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抗逆转录病毒疗法的类型和疗程是否能减轻HIV与丙型肝炎病毒合并感染患者的肝纤维化?

Do type and duration of antiretroviral therapy attenuate liver fibrosis in HIV-hepatitis C virus-coinfected patients?

作者信息

Verma Sumita, Wang Chun-Hsiang, Govindarajan Sugantha, Kanel Gary, Squires Kathleen, Bonacini Maurizio

机构信息

Division of Gastrointestinal and Liver Diseases, University of Southern California, Los Angeles, CA 90033, USA.

出版信息

Clin Infect Dis. 2006 Jan 15;42(2):262-70. doi: 10.1086/499055. Epub 2005 Dec 2.

Abstract

BACKGROUND

This study aimed to determine whether type and duration of therapy for human immunodeficiency virus (HIV) infection attenuates liver fibrosis in patients with HIV and hepatitis C virus (HCV) coinfection.

METHODS

Patients with HCV monoinfection (group 1) and HIV-HCV coinfection were retrospectively selected; the latter patients were classified into the following 3 groups: group 2, patients who received no therapy or only nucleoside reverse-transcriptase inhibitors (NRTIs); group 3, those who received highly active antiretroviral therapy (HAART); and group 4, those who initially received NRTIs followed by HAART. Fibrosis stage (scale, 0-6) and necroinflammatory score (scale, 0-18) were assessed according to the Ishak system. Data are presented as mean +/- standard deviation.

RESULTS

Three hundred eighty-one patients (296 HCV-monoinfected patients and 85 HIV-HCV-coinfected patients) were recruited. The durations of HIV therapy before liver biopsy was performed for groups 2, 3, and 4 were 3.8 +/- 2.8, 3.3 +/- 1.8, and 6.6 +/- 2.2 years. The time from HIV diagnosis to HAART initiation was shorter for group 3 than for group 4 (9.1 +/- 7.3 vs. 34.1 +/- 13.1 months; P < .0001). Groups 1 and 3 had similar fibrosis stages (3.1 +/- 2 vs. 3.4 +/- 2.4), rates of fibrosis progression (0.13 +/- 0.09 vs. 0.16 +/- 0.11 per year), and necroinflammatory scores (6.1 +/- 1.8 vs. 6.1 +/- 2.0). Groups 2 and 4 had significantly more-advanced liver disease, as determined by fibrosis stage (4.6 +/- 1.8 vs. 4.3 +/- 2.0; P < .0009), rate of fibrosis progression (0.24 +/- 0.11 vs. 0.20 +/- 0.10 per year; P < .0001), and prevalence of cirrhosis (68% vs. 55%; P < .006), compared with group 1.

CONCLUSIONS

HIC-HCV-coinfected subjects who receive HAART as their sole form of therapy have liver histology findings comparable to those for HCV-monoinfected patients. A similar degree of benefit is not observed for HIV-HCV-coinfected patients who receive no therapy, NRTIs, or HAART after NRTIs, despite having a longer duration of therapy.

摘要

背景

本研究旨在确定人类免疫缺陷病毒(HIV)感染的治疗类型和持续时间是否能减轻HIV与丙型肝炎病毒(HCV)合并感染患者的肝纤维化。

方法

回顾性选取HCV单一感染患者(第1组)和HIV-HCV合并感染患者;后者被分为以下3组:第2组,未接受治疗或仅接受核苷类逆转录酶抑制剂(NRTIs)治疗的患者;第3组,接受高效抗逆转录病毒治疗(HAART)的患者;第4组,最初接受NRTIs治疗随后接受HAART的患者。根据Ishak系统评估纤维化分期(范围0 - 6)和坏死性炎症评分(范围0 - 18)。数据以均值±标准差表示。

结果

共纳入381例患者(296例HCV单一感染患者和85例HIV-HCV合并感染患者)。第2组、第3组和第4组在进行肝活检前的HIV治疗持续时间分别为3.8±2.8年、3.3±1.8年和6.6±2.2年。第3组从HIV诊断到开始HAART的时间比第4组短(9.1±7.3个月对34.1±13.1个月;P < 0.0001)。第1组和第3组的纤维化分期相似(3.1±2对3.4±2.4),纤维化进展率相似(每年0.13±0.09对0.16±0.11),坏死性炎症评分相似(6.1±1.8对6.1±2.0)。与第1组相比,第2组和第4组的肝病更严重,这由纤维化分期(4.6±1.8对4.3±2.0;P < 0.0009)、纤维化进展率(每年0.24±0.11对0.20±0.10;P < 0.0001)和肝硬化患病率(68%对55%;P < 0.006)确定。

结论

仅接受HAART作为唯一治疗形式的HIV-HCV合并感染受试者的肝脏组织学结果与HCV单一感染患者相当。未接受治疗、接受NRTIs或接受NRTIs后再接受HAART的HIV-HCV合并感染患者,尽管治疗持续时间更长,但未观察到类似程度的获益。

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