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Alcohol Res Health. 2010;33(3):229-36.
2
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本文引用的文献

1
Chronic ethanol feeding affects proteasome-interacting proteins.长期喂食乙醇会影响与蛋白酶体相互作用的蛋白质。
Proteomics. 2009 Jul;9(13):3609-22. doi: 10.1002/pmic.200800959.
2
Liver-related deaths in HIV-infected patients between 1995 and 2005 in the French GERMIVIC Joint Study Group Network (Mortavic 2005 study in collaboration with the Mortalité 2005 survey, ANRS EN19).1995 年至 2005 年间法国 GERMIVIC 联合研究组网络(与 Mortalité 2005 调查合作的 Mortavic 2005 研究,ANRS EN19)中与肝脏相关的 HIV 感染者死亡情况。
HIV Med. 2009 May;10(5):282-9. doi: 10.1111/j.1468-1293.2008.00686.x. Epub 2009 Feb 15.
3
Hazardous drinking is associated with an elevated aspartate aminotransferase to platelet ratio index in an urban HIV-infected clinical cohort.在一个城市 HIV 感染临床队列中,危险饮酒与天门冬氨酸氨基转移酶与血小板比值指数升高相关。
HIV Med. 2009 Mar;10(3):133-42. doi: 10.1111/j.1468-1293.2008.00662.x. Epub 2008 Dec 20.
4
Implication of cytokines: Roles of tumor necrosis factor-alpha in liver injury.细胞因子的意义:肿瘤坏死因子-α在肝损伤中的作用。
Hepatol Res. 2008 Nov;38 Suppl 1:S19-28. doi: 10.1111/j.1872-034X.2008.00422.x.
5
HIV prevalence estimates--United States, 2006.2006年美国艾滋病毒流行率估计
MMWR Morb Mortal Wkly Rep. 2008 Oct 3;57(39):1073-6.
6
Increase in the non-HIV-related deaths among AIDS cases in the HAART era.高效抗逆转录病毒治疗(HAART)时代艾滋病病例中与非艾滋病相关的死亡人数增加。
Curr HIV Res. 2008 Jan;6(1):77-81. doi: 10.2174/157016208783572017.
7
Common pathogenic mechanism in development progression of liver injury caused by non-alcoholic or alcoholic steatohepatitis.非酒精性或酒精性脂肪性肝炎所致肝损伤发展进程中的常见致病机制。
J Toxicol Sci. 2007 Dec;32(5):453-68. doi: 10.2131/jts.32.453.
8
Mitochondrial toxicity of tenofovir, emtricitabine and abacavir alone and in combination with additional nucleoside reverse transcriptase inhibitors.替诺福韦、恩曲他滨和阿巴卡韦单独及与其他核苷类逆转录酶抑制剂联合使用时的线粒体毒性。
Antivir Ther. 2007;12(7):1075-85.
9
Implication of altered proteasome function in alcoholic liver injury.蛋白酶体功能改变在酒精性肝损伤中的作用
World J Gastroenterol. 2007 Oct 7;13(37):4931-7. doi: 10.3748/wjg.v13.i37.4931.
10
Liver-related deaths in persons infected with the human immunodeficiency virus: the D:A:D study.感染人类免疫缺陷病毒者的肝脏相关死亡:D:A:D研究
Arch Intern Med. 2006;166(15):1632-41. doi: 10.1001/archinte.166.15.1632.

关注肝脏:HIV 感染患者中的饮酒、高效抗逆转录病毒治疗与肝脏疾病

Focus on the liver: alcohol use, highly active antiretroviral therapy, and liver disease in HIV-infected patients.

作者信息

Barve Shirish, Kapoor Rama, Moghe Akshata, Ramirez Julio A, Eaton John W, Gobejishvili Leila, Joshi-Barve Swati, McClain Craig J

机构信息

University of Louisville, Louisville, Kentucky.

出版信息

Alcohol Res Health. 2010;33(3):229-36.

PMID:23584064
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3860514/
Abstract

Since the introduction of highly active antiretroviral therapy (HAART) in the 1990 s, liver disease is emerging as a major cause of morbidity and mortality among HIV-infected patients. This is attributed to a variety of factors, including HAART hepatotoxicity, coinfection with hepatitis B and C virus (HBV and HCV, respectively), and alcohol abuse. Several studies have examined the effects of HAART and HCV/HBV coinfection on liver toxicity. However, the impact of alcohol consumption as a cofactor for hepatotoxicity in HIV patients is only beginning to be understood. Similar to the general population, alcohol use is common in the HIV population but is often overlooked by health care providers. Approximately 25 percent of recently diagnosed HIV patients are alcohol dependent; moreover, alcohol dependence has been associated with HIV treatment failure. Alcohol/HAART interactions appear crucial for the development of liver disease in HIV patients. Recent research has shown that alcohol abuse is associated with severe hepatotoxicity in patients on HAART. Importantly, alcoholic- and HAART-induced liver disease share many potential mechanisms of injury, including altered metabolism of certain signaling molecules (i.e., cytokines) and dysfunction of some cell components (i.e., proteasomes and mitochondria).

摘要

自20世纪90年代引入高效抗逆转录病毒疗法(HAART)以来,肝脏疾病正成为HIV感染患者发病和死亡的主要原因。这归因于多种因素,包括HAART的肝毒性、与乙型和丙型肝炎病毒(分别为HBV和HCV)的合并感染以及酗酒。多项研究已探讨了HAART和HCV/HBV合并感染对肝脏毒性的影响。然而,饮酒作为HIV患者肝毒性的一个辅助因素所产生的影响才刚刚开始被了解。与普通人群类似,饮酒在HIV人群中很常见,但往往被医疗保健人员忽视。大约25%新诊断的HIV患者存在酒精依赖;此外,酒精依赖与HIV治疗失败有关。酒精/HAART相互作用似乎对HIV患者肝脏疾病的发展至关重要。最近的研究表明,酗酒与接受HAART治疗的患者严重肝毒性有关。重要的是,酒精性和HAART诱导的肝脏疾病有许多潜在的损伤机制,包括某些信号分子(即细胞因子)代谢改变和一些细胞成分(即蛋白酶体和线粒体)功能障碍。