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巴西慢性丙型肝炎合并HIV感染患者严重肝纤维化的发病率及预测因素

Incidence and predictors of severe liver fibrosis in HIV-infected patients with chronic hepatitis C in Brazil.

作者信息

Mendes-Correa Maria Cássia, Widman Azzo, Brussi Maria Luiza Paes, Guastini Cristina Fátima, Gianini Reinaldo José

机构信息

Casa da AIDS, Division of Infectious Diseases, Hospital das Clinicas, University of Säo Paulo, São Paulo, Brazil.

出版信息

AIDS Patient Care STDS. 2008 Sep;22(9):701-7. doi: 10.1089/apc.2007.0216.

Abstract

The aim of this study was to examine the incidence and factors associated with the severity of liver fibrosis in 234 coinfected patients in Brazil. Patients were cared for in our clinic, from 1996 to 2004. Eligible patients were defined as patients with documented HIV and hepatitis C virus (HCV) infections and had previously undergone a liver biopsy. Patients with persistently normal alanine aminotransferase (ALT) were also included. The variables selected for study were age, gender, risk category, history of high alcohol consumption, CD4(+) T cell count, antiretroviral therapy usage, HCV genotype and duration of HCV infection. Stage of fibrosis was scored as follows: F0, no fibrosis; F1, portal fibrosis with no septa; F2, portal fibrosis with few septa; F3, bridging fibrosis with many septa; and F4, cirrhosis. The liver fibrosis stage was F3 in 39 (16.6%) and F4 in 20(8.5%) patients. Among patients with normal ALT, the liver fibrosis stage was F3-F4 in three patients (5.6%). Predictors of severe liver fibrosis (F3-F4) by multivariate analysis were age (older patients) and genotype 3 (genotype 1 = odds ratio [OR], 0.28; 95% confidence interval [CI], 0.12 0.65). In summary, in the present study severe liver fibrosis was found in 25% of our patients and was associated with an age of more than 38 years at the time of liver biopsy as well as, HCV genotype 3. No differences were found with respect to CD4(+) T cell counts although patients with a CD4(+) T cell count greater than 50 were excluded.

摘要

本研究旨在调查巴西234例合并感染患者肝纤维化的发生率及与肝纤维化严重程度相关的因素。1996年至2004年期间,这些患者在我们的诊所接受治疗。符合条件的患者被定义为有记录的HIV和丙型肝炎病毒(HCV)感染患者,且之前接受过肝活检。谷丙转氨酶(ALT)持续正常的患者也被纳入研究。所选的研究变量包括年龄、性别、风险类别、高酒精摄入量史、CD4(+)T细胞计数、抗逆转录病毒疗法的使用、HCV基因型以及HCV感染持续时间。纤维化分期如下:F0,无纤维化;F1,无间隔的门脉纤维化;F2,有少量间隔的门脉纤维化;F3,有许多间隔的桥接纤维化;F4,肝硬化。39例(16.6%)患者的肝纤维化分期为F3,20例(8.5%)患者的肝纤维化分期为F4。在ALT正常的患者中,3例(5.6%)患者的肝纤维化分期为F3 - F4。多因素分析显示,严重肝纤维化(F3 - F4)的预测因素为年龄(年龄较大的患者)和基因型3(基因型1 = 比值比[OR],0.28;95%置信区间[CI],0.12 - 0.65)。总之,在本研究中,25%的患者存在严重肝纤维化,这与肝活检时年龄超过38岁以及HCV基因型3有关。尽管CD4(+)T细胞计数大于50的患者被排除,但在CD4(+)T细胞计数方面未发现差异。

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