Nakamura T, Matsushita S, Nishiguchi N, Kimura M, Yoshino A, Higuchi S
Division of Clinical Research, National Institute on Alcoholism, Kurihama National Hospital, Yokosuka, Japan.
Mol Psychiatry. 1999 Jan;4(1):85-8. doi: 10.1038/sj.mp.4000474.
Approximately 10% of Japanese alcoholics develop their disease despite having an inactive form of aldehyde dehydrogenase-2 (ALDH2), known as a genetic deterrent of heavy drinking due to adverse reactions after drinking. Such alcoholics are considered to be advantageous in genetic research because they should show reduced heterogeneity and possess genetic factors conferring susceptibility to alcohol dependence. Examination of the -1438 A/G polymorphism of the serotonin 2A (5HT2A) receptor gene in 225 Japanese alcoholics with inactive ALDH2 revealed the presence of significantly more of the G allele than was found in 361 control subjects. The frequency of the G allele in 282 alcoholics with active ALDH2 fell between the G allele frequencies of controls and subjects with inactive ALDH2. These data suggest that although the effect is relatively small, genetic variability in the 5HT2A receptor is involved in the development of alcohol dependence.
尽管约10%的日本酗酒者体内的乙醛脱氢酶2(ALDH2)呈无活性形式,而饮酒后出现的不良反应使这种酶被认为是大量饮酒的一种遗传阻碍,但他们仍患上了酒精性疾病。这类酗酒者在基因研究中被认为具有优势,因为他们的异质性应较低,且拥有导致酒精依赖易感性的遗传因素。对225名携带无活性ALDH2的日本酗酒者的血清素2A(5HT2A)受体基因-1438 A/G多态性进行检测发现,与361名对照者相比,G等位基因的存在显著更多。282名携带活性ALDH2的酗酒者中G等位基因的频率介于对照者和携带无活性ALDH2者的G等位基因频率之间。这些数据表明,尽管影响相对较小,但5HT2A受体的基因变异性参与了酒精依赖的发生。