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Sex differences in clinical and polysomnographic features of obstructive sleep apnea: the Turkish sleep apnea database (TURKAPNE) cohort

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Peker, Yüksel
Balcan, Mehmet Baran
Arbatlı, Semih

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Pihtili, Aylin
Kiyan, Esen
Cilli, Aykut
Altintas, Nejat
gurlu, Aylin Ozsancak
Gurkan, Canan
Annakkaya, Ali Nihat
Dursunoglu, Nese
Ogun, Hamza
Basoglu, Ozen K

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Background Previous reports from relatively small clinical cohorts have suggested that the clinical presentation of obstructive sleep apnea (OSA) differs between men and women. Objective We aimed to explore sex differences in clinical and polysomnographic features of OSA in a large nationwide registry. Methods Participants from the ongoing Turkish Sleep Apnea Database (TURKAPNE) Study from 34 centers were included in the current analysis. OSA was defined as an apnea-hypopnea index (AHI) >= 5 events/hour and was classified as mild, moderate, and severe according to AHI cut-offs 5, 15, and 30 events/hour, respectively. Results In all, 7130 patients (2259 women) were included. OSA was observed in 6323 (88.7 %), of whom 70.2 % were male and 29.8 % were female. In the OSA group, women were older (56.7 +/- 11.9 vs. 49.5 +/- 11.3 years;p < 0.001) and more obese (body mass index 34.3 +/- 7.2 vs. 31.4 +/- 5.6 kg/m(2);p < 0.001) and had lower AHI (29.8 +/- 24.1 vs. 36.8 +/- 26.2 events/h;p < 0.001) than men. Loud snoring and witnessed apnea were more common in men than in women whereas women were more frequently presented with insomnia, headache, and mood changes. Women had significantly less total sleep time, less sleep efficiency, and longer sleep latency compared with men (p < 0.001 for each). Additionally, comorbid diseases such as diabetes mellitus, hypertension, asthma, psychiatric disorders, hypothyroidism as well as drug use were more common in women than in men independent of age and obesity (p < 0.05 for each). Conclusions Our results suggest significant sex differences in clinical and polysomnographic features in this nationwide Turkish adult population. Women with OSA have more symptom burden and comorbidities despite having a less severe AHI.

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Sleep Medicine

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Elsevier

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Clinical neurology

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