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A European multicenter association study ofHTR2A receptor polymorphism in bipolar affective disorder

2000; Wiley; Volume: 96; Issue: 2 Linguagem: Inglês

10.1002/(sici)1096-8628(20000403)96

1096-8628

Isabelle Massat, Daniel Souery, Olivier Lipp, Sylvie Blairy, G N Papadimitriou, D. Dikeos, Manfred Ackenheil, S. Fuchshuber, Christiane Hilger, Radka Kaneva, Vibra Milanova, Geert R. Verheyen, Peter Raeymaekers, Luc Staner, Lilijana Oruč, Miro Jakovljević, Alessandro Serretti, Fabìo Macciardi, Christine Van Broeckhoven, Julien Mendlewicz,

Neurotransmitter Receptor Influence on Behavior

The available data on the role of 5-HT in a variety of behaviors support the hypothesis that a dysfunction in brain serotoninergic system activity contributes to vulnerability to major depression. The diversity in the electrophysiological actions of 5-HT in the central nervous system can now be categorized according to receptor subtypes and their respective effector mechanisms. In particular, the implication of central postsynaptic 5-HT2A receptor in affective disorders has been supported by findings consistent with the hypothesis of 5-HT2A receptor up-regulation in depression. For these reasons, the 5-HT2A receptor (HTR2A) gene can be considered as a candidate gene in bipolar affective disorder (BPAD). We tested the possible genetic contribution of the polymorphic DNA variation T102C in exon 1 of HTR2A (chromosome 13q14-21) gene in a large European multicentric case-control sample. Allele and genotype frequencies, as well as homo-heterozygote distributions were compared between the two groups of 309 bipolar affective disorder patients and 309 matched controls. No significant differences were observed in the allelic and genotypic (also for homo-heterozygote) distribution between BPAD and controls. These results indicate that, in our sample, the 5-HT2A receptor polymorphism studied is unlikely to play a major role in the genetic susceptibility to BPAD. Am. J. Med. Genet. (Neuropsychiatr. Genet.) 96:136-140, 2000.