Department of Molecular and Clinical Pharmacology, University of Liverpool, Liverpool, United Kingdom.
Antimicrob Agents Chemother. 2014;58(2):706-12. doi: 10.1128/AAC.02069-13. Epub 2013 Nov 11.
We modeled nevirapine (NVP) pharmacokinetics in HIV-infected Malawian patients to assess the relationship between drug exposure and patient characteristics, genetic polymorphisms, and development of hypersensitivity reaction (HSR). One thousand one hundred seventeen patients were prospectively recruited and followed for 26 weeks with multiple or single serum samples obtained in a subset of patients for NVP quantification. Single nucleotide polymorphisms (SNPs) within CYP2B6 and CYP3A4 genes were typed. Nonlinear mixed effects modeling was utilized to assess the influence of patient characteristics and host genetics on NVP apparent oral clearance (CL/F) and to explore the relationship between NVP CL/F and HSR. Published haplotype distributions were used to simulate NVP concentrations in Caucasians versus Africans. One hundred eighty patients (101 female) were included in the model; 25 experienced HSR. No associations between patient demographics or HSR and NVP CL/F were evident. A significant relationship between CYP2B6 c.983T>C and CYP2B6 c.516G>T and NVP CL/F was observed (P < 0.01). NVP CL/F was reduced by 23% and 36% in patients with CYP2B6 983TT/516TT and 983TC/516GG or GT, respectively, compared to the reference genotype. Simulated exposures suggested similar proportions (13 to 17%) of patients with subtherapeutic NVP among Caucasians and an African population. Influence of CYP2B6 polymorphisms on NVP CL/F in this population is in agreement with other reports. Our data indicate a lack of association between NVP exposure and HSR. Based on these data, dose optimization based solely on ethnicity (without individual gene testing) is unlikely to impact on risk of treatment failure or toxicity even in an African population with high carriage of poor metabolizer mutations.
我们对感染 HIV 的马拉维患者中的奈韦拉平(NVP)药代动力学进行建模,以评估药物暴露与患者特征、遗传多态性以及过敏反应(HSR)发展之间的关系。1117 名患者前瞻性入组并随访 26 周,部分患者在多个时间点或单一时间点采集血清样本以进行 NVP 定量。对 CYP2B6 和 CYP3A4 基因内的单核苷酸多态性(SNP)进行分型。利用非线性混合效应模型来评估患者特征和宿主遗传对 NVP 表观口服清除率(CL/F)的影响,并探索 NVP CL/F 与 HSR 之间的关系。使用已发表的单倍型分布来模拟白人和非洲人之间的 NVP 浓度。180 名患者(101 名女性)纳入模型;25 名患者出现 HSR。患者的人口统计学特征或 HSR 与 NVP CL/F 之间无显著相关性。CYP2B6 c.983T>C 和 CYP2B6 c.516G>T 与 NVP CL/F 之间存在显著关系(P<0.01)。与参考基因型相比,CYP2B6 983TT/516TT 和 983TC/516GG 或 GT 患者的 NVP CL/F 分别降低 23%和 36%。模拟结果表明,在白人和非洲人群中,亚治疗性 NVP 的患者比例相似(13%至 17%)。该人群中 CYP2B6 多态性对 NVP CL/F 的影响与其他报道一致。我们的数据表明,NVP 暴露与 HSR 之间没有关联。根据这些数据,即使在 CYP2B6 不良代谢突变携带率较高的非洲人群中,基于种族(不进行个体基因检测)进行剂量优化不太可能影响治疗失败或毒性的风险。