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GWAS Study

GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.

Pirastu N, Joshi PK, de Vries PS et al.

29146897 PubMed ID
GWAS Study Type
74679 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PN
Pirastu N
JP
Joshi PK
DV
de Vries PS
CM
Cornelis MC
MP
McKeigue PM
KN
Keum N
FN
Franceschini N
CM
Colombo M
GE
Giovannucci EL
SA
Spiliopoulou A
FL
Franke L
NK
North KE
KP
Kraft P
MA
Morrison AC
ET
Esko T
WJ
Wilson JF
Chapter II

Abstract

Summary of the research findings

Male pattern baldness (MPB) or androgenetic alopecia is one of the most common conditions affecting men, reaching a prevalence of ~50% by the age of 50; however, the known genes explain little of the heritability. Here, we present the results of a genome-wide association study including more than 70,000 men, identifying 71 independently replicated loci, of which 30 are novel. These loci explain 38% of the risk, suggesting that MPB is less genetically complex than other complex traits. We show that many of these loci contain genes that are relevant to the pathology and highlight pathways and functions underlying baldness. Finally, despite only showing genome-wide genetic correlation with height, pathway-specific genetic correlations are significant for traits including lifespan and cancer. Our study not only greatly increases the number of MPB loci, illuminating the genetic architecture, but also provides a new approach to disentangling the shared biological pathways underlying complex diseases.

25,662 British ancestry cases, 17,928 British ancestry controls

Chapter III

Study Statistics

Key metrics and study information

74679
Total Participants
GWAS
Study Type
Yes
Replicated
13,367 European ancestry cases, 11,851 European ancestry controls, 3,436 cases, 2,435 controls
Replication Participants
European
Ancestry
U.S., U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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