4.2 Article

Systematic analysis of dopamine receptor genes (DRD1-DRD5) in antipsychotic-induced weight gain

Journal

PHARMACOGENOMICS JOURNAL
Volume 12, Issue 2, Pages 156-164

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/tpj.2010.65

Keywords

antipsychotic-induced weight gain; schizophrenia; pharmacogenetics; dopamine receptor genes; polymorphisms; haplotypes

Funding

  1. Abbott Labs
  2. ACADIA
  3. Bristol-Myers Squibb
  4. Eli Lilly
  5. Jansse
  6. Pfizer
  7. AstraZeneca
  8. GlaxoSmithKline
  9. Memory
  10. Cephalon
  11. Minster
  12. Aryx
  13. BiolineRx
  14. Allon
  15. Bioline
  16. Forest Labs
  17. Janssen
  18. Merck
  19. Novartis
  20. Solvay
  21. Wyeth
  22. CIHR [MOP-15007, MOP-89853]
  23. NARSAD
  24. Prentiss Foundation
  25. Ritter Foundation
  26. Hintz family
  27. Peterson Family
  28. Bebensee fellowship
  29. [MH41468]

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Antipsychotic-induced weight gain has emerged as a serious complication in the treatment of patients with most antipsychotics. We have conducted the first in-depth examination of dopamine receptor genes in antipsychotic-induced weight gain. A total of 206 patients (139 of European descent and 56 African Americans) who underwent treatment for chronic schizophrenia or schizoaffective disorder were evaluated after on average over 6 weeks of treatment. Thirty-six tag single nucleotide polymorphisms (SNPs) and one variable-number tandem repeat, spanning the five dopamine receptor genes (DRD1-DRD5) were analyzed. In the total sample, we found a nominally significant association between the DRD2 rs1079598 marker and weight change using a cutoff of 7% gain (P = 0.03). When stratifying the sample according to ethnicity and antipsychotics with highest risk for weight gain, we found significant associations in three DRD2 SNPs: rs6277 (C957T), rs1079598 and rs1800497 (TaqIA). The other genes were primarily negative. We provide evidence that dopamine receptor DRD2 gene variants might be associated with antipsychotic-induced weight gain in chronic schizophrenia patients. The Pharmacogenomics Journal (2012) 12, 156-164; doi:10.1038/tpj.2010.65; published online 17 August 2010

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