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GWAS Study

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19.

Pairo-Castineira E, Rawlik K, Bretherick AD et al.

37198478 PubMed ID
GWAS Study Type
1779771 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PE
Pairo-Castineira E
RK
Rawlik K
BA
Bretherick AD
QT
Qi T
WY
Wu Y
NI
Nassiri I
MG
McConkey GA
ZM
Zechner M
KL
Klaric L
GF
Griffiths F
OW
Oosthuyzen W
KA
Kousathanas A
RA
Richmond A
MJ
Millar J
RC
Russell CD
MT
Malinauskas T
TR
Thwaites R
MK
Morrice K
KS
Keating S
MD
Maslove D
NA
Nichol A
SM
Semple MG
KJ
Knight J
SM
Shankar-Hari M
SC
Summers C
HC
Hinds C
HP
Horby P
LL
Ling L
MD
McAuley D
MH
Montgomery H
OP
Openshaw PJM
BC
Begg C
WT
Walsh T
TA
Tenesa A
FC
Flores C
RJ
Riancho JA
RA
Rojas-Martinez A
LP
Lapunzina P
YJ
Yang J
PC
Ponting CP
WJ
Wilson JF
VV
Vitart V
AM
Abedalthagafi M
LA
Luchessi AD
PE
Parra EJ
CR
Cruz R
CA
Carracedo A
FA
Fawkes A
ML
Murphy L
RK
Rowan K
PA
Pereira AC
LA
Law A
FB
Fairfax B
HS
Hendry SC
BJ
Baillie JK
Chapter II

Abstract

Summary of the research findings

Critical illness in COVID-19 is an extreme and clinically homogeneous disease phenotype that we have previously shown1 to be highly efficient for discovery of genetic associations2. Despite the advanced stage of illness at presentation, we have shown that host genetics in patients who are critically ill with COVID-19 can identify immunomodulatory therapies with strong beneficial effects in this group3. Here we analyse 24,202 cases of COVID-19 with critical illness comprising a combination of microarray genotype and whole-genome sequencing data from cases of critical illness in the international GenOMICC (11,440 cases) study, combined with other studies recruiting hospitalized patients with a strong focus on severe and critical disease: ISARIC4C (676 cases) and the SCOURGE consortium (5,934 cases). To put these results in the context of existing work, we conduct a meta-analysis of the new GenOMICC genome-wide association study (GWAS) results with previously published data. We find 49 genome-wide significant associations, of which 16 have not been reported previously. To investigate the therapeutic implications of these findings, we infer the structural consequences of protein-coding variants, and combine our GWAS results with gene expression data using a monocyte transcriptome-wide association study (TWAS) model, as well as gene and protein expression using Mendelian randomization. We identify potentially druggable targets in multiple systems, including inflammatory signalling (JAK1), monocyte-macrophage activation and endothelial permeability (PDE4A), immunometabolism (SLC2A5 and AK5), and host factors required for viral entry and replication (TMPRSS2 and RAB2A).

682 African ancestry cases, 2,540 African ancestry controls, 401 East Asian ancestry cases, 759 East Asian ancestry controls, 13,199 European ancestry cases, 745,011 European ancestry controls, 1,141 South Asian ancestry cases, 5,384 South Asian ancestry controls, 8,779 cases, 1,001,875 controls

Chapter III

Study Statistics

Key metrics and study information

1779771
Total Participants
GWAS
Study Type
No
Replicated
African unspecified, East Asian, European, South Asian, Other admixed ancestry, Hispanic or Latin American, Hispanic or Latin American
Ancestry
U.K., U.S., Spain, Saudi Arabia, Brazil
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.