Hepatotoxicity of antiretroviral drugs

被引:35
|
作者
Abrescia, N [1 ]
D'Abbraccio, M [1 ]
Figoni, M [1 ]
Busto, A [1 ]
Maddaloni, A [1 ]
De Marco, M [1 ]
机构
[1] AO D Cotugno Reg Hosp Infect Dis, Div Malattie Infett 4, I-80131 Naples, Italy
关键词
aids; HIV; HAART; antiretroviral drugs; HAART hepatotoxicity; antiretroviral drugs hepatotoxicity; management of HAART hepatotoxicity; management of antiretroviral drugs hepatotoxicity;
D O I
10.2174/138161205774580804
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The use of highly active antiretroviral therapy (HAART) has significantly slowed the HIV disease progression. However, adverse effects are now a limiting cause of HAART benefit in a substantial proportion of patients. Particularly hepatotoxicity which is a common complication occurring during every HAART regimen. All antiretroviral (ARV) drugs classes, Nucleoside/Nucleotide reverse transcriptase inhibitors (NRTI), non-Nucleoside reverse transcriptase inhibitors (nNRTI) and Protease Inhibitors (PI) may cause hepatotoxicity but in different pathways. Many risk factors have been identified for developing antiretroviral-related hepatotoxicity, however severe hepatitis remains very uncommon in patients receiving HAART, also if the incidence of hepatotoxicity is rather high. That being the case, means that every new available antiretroviral drug strongly necessities studies which can evaluate its hepatotoxicity and drug-drug interactions, to define the potential risk factors and the outcome of any side effects. This report will review the risk factors, the epidemiology and the pathogenic mechanisms of hepatotoxicity caused in every antiretroviral drug.
引用
收藏
页码:3697 / 3710
页数:14
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