Division of Maternal Fetal Medicine, Department of Gynecology & Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA
Doctoral Training Program (PhD), Graduate Training Program in Clinical Investigation (GTPCI), Johns Hopkins University School of Public Health, Baltimore, Maryland, USA.
Antimicrob Agents Chemother. 2021 Feb 17;65(3). doi: 10.1128/AAC.02168-20.
Pharmacokinetics of drugs can be affected by physiologic changes during pregnancy. Our aim was to assess the influence of covariates on tenofovir (TFV) pharmacokinetics in pregnant and postpartum women receiving tenofovir disoproxil fumarate (TDF). Population pharmacokinetic parameter estimates and the influence of covariates were assessed using nonlinear mixed-effects modeling (NONMEM 7.4). Forty-six women had intensive pharmacokinetic evaluations during the second and third trimesters of pregnancy, with another evaluation postpartum. A two-compartment pharmacokinetic model with allometric scaling for body weight and first-order absorption best described the tenofovir plasma concentration data. Apparent oral clearance (CL/F) and volume of distribution at steady state (/F) were increased during pregnancy. Weight, serum creatinine (SCr), pregnancy, albumin, and age were associated with TFV CL/F during univariate assessment, but in the multivariate analysis, changes in CL/F and /F were only associated with increased body weight and enhanced renal function. Due to greater weight and lower SCr during pregnancy, CL/F was 28% higher during pregnancy than postpartum. In the final model, CL/F (liters per hour) was described as 2.07 × (SCr/0.6) × weight, with a low between-subject variability (BSV) of 24%. The probability of target attainment (proportion exceeding area under the concentration-time curve of >1.99 μg·h/ml, the 10th percentile of average TFV exposure for nonpregnant historical controls) was 68%, 80%, 87%, and 93% above the target with 300 mg, 350 mg, 400 mg, and 450 mg of TDF, respectively, during pregnancy and 88%, 92%, 96%, and 98% above the target with same doses in postpartum women. Dose adjustment of TDF during pregnancy is not generally warranted, but any modification should be based on weight and renal function. (This study has been registered at ClinicalTrials.gov under identifier NCT00042289.).
药物的药代动力学可能会受到妊娠期间生理变化的影响。我们的目的是评估在接受富马酸替诺福韦二吡呋酯(TDF)的孕妇和产后妇女中,协变量对替诺福韦(TFV)药代动力学的影响。使用非线性混合效应模型(NONMEM 7.4)评估群体药代动力学参数估计和协变量的影响。46 名女性在妊娠的第二和第三个三个月期间进行了强化药代动力学评估,并在产后进行了另一次评估。两室药代动力学模型,体重的比例缩放和一级吸收最好地描述了替诺福韦血浆浓度数据。在妊娠期间,表观口服清除率(CL/F)和稳态分布容积(/F)增加。体重、血清肌酐(SCr)、妊娠、白蛋白和年龄与单变量评估时的 TFV CL/F 相关,但在多变量分析中,CL/F 和/F 的变化仅与体重增加和肾功能增强相关。由于妊娠期间体重增加和 SCr 降低,CL/F 在妊娠期间比产后高 28%。在最终模型中,CL/F(升/小时)描述为 2.07×(SCr/0.6)×体重,个体间变异性(BSV)低至 24%。目标达到的概率(超过浓度-时间曲线下面积的比例>1.99μg·h/ml,非妊娠历史对照的平均 TFV 暴露的第 10 百分位)分别为 300mg、350mg、400mg 和 450mgTDF 时,在妊娠期间分别为 68%、80%、87%和 93%,在产后女性中分别为 88%、92%、96%和 98%。妊娠期间一般不需要调整 TDF 的剂量,但任何调整都应基于体重和肾功能。(本研究已在 ClinicalTrials.gov 上注册,标识符为 NCT00042289。)