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GWAS Study

Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis.

Choquet H, Li W, Yin J et al.

35022708 PubMed ID
GWAS Study Type
1241538 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CH
Choquet H
LW
Li W
YJ
Yin J
BR
Bradley R
HT
Hoffmann TJ
NP
Nandakumar P
MR
Mostaedi R
TC
Tian C
AN
Ahituv N
JE
Jorgenson E
Chapter II

Abstract

Summary of the research findings

Inguinal hernias are some of the most frequently diagnosed conditions in clinical practice and inguinal hernia repair is the most common procedure performed by general surgeons. Studies of inguinal hernias in non-European populations are lacking, though it is expected that such studies could identify novel loci. Further, the cumulative lifetime incidence of inguinal hernia is nine times greater in men than women, however, it is not clear why this difference exists. We conducted a genome-wide association meta-analysis of inguinal hernia risk across 513 120 individuals (35 774 cases and 477 346 controls) of Hispanic/Latino, African, Asian and European descent, with replication in 728 418 participants (33 491 cases and 694 927 controls) from the 23andMe, Inc dataset. We identified 63 genome-wide significant loci (P < 5 × 10-8), including 41 novel. Ancestry-specific analyses identified two loci (LYPLAL1-AS1/SLC30A10 and STXBP6-NOVA1) in African ancestry individuals. Sex-stratified analyses identified two loci (MYO1D and ZBTB7C) that are specific to women, and four (EBF2, EMX2/RAB11FIP2, VCL and FAM9A/FAM9B) that are specific to men. Functional experiments demonstrated that several of the associated regions (EFEMP1 and LYPLAL1-SLC30A10) function as enhancers and show differential activity between risk and reference alleles. Our study highlights the importance of large-scale genomic studies in ancestrally diverse populations for identifying ancestry-specific inguinal hernia susceptibility loci and provides novel biological insights into inguinal hernia etiology.

461 African American or African ancestry cases, 10,141 African American or African ancestry controls, 33,379 European ancestry cases, 436,717 European ancestry controls, 433 East Asian ancestry cases, 8,318 East Asian ancestry controls, 725 Hispanic or Latin American cases, 6,883 Hispanic or Latin American controls, 435 South Asian ancestry cases, 8,482 South Asian ancestry controls, 341 mixed ancestry cases, 6,805 mixed ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1241538
Total Participants
GWAS
Study Type
Yes
Replicated
559 African American or African ancestry cases, 23,053 African American or African ancestry controls, 30,322 European ancestry cases, 580,593 European ancestry controls, 174 East Asian ancestry cases, 12,619 East Asian ancestry controls, 2,341 Hispanic or Latin American cases, 75,507 Hispanic or Latin American controls, 95 South Asian ancestry cases, 3,155 South Asian ancestry controls
Replication Participants
African American or Afro-Caribbean, African unspecified, European, East Asian, Hispanic or Latin American, South Asian, Other admixed ancestry
Ancestry
U.S., U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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