Risk factors of accelerated liver fibrosis in HIV-HCV coinfection: a matched analysis: original

Ayman B. Ibrahim, A. Shpaner, J. Nieto, S. Saab
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引用次数: 3

Abstract

Introduction: Chronic liver diseases have become a significant cause of mortality in HIV patients. Few reports have assessed risk factors for HCV disease progression in HIV infected patients. Objectives: The aim of our study was to compare the progression rate of liver fibrosis in HIV-HCV coinfected patients with that of HCV-only infected patients. We sought to identify the risk factors associated with accelerated progression rates and higher fibrosis stage. Methods: Eighteen HCV/HIV coinfected patients were matched to fifty-four HCV patients in a 1 to 3 ratio. The matching variables included duration of HCV, alcohol use, age, gender and race. Both unmatched and matched analyses were performed on estimated fibrosis progression rate and fibrosis stage separately. An ordinal logistic regression analysis was used to identify risk factors. Results: Using Metavir unit system, the mean (+ standard deviation [SD]) estimated fibrosis rates were 0.26 (+ 0.17) and 0.11 (+ 0.09) for HIV-HCV coinfected and HCV-only patients respectively (unmatched analysis p=0.001). The mean (+ SD) duration of HCV infection was 22.05 (+ 1.10) and 15.50 (+ 2.20) for coinfected and HCV-only patients, respectively. There was a statistically significant difference in the proportion of patients with stage 4 liver fibrosis between both groups (HIV-HCV 33 %, HCV 9%, P =0.004). Ordinal Logistic Regression model (unmatched analysis) suggested that duration of HCV (Odds Ratio [OR]= 1.11, 95 % confidence interval [CI] 1.03 to 1.20, P = 0.01), HIV status (OR =9.49, CI 2.39 to 37.75, P = 0.001) (overall model R2= 0.16, F = 0.0002) and age (OR=1.14, CI 1.01 to 1.28, P = 0.03) are statistically significant independent predictors of accelerated progression rate and higher fibrosis stage. Conclusions: Duration of HCV infection, age, and HIV status are significant independent predictors of accelerated fibrosis in HIV-HCV coinfected patient population. HIV-HCV coinfected patients should be counseled and their providers informed regarding the risk factors for accelerated progression of liver fibrosis. Further studies are needed to investigate the underlying biological and immunological mechanisms of accelerated liver fibrosis in HCV patients coinfected with HIV. South African Gastroenterology Review Vol.2(3) 2004: 14-17
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HIV-HCV合并感染加速肝纤维化的危险因素:一项匹配分析:原始
慢性肝病已成为HIV患者死亡的重要原因。很少有报告评估了HIV感染患者HCV疾病进展的危险因素。目的:本研究的目的是比较HIV-HCV合并感染患者与单纯hcv感染患者肝纤维化的进展率。我们试图确定与加速进展率和较高纤维化分期相关的危险因素。方法:18例HCV/HIV合并感染患者与54例HCV患者按1:3的比例配对。匹配变量包括HCV持续时间、酒精使用、年龄、性别和种族。对估计的纤维化进展率和纤维化分期分别进行了非匹配和匹配分析。采用有序逻辑回归分析确定危险因素。结果:使用Metavir单位系统,HIV-HCV合并感染和仅hcv患者的平均(+标准差[SD])估计纤维化率分别为0.26(+ 0.17)和0.11(+ 0.09)(未匹配分析p=0.001)。合并感染和单纯感染HCV的患者HCV感染的平均(+ SD)持续时间分别为22.05(+ 1.10)和15.50(+ 2.20)。两组患者发生4期肝纤维化的比例差异有统计学意义(HIV-HCV 33%, HCV 9%, P =0.004)。有序Logistic回归模型(未匹配分析)显示,HCV病程(比值比[OR]= 1.11, 95%可信区间[CI] 1.03 ~ 1.20, P = 0.01)、HIV状态(OR= 9.49, CI 2.39 ~ 37.75, P = 0.001)(总模型R2= 0.16, F = 0.0002)和年龄(OR=1.14, CI 1.01 ~ 1.28, P = 0.03)是加速进展率和较高纤维化分期的独立预测因子,具有统计学意义。结论:HCV感染持续时间、年龄和HIV状态是HIV-HCV合并感染患者纤维化加速的重要独立预测因素。应告知HIV-HCV合并感染患者,并告知其提供者肝纤维化加速进展的危险因素。HCV合并HIV患者加速肝纤维化的潜在生物学和免疫学机制有待进一步研究。南非胃肠病学评论Vol.2(3) 2004: 14-17
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South African Gastroenterology Review
South African Gastroenterology Review Medicine-Gastroenterology
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