酒精代谢基因ADH2和ADH3多态性与酗酒者对胰腺炎的易感性

Aaren Vedangi, S. Godi, Girinadh L.R.S.
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摘要

在发达国家和发展中国家,过度饮酒被认为是急性和慢性胰腺炎的主要原因。长期过量饮酒5-10年通常先于急性酒精性胰腺炎的初始发作。据观察,只有少数酗酒者(约5%)发展为胰腺炎。现在已经确定胰腺有代谢乙醇的能力。以往的研究表明,乙醇代谢主要有氧化和非氧化两种途径。乙醇氧化代谢包括将乙醇转化为乙醛,该反应由醛脱氢酶(ADH)催化,并有细胞色素P450酶(CYP2E1)和过氧化氢酶的参与。调节酒精代谢的遗传因素可诱发酒精性胰腺炎(AP)。我们调查了安得拉邦北部沿海地区ADH酶多态性与酒精性胰腺炎的关系。酒精性胰腺炎患者;n = 100),酒精对照(AC;n = 100)和健康对照(HC;N = 100)纳入研究。受试者的血样采集在EDTA包被的小瓶中。提取DNA,采用聚合酶链反应限制性片段长度多态性(PCR-RFLP)对ADH2和ADH3进行基因分型。用凝胶电泳法对产物进行分析。AP组ADH3 * 1/ * 1基因型频率分布(54%)明显高于AC组(35%)和HC组(42%),并与酒精性胰腺炎风险增加相关。ADH3 * 1/ * 1、ADH3 * 1/ * 2、ADH3 * 2/ * 2基因型的频率分布在AC和HC之间无统计学差异。AP患者ADH2 * 1/ * 1、ADH2 * 1/ * 2、ADH2 * 2/ * 2基因型频率分布与AC、HC患者比较,差异均无统计学意义。本研究表明,与ADH3 * 1/ * 2和ADH3 * 2/ * 2基因型相比,ADH3 * 1/ * 1基因型饮酒个体发生酒精性胰腺炎的风险更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymorphisms in alcohol metabolizing genes ADH2 and ADH3 and susceptibility to pancreatitis in alcoholics
In both developed and developing countries, overuse of alcohol is a considered as the major cause of acute and chronic pancreatitis. Prolonged overconsumption of alcohol for 5–10 years typically precedes the initial attack of acute alcoholic pancreatitis. It is observed that only a minority (around 5%) of alcoholics develop pancreatitis. It is now established that the pancreas has the capacity to metabolize ethanol. Previous studies have shown that there are two major pathways of ethanol metabolism, oxidative and non-oxidative. Oxidative ethanol metabolism involves the conversion of ethanol to acetaldehyde, a reaction that is catalysed by aldehyde dehydrogenase (ADH) with contributions from cytochrome P450 enzyme (CYP2E1) and possibly also catalase. Genetic factors regulating alcohol metabolism could predispose in developing alcoholic pancreatitis (AP). We investigated the association of polymorphisms in ADH enzymes with the alcoholic pancreatitis in North coastal Andhra Pradesh. Patients with alcoholic pancreatitis (AP;  n  = 100), alcoholic controls (AC;  n  = 100), and healthy controls (HC;  n  = 100) were included in the study. Blood samples were collected from the subjects in EDTA coated vials. DNA was extracted and genotyping for ADH2 and ADH3 was done by PCR-RFLP (polymerase chain reaction restriction fragment length polymorphism). The products were analysed by gel electrophoresis. The frequency distribution of ADH3 * 1/ * 1 genotype was significantly higher in AP group (54%) compared with AC (35%), and HC (42%), and was found to be associated with increased risk of alcoholic pancreatitis. There was no statistically significant difference between the frequency distribution of ADH3 * 1/ * 1, ADH3 * 1/ * 2, and ADH3 * 2/ * 2 genotypes between AC and HC. There was no statistically significant difference between the frequency distribution of ADH2 * 1/ * 1, ADH2 * 1/ * 2, and ADH2 * 2/ * 2 genotypes in AP compared with AC and HC. This study shows that carriers of ADH3 * 1/ * 1 individuals consuming alcohol are at higher risk for alcoholic pancreatitis than those with other genotypes such as ADH3 * 1/ * 2 and ADH3 * 2/ * 2.
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