首页> 美国卫生研究院文献>Disease Markers >Combined Effect of ADH1B RS1229984 RS2066702 and ADH1C RS1693482/ RS698 Alleles on Alcoholism and Chronic Liver Diseases
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Combined Effect of ADH1B RS1229984 RS2066702 and ADH1C RS1693482/ RS698 Alleles on Alcoholism and Chronic Liver Diseases

机译:ADH1B RS1229984RS2066702和ADH1C RS1693482 / RS698等位基因对酒精中毒和慢性肝病的综合影响

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摘要

The aim of this study was to analyze the combined effect of the most frequent alcohol dehydrogenase polymorphisms (Arg48His and Arg370Cys in ADH1B, Arg272Gln and Ile350Val in ADH1C) on the alcohol use habits, alcohol dependence and chronic liver diseases in Hungary.The study included men, aged 45–64 years. Altogether, 241 cases with chronic liver disease (CLD) and 666 randomly selected controls without CLD were analysed for all four polymorphisms. Associations between the polymorphisms, individually, and in combination, and excessive and problem drinking and CLD, were assessed using logistic regression.In this study we have identified a novel mutation, called ADH1B Arg370His. The ADH1C Arg272Gln and Ile350Val showed almost complete linkage. The 272Gln/350Val allele increased the risk of excessive and problem drinking in homozygous form (OR = 1.582, p = 0.035, CI = 1.034–2.421, OR = 1.780, p = 0.016, CI = 1.113–2.848, respectively). The joint analysis showed that when combined with the wild type ADH1C Arg272/Ile350 allele, the ADH1B 48His is protective against CLD (OR = 0.368, p = 0.019, CI = 0.159–0.851).The results obtained in the study help not only to clarify the effects of different ADH SNPs but to better understand how these polymorphisms modify each other’s effects in the development of alcoholism and related diseases.
机译:这项研究的目的是分析匈牙利最常见的酒精脱氢酶多态性(ADH1B中的Arg48His和Arg370Cys,ADH1C中的Arg272Gln和Ile350Val)对匈牙利人的饮酒习惯,酒精依赖和慢性肝病的综合影响。 ,年龄在45-64岁之间。总共分析了241例患有慢性肝病(CLD)的患者和666例随机选择的无CLD的对照者的所有四种多态性。使用logistic回归评估了多态性(单独和组合)与过量饮酒和问题饮酒和CLD之间的关联。在这项研究中,我们发现了一个新突变,称为ADH1B Arg370His。 ADH1C Arg272Gln和Ile350Val显示几乎完全的连接。 272Gln / 350Val等位基因增加了纯合子形式过量饮酒和饮酒困难的风险(分别为OR = 1.582,p = 0.035,CI = 1.034–2.421,OR = 1.780,p = 0.016,CI = 1.113–2.848)。联合分析表明,与野生型ADH1C Arg272 / Ile350等位基因联合使用时,ADH1B 48His具有抗CLD的保护作用(OR = 0.368,p = 0.019,CI = 0.159-0.851)。阐明了不同ADH SNP的作用,但更好地了解了这些多态性如何在酒精中毒和相关疾病的发展中相互影响。

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