Sleep Apnea is Associated With Accelerated Vascular Aging: Results From 2 European Community-Based Cohort Studies.

Raphaël Heinzer, Jean-Philippe Empana, Coen D A Stehouwer, Xavier Jouven, Manuel Sastry, Sebastian Köhler, Koen Reesink, Marleen van Greevenbroek, Harry J Crijns, Carla J van der Kallen, Pedro Marques-Vidal, Quentin Lisan, Miranda T Schram, Ronald M Henry, Pieter Dagnelie, Marie-Cécile Perier, Catherine Guibout, Frédérique Thomas, Nicolas Danchin, Stéphane Laurent, Pierre Boutouyrie, Thomas van Sloten

Journal: Journal of the American Heart Association 2021;10(15):e021318

PMID: 34308679

Abstract

Background The mechanisms underlying the association between obstructive sleep apnea (OSA) and cardiovascular disease may include accelerated vascular aging. The aim was to compare the magnitude of vascular aging in patients with high versus low risk of OSA. Methods and Results In 2 community-based studies, the PPS3 (Paris Prospective Study 3) and the Maastricht Study, high risk of OSA was determined with the Berlin questionnaire (a screening questionnaire for OSA). We assessed carotid artery properties (carotid intima-media thickness, Young's elastic modulus, carotid-femoral pulse wave velocity, carotid pulse wave velocity, carotid diameter using high precision ultrasound echography), and carotid-femoral pulse wave velocity (in the Maastricht Study only). Regression coefficients were estimated on pooled data using multivariate linear regression. A total of 8615 participants without prior cardiovascular disease were included (6840 from PPS3, 62% men, mean age 59.5±6.2 years, and 1775 from the Maastricht Study, 51% men, 58.9±8.1 years). Overall, high risk of OSA prevalence was 16.8% (n=1150) in PPS3 and 23.8% (n=423) in the Maastricht Study. A high risk of OSA was associated with greater carotid intima-media thickness (β=0.21; 0.17-0.26), Young's elastic modulus (β=0.21; 0.17-0.25), carotid-femoral pulse wave velocity (β=0.24; 0.14-0.34), carotid pulse wave velocity (β=0.31; 0.26-0.35), and carotid diameter (β=0.43; 0.38-0.48), after adjustment for age, sex, total cholesterol, smoking, education level, diabetes mellitus, heart rate, and study site. Consistent associations were observed after additional adjustments for mean blood pressure, body mass index, or antihypertensive medications. Conclusions These data lend support for accelerated vascular aging in individuals with high risk of OSA. This may, at least in part, underlie the association between OSA and cardiovascular disease.

Address: INSERM UMR 970 Integrative Epidemiology of Cardiovascular Diseases University of Paris Paris France.; Department of Otolaryngology-Head and Neck Surgery Foch HospitalSchool of MedicineUniversity Paris Saclay Paris France.; CARIM School for Cardiovascular DiseasesMaastricht University Maastricht the Netherlands.; Department of Internal MedicineMaastricht University Medical Centre Maastricht the Netherlands.; Department of Medicine Service of Internal Medicine Lausanne University Hospital and University of Lausanne Switzerland.; Department of Cardiology and Cardiovascular Research Institute MaastrichtMaastricht University Medical Center Maastricht Netherlands.; Department of Biomedical EngineeringMaastricht University Medical Centre Maastricht the Netherlands.; AP-HP Department of PharmacologyGeorges Pompidou European Hospital Paris France.; MHeNs School for Mental Health and Neuroscience Maastricht University Maastricht the Netherlands.; Department of Respiratory Medicine Maastricht University Medical Centre Maastricht The Netherlands.; Preventive and Clinical Investigation Center Paris France.; AP-HP Department of Cardiology Georges Pompidou European Hospital Paris France.; Department of EpidemiologyMaastricht University Medical Centre Maastricht the Netherlands.; Center for Investigation and Research in SleepLausanne University Hospital and University of Lausanne Switzerland.
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