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Association of alcohol-metabolizing genes with alcoholism in a Mexican Indian (Otomi) population.

机译:在墨西哥印第安人(乙女)人群中,酒精代谢基因与酒精中毒的关联。

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Association studies provide a powerful approach to link DNA variants and genetic predisposition to complex diseases. In this study, we determined the genotype and allelic frequencies of genes encoding enzymes involved in alcohol metabolism in alcoholic and nonalcoholic subjects of related ethnicity. A total of 118 individuals of Otomi Mexican Indian ancestry were included. Fifty-nine were chronic alcoholics according to WHO criteria and alcohol dependents according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM IV) criteria. They were compared to 59 teetotalers or alcohol consumers of <10 g per day. The restriction fragment length polymorphisms analyzed were ADH1B/MaeIII, ALDH2/MboII, CYP2E1/DraI, CYP2E1/RsaI, and CYP2E1/TaqI. Of the studied polymorphisms, a significant difference between alcoholic and nonalcoholic Otomies was observed only in the CYP2E1/TaqI. The common genotype in alcoholics was A1/A2 (54%), and in nonalcoholics the homozygous A2/A2 (63%) (odds ratio [OR]: 0.28; 95% confidence interval [CI]: 0.13-0.60; P=.002). The frequency of the mutant allele A1 was significantly higher in alcoholics than in nonalcoholics (41 vs. 21%; OR: 2.4; 95% CI: 1.3-4.3; P=.003). This documents the presence of a polymorphism of CYP2E1 that is overexpressed in alcoholic Otomies, in which the variant allele (A1 of CYP2E1/TaqI) is associated with increased susceptibility to alcoholism. The appreciation that this finding may be an additional factor contributing to the high frequency of liver cirrhosis in Otomies requires further investigation.
机译:关联研究提供了将DNA变异和遗传易感性与复杂疾病联系起来的有效方法。在这项研究中,我们确定了相关种族的酒精和非酒精受试者中编码与酒精代谢有关的酶的基因的基因型和等位基因频率。总共包括118个人的Otomi墨西哥印第安血统。根据世界卫生组织的标准,有59名是慢性酒精中毒,根据《精神疾病诊断和统计手册》第4版(DSM IV)标准,是酒精依赖者。将他们与每天食用<10 g的59个酒醉者或饮酒者进行比较。分析的限制性片段长度多态性是ADH1B / MaeIII,ALDH2 / MboII,CYP2E1 / DraI,CYP2E1 / RsaI和CYP2E1 / TaqI。在所研究的多态性中,仅在CYP2E1 / TaqI中观察到酒精和非酒精性割礼之间的显着差异。酗酒者的常见基因型是A1 / A2(54%),而在非酗酒者中,纯合的A2 / A2(63%)(赔率[OR]:0.28; 95%置信区间[CI]:0.13-0.60; P =。 002)。酗酒者的突变等位基因A1的频率显着高于非酗酒者(41%vs. 21%; OR:2.4; 95%CI:1.3-4.3; P = .003)。这证明了CYP2E1的多态性在酒精疗法中表达过,其中变异等位基因(CYP2E1 / TaqI的A1)与酒精中毒易感性增加相关。对这一发现可能是导致Otomies肝硬化高发的另一个因素的认识需要进一步研究。

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