Dominic L. Sykes1*†
Alyn H. Morice2†- 1Hull University Teaching Hospitals NHS Trust, Hull, United Kingdom
- 2Hull York Medical School, University of York, York, United Kingdom
In clinical practice, we commonly face adversity when encountering dysfunction of the cough reflex. Similar to ancient Roman deity Janus, it often presents with one of two opposing “faces”. Continual aberrant activation of the cough reflex, also known as chronic cough, can cause great detriment to quality of life and many of these patients are left misdiagnosed and undertreated. In contrast, loss of normal functioning of the cough reflex is the cause of a significant proportion of mortality in the elderly, primarily through the development of aspiration pneumonia. In this review we discuss both hyper- and hypo-activation of the cough reflex and how airway reflux and chronic aspiration may be involved in the aetiology and sequalae of both disease states. We detail the physiological and pharmacological mechanisms involved in cough, and how the recent development of P2X3 receptor antagonists may lead to the first pharmaceutical agent licensed for chronic cough. The treatment and prevention of loss of the cough reflex, which has been largely neglected, is also discussed as novel low-cost interventions could help prevent a number of hospital and domiciliary deaths from both acute and chronic aspiration.
Introduction
The cough reflex is a vital defense mechanism that allows the body to expel inhaled foreign objects, potential pathogens, and endogenous secretions. Dysfunction of this reflex may be crudely dichotomized into hypo and hyper-activation. Impairment of the cough reflex is associated with aspiration and is a common mode of death in elderly, demented, and neurologically impaired patients. On the other hand, excessive chronic cough causes a major decrement in quality of life and is responsible for a large proportion of health care visits.
Chronic Cough (CC) remains one of the most frequent and onerous causes of patient morbidity encountered in healthcare and is estimated to burden 9–12% of the population (Morice, 2008; Song et al., 2015). A more worrying statistic is that despite multiple visits to healthcare professionals, only half of patients receive a diagnosis to explain their debilitating symptoms (Chamberlain et al., 2015). Several drugs demonstrate significant antitussive effect for CC such as low-dose morphine sulfate (Morice et al., 2007) and gabapentin (Ryan et al., 2012), however, many patients do not benefit from such interventions, and these centrally acting drugs have large side-effect profiles. A characteristic symptom complex, consisting of hypersensitivity to external stimuli, has been detailed recently with the new paradigm of Cough Hypersensitivity Syndrome (CHS) (Morice, 2010). In this review, we aim to analyze the current evidence for the proposed mechanisms which attempt to explain the etiology of CHS. We attempt to convey the novel paradigm of airway reflux and how it should be differentiated from traditional gastro-esophageal reflux as the culprit of cough hypersensitivity through sensitization of vagal afferents.
We also explore the second “face” of cough reflex dysfunction by detailing the sequalae of cough “hypo-sensitivity.” The harmful effects of aspiration secondary to dysfunction of the cough reflex will be examined, specifically chronic aspiration and how loss of the neural mechanisms underpinning the cough reflex is the culprit of much morbidity in the elderly.
Chronic Cough: Establishing an Accurate Definition
Chronic cough has been defined by both the European Respiratory Society (ERS) and the American College of Chest Physicians (ACCP) as a persistent daily cough for > 8 weeks which should be based on a global clinical assessment of the patient’s symptoms and how they may relate to the many phenotypes of CC (Irwin et al., 2006; Morice et al., 2020). For the purposes of drug trials, patients with chronic cough have been stratified into one of two categories: Unexplained Chronic Cough (UCC), usually defined as cough with no obvious cause for > 1 years duration, and Refractory Chronic Cough (RCC), that being an unexplained chronic cough that persists despite rigorous investigation and treatment in accordance with best-practice guidelines (Gibson et al., 2016; Dicpinigaitis, 2020). We suggest that these definitions may be further simplified, with RCC being the failure of the treatment to improve a patient’s cough and UCC being the failure of the physician to identify the cause of the patient’s cough. These definitions have been shown to have little utility in the differentiation of patients with CC, as conveyed in COUGH-1 and COUGH-2 trials, where both UCC and RCC displayed similar symptom profiles (Morice et al., 2021). For the purposes of simplicity in this review, we will use the definition of CC as defined by the ERS and ACCP.
Acid Reflux and Cough
Gastro-esophageal reflux disease (GORD/GERD) is caused by the retrograde transit of gastric contents into the esophagus causing esophagitis, dyspeptic symptoms sufficient to impair quality of life, or risk of long-term complications (Moayyedi and Talley, 2006). Historically it was believed that there was a causal relationship between GORD and chronic cough, with the acidic nature of the refluxate being directly responsible for the development of an continual cough (Fitzgerald et al., 1989; Irwin et al., 1989). One of the prominent theories linking GORD and chronic cough was that of proximal esophageal acidic reflux. However, previous work has shown no difference in the frequency of proximal reflux events, as measured by impedance, and pH of reflux between chronic cough patients and healthy controls (Decalmer et al., 2012).
There is evidence to suggest that cough may be directly initiated from esophageal irritation by acid and non-acid refluxate, which led to the concept of the “esophago-bronchial reflex” (Smith and Houghton, 2013). This concept is based on the theory that there may be crosstalk at the nucleus tractus solitarius (nTS) between the stimuli from esophageal and airway neurons converging in this area, which would allow reflux-mediated irritation of the esophagus to produce a “referred” initiation of the cough reflex. Numerous animal studies have evidenced this model (Canning and Mori, 2010; Chen et al., 2017, 2018, 2019). Other animal models show that mast cell activation may cause the esophagus to become more permeable to acid, increasing vagal nociceptive C-fiber activation which may lead to hypersensitivity and therefore esophageal dysfunction (Yu et al., 2014; Zhang et al., 2014). Clinical studies have corroborated the link between esophageal exposure to gastric acid and enhanced cough sensitivity using capsaicin challenge. One study demonstrated that HCl infusion into the esophagus of GORD patients increased capsaicin cough sensitivity when compared to healthy controls (Javorkova et al., 2008). A subsequent study demonstrated that patients with both non-acid and acid reflux, as measured by esophageal multi-channel intraluminal impedance combined with pH monitoring (MII-pH), had greater levels of capsaicin cough sensitivity when compared to healthy individuals (Qiu et al., 2011).
In more recent years the theory that GORD plays a pertinent role in the development of chronic cough has been contested, predominantly due to the failure of anti-acid therapy in the treatment of chronic cough (Chang et al., 2011; Kahrilas et al., 2013). An initial trial reported no difference in subjective cough counts between those with GORD and chronic cough who had their stomach pH neutralized secondary to anti-acid therapy and those whose pH remained acidic (Ours et al., 1999), suggesting that the acidic component of reflux has little effect on cough. A further randomized controlled trial showed no difference in cough questionnaire scores at 8 weeks between patients treated with proton pump inhibitors (PPI) and those who received a placebo (Faruqi et al., 2011). Researchers have attempted to establish the link between acid reflux and cough, however, the acidity of the refluxate may be less important in the etiology of cough. In this review we aim to assess the evidence for the distinct paradigm “airway reflux,” that is total reflux both acidic and non-acidic and both within the gastrointestinal tract and extra esophageal.
What Is Airway Reflux?
Airway reflux is a distinct phenomenon from GORD. As discussed previously, GORD is defined as abnormal reflux of gastric contents, mainly considered acidic liquid and when non-acidic it is termed “volume reflux.” In contrast, airway reflux is believed to be mainly composed of fluid, either gaseous “mist” or a liquid, which may be weakly or non-acidic. This refluxate ascends through a patent esophagus and is aspirated into the upper airways, damaging the epithelium (Morice, 2013).
Airway reflux occurs as an everyday phenomenon. We all “taste” our food post-prandially on occasion. In healthy individuals, impedance monitoring detected reflux events in all participants in a “normal” cohort (Zerbib et al., 2005). A normal level of reflux and aspiration may be managed by innate defenses such as coughing and ciliary removal, which may deteriorate with increasing age. The paradigm of airway reflux has been used as an elegant explanation for the development of chronic cough (Morice, 2013). The association between cough and reflux may be historically underestimated as the term reflux was tethered to the peptic diagnostic criteria of acidic GORD.
The development of the Hull Airway Reflux Questionnaire (HARQ) has provided a validated tool to assess the likelihood of the presence of airway reflux (Morice et al., 2011). The questions that are included in the HARQ are based on what are believed to be common sequalae of gaseous, non-acidic reflux from the gastrointestinal tract. Components of the HARQ were inspired by Belafsky et al. (2002) and their Reflux Symptom Index (RSI), a tool used in the diagnosis of laryngopharyngeal reflux (LPR) which has also been termed “silent reflux”. Both of these terms are synonymous with airway reflux, “silent” reflux, whilst appropriate for voice change is inappropriate for the patient with chronic cough! The phenomena listed in the questionnaire were derived from interviews with patients with chronic cough, and are inextricably linked to the opening of the lower esophageal sphincter (Mittal and Balaban, 1997). This allows the fluid refluxate to interact with the upper and lower airways. This tool has been demonstrated to be highly sensitive in identifying those with chronic cough compared to normal volunteers with a sensitivity of 94% and a specificity of 95% (Johansson and Ternesten-Hasseus, 2016). In the recent rigorously defined cohort of CC patients participating in COUGH-1 and COUGH-2 the HARQ identified 95% of these patients as being above the upper limit of normal (Morice et al., 2021), confirming the questionnaire’s utility in the diagnosis of this patient population.
The Esophagus and Cough
Reflux and aspiration are a complex phenomenon which is an indication of a disorder of the entire upper gastrointestinal tract. Esophageal dysmotility in patients with chronic cough has been displayed in multiple studies and is believed to be a major contributor to the pathophysiology of airway reflux. Patients with esophageal dysmotility fail to clear the residual bolus of swallowed material, giving rise to esophagopharyngeal reflux (Vardar et al., 2013; Almansa et al., 2015).
What Is Cough Hypersensitivity Syndrome?
Historically, clinicians would diagnose patients with chronic cough with one of three principle categories: reactive airways (usually eosinophilic bronchitis or cough-variant asthma); rhinosinusitis (post-nasal drip); and GORD (Gibson, 2004). The lack of success in targeted therapy to these conditions (McGarvey, 2005), as well as the fact that a considerable proportion of patients do not accord to any of these categories, necessitates a review this classification. As many patients complain of hypersensitivity to external stimuli, CHS has been suggested as an umbrella term to globally encompass CC (Morice et al., 2014; Song and Morice, 2017). The introduction of the CHS has enabled us to understand cough-related disease as a hypersensitivity syndrome akin to chronic pain. Clinically, the history that a patient with CHS conveys is usually directly correlated with normally innocuous stimuli. However, hypersensitivity to external stimuli is not a universal finding in patients with chronic cough and must be differentiated from isolated airway reflux due to upper gastrointestinal pathology.
A pathophysiological basis for CHS is thought to be sensitization of vagal afferents in the upper and lower airways. Chronic airway inflammation may precipitate this sensitization, shifting the tussigen-cough response curve to the left leading to increased cough sensitivity to normally anodyne stimuli (Chung et al., 2013). There is also compelling evidence of an etiological mechanism within the central nervous system, as demonstrated by functional magnetic resonance imaging (fMRI) studies. Functional brain imaging techniques have shown significantly higher neural activity in the midbrain in patients with cough hypersensitivity compared to controls when both groups of participants were exposed to capsaicin (Ando et al., 2016). Interestingly these areas of the midbrain (nucleus cuneiformis and periaqueductal gray) are also known to display increased neural activity in patients with chronic pain (Lau and Vaughan, 2014), suggesting there may be a common pathophysiology between the two syndromes. Further to this, higher centers in the brain have been implicated in the development of cough hypersensitivity, with these higher centers having a role in suppressing the cough reflex (Mazzone et al., 2011). The failure of these inhibitory pathways lead to an aberrant cough reflex. Imaging has unveiled that there is reduced neural activation in the dorsomedial prefrontal and anterior mid-cingulate cortices in patients with cough hypersensitivity. This has been interpreted as a reduced ability to inhibit the activation of the cough reflex (Ando et al., 2016). These proposed central mechanisms are supported by the efficacy of centrally acting medications such as gabapentin and morphine sulfate in patients with chronic cough. The evidence for vagal hypersensitivity will be the main etiological mechanism discussed in this review, as the burgeoning interest in peripheral channel antagonists is increasing supported by clinical trial evidence.
Vagal Afferents and the Cough Reflex
The cough reflex is primarily mediated by sensory nerves in the airways, which largely originate from the superior (jugular) and inferior (nodose) vagal ganglia (Canning et al., 2014). Of these vagal afferents Aδ fibers are responsible for the sensation of mechanical stimuli and rapid changes in pH, and are thought to be crucial to the immediate protection against acid or foreign body aspiration (Canning et al., 2006). It is currently believed that the afferent C fibers, which constitute the majority of vagal afferent fibers, are central to the development of cough hypersensitivity (Lee and Pisarri, 2001). In vitro studies have shown that these fibers are responsible for the mediation of the sensitization to endogenous inflammatory mediators (Grace et al., 2013). Despite these physiological principles, it must be recognized that our understanding of the wandering nerve in humans is far from complete. The exact neural composition of vagal afferents in the upper and lower airways requires further study (Mazzone and Undem, 2016). Nevertheless, vagal C fibers have attracted interest in the treatment of chronic cough, largely due their mechano-/thermo-/chemo-sensitive properties.
Molecular Pharmacology of Cough
TRPV1/TRPA1 Receptors
One of the most widely studied receptors expressed on vagal C-fibers is the Transient Receptor Potential Vanilloid 1 (TRPV1) channel, a ligand gated ion channel, which is known to react to irritants such as capsaicin in the upper airway to initiate the cough reflex (Jia and Lee, 2007). The TRPV1 channel has been shown to be upregulated in patients who develop chronic cough (Groneberg et al., 2004; Mitchell et al., 2005; Morice, 2010), although whether this is a primary or secondary phenomenon remains to be established. TRPV1 has also been shown to be sensitive to extracellular pH and H+ ions which stimulate the receptors directly, and increase sensitivity of the receptor to capsaicin (Caterina et al., 1997; Tominaga et al., 1998). This may explain the reduction in cough observed in those with severe acid reflux when treated with PPI. Transient Receptor Potential Cation Channel A1 (TRPA1), which has been shown to be co-expressed with TRPV1 (Story et al., 2003), was thought to be another vital contributor to the development of cough hypersensitivity. This receptor is expressed on 20–35% of all vagal neurons and be sensitive to a litany of compounds found in common foodstuffs including mustard oils, cinnamaldehyde, perfumes, smoke and allicin sulfides (Bandell et al., 2004; Jordt et al., 2004; Macpherson et al., 2005; Bessac and Jordt, 2008). For this reason it is believed that these TRPA1 receptors may play a greater role in cough secondary to the reflux of a gaseous mist containing food particles and products of digestion (Molyneux and Morice, 2011). Despite the promising research into both receptors, clinical trials have shown novel antagonists have no clinical benefit in patients with chronic cough (Belvisi et al., 2017; Morice, 2017). Although TRPV1 and TRPA1 play a large role in physiological irritant cough, they do not appear to be crucial in the development of pathological cough, suggesting multiple cough pathways in man. Only with the serendipitous finding that purinergic receptor blockade dramatically reduced chronic cough was a novel pathological pathway uncovered.
The Role of ATP and the P2X3 Receptor
ATP is ubiquitous in the human body and is most famous for its role as the currency of energy in cellular metabolism. It also has multiple extracellular effects which can cause inflammation. It is thought that ATP is able to reach extracellular targets following release from cells in response to damage from exogenous and endogenous stimuli (Burnstock et al., 2012; Ford and Undem, 2013). One study demonstrated the mechanism in which nutritional lipid is phagocytosed by alveolar macrophages to produce lipid-laden macrophages (LLM). These LLMs generate activated macrophages which interact with other components of the innate immune system to promote the release of Damage-associated Molecular Patterns (DAMPS), also known as alarmins, which in turn can engender airway inflammation (Hayman et al., 2017). Airway inflammation will then induce the release of cytoplasmic alarmins, including ATP, which will then bind to extracellular targets to further propagate inflammation (Yang et al., 2017). The most prominent extracellular target pertaining to chronic cough is the P2X purinoceptor 3 (P2X3), a ligand gated cation channel which has been demonstrated to be expressed on vagal afferents, most commonly on nodose (inferior ganglion) vagal neurons which project C-fibers in the lower airways. Purinoreceptors are less commonly expressed the jugular (superior ganglion) neurons that are responsible for the innervation of upper airway structures (Undem et al., 2004). In the search for a link between ATP and CC, one study has shown that patients with CC demonstrate a greater response to inhaled ATP at lower concentrations, when compared with healthy controls (Fowles et al., 2017). This finding suggests that cough maybe mediated through the activation of P2X3, which has since become the main target for pharmaceutical development.
TRPV4-ATP-P2X3 Signaling
Transient receptor potential cation channel subfamily vallinoid member 4 (TRPV4) has been recently implicated as a piece in the puzzle of ATP mediated cough. These receptors are activated by a vast array of stimuli including temperature, mechanical stress, and changes in pH (Nilius et al., 2004) and are extensively expressed in the airways where they may release ATP in response to hypo-osmotic stimuli (Jia et al., 2004). This ATP efflux, mediated largely by the large conductance ion pore pannexin 1 (Dahl, 2015), was then thought to directly activate the P2X3 receptors in the sensory neurons to initiate the cough reflex. Interestingly the activation of TRPV4 has been shown to cause prolonged stimulation of Aδ fibers and had no effect on the C fibers which, as discussed previously, are stimulated with activation of TRPV1 and TRPA1 channels (Bonvini et al., 2016). One study has demonstrated that antagonism of the P2X3 receptor significantly reduced cough in response to ATP and distilled water (a hypo-osmolar stimulus for TRPV4) whilst there was no effect on the response to capsaicin- citric acid-evoked cough (Morice et al., 2019). These findings again suggested that there are at least two distinct pathways responsible for generating the cough reflex, one irritant (TRPV1/TRPA1) and one pathological (P2X3). Unfortunately, investigation of a TRPV4 antagonist was stopped early due to a rise in cough counts when compared to placebo, suggesting other ATP release mechanisms may be important in CC (Ludbrook et al., 2019).
P2X3 Inhibitors—A New Frontier for the Treatment of Chronic Cough
In recent years novel P2X3 receptor antagonists have shown much promise as a therapeutic option for patients with chronic cough (Dicpinigaitis et al., 2020). Initial proof of concept studies showed a reduction in cough frequency with P2X3 inhibitors almost 10 years ago, with all patients reporting side effects of taste disturbance (hypogeusia or ageusia) (Abdulqawi et al., 2015). Since this study, further developments of this and other P2X3 inhibitors have shown a significant reduction in objective cough count at 12-week follow-up (Morice A. et al., 2020; Niimi et al., 2020; Smith et al., 2020). Phase 3 randomized controlled trials COUGH-1 and COUGH-2 (Muccino et al., 2020) have demonstrated an 18% reduction in cough at 12 weeks and a near 15% reduction at 24 weeks vs. placebo in those treated with gefapixant. Despite a large placebo effect observed in the control group (McGarvey et al., 2020), its efficacy was confirmed and it is likely that gefapixant and other P2X3 inhibitors will soon be made widely available for patients attending cough clinics.
Aspiration and Loss of the Cough Reflex in Respiratory Disease
Aspiration is defined as the misdirection of oropharyngeal or gastric contents into the lower respiratory tract (Marik and Kaplan, 2003). One of the most frequent and fatal manifestations of aspiration in humans is aspiration pneumonia, which has historically been attributed to the impairment of the swallowing reflex (dysphagia) causing macro-aspiration of food content and has been dubiously singularized in its definition as an acute, bacterial cause of pneumonia (Mandell and Niederman, 2019). The cough reflex, and its mechanism of protecting the airways, is completely ignored in this definition. Moreover, this definition is far too narrow and the sequalae of aspiration should be thought to include pneumonia, pneumonitis, and bronchitis. It is known that the appearance of consolidation of plain radiograph is indicative of pneumonia, whereas micro-aspiration may also lead to an “aspiration bronchitis” which, because we cannot visualize it on a radiograph, has been poorly studied. In clinical practice the term “aspiration pneumonia” is used as a blanket term for all of these conditions, and is almost always treated as a bacterial infection, when in a large proportion of cases there is likely no bacterial pathogen, but rather a chemical induced injury.
Nihei et al. provided theoretical evidence for an abacterial aspiration pneumonia, conveying that mice developed a chronic form of aspiration pneumonia, with similar histopathological findings to human lung tissue, after 28 days of chronic micro-aspiration devoid of micro-organisms (Nihei et al., 2015). This is mirrored in clinical practice where studies have shown that, in those diagnosed with aspiration pneumonia, sputum cultures seldom unveil a causative pathogen (Yamanda et al., 2010; Ebihara et al., 2011b). We suggest that the etiology of these pneumoniae may be due to the acute and/or chronic aspiration of gastro-esophageal contents into the airways. Furthermore, in studies which have elucidated bacterial pathogens, they are commonly bacteria from the Proteobacteria and Firmicutes phyla (El-Solh et al., 2003; Tokuyasu et al., 2009) and mainly of the Streptococci, Klebsiella, and Escherichia genera. This is strikingly similar to the dominant organisms of the gastric microbiome (Monstein et al., 2000; Bik et al., 2006; Andersson et al., 2008; Petra et al., 2017). This is suggestive of an intrinsic etiology in which many elderly patients aspirate refluxed contents from the gastrointestinal tract, leading to the development of aspiration pneumonia. This, however, is speculative, indeed there is still much we do not know about both the gut and lung microbiomes including how and to what extent they interact with each other in health and disease.
Satoru Ebihara and his colleagues have eloquently described a new paradigm, shifting away from the classical model of dysphagia as the solitary cause of aspiration pneumonia, instead suggesting that the keystone in the prevention of aspiration pneumonia is the cough reflex (Ebihara et al., 2016). They suggest that dysphagia and impairment of the cough reflex (referred to as “dystussia”) do not develop simultaneously in those at high risk of aspiration, such as those with dementia. Indeed, there is a time lag between the development of swallowing problems and the development of aspiration pneumonia which may be due to the fact the patient’s cough reflex deteriorates later in the progression of advanced dementia. Therefore patients are still able to expel any refluxed and/or aspirated material (Mitchell et al., 2009). Studies have demonstrated that the failure of the cough reflex, as measured by the reduction in the perception of the urge-to-cough, is strongly associated with aspiration pneumonia (Sekizawa et al., 1990; Yamanda et al., 2008). The effect of neurodegeneration of the higher centers controlling the urge-to-cough motivation system (Davenport, P. W., 2009) secondary to dementia may lead to dysfunction of the cough reflex and the consequent increased risk of aspiration.
Interestingly, it has been shown that this dysfunction is caused by the degradation of the sensory rather than the motor pathways of the cough reflex, which is associated with aging (Ebihara et al., 2011a; Malandraki et al., 2011). This has led to the development of novel techniques to protect against this apparent “cough hypo-sensitivity” in the elderly. ACE inhibitors (ACEi) are well known to increase cough sensitivity (Morice et al., 1987; Shim et al., 2020), and have demonstrated some efficacy in reducing the incidence of pneumonia in both the elderly and stroke patients (Okaishi et al., 1999; Caldeira et al., 2012). Rigorous inpatient oral care, including regular teeth and oral cavity cleaning after meals by nursing staff, may help reduce the incidence of aspiration pneumonia in elderly patients (van der Maarel-Wierink et al., 2013). Increasing cough sensitivity through capsaicin-mediated activation of TRPV1 channels has been suggested as a potential protective strategy, with data suggesting improved cough reflex, as well as improved esophageal motility in patients receiving capsaicin supplementation (Ebihara et al., 2005; Nakato et al., 2017). We suggest that we should integrate these strategies into clinical practice, as they are low-cost interventions that may well save the lives of those whose cough reflex has diminished as a result of their senescence.
Cough in the elderly has been accurately described as a double-sided conundrum (Won et al., 2018) and should be addressed at both ends of the spectrum with improved regulation of the cough reflex in order to prevent morbidity associated with hyper- and hyposensitivity.
Conclusion
In this review, we have attempted to unmask both faces of the cough reflex in respiratory disease. We have used aspiration pneumonia as an obvious example of the damage caused by airway reflux and aspiration when the cough reflex has been impaired, however, there is evidence to suggest this mechanism could precipitate a plethora of respiratory disease (Morice and Dettmar(eds)., 2018). We have also presented the evidence for airway reflux as a common culprit of the development of CC and we have recounted recent development of P2X3R antagonists, such as gefapixant, which may well become the first drug to ever be licensed for the treatment of CC. Despite these developments, more research is required to reduce both morbidity and mortality associated with the two faces of the cough reflex.
Author Contributions
Both authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
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.
References
Abdulqawi, R., Dockry, R., Holt, K., Layton, G., McCarthy, B. G., Ford, A. P., et al. (2015). P2X3 receptor antagonist (AF-219) in refractory chronic cough: a randomised, double-blind, placebo-controlled phase 2 study. Lancet 385, 1198–1205. doi: 10.1016/s0140-6736(14)61255-1
Almansa, C., Smith, J. A., Morris, J., Crowell, M. D., Valdramidou, D., Lee, A. S., et al. (2015). Weak peristalsis with large breaks in chronic cough: association with poor esophageal clearance. Neurogastroenterol. Motil. 27, 431–442. doi: 10.1111/nmo.12513
Andersson, A. F., Lindberg, M., Jakobsson, H., Backhed, F., Nyren, P., and Engstrand, L. (2008). Comparative analysis of human gut microbiota by barcoded pyrosequencing. PLoS One 3:e2836. doi: 10.1371/journal.pone.0002836
Ando, A., Smallwood, D., McMahon, M., Irving, L., Mazzone, S. B., and Farrell, M. J. (2016). Neural correlates of cough hypersensitivity in humans: evidence for central sensitisation and dysfunctional inhibitory control. Thorax 71, 323–329. doi: 10.1136/thoraxjnl-2015-207425
Bandell, M., Story, G. M., Hwang, S. W., Viswanath, V., Eid, S. R., Petrus, M. J., et al. (2004). Noxious cold ion channel TRPA1 is activated by pungent compounds and bradykinin. Neuron 41, 849–857. doi: 10.1016/s0896-6273(04)00150-3
Belafsky, P. C., Postma, G. N., and Koufman, J. A. (2002). Validity and reliability of the reflux symptom index (RSI). J. Voice 16, 274–277. doi: 10.1016/s0892-1997(02)00097-8
Belvisi, M. G., Birrell, M. A., Wortley, M. A., Maher, S. A., Satia, I., Badri, H., et al. (2017). XEN-D0501, a Novel Transient Receptor Potential Vanilloid 1 Antagonist, Does Not Reduce Cough in Patients with Refractory Cough. Am. J. Respir. Crit. Care Med. 196, 1255–1263. doi: 10.1164/rccm.201704-0769oc
Bessac, B. F., and Jordt, S. E. (2008). Breathtaking TRP channels: TRPA1 and TRPV1 in airway chemosensation and reflex control. Physiology 23, 360–370. doi: 10.1152/physiol.00026.2008
Bik, E. M., Eckburg, P. B., Gill, S. R., Nelson, K. E., Purdom, E. A., Francois, F., et al. (2006). Molecular analysis of the bacterial microbiota in the human stomach. Proc. Natl. Acad. Sci. U. S. A. 103, 732–737. doi: 10.1073/pnas.0506655103
Bonvini, S. J., Birrell, M. A., Grace, M. S., Maher, S. A., Adcock, J. J., Wortley, M. A., et al. (2016). Transient receptor potential cation channel, subfamily V, member 4 and airway sensory afferent activation: role of adenosine triphosphate. J. Allergy Clin. Immunol. 138:e12.
Burnstock, G., Brouns, I., Adriaensen, D., and Timmermans, J. P. (2012). Purinergic signaling in the airways. Pharmacol. Rev. 64, 834–868. doi: 10.1124/pr.111.005389
Caldeira, D., Alarcao, J., Vaz-Carneiro, A., and Costa, J. (2012). Risk of pneumonia associated with use of angiotensin converting enzyme inhibitors and angiotensin receptor blockers: systematic review and meta-analysis. BMJ 345:e4260. doi: 10.1136/bmj.e4260
Canning, B. J., Chang, A. B., Bolser, D. C., Smith, J. A., Mazzone, S. B., McGarvey, L., et al. (2014). Anatomy and neurophysiology of cough: CHEST Guideline and Expert Panel report. Chest 146, 1633–1648.
Canning, B. J., and Mori, N. (2010). An essential component to brainstem cough gating identified in anesthetized guinea pigs. FASEB J. 24, 3916–3926. doi: 10.1096/fj.09-151068
Canning, B. J., Mori, N., and Mazzone, S. B. (2006). Vagal afferent nerves regulating the cough reflex. Respir. Physiol. Neurobiol. 152, 223–242. doi: 10.1016/j.resp.2006.03.001
Caterina, M. J., Schumacher, M. A., Tominaga, M., Rosen, T. A., Levine, J. D., and Julius, D. (1997). The capsaicin receptor: a heat-activated ion channel in the pain pathway. Nature 389, 816–824. doi: 10.1038/39807
Chamberlain, S. A., Garrod, R., Douiri, A., Masefield, S., Powell, P., Bucher, C., et al. (2015). The impact of chronic cough: a cross-sectional European survey. Lung 193, 401–408. doi: 10.1007/s00408-015-9701-2
Chang, A. B., Lasserson, T. J., Gaffney, J., Connor, F. L., and Garske, L. A. (2011). Gastro-oesophageal reflux treatment for prolonged non-specific cough in children and adults. Cochrane Database Syst. Rev. 2011:CD004823.
Chen, Z., Chen, H., Chen, F., Gu, D., Sun, L., Zhang, W., et al. (2017). Vagotomy decreases the neuronal activities of medulla oblongata and alleviates neurogenic inflammation of airways induced by repeated intra-esophageal instillation of HCl in guinea pigs. Physiol. Res. 66, 1021–1028. doi: 10.33549/physiolres.933574
Chen, Z., Gu, D., Fan, L., Zhang, W., Sun, L., Chen, H., et al. (2019). Neuronal activity of the medulla oblongata revealed by manganese-enhanced magnetic resonance imaging in a rat model of gastroesophageal reflux-related cough. Physiol. Res. 68, 119–127. doi: 10.33549/physiolres.933791
Chen, Z., Sun, L., Chen, H., Gu, D., Zhang, W., Yang, Z., et al. (2018). Dorsal Vagal Complex Modulates Neurogenic Airway Inflammation in a Guinea Pig Model With Esophageal Perfusion of HCl. Front. Physiol. 9:536. doi: 10.3389/fphys.2018.00536
Chung, K. F., McGarvey, L., and Mazzone, S. B. (2013). Chronic cough as a neuropathic disorder. Lancet Respir. Med. 1, 414–422. doi: 10.1016/s2213-2600(13)70043-2
Dahl, G. (2015). ATP release through pannexon channels. Philos. Trans. R. Soc. Lond. B Biol. Sci. 370:20140191.
Davenport, P. W. (2009). Clinical cough I: the urge-to-cough: a respiratory sensation. Handb. Exp. Pharmacol. 187, 263–276. doi: 10.1098/rstb.2014.0191
Decalmer, S., Stovold, R., Houghton, L. A., Pearson, J., Ward, C., Kelsall, A., et al. (2012). Chronic cough: relationship between microaspiration, gastroesophageal reflux, and cough frequency. Chest 142, 958–964.
Dicpinigaitis, P. (2020). Understanding the foundations of chronic cough. Am. J. Manag. Care 26, S232–S238.
Dicpinigaitis, P. V., McGarvey, L. P., and Canning, B. J. (2020). P2X3-Receptor Antagonists as Potential Antitussives: summary of Current Clinical Trials in Chronic Cough. Lung 198, 609–616. doi: 10.1007/s00408-020-00377-8
Ebihara, S., Ebihara, T., Kanezaki, M., Gui, P., Yamasaki, M., Arai, H., et al. (2011a). Aging deteriorated perception of urge-to-cough without changing cough reflex threshold to citric acid in female never-smokers. Cough 7:3. doi: 10.1186/1745-9974-7-3
Ebihara, S., Kohzuki, M., Sumi, Y., and Ebihara, T. (2011b). Sensory Stimulation to Improve Swallowing Reflex and Prevent Aspiration Pneumonia in Elderly Dysphagic People. J. Pharmacol. Sci. 115, 99–104. doi: 10.1254/jphs.10r05cp
Ebihara, S., Sekiya, H., Miyagi, M., Ebihara, T., and Okazaki, T. (2016). Dysphagia, dystussia, and aspiration pneumonia in elderly people. J. Thorac. Dis. 8, 632–639. doi: 10.21037/jtd.2016.02.60
Ebihara, T., Takahashi, H., Ebihara, S., Okazaki, T., Sasaki, T., Watando, A., et al. (2005). Capsaicin troche for swallowing dysfunction in older people. J. Am. Geriatr. Soc. 53, 824–828. doi: 10.1111/j.1532-5415.2005.53261.x
El-Solh, A. A., Pietrantoni, C., Bhat, A., Aquilina, A. T., Okada, M., Grover, V., et al. (2003). Microbiology of severe aspiration pneumonia in institutionalized elderly. Am. J. Respir. Crit. Care Med. 167, 1650–1654. doi: 10.1164/rccm.200212-1543oc
Faruqi, S., Molyneux, I. D., Fathi, H., Wright, C., Thompson, R., and Morice, A. H. (2011). Chronic cough and esomeprazole: a double-blind placebo-controlled parallel study. Respirology 16, 1150–1156. doi: 10.1111/j.1440-1843.2011.02014.x
Fitzgerald, J. M., Allen, C. J., Craven, M. A., and Newhouse, M. T. (1989). Chronic cough and gastroesophageal reflux. CMAJ 140, 520–524.
Ford, A. P., and Undem, B. J. (2013). The therapeutic promise of ATP antagonism at P2X3 receptors in respiratory and urological disorders. Front. Cell Neurosci. 7:267. doi: 10.3389/fncel.2013.00267
Fowles, H. E., Rowland, T., Wright, C., and Morice, A. (2017). Tussive challenge with ATP and AMP: does it reveal cough hypersensitivity? Eur. Respir. J. 49:1601452. doi: 10.1183/13993003.01452-2016
Gibson, P., Wang, G., McGarvey, L., Vertigan, A. E., Altman, K. W., Birring, S. S., et al. (2016). Treatment of Unexplained Chronic Cough: CHEST Guideline and Expert Panel Report. Chest 149, 27–44.
Grace, M. S., Dubuis, E., Birrell, M. A., and Belvisi, M. G. (2013). Pre-clinical studies in cough research: role of Transient Receptor Potential (TRP) channels. Pulm. Pharmacol. Ther. 26, 498–507. doi: 10.1016/j.pupt.2013.02.007
Groneberg, D. A., Niimi, A., Dinh, Q. T., Cosio, B., Hew, M., Fischer, A., et al. (2004). Increased expression of transient receptor potential vanilloid-1 in airway nerves of chronic cough. Am. J. Respir. Crit. Care Med. 170, 1276–1280. doi: 10.1164/rccm.200402-174oc
Hayman, Y. A., Sadofsky, L. R., Williamson, J. D., Hart, S. P., and Morice, A. H. (2017). The effects of exogenous lipid on THP-1 cells: an in vitro model of airway aspiration? ERJ Open Res. 3, 00026–2016. doi: 10.1183/23120541.00026-2016
Irwin, R. S., Baumann, M. H., Bolser, D. C., Boulet, L.-P., Braman, S. S., Brightling, C. E., et al. (2006). Diagnosis and management of cough executive summary: ACCP evidence-based clinical practice guidelines. Chest 129, 1S–23S.
Irwin, R. S., Zawacki, J. K., Curley, F. J., French, C. L., and Hoffman, P. J. (1989). Chronic cough as the sole presenting manifestation of gastroesophageal reflux. Am. Rev. Respir. Dis. 140, 1294–1300. doi: 10.1164/ajrccm/140.5.1294
Javorkova, N., Varechova, S., Pecova, R., Tatar, M., Balaz, D., Demeter, M., et al. (2008). Acidification of the oesophagus acutely increases the cough sensitivity in patients with gastro-oesophageal reflux and chronic cough. Neurogastroenterol. Motil. 20, 119–124.
Jia, Y., and Lee, L. Y. (2007). Role of TRPV receptors in respiratory diseases. Biochim. Biophys. Acta 1772, 915–927. doi: 10.1016/j.bbadis.2007.01.013
Jia, Y., Wang, X., Varty, L., Rizzo, C. A., Yang, R., Correll, C. C., et al. (2004). Functional TRPV4 channels are expressed in human airway smooth muscle cells. Am. J. Physiol. Lung Cell Mol. Physiol. 287, L272–L278.
Johansson, E. L., and Ternesten-Hasseus, E. (2016). Reliability and Validity of the Swedish Version of the Hull Airway Reflux Questionnaire (HARQ-S). Lung 194, 997–1005. doi: 10.1007/s00408-016-9937-5
Jordt, S. E., Bautista, D. M., Chuang, H. H., McKemy, D. D., Zygmunt, P. M., Hogestatt, E. D., et al. (2004). Mustard oils and cannabinoids excite sensory nerve fibres through the TRP channel ANKTM1. Nature 427, 260–265. doi: 10.1038/nature02282
Kahrilas, P. J., Howden, C. W., Hughes, N., and Molloy-Bland, M. (2013). Response of chronic cough to acid-suppressive therapy in patients with gastroesophageal reflux disease. Chest 143, 605–612. doi: 10.1378/chest.12-1788
Lau, B. K., and Vaughan, C. W. (2014). Descending modulation of pain: the GABA disinhibition hypothesis of analgesia. Curr. Opin. Neurobiol. 29, 159–164. doi: 10.1016/j.conb.2014.07.010
Lee, L. Y., and Pisarri, T. E. (2001). Afferent properties and reflex functions of bronchopulmonary C-fibers. Respir. Physiol. 125, 47–65.
Ludbrook, V., Hanrott, K., Marks-Konczalik, J., Kreindler, J., Bird, N., Hewens, D., et al. (2019). S27 A placebo-controlled, double-blind, randomised, crossover study to assess the efficacy, safety and tolerability of TRPV4 inhibitor GSK2798745 in participants with chronic cough. Thorax 74:A18.
Macpherson, L. J., Geierstanger, B. H., Viswanath, V., Bandell, M., Eid, S. R., Hwang, S., et al. (2005). The pungency of garlic: activation of TRPA1 and TRPV1 in response to allicin. Curr. Biol. 15, 929–934. doi: 10.1016/j.cub.2005.04.018
Malandraki, G. A., Perlman, A. L., Karampinos, D. C., and Sutton, B. P. (2011). Reduced somatosensory activations in swallowing with age. Hum. Brain Mapp. 32, 730–743. doi: 10.1002/hbm.21062
Marik, P. E., and Kaplan, D. (2003). Aspiration pneumonia and dysphagia in the elderly. Chest 124, 328–336. doi: 10.1378/chest.124.1.328
Mazzone, S. B., Cole, L. J., Ando, A., Egan, G. F., and Farrell, M. J. (2011). Investigation of the neural control of cough and cough suppression in humans using functional brain imaging. J. Neurosci. 31, 2948–2958. doi: 10.1523/jneurosci.4597-10.2011
Mazzone, S. B., and Undem, B. J. (2016). Vagal afferent innervation of the airways in health and disease. Physiol. Rev. 96, 975–1024. doi: 10.1152/physrev.00039.2015
McGarvey, L., Birring, S., Morice, A., Dicpinigaitis, P., Pavord, I., Schelfhout, J., et al. (2020). Late Breaking Abstract-Two Phase 3 Randomized Clinical Trials of Gefapixant, a P2X3 Receptor Antagonist, in Refractory or Unexplained Chronic Cough (COUGH-1 and COUGH-2). Eur. Respir. Soc. 56:3800.
McGarvey, L. P. (2005). Idiopathic chronic cough: a real disease or a failure of diagnosis? Cough 1:9.
Mitchell, J. E., Campbell, A. P., New, N. E., Sadofsky, L. R., Kastelik, J. A., Mulrennan, S. A., et al. (2005). Expression and characterization of the intracellular vanilloid receptor (TRPV1) in bronchi from patients with chronic cough. Exp. Lung Res. 31, 295–306. doi: 10.1080/01902140590918803
Mitchell, S. L., Teno, J. M., Kiely, D. K., Shaffer, M. L., Jones, R. N., Prigerson, H. G., et al. (2009). The clinical course of advanced dementia. N. Engl. J. Med. 361, 1529–1538.
Mittal, R. K., and Balaban, D. H. (1997). The esophagogastric junction. N. Engl. J. Med. 336, 924–932.
Molyneux, I. D., and Morice, A. H. (2011). Airway reflux, cough and respiratory disease. Ther. Adv. Chronic Dis. 2, 237–248. doi: 10.1177/2040622311406464
Monstein, H. J., Tiveljung, A., Kraft, C. H., Borch, K., and Jonasson, J. (2000). Profiling of bacterial flora in gastric biopsies from patients with Helicobacter pylori-associated gastritis and histologically normal control individuals by temperature gradient gel electrophoresis and 16S rDNA sequence analysis. J. Med. Microbiol. 49, 817–822. doi: 10.1099/0022-1317-49-9-817
Morice, A. (2008). Chronic cough: epidemiology. Chron. Respir. Dis. 5, 43–47. doi: 10.1177/1479972307084252
Morice, A., Birring, S., Dicpinigaitis, P., McGarvey, L., Pavord, I., Smith, J., et al. (2021). Cough Triggers and Symptoms Among Patients with Refractory or Unexplained Chronic Cough in Two Phase 3 Trials of the P2X3 Receptor Antagonist Gefapixant (COUGH-1 and COUGH-2). J. Allergy Clin. Immunol. 147:AB61.
Morice, A., Smith, J., McGarvey, L., Birring, S., Parker, S., Turner, A., et al. (2020). “Safety and efficacy of BAY 1817080, a P2X3 receptor antagonist, in patients with refractory chronic cough (RCC)”. D93 EVALUATION AND NOVEL TREATMENT APPROACH FOR CHRONIC COUGH: American Thoracic Society 2020 International Conference, (New York: American Thoracic Society), A7648.
Morice, A. H. (2010). The cough hypersensitivity syndrome: a novel paradigm for understanding cough. Lung 188, S87–S90.
Morice, A. H. (2013). Airway Reflux as a cause of respiratory disease. Breathe 9, 256–266. doi: 10.1183/20734735.000513
Morice, A. H. (2017). TRPA1 receptors in chronic cough. Pulm. Pharmacol. Ther. 47, 42–44. doi: 10.1016/j.pupt.2017.05.004
Morice, A. H., Faruqi, S., Wright, C. E., Thompson, R., and Bland, J. M. (2011). Cough hypersensitivity syndrome: a distinct clinical entity. Lung 189, 73–79. doi: 10.1007/s00408-010-9272-1
Morice, A. H., Kitt, M. M., Ford, A. P., Tershakovec, A. M., Wu, W. C., Brindle, K., et al. (2019). The effect of gefapixant, a P2X3 antagonist, on cough reflex sensitivity: a randomised placebo-controlled study. Eur. Respir. J. 54:1900439. doi: 10.1183/13993003.00439-2019
Morice, A. H., Lowry, R., Brown, M. J., and Higenbottam, T. (1987). Angiotensin-converting enzyme and the cough reflex. Lancet 2, 1116–1118. doi: 10.1016/s0140-6736(87)91547-9
Morice, A. H., Menon, M. S., Mulrennan, S. A., Everett, C. F., Wright, C., Jackson, J., et al. (2007). Opiate therapy in chronic cough. Am. J. Respir. Crit. Care Med. 175, 312–315.
Morice, A. H., Millqvist, E., Belvisi, M. G., Bieksiene, K., Birring, S. S., Chung, K. F., et al. (2014). Expert opinion on the cough hypersensitivity syndrome in respiratory medicine. Eur. Respir. J. 44, 1132–1148. doi: 10.1183/09031936.00218613
Morice, A. H., Millqvist, E., Bieksiene, K., Birring, S. S., Dicpinigaitis, P., Domingo Ribas, C., et al. (2020). ERS guidelines on the diagnosis and treatment of chronic cough in adults and children. Eur. Respir. J. 55:1901136.
Muccino, D. R., Morice, A. H., Birring, S. S., Dicpinigaitis, P. V., Pavord, I. D., Assaid, C., et al. (2020). Design and rationale of two phase 3 randomised controlled trials (COUGH-1 and COUGH-2) of gefapixant, a P2X3 receptor antagonist, in refractory or unexplained chronic cough. ERJ Open Res. 6, 00284–2020. doi: 10.1183/23120541.00284-2020
Nakato, R., Manabe, N., Shimizu, S., Hanayama, K., Shiotani, A., Hata, J., et al. (2017). Effects of Capsaicin on Older Patients with Oropharyngeal Dysphagia: a Double-Blind, Placebo-Controlled, Crossover Study. Digestion 95, 210–220. doi: 10.1159/000463382
Nihei, M., Okazaki, T., Ebihara, S., Kobayashi, M., Niu, K., Gui, P., et al. (2015). Chronic inflammation, lymphangiogenesis, and effect of an anti-VEGFR therapy in a mouse model and in human patients with aspiration pneumonia. J. Pathol. 235, 632–645. doi: 10.1002/path.4473
Niimi, A., Ishihara, H., Hida, H., and Miyazaki, S. (2020). “Phase 2a randomized, double-blind, placebo-controlled, crossover study of a P2X3 receptor antagonist S-600918: effects on health-related quality of life in patients with refractory chronic cough”. D93 EVALUATION AND NOVEL TREATMENT APPROACH FOR CHRONIC COUGH: American Thoracic Society2020 International Conference (New York: American Thoracic Society), A7647.
Nilius, B., Vriens, J., Prenen, J., Droogmans, G., and Voets, T. (2004). TRPV4 calcium entry channel: a paradigm for gating diversity. Am. J. Physiol. Cell Physiol. 286, C195–C205.
Okaishi, K., Morimoto, S., Fukuo, K., Niinobu, T., Hata, S., Onishi, T., et al. (1999). Reduction of risk of pneumonia associated with use of angiotensin I converting enzyme inhibitors in elderly inpatients. Am. J. Hypertens. 12, 778–783. doi: 10.1016/s0895-7061(99)00035-7
Ours, T. M., Kavuru, M. S., Schilz, R. J., and Richter, J. E. (1999). A prospective evaluation of esophageal testing and a double-blind, randomized study of omeprazole in a diagnostic and therapeutic algorithm for chronic cough. Am. J. Gastroenterol. 94, 3131–3138. doi: 10.1111/j.1572-0241.1999.01504.x
Petra, C. V., Rus, A., and Dumitrascu, D. L. (2017). Gastric microbiota: tracing the culprit. Clujul Med. 90, 369–376. doi: 10.15386/cjmed-854
Qiu, Z., Yu, L., Xu, S., Liu, B., Zhao, T., Lu, H., et al. (2011). Cough reflex sensitivity and airway inflammation in patients with chronic cough due to non-acid gastro-oesophageal reflux. Respirology 16, 645–652. doi: 10.1111/j.1440-1843.2011.01952.x
Ryan, N. M., Birring, S. S., and Gibson, P. G. (2012). Gabapentin for refractory chronic cough: a randomised, double-blind, placebo-controlled trial. Lancet 380, 1583–1589. doi: 10.1016/s0140-6736(12)60776-4
Sekizawa, K., Ujiie, Y., Itabashi, S., Sasaki, H., and Takishima, T. (1990). Lack of cough reflex in aspiration pneumonia. Lancet 335, 1228–1229. doi: 10.1016/0140-6736(90)92758-a
Smith, J. A., and Houghton, L. A. (2013). The oesophagus and cough: laryngo-pharyngeal reflux, microaspiration and vagal reflexes. Cough 9:12.
Smith, J. A., Kitt, M. M., Morice, A. H., Birring, S. S., McGarvey, L. P., Sher, M. R., et al. (2020). Gefapixant, a P2X3 receptor antagonist, for the treatment of refractory or unexplained chronic cough: a randomised, double-blind, controlled, parallel-group, phase 2b trial. Lancet Respir. Med. 8, 775–785.
Song, W. J., Chang, Y. S., Faruqi, S., Kim, J. Y., Kang, M. G., Kim, S., et al. (2015). The global epidemiology of chronic cough in adults: a systematic review and meta-analysis. Eur. Respir. J. 45, 1479–1481. doi: 10.1183/09031936.00218714
Song, W. J., and Morice, A. H. (2017). Cough Hypersensitivity Syndrome: a Few More Steps Forward. Allergy Asthma Immunol. Res. 9, 394–402. doi: 10.4168/aair.2017.9.5.394
Story, G. M., Peier, A. M., Reeve, A. J., Eid, S. R., Mosbacher, J., Hricik, T. R., et al. (2003). ANKTM1, a TRP-like channel expressed in nociceptive neurons, is activated by cold temperatures. Cell 112, 819–829. doi: 10.1016/s0092-8674(03)00158-2
Tokuyasu, H., Harada, T., Watanabe, E., Okazaki, R., Touge, H., Kawasaki, Y., et al. (2009). Effectiveness of meropenem for the treatment of aspiration pneumonia in elderly patients. Intern. Med. 48, 129–135. doi: 10.2169/internalmedicine.48.1308
Tominaga, M., Caterina, M. J., Malmberg, A. B., Rosen, T. A., Gilbert, H., Skinner, K., et al. (1998). The cloned capsaicin receptor integrates multiple pain-producing stimuli. Neuron 21, 531–543. doi: 10.1016/s0896-6273(00)80564-4
Undem, B. J., Chuaychoo, B., Lee, M. G., Weinreich, D., Myers, A. C., and Kollarik, M. (2004). Subtypes of vagal afferent C-fibres in guinea-pig lungs. J. Physiol. 556, 905–917. doi: 10.1113/jphysiol.2003.060079
van der Maarel-Wierink, C. D., Vanobbergen, J. N., Bronkhorst, E. M., Schols, J. M., and de Baat, C. (2013). Oral health care and aspiration pneumonia in frail older people: a systematic literature review. Gerodontology 30, 3–9. doi: 10.1111/j.1741-2358.2012.00637.x
Vardar, R., Sweis, R., Anggiansah, A., Wong, T., and Fox, M. R. (2013). Upper esophageal sphincter and esophageal motility in patients with chronic cough and reflux: assessment by high-resolution manometry. Dis. Esophagus. 26, 219–225. doi: 10.1111/j.1442-2050.2012.01354.x
Won, H. K., Yoon, S. J., and Song, W. J. (2018). The double-sidedness of cough in the elderly. Respir. Physiol. Neurobiol. 257, 65–69. doi: 10.1016/j.resp.2018.01.009
Yamanda, S., Ebihara, S., Ebihara, T., Yamasaki, M., Arai, H., and Kohzuki, M. (2010). Bacteriology of aspiration pneumonia due to delayed triggering of the swallowing reflex in elderly patients. J. Hosp. Infect. 74, 399–401. doi: 10.1016/j.jhin.2009.08.011
Yamanda, S., Ebihara, S., Ebihara, T., Yamasaki, M., Asamura, T., Asada, M., et al. (2008). Impaired urge-to-cough in elderly patients with aspiration pneumonia. Cough 4:11. doi: 10.1186/1745-9974-4-11
Yu, X., Hu, Y., and Yu, S. (2014). Effects of acid on vagal nociceptive afferent subtypes in guinea pig esophagus. Am. J. Physiol. Gastrointest. Liver Physiol. 307, G471–G478.
Zerbib, F., des Varannes, S. B., Roman, S., Pouderoux, P., Artigue, F., Chaput, U., et al. (2005). Normal values and day-to-day variability of 24-h ambulatory oesophageal impedance-pH monitoring in a Belgian-French cohort of healthy subjects. Aliment. Pharmacol. Ther. 22, 1011–1021. doi: 10.1111/j.1365-2036.2005.02677.x
Keywords: cough, chronic cough, aspiration [MeSH], airway reflux, reflux
Citation: Sykes DL and Morice AH (2021) The Cough Reflex: The Janus of Respiratory Medicine. Front. Physiol. 12:684080. doi: 10.3389/fphys.2021.684080
Received: 22 March 2021; Accepted: 09 June 2021;
Published: 29 June 2021.
Edited by:
Stuart Mazzone, The University of Melbourne, AustraliaReviewed by:
Peter V. Dicpinigaitis, Montefiore Medical Center, United StatesGiovanni Augusto Fontana, University of Florence, Italy
Mariana Brozmanova, Comenius University, Slovakia
Copyright © 2021 Sykes and Morice. 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: Dominic L. Sykes, ZG9taW5pYy5zeWtlc0BoZXkubmhzLnVr
†These authors have contributed equally to this work