Exome sequencing in a familial form of anorexia nervosa supports multigenic etiology

J Neural Transm (Vienna). 2019 Nov;126(11):1505-1511. doi: 10.1007/s00702-019-02056-2. Epub 2019 Aug 6.

Abstract

Anorexia nervosa (AN) is a severe debilitating eating disorder. To date, only very few genes that predispose to AN have been identified. An alternative to association studies is to characterize ultra-rare variants in familial forms of AN. Here, we have implemented this approach to identify pathways that contribute to the development of AN through the analysis of a family with three members suffering from AN by exome analysis. We identified three ultra-rare deleterious variants in three genes (DRD4, CCKAR, NMS), already connected to the reward pathway, that co-segregate with AN, suggesting that this pathway might be playing a predisposing role in AN at least in familial forms.

Keywords: Anorexia nervosa; CCKAR; DRD4; Exome; NMS; Reward pathway.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Anorexia Nervosa / genetics*
  • Exome Sequencing
  • Female
  • Humans
  • Pedigree