AJ, Rice-Trumble K, et al. Predictors of urinary incontinence in community-dwelling frail older adults with diabetes mellitus in a cross-sectional study. BMC Geriatr. (2014) 14:137. doi: 10.1186/1471-2318-14-137
38. Hart HE, Rutten GE, Bontje KN, Vos RC. Overtreatment of older patients with type 2 diabetes mellitus in primary care. Diabetes Obes Metab. (2018) 20:1066–9. doi: 10.1111/dom.13174
39. Abdelhafiz AH, Sinclair AJ. Deintensification of hypoglycaemic medications-use of a systematic review approach to highlight safety concerns in older people with type 2 diabetes. Diabetes Complicat. (2018) 32:444–50. doi: 10.1016/j.jdiacomp.2017.11.011
40. Alwhaibi M, Balkhi B, Alhawassi TM, Alkofide H, Alduhaim N, Alabdulali R, et al. Polypharmacy among patients with diabetes: a cross-sectional retrospective study in a tertiary hospital in Saudi Arabia. BMJ Open (2018) 8:e020852. doi: 10.1136/bmjopen-2017-020852
41. Peron EP, Ogbonna KC, Donohoe KL. Antidiabetic medications and polypharmacy. Clin Geriatr Med. (2015) 31:17–27. doi: 10.1016/j.cger.2014.08.017
42. Munshi MN. Cognitive dysfunction in older adults with diabetes: what a clinician needs to know. Diabetes Care (2017) 40:461–7. doi: 10.2337/dc16-1229
43. Majumdar SR, Hemmelgarn BR, Lin M, McBrien K, Manns BJ, Tonelli M. Hypoglycemia associated with hospitalization and adverse events in older people: population-based cohort study. Diabetes Care (2013) 36:3585–90. doi: 10.2337/dc13-0523
44. Kagansky N, Levy S, Rimon E, Cojocaru L, Fridman A, Ozer Z, et al. Hypoglycemia as a predictor of mortality in hospitalized elderly patients. Arch Intern Med. (2003) 163:1825–9. doi: 10.1001/archinte.163.15.1825
45. Migdal A, Yarandi SS, Smiley D, Umpierrez GE. Update on diabetes in the elderly and in nursing home residents. J Am Med Dir Assoc. (2011) 12:627–32. doi: 10.1016/j.jamda.2011.02.010
46. Huang CC, Weng SF, Tsai KT, Chen PJ, Lin HJ, Wang JJ, et al. Long-term mortality risk after hyperglycemic crisis episodes in geriatric patients with diabetes: a national population-based cohort study. Diabetes Care (2015) 38:746–51. doi: 10.2337/dc14-1840
47. Action to Control Cardiovascular Risk in Diabetes Study Group, Gerstein HC, Miller ME, Byington RP, Goff DC Jr, Bigger JT, et al. Effects of intensive glucose lowering in type 2 diabetes. N Engl J Med. (2008) 358:2545–59. doi: 10.1056/NEJMoa0802743
48. ADVANCE Collaborative Group, Patel A, MacMahon S, Chalmers J, Neal B, Billot L, et al. Intensive blood glucose control and vascular outcomes in patients with type 2 diabetes. N Engl J Med. (2008) 358:2560–72. doi: 10.1056/NEJMoa0802987
49. Duckworth W, Abraira C, Moritz T, Reda D, Emanuele N, Reaven PD, et al. Glucose control and vascular complications in veterans with type 2 diabetes. N Engl J Med. (2009) 360:129–39. doi: 10.1056/NEJMoa0808431
50. Palta P, Huang ES, Kalyani RR, Golden SH, Yeh H-C. Hemoglobin A1C and mortality in older adults with and without diabetes: results from the National Health and Nutrition Examination Surveys (1988–2011). Diabetes Care (2017) 40:453–60. doi: 10.2337/dci16-0042
51. Abbasi J. For patients with type 2 diabetes, what's the best target hemoglobin A1C? JAMA (2018) 319:2367–9. doi: 10.1001/jama.2018.5420
52. Lee SJ, Eng C. Goals of glycemic control in frail older patients with diabetes. JAMA (2011) 305:1350–1. doi: 10.1001/jama.2011.404
53. Garber AJ, Abrahamson MJ, Barzilay JI, Blonde L, Bloomgarden ZT, Bush MA, et al. Consensus statement by the american association of clinical endocrinologists and american college of endocrinology on the comprehensive type 2 diabetes management algorithm - 2018 executive summary. Endocr Pract. (2018) 24:91–120. doi: 10.4158/CS-2017-0153
54. Qaseem A, Wilt TJ, Kansagara D, Horwitch C, Barry MJ, Forciea MA, et al. Hemoglobin A1c Targets for glycemic control with pharmacologic therapy for non-pregnant adults with type 2 diabetes mellitus: a guidance statement update from the American college of physicians. Ann Intern Med. (2018) 168:569–76. doi: 10.7326/M17-0939
55. Giugliano D, Maiorino MI, Bellastella G, Esposito K. Dissonance among treatment algorithms for hyperglycemia in type 2 diabetes: an egalitarian dialog. J Endocrinol Invest. (2018) 1–6. doi: 10.1007/s40618-018-0893-1
56. McLaren LA, Quinn TJ, McKay GA. Diabetes control in older people. BMJ (2013) 346:f2625. doi: 10.1136/bmj.f2625
57. Davies MJ, D'Alessio DA, Fradkin J, Kernan WN, Mathieu C, Mingrone G, et al. Management of Hyperglycemia in type 2 diabetes, 2018. a consensus report by the American Diabetes Association (ADA) and the European association for the study of diabetes (EASD). Diabetes Care (2018) 41:2669–701. doi: 10.2337/dci18-0033
58. Inzucchi SE, Lipska KJ, Mayo H, Bailey CJ, McGuire DK. Metformin in patients with type 2 diabetes and kidney disease: a systematic review. JAMA (2014) 312:2668–75. doi: 10.1001/jama.2014.15298
59. Lipska KJ, Bailey CJ, Inzucchi SE. Use of metformin in the setting of mild-to-moderate renal insufficiency. Diabetes Care (2011) 34:1431–7. doi: 10.2337/dc10-2361
60. Wilcox R, Kupfer S, Erdmann E. Effects of pioglitazone on major adverse cardiovascular events in high-risk patients with type 2 diabetes: results from PROspective pioglitAzone clinical trial in macro vascular events (PROactive 10). Am Heart J. (2008) 155:712e7. doi: 10.1016/j.ahj.2008.04.032
61. Schneider CA, Ferrannini E, Defronzo R, Schernthaner G, Yates J, Erdmann E. Effect of pioglitazone on cardiovascular outcome in diabetes and chronic kidney disease. J Am Soc Nephrol. (2008) 19:182–7. doi: 10.1681/ASN.2007060678
62. Viscoli CM, Inzucchi SE, Young LH, Insogna KL, Conwit R, Furie KL, et al., IRIS Trial Investigators. Pioglitazone and risk for bone fracture: safety data from a randomized clinical trial. J Clin Endocrinol Metab. (2017) 102:914–22. doi: 10.1210/jc.2016-3237
63. Lewis JD, Habel LA, Quesenberry CP, Strom BL, Peng T, Hedderson MM, et al. Pioglitazone use and risk of bladder cancer and other common cancers in persons with diabetes. JAMA (2015) 314:265–77. doi: 10.1001/jama.2015.7996
64. Yakaryılmaz FD, Öztürk ZA. Treatment of type 2 diabetes mellitus in the elderly. World J Diabetes (2017) 8:278–85. doi: 10.4239/wjd.v8.i6.278
65. Omori K, Nomoto H, Nakamura A, Takase T, Cho KY, Ono K, et al. Reduction in glucose fluctuations in elderly patients with type 2 diabetes using repaglinide: a randomized controlled trial of repaglinide vs. sulfonylurea. J Diabetes Investig. (2019) 321:69–79. doi: 10.1111/jdi.12889
66. Inzucchi SE, Nauck MA, Hehnke U, Woerle HJ, von Eynatten M, Henry RR. Improved glucose control with reduced hypoglycaemic risk when linagliptin is added to basal insulin in elderly patients with type 2 diabetes. Diabetes Obes Metab. (2015) 17:868–77. doi: 10.1111/dom.12490
67. Barnett AH, Huisman H, Jones R, von Eynatten M, Patel S, Woerle HJ. Linagliptin for patients aged 70 years or older with type 2 diabetes inadequately controlled with common antidiabetes treatments: a randomised, double-blind, placebo controlled trial. Lancet (2013) 382:1413–23. doi: 10.1016/S0140-6736(13)61500-7
68. Esposito K, Chiodini P, Maiorino MI, Capuano A, Cozzolino D, Petrizzo M, et al. A nomogram to estimate the HbA1c response to different DPP-4 inhibitors in type 2 diabetes: a systematic review and meta-analysis of 98 trials with 24 163 patients. BMJ Open (2015) 5:e005892. doi: 10.1136/bmjopen-2014-005892
69. Rizzo MR, Barbieri M, Fava I, Desiderio M, Coppola C, Marfella R, et al. Sarcopenia in elderly diabetic patients: role of dipeptidyl peptidase 4 inhibitors. J Am Med Dir Assoc. (2016) 17:896–901. doi: 10.1016/j.jamda.2016.04.016
70. Nauck MA, Meier JJ, Cavender MA, Abd El Aziz M, Drucker DJ. Cardiovascular actions and clinical outcomes with glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors. Circulation (2017) 136:849–70. doi: 10.1161/CIRCULATIONAHA.117.028136
71. White WB, Cannon CP, Heller SR, Nissen SE, Bergenstal RM, Bakris GL, et al. Alogliptin after acute coronary syndrome in patients with type 2 diabetes. N Engl J Med. (2013) 369:1327–35. doi: 10.1056/NEJMoa1305889
72. Scirica BM, Bhatt DL, Braunwald E, Steg PG, Davidson J, Hirshberg B, et al. Saxagliptin and cardiovascular outcomes in patients with type 2 diabetes mellitus. N Engl J Med. (2013) 369:1317–26. doi: 10.1056/NEJMoa1307684
73. Green JB, Bethel MA, Armstrong PW, Buse JB, Engel SS, Garg J, et al. Effect of sitagliptin on cardiovascular outcomes in type 2 diabetes. N Engl J Med. (2015) 373:232–42. doi: 10.1056/NEJMoa1501352
74. Rosenstock J, Perkovic V, Johansen OE, Cooper ME, Kahn SE, Marx N, et al. Effect of linagliptin vs. placebo on major cardiovascular events in adults with type 2 diabetes and high cardiovascular and renal risk-The Carmelina Randomized clinical trial. JAMA (2018) 321:69–79. doi: 10.1001/jama.2018.18269. [Epub ahead of print].
75. Scirica BM, Braunwald E, Raz I, Cavender MA, Morrow DA, Jarolim P, et al. Heart failure, saxagliptin, and diabetes mellitus: observations from the SAVOR-TIMI 53 randomized trial. Circulation (2014) 130:1579–88. doi: 10.1161/CIRCULATIONAHA.114.010389
76. Zannad F, Cannon CP, Cushman WC, Bakris GL, Menon V, Perez AT, et al. Heart failure and mortality outcomes in patients with type 2 diabetes taking alogliptin versus placebo in EXAMINE: a multicentre, randomised, double-blind trial. Lancet (2015) 385:2067–76. doi: 10.1016/S0140-6736(14)62225-X
77. Bethel MA, Engel SS, Green JB, Huang Z, Josse RG, Kaufman KD, et al. Assessing the safety of sitagliptin in older participants in the trial evaluating cardiovascular outcomes with sitagliptin (TECOS). Diabetes Care (2017) 40:494–501. doi: 10.2337/dc16-1135
78. Josse RG, Majumdar SR, Zheng Y, Adler A, Bethel MA, Buse JB, et al. Sitagliptin and risk of fractures in type 2 diabetes: results from the TECOS trial. Diabetes Obes Metab. (2017) 19:78–86. doi: 10.1111/dom.12786
79. Sesti G, Antonelli Incalzi R, Bonora E, Consoli A, Giaccari A, Maggi S, et al. Management of diabetes in older adults. Nutr Metab Cardiovasc Dis. (2018) 28:206–18. doi: 10.1016/j.numecd.2017.11.007
80. Zinman B, Wanner C, Lachin JM, Fitchett D, Bluhmki E, Hantel S, et al. Empagliflozin, cardiovascular outcomes, and mortality in type 2 diabetes. N Engl J Med. (2015) 373:2117–28. doi: 10.1056/NEJMoa1504720
81. Neal B, Perkovic V, Mahaffey KW, De Zeeuw D, Fulcher G, Erondu N, et al. Canagliflozin and cardiovascular and renal events in type 2 diabetes. N Engl J Med. (2017) 377:644–57. doi: 10.1056/NEJMoa1611925
82. Birkeland KI, Jørgensen ME, Carstensen B, Persson F, Gulseth HL, Thuresson M, et al. Cardiovascular mortality and morbidity in patients with type 2 diabetes following initiation of sodium-glucose co-transporter-2 inhibitors versus other glucose-lowering drugs (CVD-REAL Nordic): a multinational observational analysis. Lancet Diabetes Endocrinol. (2017) 5:709–17. doi: 10.1016/S2213-8587(17)30258-9
83. Wanner C, Inzucchi SE, Lachin JM, Fitchett D, von Eynatten M, Mattheus M, et al. Empagliflozin and progression of kidney disease in type 2 diabetes. N Engl J Med. (2016) 375:323–34. doi: 10.1056/NEJMoa1515920
84. Perkovic V, De Zeeuw D, Mahaffey KW, Fulcher G, Erondu N, Shaw W, et al. Canagliflozin and renal outcomes in type 2 diabetes: results from the CANVAS Program randomised clinical trials. Lancet Diabetes Endocrinol. (2018) 6:691–704. doi: 10.1016/S2213-8587(18)30141-4
85. Wiviott SD, Raz I, Bonaca MP, Mosenzon O, Kato ET, Cahn A, et al. Dapagliflozin and cardiovascular outcomes in type 2 diabetes. N Engl J Med. (2019) 380:347–57. doi: 10.1056/NEJMoa1812389
86. FDA Drug Safety Communication. FDA Warns That SGLT2 Inhibitors for Diabetes May Result in a Serious Condition of Too Much Acid in the Blood. Available online at:https://www.fda.gov/Drugs/DrugSafety/ucm446845.htm (Accessed May 15, 2015).
87. Fralick M, Schneeweiss S, Patorno E. Risk of diabetic ketoacidosis after initiation of an SGLT2 inhibitor. N Engl J Med. (2017) 376:2300–2. doi: 10.1056/NEJMc1701990
88. Peters AL, Buschur EO, Buse JB, Cohan P, Diner JC, Hirsch IB. Euglycemic diabetic ketoacidosis: a potential complication of treatment with sodium-glucose cotransporter 2 inhibition. Diabetes Care (2015) 38:1687–93. doi: 10.2337/dc15-0843
89. Neal B, Perkovic V, Matthews DR. Canagliflozin and cardiovascular and renal events in type 2 diabetes. N Engl J Med. (2017) 377:2099. doi: 10.1056/NEJMc1712572
90. Watts NB, Bilezikian JP, Usiskin K, Edwards R, Desai M, Law G, et al. Effects of canagliflozin on fracture risk in patients with type 2 diabetes mellitus. J Clin Endocrinol Metabol. (2016) 101:157–66. doi: 10.1210/jc.2015-3167
91. Esposito K, Mosca C, Brancario C, Chiodini P, Ceriello A, Giugliano D. GLP-1 receptor agonists and HBA1c target of < 7% in type 2 diabetes: meta-analysis of randomized controlled trials. Curr Med Res Opin. (2011) 27:1519–28. doi: 10.1185/03007995.2011.590127
92. Abd El Aziz MS, Kahle M, Meier JJ, Nauck MA. A meta-analysis comparing clinical effects of short- or long-acting GLP-1 receptor agonists versus insulin treatment from head-to-head studies in type 2 diabetic patients. Diabetes Obes Metab. (2017) 19:216–27. doi: 10.1111/dom.12804
93. Meneilly GS, Roy-Duval C, Alawi H, Dailey G, Bellido D, Trescoli C, et al. Lixisenatide therapy in older patientswith type 2 diabetes inadequately controlled on their current antidiabetic treatment: the GetGoal-O randomized trial. Diabetes Care (2017) 40:485–93. doi: 10.2337/dc16-2143
94. Bettge K, Kahle M, Abd El Aziz MS, Meier JJ, Nauck MA. Occurrence of nausea, vomiting and diarrhoea reported as adverse events in clinical trials studying glucagon-like peptide-1 receptor agonists: a systematic analysis of published clinical trials. Diabetes Obes Metab. (2017) 19:336–47. doi: 10.1111/dom.12824
95. Marso SP, Daniels GH, Brown-Frandsen K, Kristensen P, Mann JF, Nauck MA, et al. Liraglutide and cardiovascular outcomes in type 2 diabetes. N Engl J Med. (2016) 375:311–22. doi: 10.1056/NEJMoa1603827
96. Marso SP, Bain SC, Consoli A, Eliaschewitz FG, Jódar E, Leiter LA, et al. Semaglutide and cardiovascular outcomes in patients with type 2 diabetes. N Engl J Med. (2016) 375:1834–44. doi: 10.1056/NEJMoa1607141
97. Hernandez AF, Green JB, Janmohamed S, D'Agostino RB Sr, Granger CB, Jones NP, et al. Albiglutide and cardiovascular outcomes in patients with type 2 diabetes and cardiovascular disease (Harmony Outcomes): a double-blind, randomised placebo-controlled trial. Lancet (2018) 392:1519–29. doi: 10.1016/S0140-6736(18)32261-X
98. McClean PL, Holscher C. Liraglutide can reverse memory impairment, synaptic loss and reduce plaque load in aged APP/PS1 mice, a model of Alzheimer's disease. Neuropharmacology (2014) 76:57–67. doi: 10.1016/j.neuropharm.2013.08.005
99. Bomba M, Granzotto A, Castelli V, Massetti N, Silvestri E, Canzoniero LMT, et al. Exenatide exerts cognitive effects by modulating the BDNF-TrkB neurotrophic axis in adult mice. Neurobiol Aging (2018) 64:33–43. doi: 10.1016/j.neurobiolaging.2017.12.009
100. American Diabetes Association. Pharmacologic approaches to glycemic treatment. In standards of medical care in diabetes. Diabetes Care (2017) 40:S64–74. doi: 10.2337/dc17-S011
101. U.S. Food and Drug Administration, Center for Drug Evaluation and Research. NDA 208583 Approval Letter, November 21, 2016. Available online at: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2016/208583Orig1s000TOC.cfm (Accessed November 10, 2018); U.S. Food and Drug Administration, Center for Drug Evaluation and Research. NDA 208673 approval letter, November 21, 2016. Available online at: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2016/208673Orig1_toc.cfm (Accessed November 10, 2018).
102. Rosenstock J, Handelsman Y, Vidal J, Ampudia Blasco FJ, Giorgino F, Liu M, et al. Propensity-score-matched comparative analyses of simultaneously administered fixed-ratio insulin glargine 100 U and lixisenatide (iGlarLixi) vs. sequential administration of insulin glargine and lixisenatide in uncontrolled type 2 diabetes. Diabetes Obes Metab. (2018) 20:2821–9. doi: 10.1111/dom.13462
103. Maiorino MI, Chiodini P, Bellastella G, Capuano A, Esposito K, Giugliano D. Insulin and glucagon-like peptide 1 receptor agonist combination therapy in type 2 diabetes: a systematic review and meta-analysis of randomized controlled trials. Diabetes Care (2017) 40:614–24. doi: 10.2337/dc16-1957
104. Maiorino MI, Chiodini P, Bellastella G, Scappaticcio L, Longo M, Esposito K, et al. Free and fixed-ratio combinations of basal insulin and GLP-1 receptor agonists versus basal insulin intensification in type 2 diabetes: a systematic review and meta-analysis of randomized controlled trials. Diabetes Obes Metab. (2018) 20:2309–13. doi: 10.1111/dom.13343
105. Esposito K, Chiodini P, Bellastella G, Maiorino MI, Giugliano D. Proportion of patients at HbA1c target < 7% with eight classes of antidiabetic drugs in type 2 diabetes: systematic review of 218 randomized controlled trials with 78 945 patients. Diabetes Obes Metab. (2012) 14:228–33. doi: 10.1111/j.1463-1326.2011.01512.x
106. Maiorino MI, Petrizzo M, Capuano A, Giugliano D, Esposito K. The development of new basal insulins: is there any clinical advantage with their use in type 2 diabetes? Expert Opin Biol Ther. (2014) 14:799–808. doi: 10.1517/14712598.2014.895812
107. Yale JF, Aroda VR, Charbonnel B, Sinclair AJ, Trescoli C, Cahn A, et al. Glycaemic control and hypoglycaemia risk with insulin glargine 300 U/mL versus glargine 100 U/mL: a patient-level meta-analysis examining older and younger adults with type 2 diabetes. Diabetes Metab. (2018) doi: 10.1016/j.diabet.2018.10.002. [Epub ahead of print].
108. Giugliano D, Chiodini P, Maiorino MI, Bellastella G, Esposito K. Intensification of insulin therapy with basal-bolus or premixed insulin regimens in type 2 diabetes: a systematic review and meta-analysis of randomized controlled trials. Endocrine (2016) 51:41–28. doi: 10.1007/s12020-015-0718-3
109. Paolisso G, Monami M, Marfella R, Rizzo MR, Mannucci E. Dipeptidyl peptidase-4 inhibitors in the elderly: more benefits or risks? Adv Ther. (2012) 29:218–33. doi: 10.1007/s12325-012-0008-x
Keywords: type 2 diabetes, elderly, diabetes-related comorbidities, glycemic targets, glucose lowering drugs
Citation: Longo M, Bellastella G, Maiorino MI, Meier JJ, Esposito K and Giugliano D (2019) Diabetes and Aging: From Treatment Goals to Pharmacologic Therapy. Front. Endocrinol. 10:45. doi: 10.3389/fendo.2019.00045
Received: 03 December 2018; Accepted: 21 January 2019;
Published: 18 February 2019.
Edited by:
Sandro La Vignera, Università Degli Studi di Catania, ItalyReviewed by:
Daniele Gianfrilli, Sapienza University of Rome, ItalyAldo Eugenio Calogero, Università Degli Studi di Catania, Italy
Copyright © 2019 Longo, Bellastella, Maiorino, Meier, Esposito and Giugliano. 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: Giuseppe Bellastella, Z2l1c2VwcGUuYmVsbGFzdGVsbGFAdW5pY2FtcGFuaWEuaXQ=