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基因多态性会增加丙型肝炎慢性肝病的风险及严重程度。

polymorphism increases risk for and severity of chronic hepatitis C liver disease.

作者信息

Salameh Habeeb, Masadeh Maen, Al Hanayneh Muhannad, Petros Vincent, Maslonka Matthew, Nanda Arjun, Singal Ashwani K

机构信息

Habeeb Salameh, Muhannad Al Hanayneh, Department of Internal Medicine, Division of Gastroenterology and Hepatology, University of Texas Medical Branch, Galveston, TX 77555, United States.

出版信息

World J Hepatol. 2016 Dec 18;8(35):1584-1592. doi: 10.4254/wjh.v8.i35.1584.

Abstract

AIM

To examine the association of polymorphisms in chronic hepatitis C patients and development of liver disease spectrum.

METHODS

Literature was searched systematically from PubMed/MEDLINE, EMBASE, and Cochrane search engines for full-length articles written in English that examined polymorphism in chronic hepatitis C (CHC) patients. Studies evaluating the association of polymorphism spectrum (fatty liver, steatohepatitis, cirrhosis, and hepatocellular carcinoma) of CHC were included. Pooled data are reported as OR with 95%CI. Our study endpoint was the risk of the entire liver disease spectrum including: Steatosis/fatty liver, cirrhosis, and hepatocellular carcinoma in CHC patients with polymorphisms.

RESULTS

Of 380 studies identified, a total of 53 studies were included for full-text review. Nineteen on chronic hepatitis C were eligible for analysis. Pooled ORs for rs738409 GG compared to CC and CG among patients with fatty liver was 2.214 (95%CI: 1.719-2.853). ORs among advanced fibrosis/cirrhosis were 1.762 (95%CI: 1.258-2.468). Similar odds ratios among hepatocellular carcinoma patients were 2.002 (95%CI: 1.519-2.639). Pooled ORs for rs738409 GG and CG compared to CC among patients with fatty liver were 1.750 (95%CI: 1.542-1.986). Pooled ORs for advanced fibrosis/cirrhosis patients were 1.613 (95%CI: 1.211-2.147). All analyses were homogenous and without publication bias except one. The associations were maintained after adjusting for publication bias and heterogeneity.

CONCLUSION

polymorphisms have strong association with increased risk and severity of the liver disease spectrum in CHC patients.

摘要

目的

研究慢性丙型肝炎患者基因多态性与肝病谱发展之间的关联。

方法

通过PubMed/MEDLINE、EMBASE和Cochrane搜索引擎系统检索文献,查找以英文撰写的关于慢性丙型肝炎(CHC)患者基因多态性的全文文章。纳入评估CHC基因多态性谱(脂肪肝、脂肪性肝炎、肝硬化和肝细胞癌)关联的研究。汇总数据以OR及95%置信区间(CI)报告。我们的研究终点是整个肝病谱的风险,包括:存在基因多态性的CHC患者发生脂肪变性/脂肪肝、肝硬化和肝细胞癌的风险。

结果

在识别出的380项研究中,共有53项研究纳入全文审查。其中19项关于慢性丙型肝炎的研究符合分析条件。在脂肪肝患者中,rs738409基因GG型与CC型和CG型相比,汇总OR为2.214(95%CI:1.719 - 2.853)。在进展期纤维化/肝硬化患者中,OR为1.762(95%CI:1.258 - 2.468)。在肝细胞癌患者中,类似的优势比为2.002(95%CI:1.519 - 2.639)。在脂肪肝患者中,rs738409基因GG型和CG型与CC型相比,汇总OR为1.750(95%CI:1.542 - 1.986)。进展期纤维化/肝硬化患者的汇总OR为1.613(95%CI:1.211 - 2.147)。除一项研究外,所有分析均具有同质性且无发表偏倚。在调整发表偏倚和异质性后,这些关联仍然存在。

结论

基因多态性与CHC患者肝病谱风险增加及严重程度密切相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9d/5165273/b5febb429b37/WJH-8-1584-g001.jpg

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