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Original Research

Sex differences of continuous positive airway pressure treatment on flow-mediated dilation in patients with obstructive sleep apnea syndrome

, , , , , , , , , , , , & show all
Pages 1361-1367 | Published online: 19 Aug 2015

Abstract

Introduction

There is growing research evidence suggesting the presence of endothelial dysfunction and systemic inflammation in patients with obstructive sleep apnea syndrome (OSAS). Continuous positive airway pressure (CPAP) is the most effective method for treating OSAS; nonetheless, the effects of CPAP on the aforementioned pathophysiologic pathways as well as on the systemic disease that result or coexist with the OSAS remain elusive.

Aim

To assess the effect of 3-month CPAP therapy on endothelial-dependent dilation, plasma levels of inflammatory markers, blood pressure (BP), and glucose control on male and female patients with OSAS.

Methods

Our study group consisted of 40 (24 males and 16 females) patients with no prior history of cardiovascular disease, with an apnea–hypopnea index ≥15, who were assigned to receive CPAP treatment. Measurements of flow-mediated dilation (FMD), 24-hour ambulatory BP, and blood analysis were performed at baseline and 3 months after CPAP therapy.

Results

Baseline FMD values were negatively correlated with the apnea–hypopnea index (r=−0.55, P=0.001). After 3 months of CPAP, there was an increase in the FMD values (5.40%±2.91% vs 3.13%±3.15%, P<0.05) and a significant reduction in the patients’ 24-hour systolic BP (122.82±11.88 mmHg vs 130.24±16.75 mmHg, P<0.05), diastolic BP (75.44±9.14 mmHg vs 79.68±11.09 mmHg, P<0.05), and pulse pressure (47.38±9.77 mmHg vs 52.72±11.38 mmHg, P<0.05); daytime systolic BP (125.76±12.69 mmHg vs 132.55±17.00 mmHg, P<0.05) and diastolic BP (77.88±10.39 mmHg vs 82.25±11.01 mmHg, P<0.05); nighttime systolic BP (118.17±13.16 mmHg vs 126.22±17.42 mmHg, P<0.05) and pulse pressure (46.61±10.76 mmHg vs 52.66±11.86 mmHg, P<0.05); and C-reactive protein and HbA1c levels (0.40 [0.40–0.70] mg/L vs 0.60 [0.40–0.84] mg/L and 5.45%±0.70% vs 5.95%±1.08%, respectively; P<0.05). When divided by sex, only male patients produced similar statistically significant results, while female patients failed to show such associations.

Conclusion

Our results suggest that CPAP therapy improves the endothelial function, the BP, and the glucose control in male patients with OSAS. Further research is warranted in order to verify these results and to further elucidate the impact of CPAP on the cardiovascular risk of male and female patients with OSAS.

Introduction

Obstructive sleep apnea syndrome (OSAS) is a high prevalent sleep disorder characterized by recurrent episodes of upper airway obstruction and subsequent recurrent arousal during sleep.Citation1 It is estimated that up to 5% of adults in western countries have OSAS.Citation2 According to published data, OSAS is an independent risk factor for hypertension and coronary artery disease.Citation3,Citation4 Emerging studies suggest that the repetitive episodes of hypoxia and reoxygenation, in manner similar to that of the ischemia/reperfusion injury model, promote the activation of proinflammatory pathways and disrupt the normal endothelial function.Citation5,Citation6 These mechanisms play a crucial role in the development of adverse cardiovascular events.

Continuous positive airway pressure (CPAP) is the most effective method for treating OSAS and alleviating the patients’ symptoms.Citation7 Nonetheless, the effects of CPAP therapy in the aforementioned pathophysiologic pathways as well as in the systemic disease that result or coexist with the OSAS require further elucidation. Furthermore, due to the various effects of sex hormones on the endothelial function in women, the majority of studies addressing the vascular endothelial function in OSAS have focused on men. The aim of this study was to assess the effect of 3-month CPAP therapy on endothelial-dependent dilation, plasma levels of inflammatory markers, and blood pressure (BP) and glucose control on male and female patients with OSAS.

Methods

This study was conducted in the sleep laboratory of the department of clinical therapeutics in the “Alexandra” Hospital, Athens Medical School. Informed consent was obtained from each patient, and approval was also obtained for the conduct of this study from the Investigational Review Board (IRB) of “Alexandra” General Hospital. Patients with suspected OSAS, who were referred to our department from March 2008 to March 2009, were recruited in the study.

All patients underwent attended overnight polysomnography. The determination of sleep stages, arousals, and respiratory events was performed according to the American Academy of Sleep Medicine (AASM) 2007 criteria.Citation8 Subjects with an apnea–hypopnea index (AHI) ≥15 were assigned to receive CPAP treatment and formed our study group. Patients with known cardiovascular, neuromuscular, or pulmonary disease were excluded from the study. All female patients were in the postmenopausal phase of life, and during our study period, they received no hormone replacement therapy.

A high-resolution 12.0 MHz transducer ultrasound was used to measure right and left common carotid artery diameter as well as brachial artery diameter at rest during reactive hyperemia. All patients fasted for at least 8 hours prior to the measurement. The assessment was carried out in a quiet room, at a stable temperature of 22°C–24°C, by an experienced physician, who was blinded to the patient’s sleep recordings and blood analysis. Reactive hyperemia was induced by inflation of a BP cuff, which was placed on the lower part of the arm and inflated to 250 mmHg followed by release after 5 minutes. Brachial artery diameter was measured 40 seconds and 60 seconds after cuff deflation. Flow-mediated dilation (FMD) was calculated as the ratio of change in diameter (maximum [of two measurements] − baseline) over baseline value. Endothelial function measurements were reassessed after 3 months of CPAP therapy.

At baseline and 3 months after CPAP treatment, all patients had a complete physical examination, including measurement of the body mass index (BMI; calculated as kilograms per meter squared). Full blood analysis, including blood cell count, C-reactive protein (CRP), erythrocyte sedimentation rate, glucose, total cholesterol, triglycerides, low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, and the concentration of glycated hemoglobin (HbA1c), was also performed prior and 3 months after CPAP.

Furthermore, all subjects underwent 24-hour ambulatory BP monitoring. Measurements were performed on a working day, and the subjects were asked to continue their normal daily activities. BP and heart rate readings were obtained every 30 minutes. Patients were instructed to take a diary of their activities and time of retiring to bed. BP variability was calculated as the standard deviation (SD) of the systolic and diastolic BP, during the whole day, but separately during daytime and nighttime. The recordings were repeated after 3 months of CPAP treatment.

Statistical analysis

A standard statistical software package SPSS (SPSS Inc., Chicago, IL, USA) was used in the analysis. Descriptive statistics were calculated for all variables. Categorical variables were analyzed with the chi-square test or Fisher’s exact test as appropriate. The one-sample Kolmogorov–Smirnov test was used to test if a variable was normally distributed. Normally distributed data were analyzed with the t-test, while in the absence of normal distribution, the Mann–Whitney test was used. Normally distributed data are shown as mean ± SD, while in the absence of normal distribution, values are presented as medians (25th percentile, 75th percentile). Paired-samples t-test and Wilcoxon test were used for comparison of the patients’ endothelium-dependent values, 24-hour ambulatory BP readings, and blood analysis at baseline and 3 months after CPAP therapy. The correlations between continuous variables were assessed with the Pearson’s or Spearman’s correlation test. P-values less than 0.05 were considered statistically significant. All statistical tests were also performed for male and female subjects separately.

Results

A total of 40 patients (24 males and 16 females) with a mean age of 53±12 years were recruited to the study. Patients had a mean BMI of 32±3 kg/m2, which did not change significantly during our study period. Correlation coefficients between baseline values of CRP and FMD and patients’ age, BMI, and sleep parameters are presented in . Pearson’s correlation showed that baseline FMD values were negatively correlated with AHI (r=−0.55, P=0.001). When divided by sex, only male patients produced similar statistically significant results, while female patients failed to show such associations. Patients’ endothelium-dependent values, 24-hour ambulatory BP readings, and blood analysis as a whole and separately for each sex at baseline and 3 months after CPAP therapy are presented in , respectively. Overall statistical analysis revealed a significant increase in the FMD values (5.40%±2.91% vs 3.13%±3.15%, P<0.05), and the percent change in FMD values after CPAP treatment was positively correlated with the percent of time <90% oxygen saturation (r=0.53, P=0.02) (). The patients’ 24-hour systolic BP (122.82±11.88 mmHg vs 130.24±16.75 mmHg), diastolic BP (75.44±9.14 mmHg vs 79.68±11.09 mmHg), and pulse pressure (PP) (47.38±9.77 mmHg vs 52.72±11.38 mmHg); daytime systolic BP (125.76±12.69 mmHg vs 132.55±17.00 mmHg) and diastolic BP (77.88±10.39 mmHg vs 82.25±11.01 mmHg); and nighttime systolic BP (118.17±13.16 mmHg vs 126.22±17.42 mmHg) and PP (46.61±10.76 mmHg vs 52.66±11.86 mmHg) showed a significant decrease (P<0.05). Furthermore, after 3 months of CPAP treatment, the values of CRP and HbA1c were significantly decreased (0.40 [0.40–0.70] mg/L vs 0.60 [0.40–0.84] mg/L and 5.45%±0.70% vs 5.95%±1.08%, respectively; P<0.05). In sex-stratified analysis, male patients showed a significant increase in the FMD values (5.76%±3.00% vs 3.49%±3.07%, P<0.05) and the percent change of FMD after CPAP treatment was positively correlated with the AHI (r=0.53, P=0.04). Moreover, after 3 months of CPAP treatment, patients’ 24-hour systolic BP (124.24±5.68 mmHg vs 131.14±12.83 mmHg) and diastolic BP (77.72±9.10 mmHg vs 82.06±11.18 mmHg) and nighttime systolic BP (117.02±9.47 mmHg vs 126.67±16.21 mmHg) and PP (44.87±9.37 mmHg vs 49.38±11.13 mmHg), as well as the values of CRP (0.40 [0.40–0.47] mg/L vs 0.48 [0.40–0.70] mg/L) and HbA1c (5.31%±0.65% vs 5.71%±0.68%) were significantly decreased (P<0.05). Female patients showed a trend toward increased levels of FMD values and decreased levels of BP measurements and HbA1c and CRP values; nonetheless, these associations were not statistically significant.

Table 1 Association between baseline CRP and FMD with age, BMI, and sleep parameters

Table 2 Endothelium-dependent parameters before and after CPAP

Table 3 Twenty-four-hour ambulatory blood pressure monitoring recordings before and after CPAP

Table 4 Blood test analysis before and after CPAP

Table 5 Correlation of percent change in FMD and CRP after CPAP with age, BMI, and sleep parameters

Discussion

This single-center study demonstrated that overall CPAP treatment increases the FMD, decreases the levels of CRP and HbA1c, and improves BP measurements in obstructive sleep apnea (OSA) patients. Previous studies have excluded women with OSAS due to the various effects of the menstrual cycle on the endothelial function. In order to avoid any potential bias caused by the different hormonal status, we choose to study only postmenopausal female patients. In sex-stratified analysis, only male patients provided with statistically significant results. Female patients showed a trend toward improved FMD, CRP, HbA1c values, and BP measurements; yet this trend failed to reach statistical significance, a finding possibly attributed to the small number of enrolled patients.

The measurement of endothelium-dependent dilation in response to reactive hyperemia is a noninvasive and validated method for the assessment of the endothelial function.Citation9 Alterations in endothelium-dependent dilation have been documented in patients with coronary artery disease and diabetes and recently OSAS.Citation10Citation13 The regulation of vasomotor tone, as measured by the change in the forearm blood flow after transient ischemia, appears to be regulated by the availability of nitric oxide. Researchers have shown that in the OSAS, the pathophysiologic stressors that result from the repetitive episodes of hypoxemia/reoxygenation downregulate the activity of the endothelial nitric oxide synthase and upregulate the expression of various vasoactive substances, such as endothelin-1 and angiotensin II.Citation14Citation16

In concordance with our results, previous studies have shown that endothelial dysfunction, as measured by FMD, was correlated with the severity of OSAS in terms of AHI.Citation17Citation19 Nonetheless, multivariable regression analysis by Chung et al revealed that the oxygen desaturation index was the only significant variable that correlated with the FMD, a finding not supported by our results.Citation19 Recently, data have emerged regarding the potential beneficial effects of CPAP on the endothelial function. A study by Ip et al demonstrated that the FMD was significantly improved after 4 weeks of CPAP treatment, while Bayram et al revealed that the improvement in the endothelial function was sustained after 6 months of treatment in complaint patients.Citation20 Our results confirm the beneficial impact of CPAP and revealed a positive correlation between the percent change of FMD and the percent of time <90% oxygen saturation, suggesting a greater benefit in patients with more severe OSAS.

Over the last years, a large body of evidence has demonstrated the pivotal role of inflammation in cardiovascular disease. In view of this notion, CRP has gained increasing attention as an independent risk factor for coronary disease.Citation21 In patients with OSAS, circulating levels of inflammatory markers appeared to be elevated, a finding suggestive of the presence of systemic inflammation.Citation22,Citation23 Previous reports have shown that CRP levels were correlated with the OSAS severity and the BMI; nevertheless, our study failed to show such an association.Citation19 Furthermore, although both FMD and CRP are involved in the pathophysiology of cardiovascular complications, the association between these two parameters in OSAS remains elusive. In agreement with our results, two separate studies by Chung et al and Verma et al failed to find a relationship between FMD and CRP in healthy subjects.Citation19,Citation24 Nonetheless, a study by Nystrom et al in patients with coronary artery disease revealed a correlation between endothelial dysfunction (measured with FMD) and the levels of CRP.Citation25 The different inclusion criteria among these studies may account for the observed discrepancies regarding the relationship between FMD and CRP. Even less data have been published regarding the impact of CPAP therapy on the inflammation markers. In this study, the CRP levels were significantly decreased 3 months after CPAP treatment. A previous study by Yokoe et al had also demonstrated that levels of CRP were decreased after 1 month of CPAP.Citation26 These results denote the possible beneficial role of CPAP in reducing the vascular inflammation.

The relationship between OSAS and hypertension has been well-established by many researchers. According to published literature, the use of CPAP can lead to minor improvement in BP control.Citation27 This study showed a significant decrease in 24-hour, daytime, and nighttime BP measurements after 3 months of CPAP treatment. Furthermore, current data suggest that patients with refractory hypertension and more severe OSAS appear to benefit more from CPAP treatment in terms of BP reduction.Citation28,Citation29 Our analysis provided statistically significant results in a population consisting of patients with no prior history of hypertension.

According to previous studies, OSA patients, independently of obesity, have higher prevalence of impaired glucose metabolism.Citation30 The etiology of this metabolic deregulation may be associated with the intermittent episodes of hypoxia and subsequent activation of the sympathetic nervous system and the hypothalamic-pituitary axis.Citation31 This study showed an improvement in blood glucose control, as estimated by the levels of HbA1c after CPAP treatment in nondiabetic patients. A similar study in euglycemic patients, by Papanas et al revealed that good adherence to CPAP treatment can significantly reduce HbA1c levels.Citation32 These findings denote a considerable beneficial effect of CPAP in glucose control, even in patients with no prior history of diabetes.

The limitations of this study should be noted. We recruited a rather small number of patients; this could account for the inability of this study to provide with more statistically significant associations between the examined variables. The study population consisted of patients with no prior history of cardiovascular or pulmonary disease; thus, the study results should be interpreted with caution in patients beyond this particular group.

In summary, our results suggest that in male OSA patients, CPAP therapy reverses to some degree the endothelial dysfunction and vascular inflammation and can ultimately lead to better BP and glucose control. Female patients presented with similar trends, nonetheless not statistically significant. Further well-designed prospective studies are needed to elucidate the effect of CPAP on the reduction of cardiovascular risk in male and female OSA patients.

Acknowledgments

The abstract of this paper was presented at the ERS Conference 2011 as a poster presentation with interim findings. The poster’s abstract was published in “Poster Abstracts” in European Respiratory Journal (http://erj.ersjournals.com/content/38/Suppl_55/p2227).

Disclosure

The authors report no conflicts of interest in this work.

References

  • PatilSPSchneiderHSchwartzARSmithPLAdult obstructive sleep apnea: pathophysiology and diagnosisChest2007132132533717625094
  • YoungTPeppardPEGottliebDJEpidemiology of obstructive sleep apnea: a population health perspectiveAm J Respir Crit Care Med200216591217123911991871
  • PeppardPEYoungTPaltaMSkatrudJProspective study of the association between sleep-disordered breathing and hypertensionN Engl J Med2000342191378138410805822
  • MarinJMCarrizoSJVicenteEAgustiAGLong-term cardiovascular outcomes in men with obstructive sleep apnoea-hypopnoea with or without treatment with continuous positive airway pressure: an observational studyLancet200536594641046105315781100
  • WangPZweierJLMeasurement of nitric oxide and peroxynitrite generation in the postischemic heart. Evidence for peroxynitrite-mediated reperfusion injuryJ Biol Chem19962714629223292308910581
  • LiaoJKZuluetaJJYuFSPengHBCoteCGHassounPMRegulation of bovine endothelial constitutive nitric oxide synthase by oxygenJ Clin Invest1995966266126668675632
  • BradleyTDFlorasJSObstructive sleep apnoea and its cardiovascular consequencesLancet20093739657829319101028
  • IberKAncoli-IsraelSChessonALQuanSFThe AASM Manual for the Scoring of Sleep and Associated EventsWestchester, ILAmerican Academy of Sleep Medicine2007
  • CorrettiMCAndersonTJBenjaminEJInternational Brachial Artery Reactivity Task ForceGuidelines for the ultrasound assessment of endothelial-dependent flow-mediated vasodilation of the brachial artery: a report of the International Brachial Artery Reactivity Task ForceJ Am Coll Cardiol200239225726511788217
  • SimovaIKatovaTDenchevSDiagnostic accuracy of flow-mediated dilatation and intima-media thickness for the presence of significant coronary artery diseaseJ Am Soc Hypertens20093638839420409981
  • YeboahJFolsomARBurkeGLPredictive value of brachial flow-mediated dilation for incident cardiovascular events in a population-based study: the multi-ethnic study of atherosclerosisCirculation2009120650250919635967
  • SuYLiuXMSunYMWangYYLuanYWuYEndothelial dysfunction in impaired fasting glycemia, impaired glucose tolerance, and type 2 diabetes mellitusAm J Cardiol2008102449749818678313
  • KatoMRoberts-ThomsonPPhillipsBGImpairment of endothelium-dependent vasodilation of resistance vessels in patients with obstructive sleep apneaCirculation2000102212607261011085964
  • ShiraiMPearsonJTShimouchiAChanges in functional and histological distributions of nitric oxide synthase caused by chronic hypoxia in rat small pulmonary arteriesBr J Pharmacol2003139589991012839863
  • PhillipsBGNarkiewiczKPesekCAHaynesWGDykenMESomersVKEffects of obstructive sleep apnea on endothelin-1 and blood pressureJ Hypertens1999171616610100095
  • MollerDSLindPStrungeBPedersenEBAbnormal vasoactive hormones and 24-hour blood pressure in obstructive sleep apneaAm J Hypertens200316427428012670743
  • NietoFJHerringtonDMRedlineSBenjaminEJRobbinsJASleep apnea and markers of vascular endothelial function in a large community sample of older adultsAm J Respir Crit Care Med2004169335436014551166
  • BayramNACiftciBKelesTEndothelial function in normotensive men with obstructive sleep apnea before and 6 months after CPAP treatmentSleep200932101257126319848355
  • ChungSYoonIYShinYKEndothelial dysfunction and C-reactive protein in relation with the severity of obstructive sleep apnea syndromeSleep2007308997100117702269
  • IpMSTseHFLamBTsangKWLamWKEndothelial function in obstructive sleep apnea and response to treatmentAm J Respir Crit Care Med2004169334835314551167
  • Emerging Risk Factors CollaborationKaptogeSDi AngelantonioEC-reactive protein concentration and risk of coronary heart disease, stroke, and mortality: an individual participant meta-analysisLancet2010375970913214020031199
  • ShamsuzzamanASWinnickiMLanfranchiPElevated C-reactive protein in patients with obstructive sleep apneaCirculation2002105212462246412034649
  • SchulzRMahmoudiSHattarKEnhanced release of superoxide from polymorphonuclear neutrophils in obstructive sleep apnea. Impact of continuous positive airway pressure therapyAm J Respir Crit Care Med20001622 pt 156657010934088
  • VermaSWangCHLonnEFATE InvestigatorsCross-sectional evaluation of brachial artery flow-mediated vasodilation and C-reactive protein in healthy individualsEur Heart J200425191754176015451155
  • NystromTNygrenASjoholmAPersistent endothelial dysfunction is related to elevated C-reactive protein (CRP) levels in Type II diabetic patients after acute myocardial infarctionClin Sci2005108212112815504106
  • YokoeTMinoguchiKMatsuoHElevated levels of C-reactive protein and interleukin-6 in patients with obstructive sleep apnea syndrome are decreased by nasal continuous positive airway pressureCirculation200310781129113412615790
  • DasAMKhayatRHypertension in obstructive sleep apnea: risk and therapyExpert Rev Cardiovasc Ther20097661962619505277
  • Martinez-GarciaMAGomez-AldaraviRSoler-CatalunaJJMartinezTGBernacer-AlperaBRoman-SanchezPPositive effect of CPAP treatment on the control of difficult-to-treat hypertensionEur Respir J200729595195717301092
  • PepperellJCRamdassingh-DowSCrosthwaiteNAmbulatory blood pressure after therapeutic and subtherapeutic nasal continuous positive airway pressure for obstructive sleep apnoea: a randomised parallel trialLancet2002359930220421011812555
  • PunjabiNMSorkinJDKatzelLIGoldbergAPSchwartzARSmithPLSleep-disordered breathing and insulin resistance in middle-aged and overweight menAm J Respir Crit Care Med2002165567768211874813
  • Van CauterEHolmbackUKnutsonKImpact of sleep and sleep loss on neuroendocrine and metabolic functionHorm Res200767suppl 12917308390
  • PapanasNSteiropoulosPNenaEHbA1c is associated with severity of obstructive sleep apnea hypopnea syndrome in nondiabetic menVasc Health Risk Manag2009575175619774216