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D2和D4受体基因与酒精中毒的连锁研究。

Linkage studies of D2 and D4 receptor genes and alcoholism.

作者信息

Hill S Y, Zezza N, Wipprecht G, Xu J, Neiswanger K

机构信息

Department of Psychiatry, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

出版信息

Am J Med Genet. 1999 Dec 15;88(6):676-85. doi: 10.1002/(sici)1096-8628(19991215)88:6<676::aid-ajmg18>3.0.co;2-s.

Abstract

The purpose of the present study was to evaluate two polymorphisms near the D2 receptor gene (TaqI A RFLP and C microsatellite) and a VNTR for D4. A nonparametric linkage (NPL) technique, SIBPAL, was used to test for the presence or absence of linkage in 54 multiplex alcoholic families. These families had been ascertained through two alcoholic proband siblings in order to increase the density of alcoholic cases within these pedigrees. Phenotypic definitions of alcoholism were manipulated in an effort to determine the impact of severity (signs of physical dependence, early age of onset, presence of antisocial personality disorder) on the likelihood of finding positive evidence for linkage. A regression analysis that simultaneously evaluated the allele sharing identical by descent for Feighner criteria alcoholism in affected, unaffected, and discordant sib pairs (SIBPAL) for two D2 polymorphisms and the D4 polymorphism gave no evidence for linkage. Phenotypes associated with greater alcoholism severity (presence of physical dependence symptoms, earlier onset, or comorbid antisocial personality disorder) revealed some evidence for linkage. The presence of one or more physical dependence symptoms in combination with Feighner criteria alcoholism provided some evidence favoring linkage (TaqI A and D4). Alcoholics with an earlier onset of alcoholism showed some evidence for linkage especially when the presence of physical dependence was required (e. g., morning drinking, wanted to stop drinking but could not, binges or benders, and evidence of withdrawal symptoms). Finally, alcoholics with antisocial personality disorder differed significantly in their allele sharing from nonalcoholics for both D2 polymorphisms. Am. J. Med. Genet. (Neuropsychiatr. Genet.) 88:676-685, 1999.

摘要

本研究的目的是评估D2受体基因附近的两种多态性(TaqI A限制性片段长度多态性和C微卫星)以及D4的可变数目串联重复序列。采用非参数连锁(NPL)技术SIBPAL,对54个多重酒精成瘾家庭进行连锁存在与否的检测。这些家庭是通过两名酒精成瘾先证者同胞确定的,以便增加这些家系中酒精成瘾病例的密度。对酒精中毒的表型定义进行了处理,以确定严重程度(身体依赖迹象、发病年龄早、反社会人格障碍的存在)对发现连锁阳性证据可能性的影响。一项回归分析同时评估了两个D2多态性和D4多态性在受影响、未受影响和不一致同胞对(SIBPAL)中符合Feighner标准酒精中毒的同源等位基因共享情况,未发现连锁证据。与更严重酒精中毒相关的表型(存在身体依赖症状、发病较早或合并反社会人格障碍)显示出一些连锁证据。一种或多种身体依赖症状与Feighner标准酒精中毒同时存在提供了一些支持连锁的证据(TaqI A和D4)。酒精中毒发病较早的酗酒者显示出一些连锁证据,尤其是当需要存在身体依赖时(例如,晨饮、想戒酒但戒不掉、暴饮或狂饮以及有戒断症状的证据)。最后,患有反社会人格障碍的酗酒者在两个D2多态性的等位基因共享方面与非酗酒者有显著差异。《美国医学遗传学杂志》(神经精神遗传学)88:676 - 685,1999年。

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