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多巴胺D4受体第三外显子等位基因与酗酒者寻求新奇行为的变异

Dopamine D4 receptor exon III alleles and variation of novelty seeking in alcoholics.

作者信息

Sander T, Harms H, Dufeu P, Kuhn S, Rommelspacher H, Schmidt L G

机构信息

Department of Psychiatry, University Hospital Benjamin Franklin, Berlin, Germany.

出版信息

Am J Med Genet. 1997 Sep 19;74(5):483-7. doi: 10.1002/(sici)1096-8628(19970919)74:5<483::aid-ajmg5>3.0.co;2-p.

Abstract

A dysfunction of dopaminergic neurotansmission has been implicated in alcohol-seeking behavior. Recently, a significant association between the seven-repeat allele (DRD47R) of a 16 amino acid motif in the third exon of the dopamine D4 receptor gene (DRD4) and the personality trait of novelty seeking has been reported. Our population-based association study tested the hypothesis that the DRD47R variant predisposes to high levels of novelty seeking, which may underlie alcohol-seeking behavior. The genotypes of the expressed DRD4 exon III polymorphism were determined in 197 German controls and 252 German alcohol-dependent males, of whom 92 alcoholics completed the tridimensional personality questionnaire. We found no significant differences in the DRD47R frequencies between controls and alcoholics, including two subgroups (56 alcoholics with dissocial personality disorder according to ICD-10 and 89 alcoholics with severe withdrawal symptoms) with a high level of novelty seeking. The novelty-seeking scores did not differ significantly between alcoholics (including both subgroups) carrying long alleles with six or more repeats compared with those lacking long alleles. The present results do not provide evidence that the DRD47R allele contributes a common and relevant effect to alcohol-seeking behavior in our sample of alcoholics.

摘要

多巴胺能神经传递功能障碍与觅酒行为有关。最近,有报道称多巴胺D4受体基因(DRD4)第三外显子中一个16个氨基酸基序的七重复等位基因(DRD47R)与寻求新奇的人格特质之间存在显著关联。我们基于人群的关联研究检验了这样一个假设,即DRD47R变体易导致高水平的寻求新奇,而这可能是觅酒行为的基础。在197名德国对照者和252名德国酒精依赖男性中确定了表达的DRD4外显子III多态性的基因型,其中92名酗酒者完成了三维人格问卷。我们发现对照者和酗酒者之间的DRD47R频率没有显著差异,包括两个具有高水平寻求新奇的亚组(根据国际疾病分类第10版,56名患有反社会人格障碍的酗酒者和89名有严重戒断症状的酗酒者)。携带六个或更多重复长等位基因的酗酒者(包括两个亚组)与缺乏长等位基因的酗酒者相比,寻求新奇得分没有显著差异。目前的结果没有提供证据表明DRD47R等位基因对我们酗酒者样本中的觅酒行为有共同且相关的影响。

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