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The GNB3 c.825C>T (rs5443) polymorphism and protection against fatal outcome of corona virus disease 2019 (COVID-19).
Möhlendick, Birte; Schönfelder, Kristina; Zacher, Christoph; Elsner, Carina; Rohn, Hana; Konik, Margarethe J; Thümmler, Laura; Rebmann, Vera; Lindemann, Monika; Jöckel, Karl-Heinz; Siffert, Winfried.
Affiliation
  • Möhlendick B; Institute of Pharmacogenetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Schönfelder K; Department of Nephrology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Zacher C; Institute of Pharmacogenetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Elsner C; Institute for Virology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Rohn H; Department of Infectious Diseases, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Konik MJ; Department of Infectious Diseases, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Thümmler L; Department of Infectious Diseases, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Rebmann V; Institute for Transfusion Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Lindemann M; Institute for Transfusion Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Jöckel KH; Institute for Transfusion Medicine, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Siffert W; Institute of Medical Informatics, Biometry and Epidemiology, University of Duisburg-Essen, Essen, Germany.
Front Genet ; 13: 960731, 2022.
Article de En | MEDLINE | ID: mdl-36017493
Background and aims: Albeit several factors which influence the outcome of corona virus disease (COVID-19) are already known, genetic markers which may predict the outcome of the disease in hospitalized patients are still very sparse. Thus, in this study, we aimed to analyze whether the single-nucleotide polymorphism (SNP) rs5443 in the gene GNB3, which was associated with higher T cell responses in previous studies, might be a suitable biomarker to predict T cell responses and the outcome of COVID-19 in a comprehensive German cohort. Methods: We analyzed the influence of demographics, pre-existing disorders, laboratory parameters at the time of hospitalization, and GNB3 rs5443 genotype in a comprehensive cohort (N = 1570) on the outcome of COVID-19. In a sub cohort, we analyzed SARS-CoV-2-specific T cell responses and associated GNB3 rs5443 genotypes. We investigated the influence of all factors on COVID-19 fatality in multivariable analysis. Results: We found a younger patient age, normotension or absence of diabetes mellitus or cardiovascular diseases, normal blood cell counts, and low inflammatory markers at hospital admission were protective factors against fatal course of disease. In addition, the rs5443 TT genotype was significantly associated with protection against COVID-19 fatality (OR: 0.60, 95% CI: 0.40-0.92, p = 0.02). We also observed significantly increased SARS-CoV-2-specific T cell responses in rs5443 TT genotype carriers (p = 0.01). Although we observed a significant association of the factors described previously in univariate analysis, only a younger age of the patients, normal blood cell counts, and the GNB3 rs5443 TT genotype remained independent predictors against COVID-19 fatality in multivariable analysis. Conclusion: Immutable predictors for COVID-19 fatality are relatively rare. In this study we could show that the TT genotype of the SNP rs5443 in the gene GNB3 is associated with protection against COVID-19 fatality. It was as well correlated to higher SARS-CoV-2-specific T cell responses, which could result in a milder course of disease in those patients. Based on those observations we hereby provide a further prognostic biomarker, which might be used in routine diagnostics as a predictive factor for COVID-19 mortality already upon hospitalization.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies Langue: En Journal: Front Genet Année: 2022 Type de document: Article Pays d'affiliation: Allemagne Pays de publication: Suisse

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Type d'étude: Prognostic_studies Langue: En Journal: Front Genet Année: 2022 Type de document: Article Pays d'affiliation: Allemagne Pays de publication: Suisse