Abstract
In all fields of medicine, major efforts are currently dedicated to improve the clinical, physiological and therapeutic understanding of disease, and obstructive sleep apnoea (OSA) is no exception. The personalised medicine approach is relevant for OSA, given its complex pathophysiology and variable clinical presentation, the interactions with comorbid conditions and its possible contribution to poor outcomes. Treatment with continuous positive airway pressure (CPAP) is effective, but CPAP is poorly tolerated or not accepted in a considerable proportion of OSA patients. This review summarises the available studies on the physiological phenotypes of upper airway response to obstruction during sleep, and the clinical presentations of OSA (phenotypes and clusters) with a special focus on our changing attitudes towards approaches to treatment. Such major efforts are likely to change and expand treatment options for OSA beyond the most common current choices (i.e. CPAP, mandibular advancement devices, positional treatment, lifestyle changes or upper airway surgery). More importantly, treatment for OSA may become more effective, being tailored to each patient's need.
Abstract
Physiological and clinical phenotyping of OSA patients will improve the management of the disease http://ow.ly/qSxq30f9Hp8
Introduction
The concept of personalised medicine has gained popularity among respiratory clinicians in recent years. The identification of phenotypes of asthma [1, 2] or chronic obstructive pulmonary disease (COPD) [3–5] has boosted a major change in the way we diagnose and treat these diseases and has widened our perspective for new treatments. In patients with lung cancer, innovative treatments have been developed towards specific molecular targets, with increased efficacy and improved outcomes compared to traditional chemotherapy [6, 7].
Obstructive sleep apnoea (OSA) is a highly prevalent disease, and its pathophysiology continues to be a major challenge for both basic researchers and clinicians. Some years ago, phenotyping of OSA patients was mostly perceived as an essential step to dissect the genetic background of the disease. More recently, availability of “big data” for OSA [8, 9] and sophisticated analysis techniques have considerably expanded the possibility of gaining insight into the variability of physiological traits, clinical presentations and biomarkers, with the potential application of results in clinical practice. Over the years, we have learned about the potential effects of OSA in increased cardiovascular morbidity and mortality [10], cognitive dysfunction [11] and traffic accidents [12], and its association with major diseases such as hypertension [13], diabetes [14] and cancer [15] and the relevant effects of chronic intermittent hypoxia in visceral fat [16, 17]. However, if personalised medicine has to be implemented in basic and clinical research on OSA, we are still in a very initial phase of such development, since some pieces of the puzzle have been identified, but their application in clinical practice remains limited or absent.
As highlighted in a recent review [18], there are many levels that have to be considered in dissecting the steps leading to the different phenotypes of OSA before a personalised clinical and therapeutic approach can be successfully developed (figure 1). Moreover, differences are evident between OSA in children, adults and the elderly, and little is known about the evolution of sleep disordered breathing over the lifespan. Recent studies suggest that childhood obesity increases the risk of developing OSA in adulthood [19], but the role of genetic traits is poorly understood, since studies on the genetics of OSA are limited in number and include small samples of patients [20, 21]. Heritable differences in craniofacial structures have been shown between OSA patients and controls [22, 23], but sophisticated analyses may be necessary to identify heritable traits in a complex disease such as OSA [21]. Finally, OSA shows major sex- [24] and age-related [25] differences in clinical and polysomnographic presentation, further complicating the overall clinical picture.
The complexity of obstructive sleep apnoea (OSA) for consideration in a personalised medicine approach. PSG: polysomnography; GWA: genome-wide association; EDS: excessive daytime sleepiness; PALM: Pcrit (passive critical closing pressure), arousal threshold, loop gain and muscle responsiveness; CCC: complete concentric palatal collapse; IL: interleukin; HTN: systemic hypertension. Reproduced and modified from [18] with permission.
This review focuses on recent work on the physiological and clinical aspects of OSA, including predictors of poor compliance to CPAP treatment and associated comorbidities, with regard to data suggesting individualised approaches to treatment. Readers are referred to other recent reviews for updated information on personalised medicine in OSA, including biomarkers and “omic” approaches [26–31].
Physiological traits
Current prevalence of sleep disordered breathing (SDB) is 10–17% in males and 3–9% in females [30]. The most common form of SDB is obstructive sleep apnoea (OSA), characterised by frequent breathing pauses due to sleep-related changes in muscle tone; the increased airway resistance leads to partial (hypopnoea) or complete (apnoea) upper airway collapse. The acute effects of these events include repeated drops in oxyhaemoglobin saturation, cardiovascular perturbations and cortical arousals, which fragment sleep [31].
It is clear that the pathophysiology of OSA is multifactorial, and caused not only by an impaired upper airway anatomy (i.e. anatomically narrow/collapsible airway), but also by several non-anatomical factors [32, 33], known as physiological traits, that combined have been shown to cause OSA [34, 35]. These include 1) poor upper airway anatomy which predisposes the airway to collapse; 2) poor ability of the upper airway muscles to respond to a respiratory challenge and stiffen or dilate the airway; 3) a low respiratory arousal threshold that causes an individual to arouse from sleep for very small increases in respiratory drive; and 4) a hypersensitive ventilatory control system, often referred to as a system with a high loop gain [35–37].
The contribution of each of these traits varies between patients and within different severities of disease [32], resulting in substantial heterogeneity between OSA patients, and possibly contributing to the results of continuous positive airway pressure (CPAP) treatment. Since adherence to CPAP is highly variable, an alternative approach for nonadherent patients would be to manipulate one or more of the underlying traits that contribute to OSA pathogenesis [38]. If a reliable and accurate pathophysiological pattern for each patient with OSA/hypopnoea syndrome could be identified, a customised therapy would be feasible in the future [39]. Here, we discuss the main characteristics of these traits as they relate to OSA pathophysiology.
Anatomical traits in OSA
The upper airway, from the posterior end of the nasal septum to the epiglottis, has relatively little bony or rigid support. The two primary forces tending to collapse the airway are the intraluminal negative pressure generated by the diaphragm during inspiration and the extraluminal tissue pressure from tissue and bony structures surrounding the airway [37, 40]. Different approaches have been developed to assess the functional and anatomical impairment of the upper airway in OSA, such as computed tomography (CT), magnetic resonance imaging (MRI), cephalometry, nasopharyngoscopy and drug-induced sleep endoscopy (DISE). The latter two provide information about the airway during static, awake or pharmacologically induced sleep states [41].
Upper airway anatomy
Obesity is a major cause of a narrow pharyngeal airway. Obesity can crowd the upper airway via deposition of adipose tissue in regions surrounding the airway. Recent evidence obtained using MRI suggests that many people with OSA have increased fat within their tongues compared to equally obese people without OSA [42–44]. Additionally, reduced tongue stiffness may contribute to increase upper airway collapsibility [45]. Nevertheless, some individuals gain weight without major upper airway compromise, and overweight/obese individuals without apnoea show a moderately compromised upper airway structure associated with highly responsive upper airway dilator muscles. Elucidating the mechanisms underlying other, non-anatomical traits can shed light on factors protecting against OSA [46].
The use of quantitative imaging techniques has shown differences in both the craniofacial structures and the soft tissues of the upper airway in OSA patients. Size and position of cranial bones (reduced length of mandibular body, low hyoid bone and retropositioning of the jaw) results in a reduction in pharyngeal airspace [40]. Increased upper airway length is associated with greater susceptibility to airway narrowing/collapse; the pharyngeal length is defined as the distance from the posterior nasal spine to the base of the epiglottis, which is attached to the hyoid. Consistent with this concept, an anatomically long upper airway, particularly in males, and an inferiorly displaced hyoid bone are anatomical features associated with OSA, easily detected in CT scans of the upper airway which provide three-dimensional reconstructions of the tongue and upper airway [42, 44].
Other methods have been used to evaluate the upper airway and investigate the severity and location of obstruction. Kim et al. [47] used fibre-optic nasopharyngoscopy with Muller manoeuvres to identify the anatomical level and degree of pharyngeal narrowing in OSA patients, revealing a correlation with the apnoea/hypopnoea index (AHI). Using sleep endoscopy in suspected OSA patients, Bachar et al. [48] found that the velopharynx was the most common site of obstruction (89% of patients), and most of the patients (72%) had multiple sites of obstruction. Huon et al. [41] observed more multilevel and lateral pharyngeal wall collapse in patients with severe OSA compared to body mass index (BMI)-matched mild OSA patients, by using sleep MRI. These data may explain the poor predictive value of single measurements of airway anatomy and the relatively high failure rate of uvulopalatopharyngoplasty (UPPP) surgery [49, 50].
Upper airway collapsibility: intraluminal negative pressure
The mechanics of the upper airway in sleep apnoea/hypopnoea syndrome has been interpreted by means of a collapsible resistor model characterised by its critical pressure (Pcrit) and its upstream resistance. Pcrit is the gold standard for measuring upper airway collapsibility and is defined as the minimal intraluminal airway pressure necessary to keep the collapsible segment open [51]. Therefore, if nasal CPAP is lower than Pcrit, the upper airway is collapsed during inspiration and the patient experiences apnoeas [52].
To measure Pcrit, the participant wears a CPAP mask attached to a modified CPAP device delivering both positive and negative pressures. In people with OSA, Pcrit is their therapeutic CPAP level, while in people without OSA it is ∼4–5 cmH2O. CPAP is then transiently lowered (for up to five breaths), sometimes to negative suction pressures, to induce variable degrees of airflow limitation, ideally (if arousals do not occur) until upper airway collapse. The technique relies on the assumption that CPAP reduces dilator muscle activity, which remains low following brief reductions in CPAP [51]. Pcrit is calculated by performing linear regression between the peak inspiratory flows for breaths 3–5 following the reduction in CPAP; breaths 1–2 following the transient reduction in CPAP are not included in the calculation, because lung volume changes that occur with the rapid reduction in CPAP take one or two breaths to stabilise [42, 53]. Increases in lung volumes probably exert caudal traction on the upper airway, preventing its collapse. This observation may help explain the link between obesity and OSA and other clinical observations, such as the improvement in OSA when sleeping upright [49].
The pharyngeal Pcrit is associated with obesity and hyoid position. Tongue dimensions, pharyngeal length and the distance from the mandibular plane to the hyoid are all associated with obesity variables [44]. As for the effect of body position, Pcrit increases (i.e. airway is more collapsible) in the supine sleeping position, whereas lateral positioning significantly improves passive airway anatomy/collapsibility [33]. As a consequence, a lower CPAP pressure is needed in the lateral position than in the supine position [54].
Instead of measuring Pcrit, negative expiratory pressure (NEP) can be applied noninvasively during spontaneous expiration during wakefulness to evaluate expiratory flow limitation. NEP is a simple measurement, first described to evaluate intrathoracic expiratory flow limitation in patients with COPD. It has been used to assess upper airway collapsibility in patients with suspected OSA [55]. Application of NEP while awake in the supine position is a simple and promising method that correlates with the anatomical component of upper airway collapsibility [56].
Non-anatomical traits
Upper airway dilator muscles
For upper airway dilator muscles to hold open the narrow pharyngeal airway of OSA patients and protect against collapse, the muscles must respond to collapsing forces by increasing their activity, to effectively reopen the upper airway [42]. Upper airway dilator muscles comprise phasic and tonic muscles. Activity of the phasic muscles increases during inspiration, resulting in stabilisation and expansion of the upper airway to counterbalance the effect of negative upper airway pressure; their activity is reduced but not completely abolished during expiration when pressure in the upper airway becomes positive. In contrast, the activity of tonic muscles remains constant in the respiratory cycle [40].
Upper airway dilator muscles: neural drive, responsiveness and effectiveness.
Much of the work on the influence of sleep on pharyngeal muscle control and patency in humans has focused on the genioglossus muscle (GGM) and, to a lesser extent, on the tensor palatine muscle. The GGM has an electromyogram (EMG) activity that is typically inspiratory phasic (greater activity on inspiration), and functions as a dilator of the pharyngeal airway. Meanwhile, tensor palatini activity is typically more constant (tonic) throughout the respiratory cycle [57, 58].
The neural drive to the upper airway dilator muscles is integrated at the level of brainstem motor nuclei where multiple neural inputs combine to produce a unitary output to the muscles. For example, the hypoglossal nucleus, which controls the GGM, receives inputs from premotor pacemaker neurons of the respiratory pattern generator, upper airway negative-pressure receptors, chemoreceptors and stretch receptors. During wakefulness this activity is augmented; at sleep onset the activity of the upper airway dilator muscles is diminished or lost and may underlie the airway collapse [41, 58].
OSA patients have greater EMG activity of the GGM and tensor palatini muscle during wakefulness compared to healthy controls. In contrast, during sleep, GGM activity decreases more in OSA patients than controls. The tonic activity of the tensor veli palatini muscle gradually decreases during sleep, and during slow-wave non-rapid eye movement (REM) sleep its activity is only 30% that when the subject is awake [40]. Some patients with OSA spontaneously overcome their tendency for airway collapse and have stable breathing during part of their sleep, increasing their GGM activity. During respiratory events in REM sleep, the tonic activity of the GGM is reduced even below the level during respiratory events in non-REM sleep phase 2. However, some subjects, despite activating their GGM, are not able to stabilise their breathing during sleep [59].
Upper airway muscle responsiveness depends on capability for increased activity when challenged with respiratory stimuli (such as hypercapnia and pharyngeal pressure changes) during sleep [42]. Although the tensor palatini can increase its activity in response to respiratory stimuli during sleep, it does not seem to be as sensitive as the GGM. As a result, tensor palatini activity is commonly quite low during sleep, despite elevations in both upper airway resistance and arterial carbon dioxide tension. The drive to several pharyngeal muscles appears to be reduced during sleep, as does their responsiveness to both chemical and mechanical stimuli [57]. Other studies have pointed to changes in respiratory timing and GGM activity during partial upper airway collapse; however, despite such activation, obese patients with OSA could restore airflow and ventilation less often than nonsnorers [60].
Muscle effectiveness is defined as the ability to translate the neural drive received by the upper airway muscles into airway dilation. OSA patients who have poor muscle responsiveness have poor muscle effectiveness too [42]. Muscle effectiveness can be assessed in different ways; some methods use gradual reductions in CPAP and compare responses in the passive versus active state where upper airway dilator muscles have low and high activity, respectively. Using this technique, the improvement in upper airway function with increased muscle activity was greater in healthy controls than in OSA patients [32, 46]. The mechanisms are not yet clear, but poor coordination of the neural drive to upper airway muscles during sleep, mechanically inefficient muscle (due to excess fat or muscle hypertrophy) [43] or muscle fibre type changes [45] could all be contributing factors [42, 61, 62].
Brown et al. [45] quantified the physical movement of the tongue across the respiratory cycle in patients with OSA and controls during wakefulness. In healthy controls the posterior portion of the tongue moved anteriorly in an en bloc fashion during tidal inspiration. In contrast, mild and moderate OSA patients had nonuniform tongue movement, and the tongue moved backwards into the airway in moderate OSA. While no measurements of upper airway dilator muscle activity were made in these patients, this work highlighted that there may be marked variability in effectiveness of muscle contraction (during wakefulness) and differences according to OSA severity.
Ventilatory control and loop gain
Loop gain is an engineering term that describes the stability of a system controlled by negative feedback loops [63]. In the context of OSA, in a closed loop system such as the breathing system, a perturbation in the controlled loop component (the respiratory apparatus or plant) induces changes in the feedback (blood gas tensions) received by the controller (respiratory centres), and in turn produces a compensatory response in the plant [64]. However, the initial response may result in overcorrection of arterial gas changes (“overshoot”). The ventilatory apparatus is then inhibited through the changes in arterial blood gas tensions that resulted in the initial response, and a hypopnoea ensues. If this second hypopnoea is less severe than the first, the disturbance in gas tensions will also be less severe, eliciting a lower response, ultimately resulting in stabilisation of the system. Conversely, if the overshoot results in large changes in arterial gas tensions, the cycle can continue indefinitely [64].
Mathematically, loop gain is defined as the ratio of the initial corrective response (e.g. hyperpnoea) to the initial disturbance (e.g. apnoea). If the corrective response is greater in magnitude than the disturbance (loop gain >1), then small perturbations have the potential to grow into self-sustaining oscillations and result in perpetual cycling. Conversely, loop gain <1 produces decaying oscillations, the magnitude and duration of which depend on the strength of the perturbation and are consistent with stable breathing [63]. Unstable ventilatory control is characterised by high loop gain, and probably contributes to cyclical airway obstruction by promoting airway collapse during periods of low ventilatory drive. OSA patients exhibit abnormal control of chemoreflexes, which contributes to increased loop gain.
Loop gain of the respiratory system can be measured during sleep in humans using a proportional assist ventilator (PAV) [64]. Using PAV, over one-third of OSA patients presented high loop gain, defined as an increase of >5 L·min−1 in minute ventilation in response to a 1-L·min−1 reduction in minute ventilation induced via a reduction in CPAP for 3 min under steady-state conditions. Similar to the impaired pharyngeal muscle phenotype, high loop gain is likely to be a particularly important determinant of OSA pathogenesis in people with mild to moderate impairment in upper airway anatomy [65]. These abnormalities have been shown to improve after CPAP treatment, suggesting induced rather than inherent trait abnormalities [66–69].
Arousal threshold
Obstructive respiratory events during sleep are often associated with brief awakening during sleep (cortical arousal), thereby disrupting sleep continuity. A marked activation of upper airway dilator muscles occurs during arousal [70]. Cortical arousals can be induced by a variety of stimuli and the sensory inputs responsible for respiratory-induced cortical arousals have been studied extensively [71]. In 1990, a landmark study found that increasing inspiratory efforts may be the stimulus to arousal from sleep [72]. Arousal occurs at a similar level of inspiratory effort irrespective of the cause of respiratory stimulation, i.e. hypercapnia, hypoxia or addition of a resistive load [72].
The notion that cortical arousal is required for the airway to open was rapidly accepted and arousal was assigned a “life-saving” role. However, subsequent work [73] showed that cortical arousals are not required to restore airflow at the end of a respiratory event. In fact, cortical arousals are not responsible for airway opening in ∼60% of events: 20% of events were associated with an arousal only after airway reopening, and 40% of events were not associated with any arousal [33, 71]. Amatoury et al. [74] recently reported that higher arousal intensities result in approximately two-fold greater upper airway muscle activation, but also in ∼40% greater increases in airflow and minute ventilation. Consistent with arousal intensity being a distinct trait and a contributor to OSA pathogenesis, these findings indicate that average arousal intensity is independent of the preceding respiratory stimulus; the physiological responses to arousal vary according to arousal intensity.
In summary, arousals are incidental events that occur when the thresholds for arousal and arousal-independent opening are close to each other, as they appear to be in patients with OSA. Arousals prevent deeper and more stable sleep, promote an unnecessarily high flow response at upper airway opening and help perpetuate respiratory control instability.
The physiological phenotypes of OSA: the PALM scale
A variable combination of anatomical and functional features of the upper airway occurs in OSA patients, and a better definition of the physiology of upper airway response to obstruction could allow alternative therapeutic approaches beyond CPAP. The PALM scale (Pcrit, arousal threshold, loop gain and muscle responsiveness) has been developed to better stratify OSA patients according to upper airway physiology and select appropriate interventions, as summarised in figure 2. In short, if a moderate-to-severe anatomical problem is present (PALM 1 and 2a), there is indication for CPAP treatment or other interventions that modify the upper airway (surgery, mandibular advancement device, positional therapy or lifestyle interventions). As the role of non-anatomical factors becomes more important than upper airway anatomy, one or more interventions for each physiological impairment can be chosen in order to target treatment to improve upper airway muscle function, i.e. upper airway muscle stimulation [75, 76], drugs [77], reduction of loop gain using acetazolamide [78] or increase of the arousal threshold using hypnotics [79–83]. While interested readers are referred to extensive reviews on this topic [42, 84, 85], some critical points need to be highlighted. First, the measurement of the PALM variables is still complicated in the clinical setting, as it requires full polysomnography and subsequent processing of a large amount of data. Clearly, this is hard to apply in the clinical context of large numbers of patients referred for OSA diagnosis and treatment. Second, while the physiology of respiratory events in non-REM sleep has been intensively studied, much less is known about REM sleep, a sleep phase characterised by more prolonged and severe events. Third, available interventional studies tailored to physiological traits are still small-scale, short-term, proof-of-concept studies. Since the theoretical and experimental background is quite solid and the first studies appear promising, ongoing research is likely to indicate clinically applicable treatments for specific OSA phenotypes, changing the current scenario of treatment for OSA.
The PALM (Pcrit (passive critical closing pressure), arousal threshold, loop gain and muscle responsiveness) scale approach to personalise obstructive sleep apnoea (OSA) treatment. Therapeutic interventions can be chosen according to the physiological phenotype of each patient. CPAP: continuous positive airway pressure; MAS: mandibular advancement splint; HNS: hypoglossal nerve stimulation. Reproduced and modified from [42] with permission.
Clinical phenotypes of OSA
The search for different clinical presentations of OSA has produced interesting results. Initially, OSA phenotypes were described based on the clinical characteristics of the disease, by combining anthropometrics, sleep data and comorbidities in patterns corresponding to the most common clinical presentations of OSA. More recently, cluster analysis has been applied to large series of data. In contrast to hypothesis-driven studies, cluster analysis is a sophisticated statistical methodology that combines several variables to identify groups of patients with distinct phenotypes, i.e. clusters.
In recent years, phenotype and cluster analyses have been applied to the clinical features of OSA patients, as summarised in table 1. Variability in results can be expected, since the studies differed in the variables entered in the analyses. In addition, the studies are heterogeneous in the number of patients included, and only three studies were multicentric [89, 90, 93]. Finally, the complexity of OSA can affect the results. A good example is provided by an interesting study on the polysomnographic features of mild-to-moderate OSA [86], which identified seven clinical phenotypes and six clusters. Some clinical phenotypes corresponded to two clusters each, while for other clinical phenotypes no cluster could be identified [86]. Positional OSA and sleep stage-dependent OSA appear to be variably combined in clinical practice, and other variables, such as the clinical characteristics of the patients, were not included in the analysis, possibly explaining the lack of precision in the identification of clusters.
Studies on clinical phenotypes/cluster analysis in patients with obstructive sleep apnoea (OSA)
While there may be inherent limitations in single-centre studies, as discussed above, they were important in identifying clinically relevant phenotypes to be tested in subsequent large studies. The first cluster analysis on OSA clinical phenotypes was published by the Icelandic Sleep Apnea Cohort (ISAC) research group, in >800 consecutive patients with newly diagnosed moderate-to-severe OSA [87]. Three main clusters were identified, corresponding to the “disturbed sleep”, the “minimally symptomatic” and the “excessive daytime sleepiness (EDS)” phenotypes. This study highlighted that these groups showed similar sleep variables, such as AHI or degree of obesity. EDS was often absent in OSA patients, and patients reported symptoms of insomnia rather than sleepiness. Moreover, the association of OSA and comorbidities was more frequent in the minimally symptomatic group, which included asymptomatic OSA patients with cardiovascular and respiratory comorbidities. The European Sleep Apnea Database (ESADA) study analysed similar OSA phenotypes, i.e. a combination of diurnal and nocturnal symptoms, in a multicentre large cohort [89]. Results were similar to those of Ye et al. [87] and coworkers, with an additional finding of a high prevalence of psychiatric comorbidities, especially in OSA patients reporting symptoms of insomnia.
In addition, the role of comorbidities was considered in the study by Vavougios et al. [88]. These authors identified four main clinical phenotypes, corresponding to increasing severity of OSA, and six clusters, with no OSA and mild OSA as single clusters, moderate and severe OSA each subdivided into two clusters according to the presence or absence of significant comorbidities. Two studies, the largest to date, were published in 2016 on OSA patients from two French registries [90, 93]. Bailly et al. [90] identified six clusters in the French OSA registry (>18 000 patients), corresponding to patients of different ages, with variable OSA severity and comorbidity burdens. Gagnadoux et al. [93] identified five clusters in the multicentre prospective sleep cohort of the Institut de Recherche en Santé Respiratoire des Pays de la Loire (almost 6000 patients); interestingly, two clusters featured female OSA and OSA in minimally symptomatic elderly patients.
Two additional cluster analyses were published recently, which used different variables compared to other studies. In a small single-centre study, Lacedonia et al. [91] stratified the patients with moderate-severe OSA according to the level of nocturnal hypoxaemia and identified three clusters. Severe nocturnal hypoxaemia was found in relatively young, severely obese patients who accounted for about half of the total sample, whereas elderly patients with mild nocturnal hypoxaemia and few symptoms accounted for ∼8% of the total sample. Finally, Mihaicuta et al. [92] published a detailed single-centre study including >1300 OSA patients and >600 controls, and identified eight clusters. This complex study assessed not only single comorbidities, but also their overlap in OSA patients, and identified two clusters of female OSA.
What clinical message can we derive from these studies on clinical presentations of OSA? Table 2 summarises the main clinical traits and the corresponding clusters identified in the different studies, suggesting that an overall picture of different phenotypes/clusters is slowly emerging. Pulmonologists dealing with OSA patients are becoming aware that females and elderly patients, or minimally symptomatic patients with cardiovascular or metabolic comorbidities, or OSA patients without sleepiness, do represent different presentations of the disease. It can be foreseen that clinical OSA presentations will eventually be combined with physiological phenotypes of OSA in order to choose the best treatment strategy for each individual patient.
Summary of results of cluster analyses according to clinical variables of interest in obstructive sleep apnoea (OSA) patients
Cluster analysis has also been applied to assess the outcome of CPAP treatment (table 1). In the study by Gagnadoux et al. [93], CPAP success after 6 months of treatment (expressed as mean nightly use for ≥4 h, and decrease in ESS score of ≥4 points, or improvement of ≥7 points in the 36-item Short Form survey score) was highest in cluster 3, corresponding to severe highly symptomatic OSA, and lowest in cluster 5, corresponding to the minimally symptomatic patients with significant comorbidities. At least two studies have reported poor compliance to CPAP treatment in patients with symptoms of insomnia [95, 96]. Cluster analysis has also been used to define patterns of CPAP use, since mean nightly use of CPAP incompletely describes the trajectory of CPAP use over time in single patients. Babbin et al. [94] identified four clusters of CPAP users, from the great user who used CPAP for most of the night without major variations over time, to the low user and the slow decliner, who used CPAP for insufficient time each night and tended to abandon treatment. These results are important to identify groups of patients in whom an intervention to improve compliance to CPAP treatment may be warranted. Unfortunately, the clinical characteristics of the patients according to the clusters of CPAP use were not included in the study.
Conclusions
Progress of personalised medicine in OSA and clinical application of results can be expected in the near future, since variability in clinical presentation and physiological trait-driven therapeutic strategies are increasingly recognised. Research on “-omics” (figure 1) continues, and may ultimately provide clinically useful biomarkers for adult [97] and paediatric [29, 98, 99] OSA. Examples are studies in adults and children with OSA using proteomics [29, 100], studies on miRNA in patients with OSA and resistant hypertension [101], the application of system biology to genetic studies of OSA [102] and studies on visceral fat transcriptome to assess the molecular basis of the interaction between OSA and obesity [103, 104]. A roadmap for a personalised approach to OSA has been proposed according to P4 medicine, (personalisation, prediction, prevention and patient participation in healthcare) [27, 28]. This huge effort is expected to change the current paradigm of OSA diagnosis and treatment, since AHI-based stratification of patients has revealed many pitfalls, similar to the forced expiratory volume in 1 s-based stratification of COPD patients, and is clearly insufficient to define the complexity of the disease. Moreover, the scientific community is currently experiencing a deep rethinking on the opportunity to prescribe CPAP in patients who are little or minimally symptomatic, since compliance to treatment is poor in this population, as confirmed by recent randomised controlled studies on patients with cardiovascular disease and OSA [105]. New and personalised treatment strategies for OSA are necessary and will foster better patient care, while improving our understanding of this complex disease.
Footnotes
Number 2 in the Series “Personalised medicine in respiratory diseases” Edited by Renaud Louis and Nicolas Roche
Previous articles in this series: No. 1: Chung KF. Personalised medicine in asthma: time for action. Eur Respir Rev 2017; 26: 170064.
Conflict of interest: None declared.
Provenance: Commissioned article, peer reviewed.
- Received June 15, 2017.
- Accepted August 14, 2017.
- Copyright ©ERS 2017.
ERR articles are open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0.
References
