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Moderate to Severe Obstructive Sleep Apnea Is a Risk Factor for Severe COVID-19: A Nationwide Cohort Study
Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden.
Department of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden.
Faculty of Medicine, Department of Clinical Sciences Lund, Respiratory Medicine, Allergology and Palliative Medicine, Lund University, Lund, Sweden.
Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Respiratory Medicine.ORCID iD: 0000-0003-1926-8464
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2026 (English)In: Journal of Sleep Research, ISSN 0962-1105, E-ISSN 1365-2869, Vol. 35, no 1, article id e70082Article in journal (Refereed) Published
Abstract [en]

The impact of obstructive sleep apnea (OSA) and positive airway pressure (PAP) treatment on COVID-19 severity is unclear. In this population-based, nationwide study using multi-register data, we aimed to assess if OSA is a risk factor for COVID-19 severity and how adherence to PAP treatment and clinical characteristics affect the risk. Swedish residents with COVID-19 infection January 2020-May 2022 were included. An exposed group of OSA (starting PAP treatment 2015-2019) was identified. COVID-19 severity outcome was defined as mild (non-hospitalised), severe (hospitalised) or critical (intensive care or death). Covariates included comorbidities and sociodemographics. Conditional odds ratios (COR) with 95% confidence intervals (95% CI) were estimated using multinomial logistic regression. Among 8,894,162 individuals in Sweden, 1,932,081 (21.7%) had registered COVID-19 January 2020-May 2022. OSA was identified in 11,407 (0.6%) and was associated with an increased risk of severe (COR 1.34; 95% CI 1.25-1.43) and critical (1.25; 1.11-1.42) COVID-19 after adjustment for age, sex, education and comorbidities. Stratified by PAP adherence, age and COVID-19 wave, OSA was a risk factor for more severe COVID-19 in PAP-adherent and non-adherent individuals, in people aged 40-60 but not > 60 years and not after June 2021. OSA severity, assessed with the oxygen desaturation index (ODI), was independently associated with COVID-19 severity, with the highest risks for severe (1.23; 1.01-1.52) and critical (1.76; 1.17-2.63) COVID-19 observed in ODI ≥ 30 (vs. ODI < 15). We conclude that patients with moderate to severe OSA have an increased risk of severe COVID-19, also when PAP-treated, with an independent dose-response relationship between the severity of intermittent hypoxia and COVID-19 severity.

Place, publisher, year, edition, pages
John Wiley & Sons, 2026. Vol. 35, no 1, article id e70082
Keywords [en]
CPAP, SARS‐CoV2, oxygen desaturation index, sleep disordered breathing
National Category
Infectious Medicine
Identifiers
URN: urn:nbn:se:oru:diva-120933DOI: 10.1111/jsr.70082ISI: 001481985200001PubMedID: 40325794Scopus ID: 2-s2.0-105004313776OAI: oai:DiVA.org:oru-120933DiVA, id: diva2:1956506
Funder
Swedish Heart Lung Foundation, 20210030Swedish Heart Lung Foundation, 20210581Swedish Heart Lung Foundation, 20240726Forte, Swedish Research Council for Health, Working Life and Welfare, 2024-01711Swedish Research Council Formas, 2020-02828Swedish Heart Lung Foundation, 2022068624Swedish Heart Lung Foundation, 20230392Swedish Heart Lung Foundation, 20210529Swedish Research Council, 2019-02081
Note

Funding Agencies:

This work was supported by Swedish Heart-Lung Foundation grants (20210030, 20210581, 20240726), and the underlying SCIFI-PEARL study has funding by Swedish Government grants through the agreement concerning the research and education of doctors (ALF) (ALFGBG-938453, ALFGBG-971130, ALFGBG-978954, ALFGBG-1006729), a grant from Forskningsrådet för Hälsa, arbetsliv och välfärd/Research Council for Health, Working Life, and Welfare (FORTE) (2024-01711) and previously from a joint grant from Forskningsrådet för hälsa, arbetsliv och välfärd/Research Council for Health, Working Life, and Welfare (FORTE) and Forskningsrådet för miljö, areella näringar och samhällsbyggande/Research Council for Environment, Agricultural Sciences and Spatial Planning (FORMAS) (2020-02828). M.L. was supported by grants from the Swedish Heart and Lung Foundation (2022068624) and by Swedish Government grants through the ALF-agreement (ALF-979044). A.P. was supported by the Swedish Heart and Lung Foundation (20230392) and by Swedish Government grants through the ALF-agreement (ALF-979044). M.E. was supported by an unrestricted grant from the Swedish Research Council (Dnr: 2019-02081). J.S. was supported by Swedish Government grants through the ALF-agreement (OLL-939092). L.G. was supported by Swedish Government grants through the ALF-agreement (ALFGBG-966283) and the Swedish Heart and Lung Foundation (20210529).

Available from: 2025-05-06 Created: 2025-05-06 Last updated: 2026-03-13Bibliographically approved

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