dc.contributor.author | Cetin, Meryem | |
dc.contributor.author | Cetin, Sirin | |
dc.contributor.author | Ulgen, Ayse | |
dc.contributor.author | Li, Wentian | |
dc.date.accessioned | 2024-03-12T19:29:24Z | |
dc.date.available | 2024-03-12T19:29:24Z | |
dc.date.issued | 2023 | |
dc.identifier.issn | 1246-7820 | |
dc.identifier.uri | https://doi.org/10.1016/j.tracli.2022.10.003 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12450/2296 | |
dc.description.abstract | We 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.sponsorship | Robert S Boas Center for Genomics and Human Genetics | en_US |
dc.description.sponsorship | WL 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.iso | eng | en_US |
dc.publisher | Elsevier France-Editions Scientifiques Medicales Elsevier | en_US |
dc.relation.ispartof | Transfusion Clinique Et Biologique | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | ABO blood group | en_US |
dc.subject | Anti -A antibody | en_US |
dc.subject | COVID-19 | en_US |
dc.subject | Logistic regression | en_US |
dc.title | Blood-Type-A is a COVID-19 infection and hospitalization risk in a Turkish cohort | en_US |
dc.type | article | en_US |
dc.department | Amasya Üniversitesi | en_US |
dc.authorid | Li, Wentian/0000-0003-1155-110X | |
dc.identifier.volume | 30 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 116 | en_US |
dc.identifier.endpage | 122 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.scopus | 2-s2.0-85143499136 | en_US |
dc.identifier.doi | 10.1016/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 USA | en_US |
dc.identifier.wos | WOS:000964972500001 | en_US |
dc.identifier.pmid | 36243305 | en_US |