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μ-阿片受体基因(OPRM1)多态性 A118G:在芬兰酒精依赖或饮酒人群中缺乏相关性。

μ-Opioid receptor gene (OPRM1) polymorphism A118G: lack of association in Finnish populations with alcohol dependence or alcohol consumption.

机构信息

Ministry of Social Affairs and Health, Department of Occupational Safety and Health, PO Box 33, FI-00023 Government, Finland.

出版信息

Alcohol Alcohol. 2013 Sep-Oct;48(5):519-25. doi: 10.1093/alcalc/agt050. Epub 2013 May 30.

Abstract

AIMS

The molecular epidemiological studies on the association of the opioid receptor µ-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.

摘要

目的

阿片受体 μ-1(OPRM1)基因 A118G(Asn40Asp,rs1799971)多态性与酒精使用障碍的分子流行病学研究结果存在矛盾。本研究旨在检验 A118G 多态性与酒精使用障碍和酒精消费之间的可能关联,采用三个基于大样本的研究样本进行分析。

方法

使用三种不同的基于人群的样本分析 OPRM1 A118G(Asn40Asp,rs1799971)多态性与酒精使用障碍和酒精消费之间的关联:(a)芬兰队列研究 Health 2000,包括 503 名符合 DSM-IV 酒精依赖和/或酒精滥用诊断的参与者和 506 名年龄和性别匹配的对照者;(b)芬兰队列研究 FINRISK(n=2360)和(c)赫尔辛基出生队列研究(n=1384)。后两个群体缺乏基于诊断的表型,但包含了详细的饮酒信息。

结果

我们未发现对照组与酒精依赖或滥用诊断受试者之间在基因型或等位基因分布上存在统计学显著差异。同样,在 A118G 基因型与酒精消费之间也未观察到显著影响。

结论

这些结果表明,A118G(Asn40Asp)多态性可能不会对芬兰人群中酒精使用障碍的发展产生重大影响。

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