Deng Li-Ping, Gui Xi-En, Zhang Yong-Xi, Gao Shi-Cheng, Yang Rong-Rong
Department of Infectious Diseases, Zhongnan Hospital, Wuhan University, Wuhan, Hubei Province, China.
World J Gastroenterol. 2009 Feb 28;15(8):996-1003. doi: 10.3748/wjg.15.996.
To analyze the influence of human immunodeficiency virus (HIV) infection on the course of hepatitis C virus (HCV) infection.
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.
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.
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.
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。
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。
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)。
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。