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dc.contributor.authorCetin, Meryem
dc.contributor.authorCetin, Sirin
dc.contributor.authorUlgen, Ayse
dc.contributor.authorLi, Wentian
dc.date.accessioned2024-03-12T19:29:24Z
dc.date.available2024-03-12T19:29:24Z
dc.date.issued2023
dc.identifier.issn1246-7820
dc.identifier.urihttps://doi.org/10.1016/j.tracli.2022.10.003
dc.identifier.urihttps://hdl.handle.net/20.500.12450/2296
dc.description.abstractWe have shown in an ethnically homogenous Turkey cohort with more than six thousand cases and 25 thousand controls that ABO blood types that contain anti-A antibody (O and B) are protective against COVID-19 infection and hospitalization, whereas those without the anti-A antibody (A and AB) are risks. The A + AB frequency increases from 54.7 % in uninfected controls to 57.6 % in COVID-19 outpatients, and to 62.5 % in COVID-19 inpatients. The odds-ratio (OR) for lacking of anti-A antibody risk for infection is 1.16 (95 % confidence interval (CI) 1.1-1.22, and Fisher test p-value 1.8 x 10-7). The OR for hospitaliza-tion is 1.23 (95 %CI 1.06-1.42, Fisher test p-value 0.005). A linear regression treating controls, outpatients, inpatients as three numerical levels over anti-A antibody leads to a p-value of 5.9 x 10-9. All these asso-ciations remain to be statistically significant after conditioning over age, even though age itself is a risk for both infection and hospitalization. We also attempted to correct the potential effect from vaccination, even though vaccination information is not available, by using the date of the data collection as a surro-gate to vaccination status. Although no significant association between infection/hospitalization with Rhesus blood system was found, forest plots are used to illustrate possible trends.(c) 2022 Societe francaise de transfusion sanguine (SFTS). Published by Elsevier Masson SAS. All rights reserved.en_US
dc.description.sponsorshipRobert S Boas Center for Genomics and Human Geneticsen_US
dc.description.sponsorshipWL acknowledges the support from Robert S Boas Center for Genomics and Human Genetics. There is no external funding for the data analysis work.en_US
dc.language.isoengen_US
dc.publisherElsevier France-Editions Scientifiques Medicales Elsevieren_US
dc.relation.ispartofTransfusion Clinique Et Biologiqueen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectABO blood groupen_US
dc.subjectAnti -A antibodyen_US
dc.subjectCOVID-19en_US
dc.subjectLogistic regressionen_US
dc.titleBlood-Type-A is a COVID-19 infection and hospitalization risk in a Turkish cohorten_US
dc.typearticleen_US
dc.departmentAmasya Üniversitesien_US
dc.authoridLi, Wentian/0000-0003-1155-110X
dc.identifier.volume30en_US
dc.identifier.issue1en_US
dc.identifier.startpage116en_US
dc.identifier.endpage122en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopus2-s2.0-85143499136en_US
dc.identifier.doi10.1016/j.tracli.2022.10.003
dc.department-temp[Cetin, Meryem] Amasya Univ, Fac Med, Dept Med Microbiol, Amasya, Turkiye; [Cetin, Sirin] Amasya Univ, Dept Biostat, Amasya, Turkiye; [Ulgen, Ayse; Li, Wentian] Girne American Univ, Fac Med, Dept Biostat, CY-99320 Karmi, Cyprus; [Ulgen, Ayse] Nottingham Trent Univ, Sch Sci & Technol, Dept Math, Nottingham NG11 8NF, England; [Li, Wentian] Northwell Hlth, Feinstein Inst Med Res, Robert S Boas Ctr Genom & Human Genet, Manhasset, NY USAen_US
dc.identifier.wosWOS:000964972500001en_US
dc.identifier.pmid36243305en_US


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