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Multi-omics highlights ABO plasma protein as a causal risk factor for COVID-19

Authors :
Ana I. Hernández Cordero
Philippe Joubert
Chen Xi Yang
Ke Hao
Stephen Milne
David C. Nickle
Yohan Bossé
Maarten van den Berge
Don D. Sin
Wim Timens
Xuan Li
Guided Treatment in Optimal Selected Cancer Patients (GUTS)
Groningen Research Institute for Asthma and COPD (GRIAC)
Source :
Human Genetics, HUMAN GENETICS, 140(6), 969-979. SPRINGER
Publication Year :
2020
Publisher :
Cold Spring Harbor Laboratory, 2020.

Abstract

SARS-CoV-2 is responsible for the coronavirus disease 2019 (COVID-19) and the current health crisis. Despite intensive research efforts, the genes and pathways that contribute to COVID-19 remain poorly understood. We, therefore, used an integrative genomics (IG) approach to identify candidate genes responsible for COVID-19 and its severity. We used Bayesian colocalization (COLOC) and summary-based Mendelian randomization to combine gene expression quantitative trait loci (eQTLs) from the Lung eQTL (n = 1,038) and eQTLGen (n = 31,784) studies with published COVID-19 genome-wide association study (GWAS) data from the COVID-19 Host Genetics Initiative. Additionally, we used COLOC to integrate plasma protein quantitative trait loci (pQTL) from the INTERVAL study (n = 3,301) with COVID-19 loci. Finally, we determined any causal associations between plasma proteins and COVID-19 using multi-variable two-sample Mendelian randomization (MR). The expression of 18 genes in lung and/or blood co-localized with COVID-19 loci. Of these, 12 genes were in suggestive loci (PGWAS

Details

ISSN :
03406717
Database :
OpenAIRE
Journal :
Human Genetics, HUMAN GENETICS, 140(6), 969-979. SPRINGER
Accession number :
edsair.doi.dedup.....099029ba8dfd6ebc463a712fbd028475
Full Text :
https://doi.org/10.1101/2020.10.05.20207118