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多巴胺受体D2基因TaqI a多态性与酒精依赖的男性局限性关联。

Male limited association of the dopamine receptor D2 gene TaqI a polymorphism and alcohol dependence.

作者信息

Limosin Frédéric, Gorwood Philip, Loze Jean-Yves, Dubertret Caroline, Gouya Laurent, Deybach Jean-Charles, Adès Jean

机构信息

Service de Psychiatrie du Pr Rouillon, Hôpital Albert Chenevier (AP-HP), Créteil, France.

出版信息

Am J Med Genet. 2002 Nov 1;112(4):343-6. doi: 10.1002/ajmg.10712.

Abstract

Association studies of the TaqI A allele of the dopamine receptor D2 (DRD2) gene with alcohol dependence have produced conflicting findings. Although a wide series of clinical features have been considered in the different association studies performed, very few studies specifically analyzed the role of gender. We compared the TaqI A polymorphisms of the DRD2 gene in 120 French Caucasian alcohol-dependent inpatients (62 males and 58 females) and 107 healthy ethnically matched controls (66 males and 41 females). We observed that 55% of alcohol-dependent males have at least one A1 allele, a prevalence that is significantly above that observed in the control males (38%). On the contrary, no differences were found in females between the alcohol-dependent inpatients and controls for the A1 allele prevalence. In our sample, this male-specific association was not explained by gender specificities of alcohol dependence, such as age at onset and severity measures (mean numbers of social, somatic, and withdrawal complications). On the other hand, alcohol-dependent women with the A1 allele reported more frequently a major depressive disorder (70% vs. 40%, P = 0.03). We thus replicated the allelic association of the A1 allele of the DRD2 gene with alcohol dependence, but showed a male-limited effect of this "vulnerability allele." Recent evidence for gender difference in dopamine D2-like receptor levels and affinity may explain this discrepancy.

摘要

多巴胺受体D2(DRD2)基因的TaqI A等位基因与酒精依赖的关联研究结果相互矛盾。尽管在已开展的不同关联研究中考虑了一系列广泛的临床特征,但很少有研究专门分析性别因素的作用。我们比较了120名法国白种人酒精依赖住院患者(62名男性和58名女性)和107名种族匹配的健康对照者(66名男性和41名女性)的DRD2基因TaqI A多态性。我们观察到,55%的酒精依赖男性至少有一个A1等位基因,这一患病率显著高于对照男性(38%)。相反,酒精依赖住院患者和对照女性之间的A1等位基因患病率没有差异。在我们的样本中,这种男性特异性关联无法用酒精依赖的性别特异性来解释,如发病年龄和严重程度指标(社会、躯体和戒断并发症的平均数量)。另一方面,携带A1等位基因的酒精依赖女性更频繁地报告患有重度抑郁症(70%对40%,P = 0.03)。因此,我们重复了DRD2基因A1等位基因与酒精依赖的等位基因关联,但显示出这种“易感等位基因”存在男性局限性效应。多巴胺D2样受体水平和亲和力存在性别差异的最新证据可能解释了这种差异。

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