Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35476
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dc.contributor.authorQuan, Stuart F-
dc.contributor.authorWeaver, Matthew D-
dc.contributor.authorCzeisler, Mark É-
dc.contributor.authorBarger, Laura K-
dc.contributor.authorBooker, Lauren A-
dc.contributor.authorHoward, Mark E-
dc.contributor.authorJackson, Melinda L-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorRidgers, Anna-
dc.contributor.authorRobbins, Rebecca-
dc.contributor.authorVarma, Prerna-
dc.contributor.authorRajaratnam, Shantha M W-
dc.contributor.authorCzeisler, Charles A-
dc.date2024-
dc.date.accessioned2024-09-12T00:53:25Z-
dc.date.available2024-09-12T00:53:25Z-
dc.date.issued2024-08-16-
dc.identifier.citationMedRxiv : the Preprint Server for Health Sciences 2024-08-16en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35476-
dc.description.abstractCross-sectional studies suggest that obstructive sleep apnea (OSA) is a potential risk factor for incident COVID-19 infection, but longitudinal studies are lacking. In this study, two surveys from a large general population cohort, the COVID-19 Outbreak Public Evaluation (COPE) Initiative, undertaken 147 ± 58 days apart were analyzed to determine whether the pre-existing OSA was a risk factor for the incidence of COVID-19. Of the 24,803 respondents completing the initial survey, 14,950 were negative for COVID-19; data from the follow-up survey were available for 2,325 respondents. Those with incident COVID-19 infection had a slightly higher prevalence of OSA (14.3 vs. 11.5%, p=0.068). Stratification by treatment status revealed that those untreated for their OSA were at greater risk for developing COVID-19 infection (OSA Untreated, 14.2 vs. 7.4%, p≤0.05). In a logistic regression model adjusted for comorbidities, demographic and socioeconomic factors and the interaction between vaccination status and OSA, incident COVID-19 infection was 2.15 times more likely in those with untreated OSA (aOR: 2.15, 95% CI: 1.18-3.92, p≤0.05). Stratification by treatment status revealed only untreated OSA participants were at greater risk for COVID-19 (aOR: 3.21, 95% CI: 1.25-8.23, p≤0.05). The evidence from this study confirms untreated OSA as a risk factor for acquiring COVID-19 infection and highlights the importance of actively treating and managing OSA as a preventative mechanism against COVID-19 disease.en_US
dc.language.isoeng-
dc.subjectCOVID-19en_US
dc.subjectObstructive Sleep Apneaen_US
dc.subjectSARS-CoV-2 infectionen_US
dc.titleObstructive Sleep Apnea is a Risk Factor for Incident COVID-19 Infection.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleMedRxiv : the Preprint Server for Health Sciencesen_US
dc.identifier.affiliationDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA.;Division of Sleep Medicine, Harvard Medical School, Boston, MA.en_US
dc.identifier.affiliationFrancis Weld Peabody Society, Harvard Medical School, Boston, MA.;School of Psychological Sciences, Turner Institute for Brain and Mental Health, Monash University, Melbourne, Australia.;Institute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australia.en_US
dc.identifier.affiliationDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA.;Division of Sleep Medicine, Harvard Medical School, Boston, MA.en_US
dc.identifier.affiliationInstitute for Breathing and Sleepen_US
dc.identifier.affiliationSchool of Psychological Sciences, Turner Institute for Brain and Mental Health, Monash University, Melbourne, Australia.;Institute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australia.en_US
dc.identifier.affiliationDivision of Sleep and Circadian Disorders, Brigham and Women's Hospital, Boston, MA.;Division of Sleep Medicine, Harvard Medical School, Boston, MA.en_US
dc.identifier.affiliationSchool of Psychological Sciences, Turner Institute for Brain and Mental Health, Monash University, Melbourne, Australia.en_US
dc.identifier.doi10.1101/2024.08.15.24312067en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-9474-7679en_US
dc.identifier.orcid0000-0003-3578-336Xen_US
dc.identifier.orcid0000-0003-3100-7347en_US
dc.identifier.orcid0000-0001-8547-7331en_US
dc.identifier.orcid0000-0002-0533-3715en_US
dc.identifier.orcid0000-0001-7772-1496en_US
dc.identifier.orcid0000-0003-4976-8101en_US
dc.identifier.orcid0000-0001-6481-3391en_US
dc.identifier.orcid0000-0003-1360-9387en_US
dc.identifier.orcid0000-0003-0288-2505en_US
dc.identifier.orcid0000-0001-5408-1625en_US
dc.identifier.orcid0000-0001-7527-8558en_US
dc.identifier.orcid0000-0002-7408-1849en_US
dc.identifier.pubmedid39185535-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptInstitute for Breathing and Sleep-
crisitem.author.deptRespiratory and Sleep Medicine-
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