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饮酒起始年龄是酒精使用障碍症状的一个风险因素,而 ALDH2*2 和种族会对此产生调节作用。

Age of Drinking Initiation as a Risk Factor for Alcohol Use Disorder Symptoms is Moderated by ALDH2*2 and Ethnicity.

机构信息

Department of Psychology, University of Southern California, Los Angeles, California.

Departments of Medicine and Pharmacology, Indiana University School of Medicine, Indianapolis, Indiana.

出版信息

Alcohol Clin Exp Res. 2017 Oct;41(10):1738-1744. doi: 10.1111/acer.13469. Epub 2017 Aug 28.

Abstract

BACKGROUND

An early age of drinking initiation (ADI) has been associated with increased risk for alcohol use disorders (AUDs), but the consistency of this risk across diverse samples has not been well studied. The purpose of this study was to examine whether the pathway from ADI to AUD symptoms by early adulthood is moderated by ethnicity and possessing an alcohol-metabolizing gene ALDH2*2 variant allele.

METHODS

We used multigroup structural equation modeling, including 5 groups split by ethnicity and ALDH22, to examine the consistency of the path from ADI to AUD symptoms in 604 Chinese-, Korean-, and White-American college students. We further examined the effects of ALDH22, ethnicity, and their interaction in Asians to better understand their unique contributions to the moderation.

RESULTS

The association between ADI and AUD symptoms was moderated, with ADI negatively associated with AUD symptoms among Koreans without ALDH22 and Whites, but not among Koreans with ALDH22 or Chinese regardless of ALDH22. Both ALDH22 and ethnicity within Asians contributed unique variability in the effect.

CONCLUSIONS

Ethnicity and ALDH22 altered the relationship of ADI as a risk factor for AUD symptoms. Being Chinese and possessing an ALDH22 allele within Koreans both buffered against the risk for AUD symptoms associated with earlier ADI, indicating that this relationship can be attenuated by protective factors.

摘要

背景

饮酒起始年龄较早(ADI)与酒精使用障碍(AUDs)的风险增加有关,但这种风险在不同样本中的一致性尚未得到很好的研究。本研究的目的是检验在成年早期,ADIs 向 AUD 症状发展的途径是否会受到种族和是否携带酒精代谢基因 ALDH2*2 变异等位基因的调节。

方法

我们使用多组结构方程模型,包括按种族和 ALDH22 划分的 5 个组,来检验 604 名中国、韩国和美国白人大学生中 ADI 向 AUD 症状发展的途径的一致性。我们进一步检验了 ALDH22、种族及其相互作用在亚洲人中的作用,以更好地了解它们对调节的独特贡献。

结果

ADI 与 AUD 症状之间的关联是可以调节的,在没有 ALDH22 的韩国人和白人中,ADI 与 AUD 症状呈负相关,但在有 ALDH22 的韩国人和无论是否有 ALDH22 的中国人中,ADI 与 AUD 症状之间没有关联。ALDH22 和亚洲人群体中的种族都对效应的可变性有独特的贡献。

结论

种族和 ALDH22 改变了 ADI 作为 AUD 症状风险因素的关系。中国人和韩国人携带 ALDH22 等位基因都能缓冲与早期 ADI 相关的 AUD 症状风险,这表明这种关系可以通过保护因素来减弱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39de/5626619/f2498ef76eb2/nihms898059f1.jpg

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