Drug Metabolism and Pharmacokinetics, GlaxoSmithKline, R&D, Stevenage, UK.
Simcyp Division, Certara UK Ltd., Sheffield, UK.
CPT Pharmacometrics Syst Pharmacol. 2023 Jun;12(6):808-820. doi: 10.1002/psp4.12954. Epub 2023 Apr 2.
In celiac disease (CeD), gastrointestinal CYP3A4 abundance and morphology is affected by the severity of disease. Therefore, exposure to CYP3A4 substrates and extent of drug interactions is altered. A physiologically-based pharmacokinetic (PBPK) population for different severities of CeD was developed. Gastrointestinal physiology parameters, such as luminal pH, transit times, morphology, P-gp, and CYP3A4 expression were included in development of the CeD population. Data on physiological difference between healthy and CeD subjects were incorporated into the model as the ratio of celiac to healthy. A PBPK model was developed and verified for felodipine extended-release tablet in healthy volunteers (HVs) and then utilized to verify the CeD populations. Plasma concentration-time profile and PK parameters were predicted and compared against those observed in both groups. Sensitivity analysis was carried out on key system parameters in CeD to understand their impact on drug exposure. For felodipine, the predicted mean concentration-time profiles and 5th and 95th percentile intervals captured the observed profile and variability in the HV and CeD populations. Predicted and observed clearance was 56.9 versus 56.1 (L/h) in HVs. Predicted versus observed mean ± SD area under the curve for extended release felodipine in different severities of CeD were values of 14.5 ± 9.6 versus 14.4 ± 2.1, 14.6 ± 9.0 versus 17.2 ± 2.8, and 28.1 ± 13.5 versus 25.7 ± 5.0 (ng.h/mL), respectively. Accounting for physiology differences in a CeD population accurately predicted the PK of felodipine. The developed CeD population can be applied for determining the drug concentration of CYP3A substrates in the gut as well as for systemic levels, and for application in drug-drug interaction studies.
在乳糜泻(CeD)中,胃肠道 CYP3A4 的丰度和形态受疾病严重程度的影响。因此,暴露于 CYP3A4 底物和药物相互作用的程度发生改变。针对不同严重程度的 CeD 开发了一种基于生理学的药代动力学(PBPK)人群模型。胃肠生理学参数,如腔室 pH 值、转运时间、形态、P-糖蛋白和 CYP3A4 表达,均包含在 CeD 人群模型的开发中。将健康受试者和 CeD 受试者之间生理差异的数据作为比值纳入模型,即乳糜泻与健康的比值。在健康志愿者(HV)中开发并验证了用于非洛地平缓释片的 PBPK 模型,然后利用该模型验证了 CeD 人群模型。预测了血浆浓度-时间曲线和 PK 参数,并与两组观察到的结果进行了比较。对 CeD 中的关键系统参数进行了敏感性分析,以了解它们对药物暴露的影响。对于非洛地平,预测的平均浓度-时间曲线和第 5 百分位和第 95 百分位区间捕获了 HV 和 CeD 人群中的观察到的曲线和变异性。在 HV 中,预测的清除率与观察到的清除率分别为 56.9 比 56.1(L/h)。在不同严重程度的 CeD 中,预测的与观察的非洛地平缓释片的平均(±SD)曲线下面积分别为 14.5(±9.6)比 14.4(±2.1)、14.6(±9.0)比 17.2(±2.8)和 28.1(±13.5)比 25.7(±5.0)(ng.h/mL)。在 CeD 人群中考虑生理学差异可以准确预测非洛地平的 PK。开发的 CeD 人群模型可用于确定肠道中 CYP3A 底物的药物浓度以及系统水平,也可用于药物相互作用研究。