No association of the neuropeptide Y (Leu7Pro) and ghrelin gene (Arg51Gln, Leu72Met, Gln90Leu) single nucleotide polymorphisms with eating disorders

Nord J Psychiatry. 2011 Jun;65(3):203-7. doi: 10.3109/08039488.2010.525258. Epub 2010 Nov 3.

Abstract

Background: Genetic factors likely contribute to the biological vulnerability of eating disorders.

Aims: Case-control association study on one neuropeptide Y gene (Leu7Pro) polymorphism and three ghrelin gene (Arg51Gln, Leu72Met and Gln90Leu) polymorphisms.

Methods: 114 eating disorder patients (46 with anorexia nervosa, 30 with bulimia nervosa, 38 with binge eating disorder) and 164 healthy controls were genotyped.

Results: No differences were detected between patients and controls for any of the four polymorphisms in allele frequency and genotype distribution (P > 0.05). Allele frequencies and genotypes had no significant influence on body mass index (P > 0.05) in eating disorder patients.

Conclusion: Positive findings of former case-control studies of associations between ghrelin gene polymorphisms and eating disorders could not be replicated. Neuropeptide Y gene polymorphisms have not been investigated in eating disorders before.

MeSH terms

  • Adolescent
  • Adult
  • Anorexia Nervosa / genetics
  • Binge-Eating Disorder / genetics
  • Body Mass Index
  • Bulimia Nervosa / genetics
  • Case-Control Studies
  • Feeding and Eating Disorders / genetics*
  • Female
  • Gene Frequency
  • Genetic Association Studies*
  • Genotype
  • Ghrelin / genetics*
  • Humans
  • Male
  • Middle Aged
  • Neuropeptide Y / genetics*
  • Polymorphism, Single Nucleotide / genetics*
  • Young Adult

Substances

  • Ghrelin
  • Neuropeptide Y