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Multi-omics highlights ABO plasma protein as a causal risk factor for COVID-19
- 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
- Subjects :
- Candidate gene
Quantitative Trait Loci
Genome-wide association study
Quantitative trait locus
Biology
Polymorphism, Single Nucleotide
ABO Blood-Group System
Cohort Studies
03 medical and health sciences
Risk Factors
ABO blood group system
Mendelian randomization
Genetics
Humans
Genetic Predisposition to Disease
Risk factor
Lung
Genetics (clinical)
Original Investigation
030304 developmental biology
Blood type
0303 health sciences
SARS-CoV-2
030305 genetics & heredity
COVID-19
Mendelian Randomization Analysis
Blood Proteins
Human genetics
Coronavirus
Expression quantitative trait loci
Genome-Wide Association Study
Subjects
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