南部非洲艾滋病毒感染者替诺福韦清除率的药物遗传学。

IF 1.7 3区 医学 Q4 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Pharmacogenetics and genomics Pub Date : 2023-06-01 Epub Date: 2023-03-06 DOI:10.1097/FPC.0000000000000495
Zinhle Cindi, Aida N Kawuma, Gary Maartens, Yuki Bradford, Simiso Sokhela, Nomathemba Chandiwana, Willem D Francois Venter, Roeland E Wasmann, Paolo Denti, Lubbe Wiesner, Marylyn D Ritchie, David W Haas, Phumla Sinxadi
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引用次数: 0

摘要

背景替诺福韦是非洲首选的抗逆转录病毒联合疗法(ART)方案的组成部分。在遗传多样性最丰富的非洲,很少有关于替诺福韦暴露的药物遗传学研究:我们研究了接受富马酸替诺福韦二吡呋酯(TDF)或替诺福韦阿拉非那胺(TAF)治疗的南部非洲人血浆替诺福韦清除率的药物遗传学特征:研究对象为ADVANCE试验(NCT03122262)中随机接受TAF或TDF治疗的成人。按研究臂分层的线性回归模型检验了替诺福韦清除率与无法解释的变异性之间的关联。我们调查了与先验选择的多态性的遗传相关性,然后是全基因组相关性:共有 268 名参与者(TAF 和 TDF 治疗组分别有 138 人和 130 人)可进行相关性评估。在以前与任何药物相关表型有关的多态性中,IFNL4 rs12979860与两种治疗组中更快的替诺福韦清除率有关(TAF:P = 0.003;TDF:P = 0.003)。在全基因组范围内,TAF和TDF两组中替诺福韦清除率P值最低的分别是LINC01684 rs9305223(P = 3.0 × 10-8)和基因间rs142693425(P = 1.4 × 10-8):在ADVANCE中随机接受TAF或TDF治疗的南部非洲人中,替诺福韦清除率的不明变异与免疫反应基因IFNL4的多态性有关。目前还不清楚该基因会如何影响替诺福韦的处置。
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Pharmacogenetics of tenofovir clearance among Southern Africans living with HIV.

Background: Tenofovir is a component of preferred combination antiretroviral therapy (ART) regimens in Africa. Few pharmacogenetic studies have been conducted on tenofovir exposure in Africa, where genetic diversity is greatest.

Objective: We characterized the pharmacogenetics of plasma tenofovir clearance in Southern Africans receiving tenofovir disoproxil fumarate (TDF) or tenofovir alafenamide (TAF).

Methods: Adults randomized to TAF or TDF in dolutegravir-containing arms of the ADVANCE trial (NCT03122262) were studied. Linear regression models stratified by study arm examined associations with unexplained variability in tenofovir clearance. We investigated genetic associations with polymorphisms selected a priori followed by genome-wide associations.

Results: A total of 268 participants (138 and 130 in the TAF and TDF arm, respectively) were evaluable for associations. Among polymorphisms previously associated with any drug-related phenotype, IFNL4 rs12979860 was associated with more rapid tenofovir clearance in both arms (TAF: P = 0.003; TDF: P = 0.003). Genome-wide, the lowest P values for tenofovir clearance in TAF and TDF arms were LINC01684 rs9305223 (P = 3.0 × 10-8) and intergenic rs142693425 (P = 1.4 × 10-8), respectively.

Conclusion: Among Southern Africans randomized to TAF or TDF in ADVANCE, unexplained variability in tenofovir clearance was associated with a polymorphism in IFNL4, an immune-response gene. It is unclear how this gene would affect tenofovir disposition.

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来源期刊
Pharmacogenetics and genomics
Pharmacogenetics and genomics 医学-生物工程与应用微生物
CiteScore
3.20
自引率
3.80%
发文量
47
审稿时长
3 months
期刊介绍: ​​​​Pharmacogenetics and Genomics is devoted to the rapid publication of research papers, brief review articles and short communications on genetic determinants in response to drugs and other chemicals in humans and animals. The Journal brings together papers from the entire spectrum of biomedical research and science, including biochemistry, bioinformatics, clinical pharmacology, clinical pharmacy, epidemiology, genetics, genomics, molecular biology, pharmacology, pharmaceutical sciences, and toxicology. Under a single cover, the Journal provides a forum for all aspects of the genetics and genomics of host response to exogenous chemicals: from the gene to the clinic.
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