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慢性乙型肝炎病毒感染的 HIV 患者长期使用核苷(酸)类似物的临床和病毒学结局。

Clinical and virological outcomes in HIV-infected patients with chronic hepatitis B on long-term nucleos(t)ide analogues.

机构信息

Department of Infectious Diseases, Hospital Carlos III, Madrid, Spain.

出版信息

AIDS. 2011 Jan 2;25(1):73-9. doi: 10.1097/QAD.0b013e328340fde2.

DOI:10.1097/QAD.0b013e328340fde2
PMID:21076274
Abstract

BACKGROUND

Chronic hepatitis B virus (HBV) infection is common in HIV-positive individuals and increases liver-related mortality. Nucleos(t)ide analogues with activity against both HBV and HIV are widely used in coinfected patients, but its long-term effect on liver disease is unknown.

METHODS

Clinical outcomes, HBsAg and/or HBeAg clearance, and changes in liver stiffness were longitudinally evaluated retrospectively in all HIV-HBV-coinfected individuals followed at our institution.

RESULTS

A total of 92 patients with HIV-HBV coinfection were identified, 19 of them superinfected with hepatitis delta virus. Their median time of follow-up was 35 months. Overall, 94% received lamivudine/emtricitabine and 82% tenofovir. Serum HBV-DNA was undetectable in 89%. Seven patients cleared serum HBsAg (2.6/100 patient-years), in four of them accompanied with anti-HBs seroconversion. Of note, two of them had hepatitis delta. Another 11 out of 42 HBeAg-positive patients cleared HBeAg (9/100 patient-years) and five of them experienced anti-HBe seroconversion. Liver decompensation and death occurred in eight (2.9/100 patient-years) and six (2.2/100 patient-years), respectively.At baseline, liver fibrosis was defined as null-mild (48%), moderate-advanced (28%) or cirrhosis (24%). At last visit, after a median of 40 months in 71 patients, 75% showed no changes, whereas improvement was recognized in 17% and worsening in 8%.

CONCLUSION

Most HIV-HBV-coinfected patients treated with anti-HBV active nucleos(t)ide analogues experience an amelioration of liver fibrosis progression, with low rates of hepatic decompensation and death. Serum HBeAg or HBsAg seroconversion occurs at yearly rates of 9 and 2.6%, respectively, even in patients with delta hepatitis.

摘要

背景

慢性乙型肝炎病毒(HBV)感染在 HIV 阳性个体中很常见,并且会增加与肝脏相关的死亡率。具有抗 HBV 和 HIV 活性的核苷(酸)类似物广泛用于合并感染患者,但长期对肝脏疾病的影响尚不清楚。

方法

对在本机构接受治疗的所有 HIV-HBV 合并感染患者进行了回顾性纵向评估,以评估临床结局、HBsAg 和/或 HBeAg 清除率以及肝硬度的变化。

结果

共确定了 92 例 HIV-HBV 合并感染患者,其中 19 例合并感染了乙型肝炎 delta 病毒。他们的中位随访时间为 35 个月。总体而言,94%的患者接受了拉米夫定/恩曲他滨和 82%的患者接受了替诺福韦。89%的患者血清 HBV-DNA 不可检测。7 例患者(2.6/100 患者年)清除了血清 HBsAg,其中 4 例伴有抗-HBs 血清转换。值得注意的是,其中 2 例有乙型肝炎 delta 病毒感染。42 例 HBeAg 阳性患者中,又有 11 例(9/100 患者年)清除了 HBeAg,其中 5 例发生了抗-HBe 血清转换。8 例(2.9/100 患者年)和 6 例(2.2/100 患者年)分别发生了肝功能失代偿和死亡。基线时,肝纤维化定义为无明显/轻度(48%)、中度-重度(28%)或肝硬化(24%)。在中位随访 40 个月后,71 例患者中有 75%无变化,17%有改善,8%有恶化。

结论

大多数接受抗 HBV 活性核苷(酸)类似物治疗的 HIV-HBV 合并感染患者的肝纤维化进展得到改善,肝功能失代偿和死亡的发生率较低。血清 HBeAg 或 HBsAg 血清转换的年发生率分别为 9%和 2.6%,即使在合并乙型肝炎 delta 病毒感染的患者中也是如此。

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