Comparative associations of oximetry patterns in Obstructive Sleep Apnea with incident cardiovascular disease

Author:

Sutherland Kate12ORCID,Sadr Nadi13,Bin Yu Sun12ORCID,Cook Kristina12ORCID,Dissanayake Hasthi U12,Cistulli Peter A124ORCID,de Chazal Philip125

Affiliation:

1. Sleep Research Group, Charles Perkins Centre, University of Sydney , Sydney, New South Wales , Australia

2. Northern Clinical School, Faculty of Medicine and Health, University of Sydney , Sydney, New South Wales , Australia

3. Department of Biomedical Informatics, Emory University , Atlanta, Georgia , USA

4. Department of Respiratory and Sleep Medicine, Royal North Shore Hospital , St Leonards, New South Wales , Australia

5. School of Biomedical Engineering, University of Sydney , Sydney, New South Wales , Australia

Abstract

Abstract Study Objectives Intermittent hypoxia is a key mechanism linking Obstructive Sleep Apnea (OSA) to cardiovascular disease (CVD). Oximetry analysis could enhance understanding of which OSA phenotypes are associated with CVD risk. The aim of this study was to compare associations of different oximetry patterns with incident CVD in men and women with OSA. Methods Sleep Heart Health Study data were used for analysis. n = 2878 Participants (51.8% female; mean age 63.5 ± 10.5 years) with OSA (Apnea Hypopnea Index [AHI] ≥ 5 events/h) and no pre-existing CVD at baseline or within the first 2 years of follow-up were included. Four oximetry analysis approaches were applied: desaturation characteristics, time series analysis, power spectral density, and non-linear analysis. Thirty-one resulting oximetry patterns were compared to incident CVD using proportional hazards regression models adjusted for age, race, smoking, BMI, and sex. Results There were no associations between OSA oximetry patterns and incident CVD in the total sample or in men. In women, there were some associations between incident CVD and time series analysis (e.g. SpO2 distribution standard deviation, HR 0.81, 95% CI 0.68–0.96, p = 0.014) and power spectral density oximetry patterns (e.g. Full frequency band mean HR 0.75; 95% CI 0.59–0.95; p = 0.015). Conclusions Comprehensive comparison of baseline oximetry patterns in OSA found none were related to development of CVD. There were no standout individual oximetry patterns that appear to be candidates for CVD risk phenotyping in OSA, but some showed marginal relationships with CVD risk in women. Further work is required to understand whether OSA phenotypes can be used to predict susceptibility to cardiovascular disease.

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Neurology (clinical)

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