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Randomized Controlled Trial
. 2017 Aug;72(8):729-735.
doi: 10.1136/thoraxjnl-2016-209560. Epub 2017 Jan 10.

Obstructive sleep apnoea and quality of life in Ehlers-Danlos syndrome: a parallel cohort study

Affiliations
Randomized Controlled Trial

Obstructive sleep apnoea and quality of life in Ehlers-Danlos syndrome: a parallel cohort study

Thomas Gaisl et al. Thorax. 2017 Aug.

Abstract

Background: Patients with the connective tissue disorder Ehlers-Danlos syndrome (EDS) often suffer from fatigue, excessive daytime sleepiness and impaired quality of life. Obstructive sleep apnoea (OSA) may be an underlying cause for these symptoms but its prevalence in this population is unclear.

Methods: In this prospective parallel-cohort study, we included 100 adult patients with EDS (46% hypermobile-type, 35% classical-type and 19% other), which were one-to-one matched to 100 healthy adult controls according to sex, age, weight and height. Participants underwent structured interviews (including short-form 36) and level-3 respiratory polygraphy. OSA was defined as apnoea-hypopnea index ≥5/hour. Photographic craniofacial phenotyping was conducted in a subgroup. Conditional logistic regression was used to compare the prevalence of OSA.

Results: In patients with EDS, OSA prevalence was 32% versus 6% in the matched control group (OR 5.3 (95% CI 2.5 to 11.2); p<0.001). The EDS group reported impaired quality of life in all dimensions (p<0.05) and significantly higher excessive daytime sleepiness measured by the Epworth Sleepiness Scale (median (quartiles) 11 (7-14) vs 7 (5-10); p<0.001). OSA severity was positively associated with daytime sleepiness and lower quality of life in the EDS group. There was no evidence of a difference between the two study groups in terms of craniofacial phenotypes.

Conclusions: The prevalence of OSA is higher in patients with EDS than in a matched control group. This is of clinical relevance as it is associated with fatigue, excessive daytime sleepiness and impaired quality of life. Further studies are needed to assess the clinical benefit of OSA treatment in patients with EDS.

Trial registration number: NCT02435745.

Keywords: Clinical Epidemiology; Connective tissue disease associated lung disease; Sleep apnoea.

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Conflict of interest statement

Competing interests: PAC reports grants, non-financial support and other from ResMed, grants, non-financial support and other from SomnoMed, grants and personal fees from Exploramed, personal fees and non-financial support from Zephyr Sleep Technologies, personal fees from NovoNordisk, other from Fisher & Paykel Healthcare, personal fees from Quintessence Publishing, personal fees from UpToDate, all outside the scope of the submitted work.

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