Machine Learning‐Based Prediction of Escitalopram and Sertraline Side Effects With Pharmacokinetic Data in Children and Adolescents

舍曲林 依西酞普兰 重性抑郁障碍 医学 中止 药代动力学 耐受性 重性抑郁发作 内科学 不利影响 精神科 焦虑 氢化可的松 扁桃形结构 抗抑郁药
作者
Ethan A. Poweleit,Samuel Vaughn,Zeruesenay Desta,Judith W. Dexheimer,Jeffrey R. Strawn,Laura B. Ramsey
出处
期刊:Clinical Pharmacology & Therapeutics [Wiley]
卷期号:115 (4): 860-870 被引量:6
标识
DOI:10.1002/cpt.3184
摘要

Selective serotonin reuptake inhibitors (SSRI) are the first‐line pharmacologic treatment for anxiety and depressive disorders in children and adolescents. Many patients experience side effects that are difficult to predict, are associated with significant morbidity, and can lead to treatment discontinuation. Variation in SSRI pharmacokinetics could explain differences in treatment outcomes, but this is often overlooked as a contributing factor to SSRI tolerability. This study evaluated data from 288 escitalopram‐treated and 255 sertraline‐treated patients ≤ 18 years old to develop machine learning models to predict side effects using electronic health record data and Bayesian estimated pharmacokinetic parameters. Trained on a combined cohort of escitalopram‐ and sertraline‐treated patients, a penalized logistic regression model achieved an area under the receiver operating characteristic curve (AUROC) of 0.77 (95% confidence interval (CI): 0.66–0.88), with 0.69 sensitivity (95% CI: 0.54–0.86), and 0.82 specificity (95% CI: 0.72–0.87). Medication exposure, clearance, and time since the last dose increase were among the top features. Individual escitalopram and sertraline models yielded an AUROC of 0.73 (95% CI: 0.65–0.81) and 0.64 (95% CI: 0.55–0.73), respectively. Post hoc analysis showed sertraline‐treated patients with activation side effects had slower clearance ( P = 0.01), which attenuated after accounting for age ( P = 0.055). These findings raise the possibility that a machine learning approach leveraging pharmacokinetic data can predict escitalopram‐ and sertraline‐related side effects. Clinicians may consider differences in medication pharmacokinetics, especially during dose titration and as opposed to relying on dose, when managing side effects. With further validation, application of this model to predict side effects may enhance SSRI precision dosing strategies in youth.
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