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日本患者酒精代谢酶基因多态性与酒精性肝硬化:多变量分析

Polymorphisms in alcohol metabolizing enzyme genes and alcoholic cirrhosis in Japanese patients: a multivariate analysis.

作者信息

Yamauchi M, Maezawa Y, Mizuhara Y, Ohata M, Hirakawa J, Nakajima H, Toda G

机构信息

First Department of Internal Medicine, Jikei University School of Medicine, Tokyo, Japan.

出版信息

Hepatology. 1995 Oct;22(4 Pt 1):1136-42. doi: 10.1016/0270-9139(95)90621-5.

Abstract

Alcohol dehydrogenase (ADH), aldehyde dehydrogenase (ALDH), and P450IIE1 are the primary enzymes that catalyze the conversion of ethanol to acetaldehyde and then to acetate. Genetic polymorphisms have been reported in ADH2, ADH3, ALDH2, and the 5'-flanking region of P450IIEI. In this study, we used multivariate analysis to determine which genetic polymorphisms in alcohol metabolizing enzymes were independently associated with the development of alcoholic cirrhosis. Thirty-four noncirrhotic alcoholic patients, including 27 with fatty liver and 7 with nonspecific changes, and 46 patients with alcoholic liver cirrhosis were studied. Restriction fragment length polymorphisms (RFLPs) in the ADH2 and P450IIE1 genes were detected by digestion of polymerase chain reaction (PCR)-amplified DNA with MaeIII and RsaI, respectively. In the ALDH2 gene, RFLPs were detected by differences in the MboII site after PCR amplification. By multivariate analysis of four significant factors including total alcohol intake, ADH, ALDH, and P450IIE1 using the multiple logistic regression model, genotype ADH2(2)/ADH2(2) (P = .029) and genotype c1/c1 of P450IIE1 (P = .013) were found to be independently associated with alcoholic cirrhosis. The odds ratios for ADH2(2)/ADH2(2) genotype and the type A genotype of P450IIE1 (c1/c1) were 4.600 and 4.006, respectively. These results suggest that ADH2 and P450IIE1 gene polymorphisms may be independently associated with the development of alcoholic liver cirrhosis in Japan.

摘要

乙醇脱氢酶(ADH)、乙醛脱氢酶(ALDH)和细胞色素P450IIE1是催化乙醇转化为乙醛进而转化为乙酸盐的主要酶。已报道ADH2、ADH3、ALDH2以及细胞色素P450IIE1的5'侧翼区存在基因多态性。在本研究中,我们采用多变量分析来确定酒精代谢酶中的哪些基因多态性与酒精性肝硬化的发生独立相关。我们研究了34例非肝硬化酒精性患者,其中包括27例脂肪肝患者和7例非特异性改变患者,以及46例酒精性肝硬化患者。分别用MaeIII和RsaI消化聚合酶链反应(PCR)扩增的DNA,检测ADH2和细胞色素P450IIE1基因中的限制性片段长度多态性(RFLP)。在ALDH2基因中,通过PCR扩增后MboII位点的差异检测RFLP。使用多元逻辑回归模型对总酒精摄入量、ADH、ALDH和细胞色素P450IIE1这四个重要因素进行多变量分析,发现ADH2(2)/ADH2(2)基因型(P = 0.029)和细胞色素P450IIE1的c1/c1基因型(P = 0.013)与酒精性肝硬化独立相关。ADH2(2)/ADH2(2)基因型和细胞色素P450IIE1的A型基因型(c1/c1)的比值比分别为4.600和4.006。这些结果表明,在日本,ADH2和细胞色素P450IIE1基因多态性可能与酒精性肝硬化的发生独立相关。

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