Excess of allele1 for α3 subunit GABA receptor gene (GABRA3) in bipolar patients: a multicentric association study View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2002-02

AUTHORS

I Massat, D Souery, J Del-Favero, L Oruc, M M Noethen, D Blackwood, M Thomson, W Muir, G N Papadimitriou, D G Dikeos, R Kaneva, A Serretti, R Lilli, E Smeraldi, M Jakovljevic, V Folnegovic, M Rietschel, V Milanova, F Valente, C Van Broeckhoven, J Mendlewicz

ABSTRACT

The available data from preclinical and pharmacological studies on the role of gamma amino butyric acid (GABA) support the hypothesis that a dysfunction in brain GABAergic system activity contributes to the vulnerability to bipolar affective disorders (BPAD). Moreover, the localization of the alpha3 subunit GABA receptor GABRA3 gene on the Xq28, a region of interest in certain forms of bipolar illness, suggests that GABRA3 may be a candidate gene in BPAD. In the present study, we tested the genetic contribution of the GABRA3 dinucleotide polymorphism in a European multicentric case-control sample, matched for sex and ethnogeographical origin. Allele and genotype (in females) frequencies were compared in 185 BPAD patients and 370 controls. A significant increase of genotype 1-1 was observed in BPAD females compared to controls (P=0.0004). Furthermore, when considering recessivity of allele 1 (females with genotype 1-1 and males carrying allele 1), results were even more significant (P= 0.00002). Our findings suggest that the GABRA3 polymorphism may confer susceptibility to or may be in linkage disequilibrium with another gene involved in the genetic etiology of BPAD. More... »

PAGES

201

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/sj.mp.4000953

DOI

http://dx.doi.org/10.1038/sj.mp.4000953

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1008387861

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/11840313


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