O'Shea Taryn, Thomas Nathaniel, Webb Bradley Todd, Dick Danielle M, Kendler Kenneth S, Chartier Karen G
a Virginia Commonwealth University , School of Social Work , Richmond , VA , USA.
b Virginia Commonwealth University , Virginia Institute for Psychiatric and Behavioral Genetics , Richmond , VA , USA.
Am J Drug Alcohol Abuse. 2017 Nov;43(6):678-685. doi: 10.1080/00952990.2017.1314489. Epub 2017 May 4.
The ALDH2*2 allele (A-allele) at rs671 is more commonly carried by Asians and is associated with alcohol-related flushing, a strong adverse reaction to alcohol that is protective against drinking. Social factors, such as having friends who binge drink, also contribute to drinking in Asian youth.
This study examined the interplay between ALDH22, peer drinking, and alcohol consumption in college students. We hypothesized that the relationship between ALDH22 and standard grams of ethanol per month would vary based on the level of peer drinking.
Subjects (N = 318, 63.25% female) were East Asian college students in the United States who reported drinking alcohol. Data were from the freshman year of a university survey that included a saliva DNA sample. ALDH22 status was coded ALDH22(+) (A/G and A/A genotypes) and ALDH2*2(-) (G/G genotype). Peer drinking was students' perception of how many of their friends "got drunk".
Main effects of ALDH22(-) and having more friends who got drunk were associated with greater alcohol consumption. The ALDH22 × peer drunkenness interaction showed a stronger positive association with alcohol consumption for ALDH22(-) versus ALDH22(+) at increasing levels of peer drunkenness. Follow-up comparisons within each peer drunkenness level identified significantly higher alcohol consumption for ALDH22(-) compared to ALDH22(+) at the all friends got drunk level.
There was evidence of a stronger effect for ALDH22(-) compared to ALDH22(+) with greater alcohol use when students were more exposed to peer drinking. Findings contribute to a growing literature on the interrelationships between genetic influences and more permissive environments for alcohol consumption.
rs671位点的乙醛脱氢酶2*2等位基因(A等位基因)在亚洲人中携带更为普遍,且与酒精相关的脸红有关,这是一种对饮酒的强烈不良反应,具有防止饮酒的作用。社会因素,如拥有酗酒的朋友,也会促使亚洲青少年饮酒。
本研究探讨了乙醛脱氢酶22、同伴饮酒与大学生酒精消费之间的相互作用。我们假设,乙醛脱氢酶22与每月乙醇标准摄入量之间的关系会因同伴饮酒水平的不同而有所变化。
研究对象(N = 318,63.25%为女性)是美国的东亚裔大学生,他们均报告有饮酒行为。数据来自大学调查的一年级阶段,其中包括唾液DNA样本。乙醛脱氢酶22状态被编码为乙醛脱氢酶22(+)(A/G和A/A基因型)和乙醛脱氢酶2*2(-)(G/G基因型)。同伴饮酒情况是指学生对有多少朋友“喝醉过”的认知。
乙醛脱氢酶22(-)以及有更多喝醉朋友这两个主效应均与更高的酒精消费量相关。乙醛脱氢酶22×同伴醉酒的交互作用表明,在同伴醉酒水平不断升高的情况下,与乙醛脱氢酶22(+)相比,乙醛脱氢酶22(-)与酒精消费之间的正相关更强。在每个同伴醉酒水平内的后续比较发现,在所有朋友都喝醉的水平下,乙醛脱氢酶22(-)的酒精消费量显著高于乙醛脱氢酶22(+)。
有证据表明,当学生更多地接触到同伴饮酒时,与乙醛脱氢酶22(+)相比,乙醛脱氢酶22(-)对酒精使用的影响更强。这些发现为关于遗传影响与更宽松的饮酒环境之间相互关系的不断增多的文献提供了补充。