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GWAS Study

A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers.

Zhao X, Wu X, Xiao J et al.

37636041 PubMed ID
GWAS Study Type
2845029 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZX
Zhao X
WX
Wu X
XJ
Xiao J
ZL
Zhang L
HY
Hao Y
XC
Xiao C
ZB
Zhang B
LJ
Li J
JX
Jiang X
Chapter II

Abstract

Summary of the research findings

Little is known regarding the long-term adverse effects of COVID-19 on female-specific cancers, nor the shared genetic influences underlying these conditions. We performed a comprehensive genome-wide cross-trait analysis to investigate the shared genetic architecture between COVID-19 (infection, hospitalization, and critical illness) with three female-specific cancers (breast cancer (BC), epithelial ovarian cancer (EOC), and endometrial cancer (EC)). We identified significant genome-wide genetic correlations with EC for both hospitalization (rg = 0.19, p = 0.01) and critical illness (rg = 0.29, p = 3.00 × 10-4). Mendelian randomization demonstrated no valid association of COVID-19 with any cancer of interest, except for suggestive associations of genetically predicted hospitalization (ORIVW = 1.09, p = 0.04) and critical illness (ORIVW = 1.06, p = 0.04) with EC risk, none withstanding multiple correction. Cross-trait meta-analysis identified 20 SNPs shared between COVID-19 with BC, 15 with EOC, and 5 with EC; and transcriptome-wide association studies revealed multiple shared genes. Findings support intrinsic links underlying these complex traits, highlighting shared mechanisms rather than causal associations.

133,384 European ancestry breast cancer cases, 122,616 European ancestry COVID-19 cases, 2,589,029 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

2845029
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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