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Polymorphisms in the transforming growth factor-beta gene (TGF-beta) and the risk of advanced alcoholic liver disease.

机译:转化生长因子-β基因(TGF-beta)的多态性和晚期酒精性肝病的风险。

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BACKGROUND/AIMS: There are wide interindividual differences in the risk of developing alcoholic cirrhosis. Transforming growth factor beta(1) (TGF-beta(1)) is the main cytokine involved in liver fibrogenesis. The TGF-beta(1) gene is polymorphic at several sites and these polymorphisms are probably related to differences in the rate of TGF-beta(1) synthesis. Our aim has been to analyse the influence of the TGF-beta(1) gene polymorphisms in the predisposition to advanced alcoholic liver disease (ALD) in ethanol abusers. METHODS: TGF-beta(1) single nucleotide polymorphisms at positions -509 (C or T), +869 (C or T, codon 10), and +915 (C or G, codon 25) were examined in 165 alcoholics with advanced ALD and in 185 healthy controls. RESULTS: Among the 94 male patients with oesophageal varices, those carrying the GG genotype at position +915 were diagnosed at an older age than the remaining patients (age 52.1 years, standard deviation (SD) 9.9 vs. 45 SD 13.4, P=0.012). No other statistically significant differences were found in the distribution of the three TGF-beta(1) polymorphisms analysed individually or as combined haplotypes. CONCLUSIONS: The polymorphisms at the TGF-beta(1) gene analysed in this study are probably not related to the risk of advanced ALD.
机译:背景/目的:发生酒精性肝硬化的风险存在个体差异。转化生长因子β(1)(TGF-β(1))是参与肝纤维化的主要细胞因子。 TGF-beta(1)基因在几个位点是多态的,这些多态性可能与TGF-beta(1)合成速率的差异有关。我们的目标是分析乙醇滥用者中TGF-beta(1)基因多态性对晚期酒精性肝病(ALD)易感性的影响。方法:在165名酒精中毒患者中,对-509(C或T),+ 869(C或T,密码子10)和+915(C或G,密码子25)的TGF-beta(1)单核苷酸多态性进行了检查。 ALD和185个健康对照。结果:在94例男性食管静脉曲张患者中,携带GG基因型+915位的患者被诊断为比其余患者年龄更大(年龄52.1岁,标准差(SD)9.9比45 SD 13.4,P = 0.012) )。在单独或作为组合单倍型分析的三个TGF-beta(1)多态性的分布中未发现其他统计显着差异。结论:在这项研究中分析的TGF-beta(1)基因的多态性可能与晚期ALD的风险无关。

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