CYP2B6*6 and CYP2B6*18 Predict Long-Term Efavirenz Exposure Measured in Hair Samples in HIV-Positive South African Women

被引:0
作者
Roehrich, Carola R. [1 ]
Droegemoeller, Britt I. [1 ]
Ikediobi, Ogechi [2 ]
van der Merwe, Lize [3 ,4 ]
Grobbelaar, Nelis [5 ]
Wright, Galen E. B. [1 ]
McGregor, Nathaniel [1 ,6 ]
Warnich, Louise [1 ]
机构
[1] Univ Stellenbosch, Dept Genet, Private Bag 11, ZA-7602 Stellenbosch, South Africa
[2] Univ Calif San Francisco, Dept Pharm, San Francisco, CA USA
[3] Univ Stellenbosch, Dept Mol Biol & Human Genet, ZA-7505 Tygerberg, South Africa
[4] Univ Western Cape, Dept Stat, ZA-7535 Bellville, South Africa
[5] TC Newman HIV Clin, Paarl, South Africa
[6] Univ Stellenbosch, Dept Psychiat, ZA-7505 Tygerberg, 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
ANTIRETROVIRAL THERAPY; INFECTED PATIENTS; PLASMA-CONCENTRATIONS; CYP2B6; VARIANTS; SEX-DIFFERENCES; ENZYME GENES; POPULATION; PHARMACOKINETICS; PHARMACOGENETICS; POLYMORPHISM;
D O I
10.1089/aid.2015.0048
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Long-term exposure to efavirenz (EFV) measured in hair samples may predict response to antiretroviral treatment (ART). Polymorphisms in CYP2B6 are known to alter EFV levels. The aim of this study was to assess the relationship between CYP2B6 genotype, EFV levels measured in hair, and virological outcomes on ART in a real-world setting. We measured EFV levels in hair from HIV-positive South African females who had been receiving EFV-based treatment for at least 3 months from the South African Black (SAB) (n=81) and Cape Mixed Ancestry (CMA) (n=53) populations. Common genetic variation in CYP2B6 was determined in 15 individuals from each population using bidirectional Sanger sequencing. Prioritized variants (n=16) were subsequently genotyped in the entire patient cohort (n=134). The predictive value of EFV levels in hair and selected variants in CYP2B6 on virological treatment outcomes was assessed. Previously described alleles (CYP2B6*2, CYP2B6*5, CYP2B6*6, CYP2B6*17, and CYP2B6*18), as well as two novel alleles (CYP2B6*31 and CYP2B6*32), were detected in this study. Compared to noncarriers, individuals homozygous for CYP2B6*6 had approximate to 109% increased EFV levels in hair (p=.016) and CYP2B6*18 heterozygotes demonstrated 82% higher EFV hair levels (p=.0006). This study confirmed that alleles affecting CYP2B6 metabolism and subsequent EFV exposure are present at significant frequencies in both the SAB and CMA populations. Furthermore, this study demonstrated that the use of hair samples for testing EFV concentrations may be a useful tool in determining long-term drug exposure in resource-limited countries.
引用
收藏
页码:529 / 538
页数:10
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