Souery D, Lipp O, Mahieu B, Mendelbaum K, De Martelaer V, Van Broeckhoven C, Mendlewicz J
Department of Psychiatry, University Clinics of Brussels, Erasme Hospital, Free University of Brussels, Belgium.
Am J Med Genet. 1996 Nov 22;67(6):551-5. doi: 10.1002/(SICI)1096-8628(19961122)67:6<551::AID-AJMG7>3.0.CO;2-K.
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.
尽管有充分证据表明遗传因素参与情感障碍的病因(来自双胞胎收养和家族研究),但连锁和关联方法仍在探索这些疾病中遗传因素的本质。已经描述了有趣的可检验假设,包括参与儿茶酚胺神经传递的候选基因。我们研究了69名双相情感障碍患者和69名匹配的对照(年龄、性别和地理来源匹配),以检测与以下基因的DNA标记的关联和连锁不平衡:酪氨酸羟化酶基因、多巴胺转运体基因以及多巴胺D2和D3受体基因。在我们的样本中,双相情感障碍与这四个候选基因之间不存在关联和连锁不平衡。