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韩国人群酒精中毒的主要遗传成分。

Major genetic components underlying alcoholism in Korean population.

作者信息

Kim Dai-Jin, Choi Ihn-Geun, Park Byung Lae, Lee Boung-Chul, Ham Byung-Joo, Yoon Sujung, Bae Joon Seol, Cheong Hyun Sub, Shin Hyoung Doo

机构信息

Department of Psychiatry, Holy Family Hospital, College of Medicine, Catholic University of Korea, Sosa-dong, Wonmi-Gu, Pucheon, Kyounggi-do 420-717, Republic of Korea.

出版信息

Hum Mol Genet. 2008 Mar 15;17(6):854-8. doi: 10.1093/hmg/ddm357. Epub 2007 Dec 4.

Abstract

Alcohol metabolism is one of the biological determinants that could significantly be influenced by genetic polymorphisms in alcohol-metabolism genes. Alcohol dehydrogenase (ADH) converts alcohol to acetaldehyde, and aldehyde dehydrogenase (ALDH) converts acetaldehyde to acetate. The well-known genetic polymorphisms in ADH1B(His47Arg) and ALDH2(Glu487Lys) have dramatic effects on the rate of metabolizing alcohol and acetaldehyde, respectively. The protective allele of ADH1B (ADH1B47His) encodes for a rapid ethanol-metabolizing enzyme, and the susceptible allele of the ALDH2 (ALDH2487Lys) is strongly associated with decreased rate of metabolizing acetaldehyde. However, the combined genetic effects of both functional polymorphisms have not been clarified. The combined analysis of two polymorphisms among a Korean population (n = 1,032) revealed dramatic genetic effects on the risk of alcoholism. Individuals bearing susceptible alleles at both loci have 91 times greater risk for alcoholism [odds ratio (OR) = 91.43, P = 1.4 x 10(-32)] and individuals bearing one susceptible and one protective allele at either loci have 11 times greater risk (OR = 11.40, P = 3.5 x 10(-15)) compared with subjects who have both protective alleles. The attributable fraction of those genetic factors, calculated based on population controls, indicates that alcoholism in 86.5% of alcoholic patients can be attributed to the detrimental effect of ADH1B47Arg and/or ALDH2487Glu in Korean population.

摘要

酒精代谢是生物决定因素之一,可能会受到酒精代谢基因中基因多态性的显著影响。乙醇脱氢酶(ADH)将酒精转化为乙醛,而乙醛脱氢酶(ALDH)将乙醛转化为乙酸。ADH1B(His47Arg)和ALDH2(Glu487Lys)中著名的基因多态性分别对酒精和乙醛的代谢速率有显著影响。ADH1B的保护性等位基因(ADH1B47His)编码一种快速代谢乙醇的酶,而ALDH2的易感等位基因(ALDH2487Lys)与乙醛代谢速率降低密切相关。然而,这两种功能多态性的联合遗传效应尚未明确。对韩国人群(n = 1032)中两种多态性的联合分析揭示了对酒精中毒风险的显著遗传效应。与具有两个保护性等位基因的受试者相比,在两个位点都携带易感等位基因的个体患酒精中毒的风险高91倍[比值比(OR)= 91.43,P = 1.4×10⁻³²],在任何一个位点携带一个易感等位基因和一个保护性等位基因的个体患酒精中毒的风险高11倍(OR = 11.40,P = 3.5×10⁻¹⁵)。基于人群对照计算的这些遗传因素的归因分数表明,在韩国人群中,86.5%的酒精中毒患者可归因于ADH1B47Arg和/或ALDH2487Glu的有害影响。

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