Department of Hospital Pharmacy, Erasmus Medical Center, Rotterdam, The Netherlands.
Department of Child and Adolescent Psychiatry/Psychology, Erasmus Medical Center, Rotterdam, the Netherlands.
Br J Clin Pharmacol. 2023 Oct;89(10):3026-3036. doi: 10.1111/bcp.15800. Epub 2023 Jun 13.
Aripiprazole is one of the most commonly prescribed antipsychotic drugs to children and adolescents worldwide, but it is associated with serious side-effects, including weight gain. This study assessed the population pharmacokinetics of aripiprazole and its active metabolite and investigated the relationship between pharmacokinetic parameters and body mass index (BMI) in children and adolescents with autism spectrum disorder (ASD) and behavioural problems. Secondary outcomes were metabolic, endocrine, extrapyramidal and cardiac side-effects and drug effectiveness.
Twenty-four children and adolescents (15 males, 9 females) aged 6-18 years were included in a 24-week prospective observational trial. Drug plasma concentrations, side-effects and drug effectiveness were measured at several time points during follow-up. Relevant pharmacokinetic covariates, including CYP2D6, CYP3A4, CYP3A5 and P-glycoprotein (ABCB1) genotypes, were determined. Nonlinear mixed-effects modelling (NONMEM®) was used for a population pharmacokinetic analysis with 92 aripiprazole and 91 dehydro-aripiprazole concentrations. Subsequently, model-based trough concentrations, maximum concentrations and 24-h area under the curves (AUCs) were analysed to predict outcomes using generalized and linear mixed-effects models.
For both aripiprazole and dehydro-aripiprazole, one-compartment models best described the measured concentrations, with albumin and BMI as significant covariates. Of all the pharmacokinetic parameters, higher sum (aripiprazole plus dehydro-aripiprazole) trough concentrations best predicted higher BMI z-scores (P < .001) and higher Hb1Ac levels (P = .03) during follow-up. No significant association was found between sum concentrations and effectiveness.
Our results indicate a threshold with regard to safety, which suggests that therapeutic drug monitoring of aripiprazole could potentially increase safety in children and adolescents with ASD and behavioural problems.
阿立哌唑是全球儿童和青少年最常开的抗精神病药物之一,但它与严重的副作用有关,包括体重增加。本研究评估了阿立哌唑及其活性代谢物的群体药代动力学,并研究了自闭症谱系障碍(ASD)和行为问题儿童和青少年的药代动力学参数与体重指数(BMI)之间的关系。次要结局是代谢、内分泌、锥体外系和心脏副作用以及药物疗效。
24 名 6-18 岁的儿童和青少年(15 名男性,9 名女性)纳入了一项为期 24 周的前瞻性观察性试验。在随访期间的多个时间点测量药物血浆浓度、副作用和药物疗效。确定了相关的药代动力学协变量,包括 CYP2D6、CYP3A4、CYP3A5 和 P-糖蛋白(ABCB1)基因型。使用非线性混合效应模型(NONMEM®)进行群体药代动力学分析,共分析了 92 个阿立哌唑和 91 个脱氢阿立哌唑浓度。随后,使用广义和线性混合效应模型分析基于模型的谷浓度、峰浓度和 24 小时 AUC 来预测结局。
对于阿立哌唑和脱氢阿立哌唑,单室模型最能描述测量的浓度,白蛋白和 BMI 是显著的协变量。在所有药代动力学参数中,较高的总和(阿立哌唑加脱氢阿立哌唑)谷浓度最好地预测了随访期间较高的 BMI z 评分(P < 0.001)和较高的 Hb1Ac 水平(P = 0.03)。总和浓度与疗效之间没有显著关联。
我们的结果表明存在一个安全性的阈值,这表明对 ASD 和行为问题儿童和青少年的阿立哌唑进行治疗药物监测可能会提高安全性。