An Exploratory Model-Informed Precision Dosing Strategy for Atomoxetine Treatment in Chinese Children with ADHD: Integrating Body Weight and CYP2D6 Pharmacogenetics Across Potential Real-World Clinical Scenarios
Objective: We aimed to develop and evaluate population pharmacokinetic (PopPK) models of atomoxetine incorporating clinically available patient information and to explore model-informed dose selection in Chinese children and adolescents with attention-deficit/hyperactivity disorder (ADHD). Methods: This retrospective single-center study included a model-building dataset of 102 patients (247 concentrations) and a patient-level holdout dataset of 65 patients (65 concentrations collected approximately 2 h post-dose). A one-compartment model with first-order absorption and elimination was developed. Body weight (BW) and alternative representations of CYP2D6 genetic information—rs1065852 genotype, activity score (AS), and predicted phenotype—were evaluated. Monte Carlo simulations evaluated steady-state 2 h post-dose concentrations (C2h) across doses of 0.5–1.4 mg/kg/day; the model-informed dose was the lowest evaluated dose, achieving ≥75% probability of reaching the exploratory C2h threshold of 268 ng/mL. Results: BW affected apparent clearance (CL/F) and volume of distribution, whereas rs1065852 genotype and AS additionally explained CL/F variability. In the holdout dataset, population predictions had limited bias (MdPE, 1.41–3.09%) but modest precision (MdAPE, 33.75–37.83%); CYP2D6-informed models improved selected performance measures. Simulation-derived doses ranged from 1.0 to 1.4 mg/kg/day across subgroups. No evaluated dose achieved the probability of target attainment (PTA) criterion for AS = 2 at any BW, or for the CC+CT and AS = 1.5 subgroups weighing 17–<30 kg. Alternative Ka assumptions changed median C2h by at most 3.99% and PTA by 3.58 percentage points. Conclusions: BW and CYP2D6 genetic information explained part of atomoxetine pharmacokinetic variability and influenced simulated concentration attainment. These model-informed findings are exploratory and require prospective, multicenter validation against efficacy, tolerability, and safety outcomes before clinical implementation.
Authors
- Fan Lin (ORCID: https://orcid.org/0000-0002-1372-0256)
- Feng Chen (ORCID: https://orcid.org/0000-0003-4800-6762)
- Jian Huang (ORCID: https://orcid.org/0000-0001-7315-4252)
- Qianqi Liu (ORCID: https://orcid.org/0000-0003-0405-4682)
- Hong‐Li Guo (ORCID: https://orcid.org/0000-0002-6660-8145)
- Xin Xu (ORCID: https://orcid.org/0000-0002-0479-6988)
- Yuanyuan Zhang (ORCID: https://orcid.org/0000-0002-5708-9718)
- Yue Li
- Jie Wang
- Dan-Dan Wu
Institutions
- China Pharmaceutical University (CN)
- Nanjing Children's Hospital (CN)
- Second Affiliated Hospital of Nanjing Medical University (CN)
- Nanjing Medical University (CN)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2026-11-01
- DOI
- https://doi.org/10.3390/pharmaceutics18111401
- Primary Topic
- Pharmaceutical studies and practices
- Type
- article
- Field-Weighted Citation Impact
- 0.00