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首页> 外文期刊>Alcohol and Alcoholism >THE ROLE OF GENETIC POLYMORPHISMS IN ALCOHOLIC LIVER DISEASE
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THE ROLE OF GENETIC POLYMORPHISMS IN ALCOHOLIC LIVER DISEASE

机译:遗传多态性在酒精性肝病中的作用

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摘要

Chronic alcohol consumption is a major cause of liver cirrhosis which, however, develops in only a minority of heavy drinkers. Evidence from twin studies indicates that genetic factors account for at least 50% of individual susceptibility. The contribution of genetic factors to the development of diseases may be investigated either by means of animal experiments, through linkage studies in families of affected patients, or population based case–control studies. With regard to the latter, single nucleotide polymorphisms of genes involved in the degradation of alcohol, antioxidant defense, necroinflammation, and formation and degradation of extracellular matrix are attractive candidates for studying genotype–phenotype associations. However, many associations in early studies were found to be spurious and could not be confirmed in stringently designed investigations. Therefore, future genotype–phenotype studies in alcoholic liver disease should meet certain requirements in order to avoid pure chance observations due to a lack of power, false functional interpretation, and insufficient statistical evaluation.
机译:长期饮酒是肝硬化的主要原因,但仅少数饮酒者会发展为酒精。双胞胎研究的证据表明,遗传因素至少占个体易感性的50%。遗传因素对疾病发展的贡献可以通过动物实验,对患病患者家属的连锁研究或基于人群的病例对照研究进行调查。关于后者,涉及酒精降解,抗氧化剂防御,坏死性炎症以及细胞外基质形成和降解的基因的单核苷酸多态性是研究基因型与表型关联的诱人候选物。但是,在早期研究中发现许多关联是虚假的,无法在严格设计的研究中得到证实。因此,酒精性肝病的未来基因型-表型研究应满足一定的要求,以避免由于缺乏能力,错误的功能解释和不足的统计评估而出现单纯的偶然观察。

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