Pharmacogenetics of CYP2B6, CYP2A6 and UGT2B7 in HIV treatment in African populations: focus on efavirenz and nevirapine

被引:29
作者
Colic, Antoinette [1 ]
Alessandrini, Marco [2 ]
Pepper, Michael S. [2 ]
机构
[1] Univ Pretoria, Fac Nat & Agr Sci, Sch Biol Sci, Dept Biochem, ZA-0001 Pretoria, South Africa
[2] Univ Pretoria, Dept Immunol, Fac Hlth Sci, Inst Cellular & Mol Med, ZA-0001 Pretoria, South Africa
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
Drug metabolism; hepatotoxicity; HIV/AIDS; inter-ethnic variability; neurotoxicity; CYTOCHROME P4502B6 CYP2B6; INFECTED PATIENTS; PLASMA-CONCENTRATIONS; HIV/AIDS TREATMENT; HIGH PREVALENCE; DRUG EFAVIRENZ; IN-VITRO; METABOLISM; POLYMORPHISMS; THERAPY;
D O I
10.3109/03602532.2014.982864
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The CYP450 and UGT enzymes are involved in phase I and phase II metabolism of the majority of clinically prescribed drugs, including the non-nucleoside reverse transcriptase inhibitors, efavirenz and nevirapine, used in the treatment of HIV/AIDS. Variations in the activity of these enzymes due to gene polymorphisms can affect an individual's drug response or may lead to adverse drug reactions. There is an inter-ethnic distribution in the frequency of these polymorphisms, with African populations exhibiting higher genetic diversity compared to other populations. African specific alleles with clinical relevance have also emerged. Given the high prevalence of HIV/AIDS in sub-Saharan Africa, understanding the frequency of pharmacogenetically relevant alleles in populations of African origin, and their impact on efavirenz and nevirapine metabolism, is becoming increasingly critical. This review aims to investigate ethnic variation of CYP2B6, CYP2A6 and UGT2B7, and to understand the pharmacogenetic relevance when comparing frequencies in African populations to other populations worldwide.
引用
收藏
页码:111 / 123
页数:13
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