Mitochondrial dysfunction and antiretroviral nucleoside analog toxicities: what is the evidence?

被引:82
作者
Dagan, T
Sable, C
Bray, J
Gerschenson, M
机构
[1] NHLBI, Div Heart & Vasc Dis, NIH, Bethesda, MD 20892 USA
[2] Childrens Natl Med Ctr, Dept Cardiol, Washington, DC 20010 USA
[3] George Washington Univ, Sch Publ Hlth & Hlth Serv, Ctr Hlth Serv Res & Policy, Forum Collaborat HIV Res, Washington, DC 20006 USA
关键词
cardiovascular; hepatic; human immunodeficiency virus; lactic acidosis; lipodystrophy; myopathies; neuropathy; nucleoside analog reverse transcriptase inhibitors; pancreatitis;
D O I
10.1016/S1567-7249(02)00003-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial dysfunction has been associated with long-term toxicities of human immunodeficiency virus (HIV) therapy, particularly with the nucleoside analog reverse transcriptase inhibitors (NRTIs). Lactic acidosis, hepatic steatosis, myopathies, cardiomyopathies, neuropathies, and lipodystrophy are frequently attributed to mitochondrial toxicity. Since mitochondrial toxicity could pose a major threat to the long-term success of HIV therapy, the scientific evidence underlying an association between mitochondrial toxicity and antiretroviral therapies, must be carefully examined. There is some data to support the association between NRTIs and mitochondria dysfunction. In this review, we examine human, animal, and in vitro data implicating mitochondrial dysfunction as the causal mechanism of NRTI-associated toxicity in HIV-infected patients. Published by Elsevier Science B.V. and Mitochondria Research Society.
引用
收藏
页码:397 / 412
页数:16
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