TY - JOUR T1 - Obstructive sleep apnoea and quality of life in Ehlers-Danlos syndrome: a parallel cohort study JF - Thorax JO - Thorax SP - 729 LP - 735 DO - 10.1136/thoraxjnl-2016-209560 VL - 72 IS - 8 AU - Thomas Gaisl AU - Cecilia Giunta AU - Daniel J Bratton AU - Kate Sutherland AU - Christian Schlatzer AU - Noriane Sievi AU - Daniel Franzen AU - Peter A Cistulli AU - Marianne Rohrbach AU - Malcolm Kohler Y1 - 2017/08/01 UR - http://thorax.bmj.com/content/72/8/729.abstract N2 - 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. ER -