Mixture regression analysis on age at onset in bipolar disorder patients: investigation of the role of serotonergic genes

Eur Neuropsychopharmacol. 2010 Sep;20(9):663-70. doi: 10.1016/j.euroneuro.2010.04.001. Epub 2010 May 8.

Abstract

Bipolar Disorder (BPD) is a complex psychiatric disease with a relevant underlying genetic basis. HTR2A T102C, HTR2C Cys23Ser, SLC6A4 5-HTTLPR and rs25531 polymorphisms were genotyped in 230 BPD patients and inserted as covariates in a mixture regression model of age at onset (AAO). 5-HTTLPR polymorphism associated with early onset component under recessive and additive model. HTR2A T102C, HTR2C Cys23Ser and 5-HTTLPR interaction terms associated with early onset component under dominant, recessive and additive model. These findings suggest a role of genes codifying for elements of the serotonergic system in influencing the AAO in BPD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • Bipolar Disorder / epidemiology
  • Bipolar Disorder / genetics*
  • Female
  • Genotype
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Receptor, Serotonin, 5-HT2A / genetics
  • Receptor, Serotonin, 5-HT2C / genetics
  • Regression Analysis
  • Serotonin Plasma Membrane Transport Proteins / genetics*

Substances

  • Receptor, Serotonin, 5-HT2A
  • Receptor, Serotonin, 5-HT2C
  • SLC6A4 protein, human
  • Serotonin Plasma Membrane Transport Proteins