Skip to main content
Free AccessCPAP

Outcome of CPAP Treatment on Intimate and Sexual Relationships in Men with Obstructive Sleep Apnea

Published Online: by:22


Study Objectives:

To examine intimate and sexual relationships in patients with obstructive sleep apnea (OSA), the association with daytime sleepiness, and the change in these outcomes with continuous positive airway pressure treatment (CPAP).


Pre-post test, quasi-experimental study


Seven sleep disorders centers in the US and Canada


123 males with OSA (AHI ≥ 20), aged 21 to 60 years


Nasal CPAP for ≥ 3 months

Measurements and Results:

Compared to normal values, at baseline patients were significantly sleepier, as measured by the Multiple Sleep Latency Test and Epworth Sleepiness Scale. They were also more impaired in intimate and sexual relationships, as measured by the Intimate and Sexual Relationships subscale of the Functional Outcomes of Sleep Questionnaire. Neither race nor marital status was significantly associated with impaired intimate and sexual relationships. Following treatment, patients were significantly more alert and had reported improved intimate and sexual relationships, with the greatest change occurring in those with the most disease severity.


OSA has an adverse impact on intimate and sexual relationships that is related to subjective sleepiness and improved with CPAP treatment.


Reishtein JL; Maislin G; Weaver TE. Outcome of CPAP treatment on intimate and sexual relationships in men with obstructive sleep apnea. J Clin Sleep Med 2010;6(3):221-226


Intimate and sexual relationships are important aspects of quality of life, as they reinforce human connections, aliveness, and caring.1 However, for some individuals with obstructive sleep apnea (OSA), this essential behavior may be adversely affected. Indeed, 30% to 68% of men with OSA suffer from some level of sexual dysfunction,2,3 and loss of interest in sex has been associated with the number of apneic events and level of oxygen desaturation.36


Current Knowledge/Study Rationale: Many studies of OSA and the effects of treatment on functional status of patients fail to include sexual function as a variable, and thus little is known about this important aspect of life. This secondary analysis using data from an investigation of the effect of CPAP treatment on the lives of people with OSA compared subjective self-reported intimate and sexual relationships before and after CPAP treatment.

Study Impact: In demonstrating that people who have OSA have impaired intimate and sexual relationships that generally normalize following CPAP treatment, this study has revealed another benefit of CPAP and a potential stimulus for improved adherence to treatment.

The impairments in sexual functioning associated with OSA, including the impact on relationships and negative effect on desire, arousal, and orgasm, have not been well described. The limited studies that have examined alterations in intimate and sexual behavior in this population have utilized small samples and have only explored one aspect of intimacy and sexual functioning.2,3,7,8 Moreover, the efficacy of CPAP in improving sexual dysfunction has been poorly documented.3,7,9 For example, Zhuraviev and colleagues treated 5 men who had both OSA and erectile dysfunction with CPAP for 6 months. Even though sleep phases normalized, no changes occurred in the men's sexual function.8

The purposes of this study were to examine OSA patients' perceptions of their intimate and sexual relationships, the association with daytime sleepiness, and degree of impairment compared to normal values, and to document change in this behavior with CPAP treatment. We hypothesized that (1) compared to normal values on the Intimate and Sexual Relationships subscale of the Functional Outcomes of Sleep Questionnaire (FOSQ),10 scores for individuals with OSA, especially for men with more severe disease, would indicate greater impairment; (2) limitations in sexual functioning would be associated with both objective and subjective sleepiness; and (3) following 3 months of CPAP treatment there would be improvement in scores on the intimate and sexual relationships subscale as well as on measures of objective and subjective sleepiness.



This article is a secondary analysis of data gathered during a larger prospective study of CPAP effectiveness.11 Participants were recruited from 7 sleep disorders centers in the US and Canada. The institutional review boards at each agency approved the original study protocol.

Potential participants were recruited at a sleep disorders center if they were 21 to 60 years old, if they had an apnea hypopnea index (AHI) ≥ 20 events per hour/sleep, and were candidates for CPAP treatment. Exclusion criteria were: coexisting sleep disorder, history of sedative-hypnotic use, cerebrovascular accident, chronic obstructive pulmonary disease, other pulmonary disease, or congestive heart failure.


The procedure for this study has been reported previously.11,12 Briefly, patients who had been referred to a participating sleep disorders center for evaluation of sleep were approached by the physician supervising the sleep study. The research project was explained and written informed consent was obtained. The physician managing the patient's care and soliciting participation in the study did not participate in data collection.

As part of their routine medical care, participants suspected of having OSA underwent a full night PSG followed by a night of CPAP titration (74.3% of sample) or a split night study (24.8% of sample). Before beginning CPAP treatment, participants underwent a day of testing that included completion of the instruments described above, as well as a neurobehavioral assessment battery, the Psychomotor Vigilance Task, and the Multiple Sleep Latency Test (MSLT). Only the results from the MSLT, ESS, and FOSQ are reported here. Upon completion of testing, subjects received instruction in use of the CPAP machine and commenced treatment. After they had used CPAP ≥ 3 months, participants returned to the sleep disorders center and underwent the same testing as they did pre-treatment. The subjects slept at home prior to the day of testing using their CPAP machine.



All subjects underwent nocturnal polysomnography (PSG) in the sleep laboratory as part of their routine clinical care. The number of apneas and hypopneas per hour was determined by a full PSG that included electroencephalogram, electrooculogram, electromyogram, and electrocardiogram. A finger pulse oximeter measured oxygen saturation, nasal thermistors measured airflow, and respiratory inductance plethysmography measured thoracic and abdominal respiratory movement.13 Sleep stages were scored using the protocol of Rechtschaffen and Kales.14 For analysis purposes, participants with sleep apnea were classified by AHI into 3 levels of severity: AHI of 20 to ≤ 40, AHI 40 to ≤ 60, and AHI > 60. No desaturation cutoff point was used to determine either diagnosis or disease severity classification.

Intimate and Sexual Relationships

Intimate and sexual relationships were assessed using the Intimate and Sexual Relationships subscale of the Functional Outcomes of Sleep Questionnaire (FOSQ).10 This disease-specific, self-administered instrument contains 30 questions and 5 stand-alone subscales: General Productivity, Vigilance, Social Outcome, Activity Level, and Intimate and Sexual Relationships. Respondents rate each activity for degree of difficulty on a 5-point Likert scale, with higher scores indicating better function. There is also an option to indicate nonperformance of an activity for reasons unrelated to sleepiness. The FOSQ was designed to make each subscale psychometrically strong and capable of being used independently. This paper reports on values for the Intimate and Sexual Relationships subscale: a general evaluation of how intimate behaviors and sexual relationships have been affected by sleepiness or tiredness, consisting of questions related to desire for intimacy or sex, ability to become sexually aroused, and ability to have an orgasm. The FOSQ has been used in numerous studies of sleep outcomes and has demonstrated reliability and validity.1519 Cronbach α for the Intimate and Sexual Relationships subscale was originally reported as 0.8910 and was 0.90 in this study.


Objective daytime sleepiness was measured using the MSLT.2022 The MSLT is measured by polysomnogram, the time required for the subject to fall asleep (latency time) in a 20-min period and is administered every 2 h starting at 10:00. The MSLT is a sensitive and valid measure of physiologic sleepiness and response to treatment.23,24 Sleep was terminated with the first epoch of stage 1 sleep to avoid sleep recovery effects on subsequent naps and neurobehavioral testing (results not reported here), as recommended by Carskadon and colleagues when the MSLT is used in research.21 The MSLT value was the average time of 4 latencies to sleep.

Subjective sleepiness was measured using the Epworth Sleepiness Scale (ESS).25,26 A score ≥ 11 indicates manifest sleepiness.26 The ESS has a single factor structure,27 and has demonstrated both test-retest reliability (r = 0.82) and internal consistency (Cronbach α = 0.88) in patients with OSA.28,29 It is a validated clinical and research tool in the assessment of daytime sleepiness.26


Subjects received the CPAP device and mask prescribed for them by the physician managing their sleep apnea. Adherence to CPAP treatment was documented using an overt monitor attached to the CPAP machine.30 This external monitor employs a microprocessor that utilizes an algorithm for the detection of mask-on pressure. The electric cord of the CPAP machine was plugged into the adherence monitor. Subjects were instructed to turn their CPAP device on and off via the monitor activation switch. The monitor is also attached to the CPAP apparatus via high-pressure tubing connected to a “T” tube inserted in its outflow port. A pressure transducer housed in the monitor senses the circuit pressure level and records mask-off events when the therapeutic pressure drops > 5 cm for ≥ 10 sec. Thus, the duration of therapeutic pressure delivery per day and number of missed days of use can be determined. Subjects were informed that their CPAP use was being monitored.

Statistical Analysis

SAS software was used to analyze the data. As data was not normally distributed, Spearman correlations were used to determine the relationship between sleepiness measures and the Intimate and Sexual Relationships subscale. Paired t-tests were used to assess the significance of the change from pre to post treatment on all items. Analyses of covariance (ANCOVA) were conducted, with post hoc tests, to determine differences among the severity groups. Key variables (age and BMI) were used as covariates after significant differences were demonstrated among OSA severity groups. Categorical variables were compared using χ2 statistics. Effect sizes were calculated by dividing the mean change score by the standard deviation of the change.31 Statistical significance was set at p < 0.05.



One hundred seventy-six people met inclusion criteria for this study. Ten subjects failed to return for follow-up testing, and CPAP adherence data for 17 subjects (10% of total) was lost because of technical problems (broken monitor transformer, failed monitor battery, corrupted electronic data). Because of the relatively small number of female participants (10% of total) in the study, and the subjective differences in sexual expression between men and women, this analysis is based on data from 123 male participants only (77% of the men in the original sample).

As shown in Table 1, the sample analyzed for this report primarily consisted of middle-aged, obese white men with severe sleep apnea (mean AHI = 66.90 ± 28.70, range 20–155.9). By design, there were significant differences in the mean AHI between the 3 disease severity groups. As expected, there were also robust differences in age between the least and most severe groups as well as significantly higher BMI in the > 60 group compared to the AHI 40 to < 60 group.

Table 1 Demographic characteristics of participants

All males with OSA n = 123AHI 20 to < 40 n = 29AHI 40 to < 60 n = 23AHI > 60 n = 71
Age years
BMI kg/m2
Marital Statusb

aNot all subjects indicated race;

bNo widowers were in sample

*p < 0.05;

**p < 0.001


At baseline, the mean score for all participants on the Intimate and Sexual Relationships subscale (3.17 ± 0.79) was significantly lower than the normal value for this subscale (3.93 ± 0.17, p < 0.001).10 This was a clinically meaningful difference with a large effect size of 0.96. Prior to treatment, there were no significant differences between disease severity groups (see Table 2). As displayed in Table 2, at baseline, 70% of the participants had an MSLT value < 10 min (mean = 7.26 ± 5.29) and an ESS ≥ 11 (mean = 14.48 ± 4.90). There were no significant differences in mean MSLT scores between disease severity groups, but scores on the ESS were significantly different between AHI 40 to < 60 and AHI > 60 groups.

Table 2 Comparisons of variables among OSA-severity groups

OutcomeInstrumentGroupBaseline (Mean ± SD)Post treatment (Mean ± SD)Change Score (Mean ± SD)pEffect Size*
Intimate/Sexual RelationshipsFOSQAll OSA subjects3.17 ± 0.793.62 ± 0.590.44 ± 0.73< 0.0010.61
AHI 20 to < 403.30 ± 0.793.55 ± 0.680.25 ± 0.73ns0.34
AHI 40 to ≤ 603.22 ± 0.723.59 ± 0.700.37 ± 0.70ns0.53
AHI > 603.10 ± 0.81)3.65 ± 0.520.55 ± 0.72< 0.0010.76

SleepinessMSLTAll OSA subjects7.26 ± 5.299.24 ± 6.012.04 ± 4.85< 0.0010.42
AHI 20 to < 408.55 ± 5.419.52 ± 5.750.93 ± 4.41ns0.21
AHI 40 to ≤ 607.78 ± 4.508.74 ± 6.050.66 ± 5.03ns0.13
AHI > 606.56 ± 5.429.29 ± 6.192.97 ± 4.84< 0.010.61

ESSAll OSA subjects14.48 ± 4.908.39 ± 5.03−6.14 ± 0.97< 0.0016.33
AHI 20 to < 4013.40 ± 4.9710.33 ± 5.80b−2.80 ± 4.92< 0.050.57
AHI 40 to ≤ 6013.05 ± 4.63a8.30 ± 5.13−4.95 ± 5.52< 0.010.90
AHI>6015.32 ± 4.84a7.64 ± 4.50b−7.82 ± 5.90< 0.011.33

*Effect Size: mean of change scores/SD change;

asignificant difference at baseline between these two groups, p < 0.05;

bsignificant difference post treatment between these two groups, p < 0.05

The impact of perceived daytime sleepiness on the ability to be intimate and engage in sexual relationships was indicated by a moderate correlation between the Intimate and Sexual Relationships scale and subjective sleepiness (rs = −0.35, p < 0.0001). However, there was no significant association between intimate and sexual relationships and objectively measured sleepiness (rs = 0.04). More than half of the OSA participants reported that sleepiness had affected at least one behavior on the Intimacy and Sexual relationships scale (desire, arousal, or orgasm). Indeed, 63% reported problems with relationships, 69% experienced reduced desire, 46% decreased arousal, and 29% difficulty achieving orgasm (see Table 3).

Table 3 Proportion of participants reporting difficulty with intimacy and sexual relationships

Post CPAP40%**34%**2%**18%*

Change in proportion baseline to post treatment;

*p < 0.05;

**p < 0.001

Post Treatment

Participants used CPAP a mean of 4.75 ± 2.12 h/ night. There were no significant differences in CPAP use between disease severity groups. Mean Intimate and Sexual Relationships score for the OSA sample pre-treatment was weakly correlated with the number of days on which CPAP was subsequently used (rs = 0.17, p = 0.05).

Post-treatment scores for Intimacy and Sexual Relationships subscale, MSLT, and ESS are shown in Table 2. As hypothesized, following 3 months of CPAP treatment, the Intimate and Sexual Relationships subscale mean score for the total sample (3.62 ± 0.59, p < 0.0001) demonstrated clinically important improvement as indicated by a moderate effect size (mean change 0.44 ± 0.73, effect size, 0.61). The magnitude of the change (effect size) in intimacy and sexual function following treatment increased across disease severity groups, with the least severe OSA participants achieving the smallest change, and the greatest improvement being realized by the most severe group (effect sizes for three groups = 0.34, 0.53, and 0.77, respectively). However, only in the group with the highest AHI (AHI ≥ 60) was this change statistically significant.

There were large changes in subjective sleepiness following treatment (ESS scores −6.15 ± 5.97, effect size 1.03, p < 0.001). Similar to the changes in intimacy and sexual function, the smallest change in subjective sleepiness occurred in the less severe group and the largest change in the group with the highest level of disease severity, all changes within severity groups were statistically reliable. Although not as robust, the mean change in objective sleepiness (MSLT scores) was also statistically significant (2.03 ± 4.85 min, effect size 0.42, p = 0.003). Moderate effect sizes in the MSLT following treatment were observed for persons with the highest levels of disease severity (effect size 0.61, p < 0.01).

The degree of change post-treatment for intimate behaviors and sexual function was significantly related to both objective and subjective sleepiness (rs = 0.31 and −0.31, respectively, p < 0.009). The change in the Intimate and Sexual Relationships score was not significantly correlated with age, BMI, AHI, or CPAP use (h /day, proportion of days with any CPAP use, or proportion of days when CPAP use was more than either 4 or 6 h).

With CPAP treatment, scores for the total sample on the Intimacy and Sexual Relationships subscale, although much improved, remained significantly different from normal values (p < 0.01). However as shown in Table 3, following treatment the proportion of participants indicating problems with relationships, desire, arousal, and orgasm significantly decreased (40%, 34%, 2%, and 18%, respectively).


This is the first large study that has examined how people who have OSA perceive their intimate and sexual relationships. Compared to people without OSA, men with OSA have poorer intimate and sexual relationships which are significantly related to daytime sleepiness. Following treatment with CPAP, intimate and sexual functioning improves substantially, with the most severely affected showing the largest improvement. This improvement is robustly related to changes in daytime sleepiness.

Our findings of diminished intimate and sexual functioning in men with OSA are consistent with findings in other smaller studies.5,16,3234 For example, in a study of mild OSA, Barnes found that compared to the normal value for the Intimate and Sexual Relationships subscale score, participants (N = 42) had reduced intimate and sexual activity scores of clinical importance.32 Bradshaw and colleagues also reported limitations in intimate and sexual behavior of OSA patients to be of similar magnitude (2.88 ± 0.88) to that found in our study.16 In 59 men who snored or had other symptoms of OSA, 59.3% of those who had OSA confirmed by PSG also reported erectile dysfunction, as indicated by low scores on the Korean version of the International Index of Erectile Function, while 29.6% of the men who did not have OSA reported erectile dysfunction.34 In a study of 15 men treated with CPAP for 12 weeks, scores on the International Index of Erectile Function, which assesses intercourse satisfaction and overall satisfaction, increased significantly.33 In a study of 50 patients with erectile dysfunction and presumed OSA based on clinical history, Teloken and colleagues demonstrated significant differences between those manifesting sleepiness (ESS scores > 10) and those who did not (ESS ≤ 10) on the total and erectile function domains of the International Index of Erectile Function.5 However, unlike our findings, they did not report differences between the two groups on the domains of intercourse satisfaction, orgasm, libido, and overall satisfaction. Without having polysomnographic confirmation of OSA for the participants, it is difficult to know whether differences in findings between the Teloken study and our investigation are related to disease severity, measures employed, or other factors related to OSA.

Most of the investigations of the relationship between OSA and intimate relationships and sexual functioning have focused on the ability to have an erection. In 1981, Schmidt and Wise noted the association between OSA and erectile dysfunction, with 46% of the 15 participants having abnormal nocturnal penile tumescence, with measurements that were significantly lower than those with psychogenic impotence or normal men.35 Examining the prevalence of OSA in a sample of 1,025 patients with ED, Hirshkowitz and associates found that 91% had an AHI > 5, indicative of OSA.36 We did not find differences in scores on the Intimacy and Sexual Relationship score between levels of disease severity. However, using cut points for respiratory disturbance similar to our study, but including patients with mild OSA, Margel and coworkers did find a significant dose-response association between severity of ED as measured by the International Index of Erectile Function and the respiratory disturbance index.37 These inconsistencies could be due to the wider spectrum of disease severity evaluated, measures used to evaluate intimate and sexual behavioral, and greater number of participants at each category of respiratory disturbance employed.

Several possible physiologic mechanisms have been explored for decreased intimate and sexual relationships in OSA. Those who are sleepier, as we found, may be less interested and more impaired in sexual activity. Indeed, Barnes and colleagues also found among a group of 98 men with OSA, those with ED were significantly sleepier in the daytime than those without ED.32 Margel and colleagues reported that morning tiredness was predictive of sexual satisfaction and being able to have a morning erection.37 In addition to excessive sleepiness, other potential mechanisms have been considered, including hormone levels as well as hypoxic-induced neural dysfunction affecting the erectile process. Comparing 10 men who had OSA with 5 healthy controls, Luboshitzky and others found that the OSA patients had lower mean luteinizing hormone (LH) and testosterone levels, secreting less LH and testosterone during sleep.38 In a study of testosterone levels in 1312 men selected from a study of osteoporosis in elderly men, Barrett-Connor and colleagues found that men in the lowest testosterone quartile had higher AHI (p = 0.02) and spent more of their sleep time with oxygen saturation less than 90% (p = 0.0001).39

In a rodent model of intermittent hypoxemia during daylight hours analogous to that experienced by patients with OSA, Soukhova-O'Hare evaluated the impact of chronic intermittent hypoxemia on sexual function and erectile activity, particularly changes in endothelial nitric oxide, which mediates penile erection, and phosphodiesterase enzyme type 5, which metabolizes cGMP into 5′GMP inhibiting the erectile process.40 In addition to finding ED in mice exposed to chronic hypoxemia, this team also documented that chronic intermittent hypoxemia produced a 55% decrease in the number of daily spontaneous erections that were reversed after 6 weeks of recovery in normoxia. Associated with this decrease in erectile functioning was reduced endothelial nitric oxide expression. They also found reduced sexual drive and mating activity. These effects were not testosterone-dependent, and no disruptions of testicular anatomy, including the number and appearance of Leidig and Sertoli cells, were found. Thus, the findings from these studies suggest that the effect of OSA on intimate and sexual behaviors may be multifactorial.

We found, as have others, that intimate and sexual activity recovers following CPAP treatment. A clinically meaningful change was found in our sample following 3 months of treatment and increased across disease severity groups. Similarly, Bradshaw and associates demonstrated significant increased in the Intimate and Sexual Relationships score in participants who received 2 weeks of CPAP treatment.16 Akashiba and colleagues reported that in patients with severe OSA, following 6 weeks CPAP treatment, Intimacy and Sexual Relationships scores improved 2.59 points.41 Using other outcome measures, Margel and colleagues3 documented improvement on the International Index of Erectile Function-5 in 20% of patients with OSA after being treated with CPAP for more than a year, and Goncalves and colleagues7 reported ED resolved in 13 of 17 OSA patients treated for one month with CPAP.

Not all studies show improvement in intimate and sexual functioning associated with CPAP therapy. Margel and coworkers found that 62% of their participants showed no change in the International Index of Erectile Function-5 after CPAP treatment, with 18% having a worse score.3 Massie and Hart found that 3 weeks of CPAP treatment did not lead to significant change in Intimacy and Sexual Relationships among 39 people with severe OSA.18 A trial of 8 weeks of CPAP in 80 people with mild OSA also did not demonstrate significant improvement.32 Zhuraviev and colleagues found no improvement in sexual function of five men with both OSA and ED following 6 months of CPAP treatment, even though their sleep normalized,8 and Hoekema and colleagues found non-significant improvements in self-reported erectile dysfunction and sexual dissatisfaction in 27 men with OSA following 2 months CPAP treatment.42 It may be that compared to other outcomes, such as daytime sleepiness, changes in intimacy and sexual relationships may take longer to be realized or noticed, given its social nature. Differences in level of disease severity, degree of treatment experience, and presence of a type II error, may be other reasons for the inconsistent results. Larger controlled trials with optimal levels of adherence are needed to more adequately understand the contribution of CPAP treatment to the recovery of intimacy and sexual activity in this population.

Despite significant improvement following 3 months of CPAP therapy, with decreased proportions of the sample reporting difficulty in desire, intimacy, arousal, and orgasm, we also found that the mean Intimacy and Sexual Relationships subscale score for the sample was not at normal levels. We have previously reported residual impairment in optimally adherent patients.11 Indeed, 43% of OSA patients using CPAP for 3 months still experienced reduced daily functioning even with nightly use > 6 hours.11 In a sample of optimally adherent CPAP-treated patients with residual daytime sleepiness and impaired intimate and sexual functioning, significant improvement occurred with modafinil treatment.19


The present study is the only large multicenter investigation to have explored OSA patients' subjective assessments of their intimate and sexual relationships both before and after treatment. The results of this study demonstrate again that OSA affects patients' waking function, and emphasizes the benefits of CPAP treatment in an area of function not often investigated within the context of sleepiness. It points out the necessity of evaluating all areas of function when assessing a person's complaints of excessive daytime sleepiness and including this important area of functioning in the assessment of treatment effectiveness.


This was not an industry supported study. Dr. Weaver has received research support from Respironics Respiratory and Sleep Research Foundation and Cephalon; has consulted for Apnex Medical and Cephalon; has FOSQ license agreements with Sanofi-Aventis, Merck, N.V. Organon, Apnex Medical, Ventus Medical, GlaxoSmithKline, and Philips Respironics; and has received the use of research equipment from Respironics and Protech. The other authors have indicated no financial conflicts of interest.


  • 1 Wilmoth MCSexuality in chronic illness: impact and interventions2002BostonJones and Bartlett

    Google Scholar
  • 2 Guilleminault CEldridge FLTilkian Asleep apnea syndrome due to upper airway obstruction: a review of 25 casesArch Intern Med19771374

    CrossrefGoogle Scholar
  • 3 Margel DTal RLivne PMPillar GPredictors of erectile function improvement in obstructive sleep apnea patients with long-term CPAP treatmentInt J Impot Res20051718690, 15510189

    CrossrefGoogle Scholar
  • 4 Arruda-Olson AMOlson LJNehra ASomers VKSleep apnea and cardiovascular disease. Implications for understanding erectile dysfunctionHerz200328298303, 12825145

    CrossrefGoogle Scholar
  • 5 Teloken PESmith EBLodowsky CFreedom TMulhall JPDefining association between sleep apnea syndrome and erectile dysfunctionUrology20066710337, 16698364

    CrossrefGoogle Scholar
  • 6 Watson RGreenberg GBakos LSleep apnea and depressionSleep Res1987166

    Google Scholar
  • 7 Goncalves MAGuilleminault CRamos EPalha APaiva TErectile dysfunction, obstructive sleep apnea syndrome and nasal CPAP treatmentSleep Med200563339, 15946896

    CrossrefGoogle Scholar
  • 8 Zhuravlev VNFrank MAGomzhin AISexual functions of men with obstructive sleep apnoea syndrome and hypogonadism may improve upon testosterone administration: a pilot studyAndrologia2009411935, 19400854

    CrossrefGoogle Scholar
  • 9 Luboshitzky RLavie LShen-Orr ZLavie PPituitary-gonadal function in men with obstructive sleep apnea. The effect of continuous positive airways pressure treatmentNeuro Endocrinol Lett2003244637, 15073577

    Google Scholar
  • 10 Weaver TELaizner AMEvans LK, et al.An instrument to measure functional status outcomes for disorders of excessive sleepinessSleep19972083543, 9415942

    Google Scholar
  • 11 Weaver TEMaislin GDinges DF, et al.Relationship between hours of CPAP use and achieving normal levels of sleepiness and daily functioningSleep20073071119, 17580592

    CrossrefGoogle Scholar
  • 12 Chasens ERPack AIMaislin GDinges DFWeaver TEClaustrophobia and adherence to CPAP treatmentWest J Nurs Res20052730721, 15781905

    CrossrefGoogle Scholar
  • 13 American Academy of Sleep MedicineSleep-related breathing disorders in adults: recommendations for syndrome definition and measurement techniques in clinical research. The Report of an American Academy of Sleep Medicine task forceSleep19992266789, 10450601

    CrossrefGoogle Scholar
  • 14 Rechtschaffen AKales AA manual for standardized terminology: techniques and scoring system for sleep stages of human subjects1968Los AngelesUCLA Brain Information Service/Brain Research Institute

    Google Scholar
  • 15 Blanco JZamarron CAbeleira Pazos MTLamela CSuarez Quintanilla DProspective evaluation of an oral appliance in the treatment of obstructive sleep apnea syndromeSleep Breath20059205, 15785917

    CrossrefGoogle Scholar
  • 16 Bradshaw DARuff GAMurphy DPAn oral hypnotic medication does not improve continuous positive airway pressure compliance in men with obstructive sleep apneaChest2006130136976, 17099012

    CrossrefGoogle Scholar
  • 17 Faccenda JFMackay TWBoon NADouglas NJRandomized placebo-controlled trial of continuous positive airway pressure on blood pressure in the sleep apnea-hypopnea syndromeAm J Respir Crit Care Med20011633448, 11179104

    CrossrefGoogle Scholar
  • 18 Massie CAHart RWClinical outcomes related to interface type in patients with obstructive sleep apnea/hypopnea syndrome who are using continuous positive airway pressureChest200312311128, 12684301

    CrossrefGoogle Scholar
  • 19 Schwartz JRLHirshkowitz MErman MKSchmidt-Nowara WModafinil as adjunct therapy for daytime sleepiness in obstructive sleep apnea: a 12-week, open-label studyChest200312421929, 14665500

    CrossrefGoogle Scholar
  • 20 Carskadon MADement WCThe multiple sleep latency test: what does it measure?Sleep19825Suppl 2S6772, 7156656

    CrossrefGoogle Scholar
  • 21 Carskadon MADement WCMitler MMRoth TWestbrook PRKeenan SGuidelines for the multiple sleep latency test (MSLT): a standard measure of sleepinessSleep1986951924, 3809866

    CrossrefGoogle Scholar
  • 22 Mitler MMCarskadon MAHirshkowitz MKryger MRoth TDement WCEvaluating sleepinessPrinciples and practice of sleep medicine20054th ed.PhiladelphiaElsevier Saunders141723

    CrossrefGoogle Scholar
  • 23 Seneviratne UPuvanendran KExcessive daytime sleepiness in obstructive sleep apnea: prevalence, severity, and predictorsSleep Med2004533943, 15222989

    CrossrefGoogle Scholar
  • 24 Sforza ELugaresi EDaytime sleepiness and nasal continuous positive airway pressure therapy in obstructive sleep apnea syndrome patients: effects of chronic treatment and 1-night therapy withdrawalSleep199518195201, 7610316

    Google Scholar
  • 25 Johns MWDaytime sleepiness, snoring, and obstructive sleep apnea. the Epworth Sleepiness ScaleChest19931033036, 8417909

    CrossrefGoogle Scholar
  • 26 Johns MWSensitivity and specificity of the multiple sleep latency test (MSLT), the maintenance of wakefulness test and the Epworth Sleepiness Scale: failure of the MSLT as a gold standardJ Sleep Res20009511, 10733683

    CrossrefGoogle Scholar
  • 27 Johns MWA new method for measuring daytime sleepiness: the Epworth sleepiness scaleSleep199114540545, 1798888

    CrossrefGoogle Scholar
  • 28 Hardinge FMPitson DJStradling JRUse of the Epworth Sleepiness Scale to demonstrate response to treatment with nasal continuous positive airways pressure in patients with obstructive sleep apnoeaRespir Med19958961720, 7494915

    CrossrefGoogle Scholar
  • 29 Johns MWSleepiness in different situations measured by the Epworth Sleepiness ScaleSleep19941770310, 7701181

    CrossrefGoogle Scholar
  • 30 Kribbs NBPack AIKline LR, et al.Objective measurement of patterns of nasal CPAP use by patients with obstructive sleep apneaAm Rev Respir Dis199314788795, 8466125

    CrossrefGoogle Scholar
  • 31 Cohen JStatistical power analysis for the behavioral sciences19772nd ed.New YorkAcademic Press

    Google Scholar
  • 32 Barnes MMcEvoy RDBanks S, et al.Efficacy of positive airway pressure and oral appliance in mild to moderate obstructive sleep apneaAm J Respir Crit Care Med200417065664, 15201136

    CrossrefGoogle Scholar
  • 33 Karkoulias KPerimenis PCharokopos N, et al.Does CPAP therapy improve erectile dysfunction in patients with obstructive sleep apnea syndrome?Clinica Terapeutica20071585158, 18265717

    Google Scholar
  • 34 Shin HWRha YCHan DH, et al.Erectile dysfunction and disease-specific quality of life in patients with obstructive sleep apneaInt J Impot Res20082054953, 18997807

    CrossrefGoogle Scholar
  • 35 Schmidt HSWise HASignificance of impaired penile tumescence and associated polysomnographic abnormalities in the impotent patientJ Urol198112634852, 7277596

    CrossrefGoogle Scholar
  • 36 Hirshkowitz MKaracan IArcasoy MOAcik GNarter EMWilliams RLPrevalence of sleep apnea in men with erectile dysfunctionUrology1990362324, 2392814

    CrossrefGoogle Scholar
  • 37 Margel DCohen MLivne PMPillar GSevere, but not mild, obstructive sleep apnea syndrome is associated with erectile dysfunctionUrology2004635459, 15028455

    CrossrefGoogle Scholar
  • 38 Luboshitzky RAviv AHefetz A, et al.Decreased pituitary-gonadal secretion in men with obstructive sleep apneaJ Clin Endocrinol Metab20028733948, 12107256

    CrossrefGoogle Scholar
  • 39 Barrett-Connor EDam TTStone KHarrison SLRedline SOrwoll EOsteoporotic Fractures in Men Study GroupThe association of testosterone levels with overall sleep quality, sleep architecture, and sleep-disordered breathingJ Clin Endocrinol Metab20089326029, 18413429

    CrossrefGoogle Scholar
  • 40 Soukhova-O'Hare GKShah ZALei ZNozdrachev ADRao CVGozal DErectile dysfunction in a murine model of sleep apneaAm J Respir Crit Care Med200817864450, 18535258

    CrossrefGoogle Scholar
  • 41 Akashiba TKawahara SAkahoshi T, et al.Relationship between quality of life and mood or depression in patients with severe obstructive sleep apnea syndromeChest20021228615, 12226024

    CrossrefGoogle Scholar
  • 42 Hoekema AStel AStegenga BSexual function and obstructive sleep apnea-hypopnea: a randomized clinical trial evaluating the effects of oral-appliance and continuous positive airway pressure therapyJ Sexual Med20074115362

    CrossrefGoogle Scholar