Nucleoside analogues and neuropathy in the era of HAART

被引:53
作者
Cherry, CL
McArthur, JC
Hoy, JF
Wesselingh, SL
机构
[1] Alfred Hosp, Dept Infect Dis & Microbiol, Melbourne, Vic 3181, Australia
[2] Monash Univ, Dept Med, Melbourne, Vic 3004, Australia
[3] Johns Hopkins Univ, Dept Neurol, Baltimore, MD 21218 USA
[4] Johns Hopkins Univ, Dept Epidemiol, Baltimore, MD 21218 USA
关键词
nucleoside analogues; neuropathy; mitochondrial DNA; HIV;
D O I
10.1016/S1386-6532(02)00118-X
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Sensory neuropathies occur commonly in the setting of HIV infection. Sensory neuropathy (SN) is clearly associated with HIV itself, and in this context develops in association with increased macrophage activation in the peripheral nervous system. A clinically identical SN may also occur as a consequence of exposure to some HIV treatments. In this setting, impaired mitochondrial function is thought to play a role in the development of neurological dysfunction. Objective: This review explores the evidence for the neurotoxicity of HIV and HIV treatments, the effect of nucleoside reverse transcriptase inhibitors on mitochondria, and the likely associations between these. Conclusions: Dideoxynucleotide drugs are commonly associated with SN. The nucleoside reverse transcriptase inhibitors inhibit mitochondrial DNA synthesis and may thus exacerbate existing viral-induced nerve damage. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:195 / 207
页数:13
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