Serotonin transporter regulatory region polymorphism is associated with anorexia nervosa

Am J Med Genet B Neuropsychiatr Genet. 2004 Jul 1;128B(1):114-7. doi: 10.1002/ajmg.b.30022.

Abstract

Several lines of evidence support possible serotonin transporter (5-HTT) involvement in modulating eating disorders (ED). The 5-HTT gene is a good candidate for genetic studies on the course of ED, despite controversy concerning the association between polymorphism in the 5-HTT gene promoter region (5-HTTLPR) and ED. Comparison of 5-HTTLPR distribution in 195 female Japanese ED patients and 290 age- and gender-matched control subjects facilitated examining the association between the course of the disease and 5-HTTLPR in 138 of 195 ED subjects. The 5-HTTLPR S allele frequency was significantly higher in subjects with anorexia nervosa (AN) than in control subjects. Among subjects observed > or =3 years, the S allele frequency was significantly higher in those diagnosed as AN at ED onset than in those diagnosed as AN in this study. The 5-HTTLPR S allele might play some role in the development of AN with persistent disease.

MeSH terms

  • Adult
  • Anorexia Nervosa / genetics*
  • Case-Control Studies
  • Feeding and Eating Disorders / genetics
  • Female
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Japan / epidemiology
  • Membrane Glycoproteins / genetics*
  • Membrane Transport Proteins / genetics*
  • Molecular Epidemiology
  • Nerve Tissue Proteins / genetics*
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic / genetics
  • Serotonin Plasma Membrane Transport Proteins

Substances

  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins