Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/35143
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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.authorLane, Rashon I-
dc.contributor.authorMcDonald, Christine F-
dc.contributor.authorRidgers, Anna-
dc.contributor.authorRobbins, Rebecca-
dc.contributor.authorVarma, Prerna-
dc.contributor.authorWiley, Joshua F-
dc.contributor.authorRajaratnam, Shantha M W-
dc.contributor.authorCzeisler, Charles A-
dc.date2024-
dc.date.accessioned2024-02-29T04:11:05Z-
dc.date.available2024-02-29T04:11:05Z-
dc.date.issued2024-06-
dc.identifier.citationThe American Journal of Medicine 2024-06; 137(6)en_US
dc.identifier.issn1555-7162-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/35143-
dc.description.abstractObstructive sleep apnea is associated with COVID-19 infection. Less clear is whether obstructive sleep apnea is a risk factor for the development of Post-Acute Sequelae of SARS-CoV-2 infection (PASC). Cross-sectional survey of a general population of 24,803 U.S. adults to determine the association of obstructive sleep apnea with PASC. COVID-19 infection occurred in 10,324 (41.6%) participants. Prevalence of persistent (> 3 months post infection) putative PASC-related physical and mental health symptoms ranged from 6.5% (peripheral edema) to 19.6% (nervous/anxious). In logistic regression models, obstructive sleep apnea was associated with all putative PASC-related symptoms with the highest adjusted odds ratios (aOR) being fever (2.053) and nervous/anxious (1.939). In 4 logistic regression models of overall PASC derived from elastic net regression, obstructive sleep apnea was associated with PASC (range of aORs: 1.934-2.071); this association was mitigated in those with treated obstructive sleep apnea. In the best fitting overall model requiring ≥3 symptoms, PASC prevalence was 21.9%. In a general population sample, obstructive sleep apnea is associated with the development of PASC-related symptoms and a global definition of PASC. Treated obstructive sleep apnea mitigates the latter risk. The presence of 3 or more PASC symptoms may be useful in identifying cases and for future research.en_US
dc.language.isoeng-
dc.subjectCOVID-19en_US
dc.subjectLong COVIDen_US
dc.subjectObstructive Sleep Apneaen_US
dc.subjectPASCen_US
dc.subjectPost-Acute Sequelae of SARS-CoV-2 infectionen_US
dc.titleAssociation of Obstructive Sleep Apnea with Post-Acute Sequelae of SARS-CoV-2 infection.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleThe American Journal of Medicineen_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, Victoria, 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.affiliationTurner Institute for Brain and Mental Health, Monash University, Clayton, Victoria, Australia; Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationSchool of Psychological Sciences, Turner Institute for Brain and Mental Health, Monash University, Melbourne, Victoria, 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.en_US
dc.identifier.affiliationDepartment of Medicine, The University of Melbourne, Melbourne, Victoria, Australia; Department of Respiratory and Sleep Medicine, Austin Health, Heidelberg, Victoria, Australia; Faculty of Medicine, Monash University, Melbourne Australia.en_US
dc.identifier.affiliationRespiratory and Sleep Medicineen_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, Victoria, Australia.en_US
dc.identifier.doi10.1016/j.amjmed.2024.02.023en_US
dc.type.contentTexten_US
dc.identifier.pubmedid38401674-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
item.languageiso639-1en-
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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