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GWAS Study

Discovery of novel ancestry specific genes for androgens and hypogonadism in Million Veteran Program Men.

Pagadala MS, Teerlink CC, Jasuja GK et al.

40316537 PubMed ID
GWAS Study Type
95184 Participants
336 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PM
Pagadala MS
TC
Teerlink CC
JG
Jasuja GK
PM
Palnati M
AT
Anglin-Foote T
CN
Chang NN
DR
Deka R
LK
Lee KM
AF
Agiri FY
AT
Amariuta T
ST
Seibert TM
RB
Rose BS
PK
Pridgen KM
LJ
Lynch JA
CH
Carter HK
PM
Panizzon MS
HR
Hauger RL
Chapter II

Abstract

Summary of the research findings

Given the various roles of testosterone in men's health, we conducted a multi-ancestral genetic analysis of total testosterone, free testosterone, SHBG, and hypogonadism in men within the Million Veteran Program (MVP). Here we identified 157 significant testosterone genetic variants, of which 8 have significant ancestry-specific associations. These variants implicate several genes, including SERPINF2, PRPF8, BAIAP2L1, SHBG, PRMT6, and PPIF, related to liver function. Genetic regulators of testosterone have cell type-specific effects in the testes, liver, and adrenal gland and are associated with disease risk. We conducted a meta-analysis amongst ancestry groups to identify 188 variants significantly associated with testosterone, of which 22 are novel associations. We constructed genetic scores for total testosterone, SHBG levels, and hypogonadism and find that men with higher testosterone genetic scores have lower odds of diabetes, hyperlipidemia, gout, and cardiac disorders. These findings provide insight into androgen regulation and identify novel variants for disease risk stratification.

95,184 European ancestry males

Chapter III

Study Statistics

Key metrics and study information

95184
Total Participants
GWAS
Study Type
No
Replicated
European, African American or Afro-Caribbean, Hispanic or Latin American, East Asian
Ancestry
U.S.
Recruitment Country
Chapter IV

AI-Generated Summary

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