首页> 外文期刊>Alcohol and alcoholism: international journal of the Medical Council on Alcoholism >mu-Opioid Receptor Gene (OPRM1) Polymorphism A118G: Lack of Association in Finnish Populations with Alcohol Dependence or Alcohol Consumption
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mu-Opioid Receptor Gene (OPRM1) Polymorphism A118G: Lack of Association in Finnish Populations with Alcohol Dependence or Alcohol Consumption

机译:mu阿片受体基因(OPRM1)多态性A118G:酒精依赖或饮酒的芬兰人口缺乏联系。

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Aims: The molecular epidemiological studies on the association of the opioid receptor mu-1 (OPRM1) polymorphism A118G (Asn40Asp, rs1799971) and alcohol use disorders have given conflicting results. The aim of this study was to test the possible association of A118G polymorphism and alcohol use disorders and alcohol consumption in three large cohort-based study samples. Methods: The association between the OPRM1 A118G (Asn40Asp, rs1799971) polymorphism and alcohol use disorders and alcohol consumption was analyzed using three different population-based samples: (a) a Finnish cohort study, Health 2000, with 503 participants having a DSM-IV diagnosis for alcohol dependence and/or alcohol abuse and 506 age- and sex-matched controls; (b) a Finnish cohort study, FINRISK (n = 2360) and (c) the Helsinki Birth Cohort Study (n = 1384). The latter two populations lacked diagnosis-based phenotypes, but included detailed information on alcohol consumption. Results: We found no statistically significant differences in genotypic or allelic distribution between controls and subjects with alcohol dependence or abuse diagnoses. Likewise no significant effects were observed between the A118G genotype and alcohol consumption. Conclusion: These results suggest that A118G (Asn40Asp) polymorphism may not have a major effect on the development of alcohol use disorders at least in the Finnish population.
机译:目的:关于阿片受体mu-1(OPRM1)多态性A118G(Asn40Asp,rs1799971)与饮酒障碍的关联的分子流行病学研究得出了相互矛盾的结果。这项研究的目的是在三个大型的队列研究样本中检验A118G多态性与酒精使用障碍和饮酒的可能关联。方法:使用三个基于人群的样本分析了OPRM1 A118G(Asn40Asp,rs1799971)多态性与饮酒障碍和饮酒之间的关联:(a)芬兰队列研究,健康2000,有503名参与者参加了DSM-IV诊断酒精依赖和/或酒精滥用以及506个年龄和性别匹配的对照; (b)芬兰队列研究FINRISK(n = 2360),以及(c)赫尔辛基出生队列研究(n = 1384)。后两个人群缺乏基于诊断的表型,但包括有关饮酒的详细信息。结果:我们发现对照组和患有酒精依赖或滥用诊断的受试者之间在基因型或等位基因分布上没有统计学上的显着差异。同样,在A118G基因型和饮酒量之间也没有观察到明显的影响。结论:这些结果表明,至少在芬兰人群中,A118G(Asn40Asp)多态性可能不会对酒精使用障碍的发生产生重大影响。

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