Uncovering associations between pre-existing conditions and COVID-19 Severity: A polygenic risk score approach across three large biobanks.


Journal

PLoS genetics
ISSN: 1553-7404
Titre abrégé: PLoS Genet
Pays: United States
ID NLM: 101239074

Informations de publication

Date de publication:
19 Dec 2023
Historique:
received: 09 08 2023
accepted: 05 12 2023
medline: 19 12 2023
pubmed: 19 12 2023
entrez: 19 12 2023
Statut: aheadofprint

Résumé

To overcome the limitations associated with the collection and curation of COVID-19 outcome data in biobanks, this study proposes the use of polygenic risk scores (PRS) as reliable proxies of COVID-19 severity across three large biobanks: the Michigan Genomics Initiative (MGI), UK Biobank (UKB), and NIH All of Us. The goal is to identify associations between pre-existing conditions and COVID-19 severity. Drawing on a sample of more than 500,000 individuals from the three biobanks, we conducted a phenome-wide association study (PheWAS) to identify associations between a PRS for COVID-19 severity, derived from a genome-wide association study on COVID-19 hospitalization, and clinical pre-existing, pre-pandemic phenotypes. We performed cohort-specific PRS PheWAS and a subsequent fixed-effects meta-analysis. The current study uncovered 23 pre-existing conditions significantly associated with the COVID-19 severity PRS in cohort-specific analyses, of which 21 were observed in the UKB cohort and two in the MGI cohort. The meta-analysis yielded 27 significant phenotypes predominantly related to obesity, metabolic disorders, and cardiovascular conditions. After adjusting for body mass index, several clinical phenotypes, such as hypercholesterolemia and gastrointestinal disorders, remained associated with an increased risk of hospitalization following COVID-19 infection. By employing PRS as a proxy for COVID-19 severity, we corroborated known risk factors and identified novel associations between pre-existing clinical phenotypes and COVID-19 severity. Our study highlights the potential value of using PRS when actual outcome data may be limited or inadequate for robust analyses.

Identifiants

pubmed: 38113267
doi: 10.1371/journal.pgen.1010907
pii: PGENETICS-D-23-00893
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1010907

Informations de copyright

Copyright: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: LGF is a Without Compensation (WOC) employee at the VA Ann Arbor, a United States government facility. SB is a paid statistical reviewer for PLOS Medicine.

Auteurs

Lars G Fritsche (LG)

Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.
Center for Precision Health Data Science, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.

Kisung Nam (K)

Graduate School of Data Science, Seoul National University, Seoul, South Korea.

Jiacong Du (J)

Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.
Center for Precision Health Data Science, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.

Ritoban Kundu (R)

Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.
Center for Precision Health Data Science, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.

Maxwell Salvatore (M)

Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.
Center for Precision Health Data Science, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.

Xu Shi (X)

Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.

Seunggeun Lee (S)

Graduate School of Data Science, Seoul National University, Seoul, South Korea.

Stephen Burgess (S)

MRC Biostatistics Unit, University of Cambridge, Cambridge, United Kingdom.
Cardiovascular Epidemiology Unit, University of Cambridge, Cambridge, United Kingdom.

Bhramar Mukherjee (B)

Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.
Center for Precision Health Data Science, University of Michigan School of Public Health, Ann Arbor, Michigan, United States of America.
Michigan Institute for Data Science, University of Michigan, Ann Arbor, Michigan, United States of America.

Classifications MeSH