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GWAS Study

Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals.

Ågren R, Patil S, Zhou X et al.

37315093 PubMed ID
GWAS Study Type
653751 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ÅR
Ågren R
PS
Patil S
ZX
Zhou X
SK
Sahlholm K
PS
Pääbo S
ZH
Zeberg H
Chapter II

Abstract

Summary of the research findings

Dupuytren's disease is characterized by fingers becoming permanently bent in a flexed position. Whereas people of African ancestry are rarely afflicted by Dupuytren's disease, up to ∼30% of men over 60 years suffer from this condition in northern Europe. Here, we meta-analyze 3 biobanks comprising 7,871 cases and 645,880 controls and find 61 genome-wide significant variants associated with Dupuytren's disease. We show that 3 of the 61 loci harbor alleles of Neandertal origin, including the second and third most strongly associated ones (P = 6.4 × 10-132 and P = 9.2 × 10-69, respectively). For the most strongly associated Neandertal variant, we identify EPDR1 as the causal gene. Dupuytren's disease is an example of how admixture with Neandertals has shaped regional differences in disease prevalence.

7,871 European ancestry cases, 645,880 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

653751
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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