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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.

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。

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