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人类免疫缺陷病毒感染对丙型肝炎病毒感染病程的影响:一项荟萃分析。

Impact of human immunodeficiency virus infection on the course of hepatitis C virus infection: a meta-analysis.

作者信息

Deng Li-Ping, Gui Xi-En, Zhang Yong-Xi, Gao Shi-Cheng, Yang Rong-Rong

机构信息

Department of Infectious Diseases, Zhongnan Hospital, Wuhan University, Wuhan, Hubei Province, China.

出版信息

World J Gastroenterol. 2009 Feb 28;15(8):996-1003. doi: 10.3748/wjg.15.996.

Abstract

AIM

To analyze the influence of human immunodeficiency virus (HIV) infection on the course of hepatitis C virus (HCV) infection.

METHODS

We performed a meta-analysis to quantify the effect of HIV co-infection on progressive liver disease in patients with HCV infection. Published studies in the English or Chinese-language medical literature involving cohorts of HIV-negative and -positive patients coinfected with HCV were obtained by searching the PUBMED, EMBASE and CBM. Data were extracted independently from relevant studies by 2 investigators and used in a fixed-effect meta analysis to determine the difference in the course of HCV infection in the 2 groups.

RESULTS

Twenty-nine trails involving 16750 patients were identified including the outcome of histological fibrosis or cirrhosis or de-compensated liver disease or hepatocellular carcinoma or death. These studies yielded a combined adjusted odds ratio (OR) of 3.40 [95% confidence interval (CI) = 2.45 and 4.73]. Of note, studies that examined histological fibrosis/cirrhosis, decompensated liver disease, hepatocellular carcinoma or death had a pooled OR of 1.47 (95% CI = 1.27 and 1.70), 5.45 (95% CI = 2.54 and 11.71), 0.76 (95% CI = 0.50 and 1.14), and 3.60 (95% CI = 3.12 and 4.15), respectively.

CONCLUSION

Without highly active antiretroviral therapies (HAART), HIV accelerates HCV disease progression, including death, histological fibrosis/cirrhosis and decompensated liver disease. However, the rate of hepatocellular carcinoma is similar in persons who had HCV infection and were positive for HIV or negative for HIV.

摘要

目的

分析人类免疫缺陷病毒(HIV)感染对丙型肝炎病毒(HCV)感染病程的影响。

方法

我们进行了一项荟萃分析,以量化HIV合并感染对HCV感染患者进展性肝病的影响。通过检索PUBMED、EMBASE和中国生物医学文献数据库(CBM),获取英文或中文医学文献中发表的涉及HCV合并感染的HIV阴性和阳性患者队列的研究。由2名研究人员独立从相关研究中提取数据,并用于固定效应荟萃分析,以确定两组中HCV感染病程的差异。

结果

共纳入29项研究,涉及16750例患者,研究结局包括组织学纤维化或肝硬化、失代偿性肝病、肝细胞癌或死亡。这些研究得出的合并调整优势比(OR)为3.40[95%置信区间(CI)=2.45至4.73]。值得注意的是,研究组织学纤维化/肝硬化、失代偿性肝病、肝细胞癌或死亡的研究的合并OR分别为1.47(95%CI=1.27至1.70)、5.45(95%CI=2.54至11.71)、0.76(95%CI=0.50至1.14)和3.60(95%CI=3.12至4.15)。

结论

在没有高效抗逆转录病毒疗法(HAART)的情况下,HIV会加速HCV疾病进展,包括死亡、组织学纤维化/肝硬化和失代偿性肝病。然而,HCV感染且HIV阳性或HIV阴性者的肝细胞癌发生率相似。

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