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

Mol Biol Evol. 2023 Jun 1;40(6):msad130. doi: 10.1093/molbev/msad130.

Abstract

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.

Keywords: Dupuytren's disease; EPDR1; Neandertals; genome-wide association studies; risk variant; splicing quantitative trait loci.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Dupuytren Contracture* / genetics
  • Humans
  • Male
  • Neanderthals* / genetics
  • Risk Factors