Association of the alpha 2A adrenergic receptor -1291C/G polymorphism and antipsychotic-induced weight gain in European-Americans

Pharmacogenomics. 2009 Jul;10(7):1169-76. doi: 10.2217/pgs.09.43.

Abstract

Aims: To investigate the -1291 C/G promoter polymorphism (rs1800544) of the adrenergic alpha-2A receptor (ADRA2A) with clozapine-/olanzapine-induced weight gain in European-Americans and African-Americans. The alpha-adrenergic receptors inhibit lipolysis in the adipose tissue and are involved in weight gain regulation. Moreover, two previous studies indicated an association with antipsychotic-induced weight gain with the same polymorphism in Asian populations.

Materials & methods: We analyzed a relatively large (n=129) and well-characterized group of patients and monitored them for a period of 6-14 weeks. Our refined sample consisted of 60 European-Americans and 39 African-Americans on clozapine or olanzapine, prospectively.

Results: In European-Americans, we observed a significant difference in weight gain across the genotypic categories (p=0.046). The carriers of the C allele gained more weight compared with the subjects homozygous for the GG allele (CC + CG vs GG; 3.73 +/- 4.13 kg vs 0.23 +/- 2.92 kg; p=0.013). We did not find a significant association in African-Americans, although the sample size was probably too small.

Conclusion: Our observations suggest a possible role of ADRA2A polymorphisms in clozapine-/olanzpaine-induced weight gain in subjects of European descent.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antipsychotic Agents / adverse effects*
  • Black or African American / genetics
  • Double-Blind Method
  • Female
  • Genome-Wide Association Study / methods
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Genetic / genetics*
  • Prospective Studies
  • Receptors, Adrenergic, alpha-2 / genetics*
  • Weight Gain / drug effects*
  • Weight Gain / genetics*
  • White People / genetics*

Substances

  • ADRA2A protein, human
  • Antipsychotic Agents
  • Receptors, Adrenergic, alpha-2