Neurological and Psychiatric Adverse Effects of Antiretroviral Drugs

被引:127
作者
Abers, Michael S. [1 ]
Shandera, Wayne X. [1 ]
Kass, Joseph S. [1 ]
机构
[1] Baylor Coll Med, Houston, TX 77030 USA
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; HIV-INFECTED PATIENTS; EFAVIRENZ DOSE REDUCTION; REVERSE-TRANSCRIPTASE INHIBITORS; HEREDITARY OPTIC NEUROPATHY; PERSISTENT MITOCHONDRIAL DYSFUNCTION; UNINFECTED CHILDREN BORN; GUILLAIN-BARRE-SYNDROME; ACETYL-L-CARNITINE; QUALITY-OF-LIFE;
D O I
10.1007/s40263-013-0132-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Antiretroviral drugs are associated with a variety of adverse effects on the central and peripheral nervous systems. The frequency and severity of neuropsychiatric adverse events is highly variable, with differences between the antiretroviral classes and amongst the individual drugs in each class. In the developing world, where the nucleoside reverse transcriptase inhibitor (NRTI) stavudine remains a commonly prescribed antiretroviral, peripheral neuropathy is an important complication of treatment. Importantly, this clinical entity is often difficult to distinguish from human immunodeficiency virus (HIV)-induced peripheral neuropathy. Several clinical trials have addressed the efficacy of various agents in the treatment of NRTI-induced neurotoxicity. NRTI-induced neurotoxicity is caused by inhibition of mitochondrial DNA polymerase. This mechanism is also responsible for the mitochondrial myopathy and lactic acidosis that occur with zidovudine. NRTIs, particularly zidovudine and abacavir, may also cause central nervous system (CNS) manifestations, including mania and psychosis. The non-nucleoside reverse transcriptase inhibitor (NNRTI) efavirenz is perhaps the antiretroviral most commonly associated with CNS toxicity, causing insomnia, irritability and vivid dreams. Recent studies have suggested that the risk of developing these adverse effects is increased in patients with various cytochrome P450 2B6 alleles. Protease inhibitors cause perioral paraesthesias and may indirectly increase the relative risk of stroke by promoting atherogenesis. HIV integrase inhibitors, C-C chemokine receptor type 5 (CCR5) inhibitors and fusion inhibitors rarely cause neuropsychiatric manifestations.
引用
收藏
页码:131 / 145
页数:15
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