Mangal Naveen, James Margaret O, Stacpoole Peter W, Schmidt Stephan
Center for Pharmacometrics & Systems Pharmacology, College of Pharmacy, University of Florida, Orlando, FL, USA.
Department of Medicinal Chemistry, College of Pharmacy, University of Florida, Gainesville, FL, USA.
J Clin Pharmacol. 2018 Feb;58(2):212-220. doi: 10.1002/jcph.1009. Epub 2017 Sep 15.
Dichloroacetate (DCA) is an investigational drug used to treat congenital lactic acidosis and other mitochondrial disorders. Response to DCA therapy in young children may be suboptimal following body weight-based dosing. This is because of autoinhibition of its metabolism, age-dependent changes in pharmacokinetics, and polymorphisms in glutathione transferase zeta 1 (GSTZ1), its primary metabolizing enzyme. Our objective was to predict optimal DCA doses for the treatment of congenital lactic acidosis in children. Accordingly, a semimechanistic pharmacokinetic-enzyme turnover model was developed in a step-wise approach: (1) a population pharmacokinetic model for adults was developed; (2) the adult model was scaled to children using allometry and physiology-based scaling; and (3) the scaled model was externally qualified, updated with clinical data, and optimal doses were projected. A 2-compartment model accounting for saturable clearance and GSTZ1 enzyme turnover successfully characterized the DCA PK in adults and children. DCA-induced inactivation of GSTZ1 resulted in phenoconversion of all subjects into slow metabolizers after repeated dosing. However, rate and extent of inactivation was 2-fold higher in subjects without the wild-type EGT allelic variant of GSTZ1, resulting in further phenoconversion into ultraslow metabolizers after repeated DCA administration. Furthermore, DCA-induced GSTZ1 inactivation rate and extent was found to be 25- to 30-fold lower in children than in adults, potentially accounting for the observed age-dependent changes in PK. Finally, a 12.5 and 10.6 mg/kg twice-daily DCA dose was optimal in achieving the target steady-state trough concentrations (5-25 mg/L) for EGT carrier and EGT noncarrier children, respectively.
二氯乙酸(DCA)是一种用于治疗先天性乳酸性酸中毒和其他线粒体疾病的研究性药物。基于体重给药时,幼儿对DCA治疗的反应可能不理想。这是由于其代谢的自抑制、药代动力学的年龄依赖性变化以及其主要代谢酶谷胱甘肽转移酶ζ1(GSTZ1)的多态性。我们的目标是预测治疗儿童先天性乳酸性酸中毒的最佳DCA剂量。因此,采用逐步方法建立了一个半机制药代动力学-酶周转模型:(1)建立了成人的群体药代动力学模型;(2)使用异速生长法和基于生理学的标度法将成人模型标度至儿童;(3)对标度后的模型进行外部验证,用临床数据更新,并预测最佳剂量。一个考虑饱和清除率和GSTZ1酶周转的二室模型成功地表征了成人和儿童的DCA药代动力学。DCA诱导的GSTZ1失活导致所有受试者在重复给药后转变为慢代谢者。然而,没有GSTZ1野生型EGT等位基因变体的受试者的失活速率和程度高2倍,导致在重复给予DCA后进一步转变为超慢代谢者。此外,发现儿童中DCA诱导的GSTZ1失活速率和程度比成人低25至30倍,这可能解释了观察到的药代动力学的年龄依赖性变化。最后,对于EGT携带者和非携带者儿童,分别以每日两次12.5和10.6 mg/kg的DCA剂量最适合达到目标稳态谷浓度(5-25 mg/L)。