Overview of genetic research in anorexia nervosa: The past, the present and the future

Marek K Brandys, Carolien G F de Kovel, Martien J Kas, Annemarie A van Elburg, Roger A H Adan

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

BACKGROUND: Even though the evidence supporting the presence of a heritable component in the aetiology of anorexia nervosa (AN) is strong, the underlying genetic mechanisms remain poorly understood. The recent publication of a genome-wide association study (GWAS) of AN (Boraska, Mol Psychiatry, 2014) was an important step in genetic research in AN.

OBJECTIVE: To briefly sum up strengths and weaknesses of candidate-gene and genome-wide approaches, to discuss the genome-wide association studies of AN and to make predictions about the genetic architecture of AN by comparing it to that of schizophrenia (since the diseases share some similarities and genetic research in schizophrenia is more advanced).

METHOD: Descriptive literature review.

RESULTS: Despite remarkable efforts, the gene-association studies in AN did not advance our knowledge as much as had been hoped, although some results still await replication.

DISCUSSION: Continuous effort of participants, clinicians and researchers remains necessary to ensure that genetic research in AN follows a similarly successful path as in schizophrenia. Identification of genetic susceptibility loci provides a basis for follow-up studies. © 2015 Wiley Periodicals, Inc. (Int J Eat Disord 2015; 48:814-825).

Original languageEnglish
Pages (from-to)814-25
Number of pages12
JournalInternational Journal of Eating Disorders
Volume48
Issue number7
DOIs
Publication statusPublished - Nov 2015

Keywords

  • genome-wide association
  • anorexia nervosa
  • genetic overlap between disorders
  • genetic architecture
  • heritability
  • candidate gene

Fingerprint

Dive into the research topics of 'Overview of genetic research in anorexia nervosa: The past, the present and the future'. Together they form a unique fingerprint.

Cite this