Insulin Sensitivity and Insulin Resistance in Non-Diabetic Middle-Aged Patients with Obstructive Sleep Apnoea Syndrome

1. INTRODUCTION

Obstructive sleep apnoea syndrome (OSAS) is characterized by repetitive episodes of partial or complete occlusion of the upper airway during sleep. These episodes are associated with recurrent oxyhaemoglobin desaturation, frequent arousals and sleep fragmentation [1]. Its prevalence is estimated at 10-17% for men and 3-9% for women among adults in developed countries [2]. OSAS is associated with increased prevalence of automobile and occupational accidents, impaired quality of life, reduced work productivity, as well as cardiovascular and cerebrovascular morbidity [3-6].

OSAS has been linked with abnormal glucose metabolism, insulin resistance (IR) and development of type 2 diabetes independently of obesity [7]. IR plays an important role in the development of diabetes mellitus and represents a recognized risk factor for cardiovascular disease [8]. The prevalence of prediabetes in OSAS ranges between 20 and 67% and it is higher than in non-apnoeic subjects [9]. Previous data suggest that exposure to intermittent hypoxia and sleep fragmentation leads to alterations in insulin sensitivity and glucose disposal [10]. However, it is still unclear whether OSAS may lead to the development of diabetes. Additionally, there is still controversy on whether continuous positive airway pressure (CPAP) treatment of OSAS exerts beneficial effects on IR and prevention of diabetes mellitus [11, 12].

The aim of the present study was to investigate the effects of OSAS on IR in patients without diabetes.

2. PATIENTS AND METHODS

We included consecutive patients referred to the sleep laboratory of our institution during a 6-month period, between May and November 2016, with symptoms suggestive of sleep-disordered breathing. The study was performed in accordance with the Helsinki Declaration of Human Rights, as revised in 2013 [13], and the patients gave their informed consent.

Exclusion criteria were: known diabetes mellitus; chronic renal or hepatic failure; chronic inflammatory diseases; cancer; systemic steroid treatment and hormonal replacement therapy. Diagnosis of diabetes mellitus was based on medical history or fasting plasma glucose ≥126 mg/dl [14].

Data on previous medical history, current medication use, tobacco smoking and alcohol consumption were recorded. Height, weight, body-mass index (BMI) [weight (kg)/height² (m)], neck, waist and hip circumference and waist/hip ratio were measured using standardized techniques.

Sleepiness was evaluated using the Greek version of the Epworth Sleepiness Scale (ESS) [15], a self-administered questionnaire evaluating the possibility of falling asleep in a variety of situations [maximum score: 24; score >10 indicative of excessive daytime sleepiness]. Pulmonary function testing, arterial blood gases and a 12-lead electrocardiographic examination before sleep study were also performed.

3. RESULTS

A total of 69 patients (60 males and 9 females), aged 49 ± 12.7 years were included. The anthropometric and sleep characteristics of patients are presented in Tables (1 and 2) respectively. Laboratory results and measurements of the study population are presented in Table 3. Among patients included in the study, 26 (37.7%) were tobacco smokers, 13 (18.8%) were receiving statins and 21 (30.4%) were on anti-hypertensive treatment.

HOMA-IR was positively associated with BMI (ρ=0.364, p=0.002), time with oxyhaemoglobin saturation <90% (ρ=0.291, p=0.015) (Fig. 1a), ESS score (ρ=0.293, p=0.019) (Fig. 2a), arousal index (ρ=0.268, p=0.027) (Fig. 2b) and negatively associated with average oxyhaemoglobin saturation (ρ=-0.398, p=0.001) (Fig. 1b) and minimum oxyhaemoglobin saturation (ρ=-0.327, p=0.006) (Fig. 1c).

QUICKI was positively associated with forced vital capacity (r=0.301, p=0.014), average oxyhaemoglobin saturation (r=0.443, p<0.001) (Fig. 1b), minimum oxyhaemoglobin saturation (ρ=0.318, p=0.008) (Fig. 1c), and negatively associated with sleep stage transitions (r=-0.266, p=0.032) (Fig. 3a), oxygen desaturation index (r=-0.404, p=0.005) (Fig. 3b), time with oxyhaemoglobin saturation <90% (r=-0.311, p=0.019) (Fig. 1a), ESS score (r=-0.299, p=0.016) (Fig. 2a) and arousal index (r=-0.344, p=0.004) (Fig. 2b).

There was no association between HOMA-IR, QUICKI and serum lipids, CRP, renal or hepatic function markers. Correlation analysis between HOMA-IR, QUICKI with anthropometric and sleep parameters is presented in Table 4.

After adjustment for age and BMI, HOMA-IR was associated with sleep stage transitions (β=0.441, p<0.001), time with oxyhaemoglobin saturation <90% (β=0.284, p=0.025), average oxyhaemoglobin saturation (β=-0.400, p=0.001), minimum oxyhaemoglobin saturation (β=-0.374, p=0.002) and arousal index (β=0.256, p=0.041). QUICKI was associated with oxygen desaturation index (β=-0.364, p=0.017), sleep stage transitions (β=-0.259, p=0.041), ESS score (β=-0.255, p=0.047), minimum oxyhaemoglobin saturation (β=0.320, p=0.007) and arousal index (r=-0.304, p=0.012).

Fasting glucose serum levels were positively correlated with proportion of sleep stage 1 in total sleep time (r=0.332, p=0.006) and negatively with minimum oxyhaemoglobin saturation (r=-0.258, p=0.032). There was no association between systolic blood pressure or diastolic blood pressure and any of the sleep parameters.

4. DISCUSSION

The major finding of this study is that surrogate markers of IR (evaluated by HOMA-IR and QUICKI) in OSAS patients without diabetes mellitus were associated with indices of hypoxia, sleep fragmentation during sleep, daytime sleepiness and respiratory function.

OSAS per se may lead to IR through several intermediary pathways. That process is multifactorial and involves sympathetic overactivity, systemic and adipose tissue inflammation along with hormonal disorders [19, 20]. Sleep deprivation promotes a pro-inflammatory state, with increased levels of interleukin-6, tumour necrosis factor-α and adiponectin, factors also involved in the development of IR [19]. In an animal study, sleep fragmentation reduced insulin sensitivity by increasing macrophage number and infiltration in adipose tissue along with an increase of nicotinamide adenine dinucleotide phosphate oxidase activity [21]. Increased sympathetic tone associated with apnoeic events and intermittent hypoxia has been linked with both IR and metabolic syndrome [22]. Increased catecholamine, cortisol and growth hormone concentrations, described in OSAS, negatively affect insulin activity and glucose metabolism [19].

In the present study, IR was associated with sleep fragmentation, as expressed by increased sleep stage transitions and arousal index. In healthy individuals, it has been shown that sleep fragmentation for two nights decreased insulin sensitivity (p<0.001) and glucose effectiveness (p<0.01), with increased morning cortisol levels and sympathetic activity [23]. In another study involving young healthy adults, selective suppression of slow-wave sleep resulted in decreased insulin sensitivity [24]. Bulcun et al. [25] compared disorders of glucose metabolism, evaluated by oral glucose tolerance test between 112 untreated OSAS patients and 19 non-apnoeic control subjects. The rate of disorders of glucose metabolism was higher in OSAS patients compared with controls (50.8 vs 15.7%, p=0.005). Arousal index, ESS and BMI were independent significant predictors of IR [25]. The recurrent arousals seen in OSAS patients may have negative impact on glucose metabolism through common pathophysiologic mechanisms activated during sleep deprivation/disruption.

Excessive daytime sleepiness is an established risk factor for the development of both hypertension and diabetes mellitus [26]. In our study, IR was associated with excessive daytime sleepiness, as expressed by the validated ESS questionnaire score. Moreover, our results are consistent with those of previous studies. Barceló et al. [27] evaluated IR in 44 OSAS patients matched for age and BMI (22 with and 22 without excessive daytime sleepiness) and 23 healthy controls. IR was assessed by HOMA-IR and excessive daytime sleepiness by the ESS and multiple sleep latency tests. Patients with excessive daytime sleepiness exhibited higher plasma glucose and insulin levels, as well as increased IR, compared with those free from sleepiness and with controls [27]. In the same study, 3 months of CPAP treatment in 35 patients, reduced insulin levels (p=0.03) and HOMA-IR (p=0.007) in subjects with excessive daytime sleepiness, but not in those without excessive daytime sleepiness [27]. In another study that included 25, otherwise healthy, OSAS patients with somnolence and 25 age- and BMI-matched, non-somnolent controls, the former had higher serum glucose (p=0.045), fasting insulin (p=0.012) and HOMA-IR (p=0.027) than the latter [28]. HOMA-IR was positively associated with ESS (p=0.005) and negatively with average oxyhaemoglobin saturation (p=0.031) [28].

Results from the present study indicate an association between hypoxia indices during sleep and IR. The effect of hypoxia on IR has been the subject of interest for previous studies involving OSAS. Ip et al. [29] investigated IR in 185 OSAS patients and 85 non-apnoeic subjects. Fasting serum insulin levels and HOMA-IR were higher in OSAS patients compared with healthy controls (p=0.001 and p<0.001, respectively) [29]. Minimum oxygen saturation (p=0.022) and AHI (p=0.044) were independent predictors of HOMA-IR [29]. In another study, enrolling 56 normoglycaemic OSAS patients [30], fasting insulin had shown negative associations with average oxyhaemoglobin saturation (p=0.002) and minimum oxyhaemoglobin saturation (p=0.048), but positive correlations with percentage of time with oxyhaemoglobin saturation <90% (p=0.018) during sleep. HOMA-IR was also correlated with average oxyhaemoglobin saturation levels (r=-0.349, p=0.008) [30]. After 6 months of CPAP therapy, only the patients, who had good adherence to treatment, demonstrated a significant decrease in glycated haemoglobin (HbA_1c) [30]. The underlying mechanism by which intermittent hypoxia induces IR still remains unclear, but recent data suggest that hypoxia-mediated inflammation of the adipose tissue may be an important contributor [31]. Hypoxia is the major determinant of renal function in OSAS patients as well [32, 33].

The QUICKI index is used for the evaluation of insulin sensitivity and is determined by a mathematical transformation, which estimates serum levels of fasting glucose and fasting insulin [17]. In populations other than OSAS, QUICKI has so far demonstrated a better linear correlation with the reference glucose clamp method than other indexes, including HOMA-IR [17, 34, 35]. In OSAS, however, the use of QUICKI is limited mainly to paediatric populations [36].

The present study has several limitations. First, the study population was small and mainly consisted of males referred for sleep disordered breathing. However, this reflects the distribution of consecutive subjects referred to a sleep laboratory related to sleep breathing disorders. Moreover, our data were obtained from middle-aged adults and so we cannot extrapolate results from those findings to older OSAS patients. However, in regression analysis, age was not an influencing factor for the sleep parameters considered. The use of statins, anti-hypertensive drugs and tobacco smoking variably affect insulin resistance and risk of diabetes [37-39]. In the current study, a small number of participants were receiving statins and blood pressure lowering drugs or were tobacco smokers, thus these parameters were not considered in our analysis. Finally, we did not examine the effect of CPAP treatment on glucose metabolism in OSAS patients, a subject that produced conflicting results among studies [40].

In conclusion, our results suggest that OSAS is independently associated with IR in patients without diabetes mellitus. Recurrent hypoxia and sleep fragmentation appear to play an important role in this process. These results should be interpreted in the context of our increasing insight into both the vascular disease risk associated with OSAS [41, 42] and the many comorbidities of the metabolic syndrome [43, 44]. Further studies are needed to evaluate the long-term impact of IR on the incidence of cardiovascular disease in OSAS patients.

REFERENCES