Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait

dc.contributor.authorVerma, Anurag
dc.contributor.authorHuffman, Jennifer E.
dc.contributor.authorGao, Lina
dc.contributor.authorMinnier, Jessica
dc.contributor.authorWu, Wen-Chih
dc.contributor.authorCho, Kelly
dc.contributor.authorHo, Yuk-Lam
dc.contributor.authorGorman, Bryan R.
dc.contributor.authorPyarajan, Saiju
dc.contributor.authorRajeevan, Nallakkandi
dc.contributor.authorGarcon, Helene
dc.contributor.authorJoseph, Jacob
dc.contributor.authorMcGeary, John E.
dc.contributor.authorSuzuki, Ayako
dc.contributor.authorReaven, Peter D.
dc.contributor.authorWan, Emily S.
dc.contributor.authorLynch, Julie A.
dc.contributor.authorPetersen, Jeffrey M.
dc.contributor.authorMeigs, James B.
dc.contributor.authorFreiberg, Matthew S.
dc.contributor.authorGatsby, Elise
dc.contributor.authorLynch, Kristine E.
dc.contributor.authorZekavat, Seyedeh Maryam
dc.contributor.authorNatarajan, Pradeep
dc.contributor.authorDalal, Sharvari
dc.contributor.authorJhala, Darshana N.
dc.contributor.authorArjomandi, Mehrdad
dc.contributor.authorBonomo, Robert A.
dc.contributor.authorThompson, Trevor K.
dc.contributor.authorPathak, Gita A.
dc.contributor.authorZhou, Jin J.
dc.contributor.authorDonskey, Curtis J.
dc.contributor.authorMadduri, Ravi K.
dc.contributor.authorWells, Quinn S.
dc.contributor.authorGelernter, Joel
dc.contributor.authorHuang, Rose D. L.
dc.contributor.authorPolimanti, Renato
dc.contributor.authorChang, Kyong-Mi
dc.contributor.authorLiao, Katherine P.
dc.contributor.authorTsao, Philip S.
dc.contributor.authorSun, Yan V.
dc.contributor.authorWilson, Peter W. F.
dc.contributor.authorO'Donnell, Christopher J.
dc.contributor.authorHung, Adriana M.
dc.contributor.authorGaziano, J. Michael
dc.contributor.authorHauger, Richard L.
dc.contributor.authorIyengar, Sudha K.
dc.contributor.authorLuoh, Shiuh-Wen
dc.contributor.authorVA Million Veteran Program COVID-19 Science Initiative
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-11-26T12:29:59Z
dc.date.available2024-11-26T12:29:59Z
dc.date.issued2022
dc.description.abstractImportance: Sickle cell trait (SCT), defined as the presence of 1 hemoglobin beta sickle allele (rs334-T) and 1 normal beta allele, is prevalent in millions of people in the US, particularly in individuals of African and Hispanic ancestry. However, the association of SCT with COVID-19 is unclear. Objective: To assess the association of SCT with the prepandemic health conditions in participants of the Million Veteran Program (MVP) and to assess the severity and sequelae of COVID-19. Design, setting, and participants: COVID-19 clinical data include 2729 persons with SCT, of whom 353 had COVID-19, and 129 848 SCT-negative individuals, of whom 13 488 had COVID-19. Associations between SCT and COVID-19 outcomes were examined using firth regression. Analyses were performed by ancestry and adjusted for sex, age, age squared, and ancestral principal components to account for population stratification. Data for the study were collected between March 2020 and February 2021. Exposures: The hemoglobin beta S (HbS) allele (rs334-T). Main outcomes and measures: This study evaluated 4 COVID-19 outcomes derived from the World Health Organization severity scale and phenotypes derived from International Classification of Diseases codes in the electronic health records. Results: Of the 132 577 MVP participants with COVID-19 data, mean (SD) age at the index date was 64.8 (13.1) years. Sickle cell trait was present in 7.8% of individuals of African ancestry and associated with a history of chronic kidney disease, diabetic kidney disease, hypertensive kidney disease, pulmonary embolism, and cerebrovascular disease. Among the 4 clinical outcomes of COVID-19, SCT was associated with an increased COVID-19 mortality in individuals of African ancestry (n = 3749; odds ratio, 1.77; 95% CI, 1.13 to 2.77; P = .01). In the 60 days following COVID-19, SCT was associated with an increased incidence of acute kidney failure. A counterfactual mediation framework estimated that on average, 20.7% (95% CI, -3.8% to 56.0%) of the total effect of SCT on COVID-19 fatalities was due to acute kidney failure. Conclusions and relevance: In this genetic association study, SCT was associated with preexisting kidney comorbidities, increased COVID-19 mortality, and kidney morbidity.
dc.identifier.citationVerma A, Huffman JE, Gao L, et al. Association of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait. JAMA Intern Med. 2022;182(8):796-804. doi:10.1001/jamainternmed.2022.2141
dc.identifier.urihttps://hdl.handle.net/1805/44721
dc.language.isoen_US
dc.publisherAmerican Medical Association
dc.relation.isversionof10.1001/jamainternmed.2022.2141
dc.relation.journalJAMA Internal Medicine
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectAcute kidney injury
dc.subjectCOVID-19
dc.subjectSickle cell trait
dc.subjectHemoglobins
dc.titleAssociation of Kidney Comorbidities and Acute Kidney Failure With Unfavorable Outcomes After COVID-19 in Individuals With the Sickle Cell Trait
dc.typeArticle
ul.alternative.fulltexthttps://pmc.ncbi.nlm.nih.gov/articles/PMC9237798/
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