Herman Aryeh I, Philbeck John W, Vasilopoulos Nicholas L, Depetrillo Paolo B
Unit of Clinical and Biochemical Pharmacology, Laboratory of Clinical Studies, Intramural Research Program, National Institutes on Alcohol Abuse and Alcoholism, NIH 10/3C103, 10 Center Drive, MSC 1256, Bethesda, MD 20892-1256, USA.
Alcohol Alcohol. 2003 Sep-Oct;38(5):446-9. doi: 10.1093/alcalc/agg110.
In the present study, differences in alcohol consumption behaviour associated with the presence of the short variant (S) of the serotonin transporter promoter polymorphism (5-HTTLPR) was investigated in a Caucasian subset (n = 204) of 268 college students.
Students who were homozygous for the S allele were more likely to engage in binge-drinking behaviour, drank more alcohol per occasion, and reported drinking to get drunk more often.
In this Caucasian sample, the 5-HTTLPR strongly influences alcohol consumption in late pubescence.
在本研究中,我们在268名大学生的白种人亚组(n = 204)中,研究了与血清素转运体启动子多态性(5-HTTLPR)短变体(S)的存在相关的饮酒行为差异。
S等位基因纯合的学生更有可能出现暴饮行为,每次饮酒量更多,且报告称更常为了喝醉而饮酒。
在这个白种人样本中,5-HTTLPR对青春期后期的酒精消费有强烈影响。