Association study of bipolar disorder with candidate genes involved in catecholamine neurotransmission: DRD2, DRD3, DAT1, and TH genes

✍ Scribed by Souery, Daniel; Lipp, Olivier; Mahieu, Brigite; Mendelbaum, Karin; De Martelaer, Viviane; Broeckhoven, Christine Van; Mendlewicz, Julien

• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 600 KB
• Volume: 67
• Category: Article
• ISSN: 0148-7299
• DOI: 10.1002/(sici)1096-8628(19961122)67:6<551::aid-ajmg7>3.0.co;2-k

✦ Synopsis

Despite strong evidence for genetic involvement in the etiology of affective disorders (from twin adoption and family studies), linkage and association methodologies are still exploring the nature of genetic factors in these diseases. Interesting testable hypotheses have been described, including candidate genes involved in catecholamine neurotransmission. We studied 69 bipolar patients and 69 matched controls (for age, sex, and geographical origin) for association and linkage disequilibrium with DNA markers at the following genes: the tyrosine hydroxylase gene, dopamine transporter gene, and dopamine D2 and D3 receptor genes. Association and linkage disequilibrium were excluded between bipolar affective disorder and these four candidate genes in our sample.