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表皮生长因子 rs4444903 G/G 基因型与慢性丙型肝炎患者年轻时发生晚期纤维化的相关性。

Association between the epidermal growth factor rs4444903 G/G genotype and advanced fibrosis at a young age in chronic hepatitis C.

机构信息

Department of Laboratory Medicine, University of Udine, Italy.

出版信息

Cytokine. 2012 Jan;57(1):68-73. doi: 10.1016/j.cyto.2011.10.018. Epub 2011 Nov 27.

Abstract

BACKGROUND

The epidermal growth factor (EGF) rs4444903 A>G polymorphism has been associated with the development of liver cancer, which commonly complicates cirrhosis of viral origin; however, whether this polymorphism might be associated with fibrosis progression in chronic viral hepatitis is unknown. The present study was performed to assess the allelic and genotypic frequencies of the rs4444903 A>G polymorphism in patients with chronic hepatitis C virus HCV infection and to ascertain whether this polymorphism might be an independent predictor of the degree of fibrosis.

METHODS

An RFLP-PCR technique was used to genotype 645 patients (211 with cirrhosis); 528 were referred for the diagnosis and treatment of chronic hepatitis C, and 117 were transplanted for HCV-related end stage liver disease. A group of 428 healthy subjects served as a control. All the subjects were of Caucasian ethnicity.

RESULTS

The EGF rs4444903 A>G polymorphism genotype frequencies in HCV chronic infected patients were as follows: A/A=227 (35.3%), A/G=328 (50.9%), and G/G=90 (14.8%). Genotype frequencies were found to differ between patients with an Ishak staging score⩽2 (A/A=117, A/G=157, G/G=34) and patients with a score>2 (A/A=110, A/G=171, G/G=56, p=0.038). A highly significant linear relationship between increasing stage scores and EGF genotype was detected in younger patients (A/A: 2.02±0.18, A/G: 2.55±0.17, G/G: 3.00±0.32, p=0.008). However, no significant association was detected between the stage score and EGF genotype in older patients (A/A: 3.79±0.19, A/G: 3.64±0.15, G/G: 3.98±0.30 p=0.579).

CONCLUSIONS

The EGF rs4444903 A>G polymorphism may facilitate liver fibrosis progression in Caucasian patients with chronic hepatitis C, especially in younger patients.

摘要

背景

表皮生长因子(EGF)rs4444903 A>G 多态性与肝癌的发生有关,肝癌常合并病毒性起源的肝硬化;然而,这种多态性是否与慢性病毒性肝炎的纤维化进展有关尚不清楚。本研究旨在评估慢性丙型肝炎病毒(HCV)感染患者中 rs4444903 A>G 多态性的等位基因和基因型频率,并确定该多态性是否可作为纤维化程度的独立预测因子。

方法

采用 RFLP-PCR 技术对 645 例患者(211 例肝硬化)进行基因分型;528 例患者因慢性丙型肝炎的诊断和治疗而就诊,117 例患者因 HCV 相关终末期肝病而接受移植。428 例健康受试者作为对照组。所有受试者均为白种人。

结果

HCV 慢性感染患者 EGF rs4444903 A>G 多态性基因型频率如下:A/A=227(35.3%),A/G=328(50.9%),G/G=90(14.8%)。发现 Ishak 分期评分⩽2 的患者(A/A=117,A/G=157,G/G=34)和评分>2 的患者(A/A=110,A/G=171,G/G=56,p=0.038)之间的基因型频率存在差异。在年轻患者中,发现随着分期评分的升高,EGF 基因型呈显著线性关系(A/A:2.02±0.18,A/G:2.55±0.17,G/G:3.00±0.32,p=0.008)。然而,在年龄较大的患者中,分期评分与 EGF 基因型之间无显著相关性(A/A:3.79±0.19,A/G:3.64±0.15,G/G:3.98±0.30,p=0.579)。

结论

EGF rs4444903 A>G 多态性可能促进白人慢性丙型肝炎患者的肝纤维化进展,尤其是在年轻患者中。

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