Trajectories and Predictors for the Development of Clinically Significant Weight Gain in Children and Adolescents Prescribed Second-Generation Antipsychotics.

IF 1.5 4区 医学 Q2 PEDIATRICS Journal of child and adolescent psychopharmacology Pub Date : 2024-05-01 Epub Date: 2024-02-26 DOI:10.1089/cap.2023.0071
Ning Lyu, Paul J Rowan, Susan Abughosh, Tyler J Varisco, Ying Lin, Hua Chen
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Abstract

Background: As many as 60% of pediatric patients taking second-generation antipsychotics (SGA) experience weight gain (antipsychotic-induced weight gain). However, the subgroup that experienced substantial weight increase was poorly understood. This study aimed to identify the development and predictors of clinically significant weight gain (CSWG) among pediatric SGA recipients. Methods: A retrospective analysis of the 2016 to 2021 IQVIA Ambulatory EMR-US database was conducted. The study cohort comprised SGA-naive patients ages 5 to 19, continuously prescribed SGA for ≥90 days. CSWG was defined as a weight gain in BMI z-score >0.5. The development of CSWG was described using the group-based trajectory model approach, and multinomial logistic regression analysis was conducted to examine the risk factors associated with the CSWG trajectories. Results: Of the 16,262 SGA recipients who met the inclusion criteria, 4 distinctive CSWG trajectories were identified: (1) Rapid (14.6%), (2) Gradual (12.6%), (3) Transit (7%), and (4) no CSWG (65.8%). Factors associated with a higher likelihood of having rapid or gradual CSWG versus nonsignificant weight gain were being younger (OR [95% CI] = 12-17 vs. 5-11, Rapid, 0.727 [0.655-0.806]; Gradual, 0.776 [0.668-0.903]), male (Rapid, 1.131 [1.021-1.253]), non-Hispanic White (Black vs. White: Rapid, 0.833 [0.709-0.98]), with lower baseline BMI z-score (Rapid, 0.376 [0.361-0.392]; Gradual, 0.449 [0.424-0.476]), and receiving olanzapine as the initial SGA (Rapid, 1.38 [1.093-1.74]). The Area under the Receiver operating characteristic (ROC) Curve for the comparison of rapid and gradual CSWG with no CSWG trajectory were 0.83 and 0.80, respectively. Conclusions: SGA recipients experienced four distinctive CSWG trajectories (Rapid, Gradual, Transient, and No CSWG). The risk of CSWG could be predicted using patient characteristics at the SGA initiation. This insight highlights the importance of personalized monitoring and timely intervention strategies for at-risk individuals who experienced persistent CSWG in real practice.

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处方第二代抗精神病药物的儿童和青少年出现临床显著体重增加的轨迹和预测因素。
背景:多达 60% 的服用第二代抗精神病药物 (SGA) 的儿童患者会出现体重增加(抗精神病药物引起的体重增加)。然而,人们对体重大幅增加的亚组却知之甚少。本研究旨在确定儿科 SGA 服用者中临床显著体重增加(CSWG)的发生和预测因素。研究方法对 2016 年至 2021 年 IQVIA Ambulatory EMR-US 数据库进行了回顾性分析。研究队列包括年龄在 5 至 19 岁、连续服用 SGA ≥ 90 天的未服用 SGA 的患者。CSWG的定义是体重指数(BMI)z-score的体重增加>0.5。采用基于群体的轨迹模型方法描述了 CSWG 的发展过程,并进行了多项式逻辑回归分析,以研究与 CSWG 轨迹相关的风险因素。研究结果在符合纳入标准的 16,262 名 SGA 接收者中,发现了 4 种不同的 CSWG 轨迹:(1)快速(14.6%);(2)渐进(12.6%);(3)中转(7%);(4)无 CSWG(65.8%)。与体重快速或逐渐增加相比,体重无明显增加的可能性更大的相关因素是:年轻(OR [95% CI] = 12-17 vs. 5-11,快速,0.727 [0.655-0.806];逐渐,0.776 [0.668-0.903])、男性(快速,1.131 [1.021-1.253])、非西班牙裔白人(黑人 vs. 白人:快速,0.833 [0.709-0.98])、基线体重指数 z 值较低者(快速,0.376 [0.361-0.392];渐进,0.449 [0.424-0.476]),以及接受奥氮平作为初始 SGA 者(快速,1.38 [1.093-1.74])。快速和渐进 CSWG 与无 CSWG 轨迹比较的接收者操作特征曲线下面积分别为 0.83 和 0.80。结论:SGA 受者经历了四种不同的 CSWG 轨迹(快速、渐进、短暂和无 CSWG)。根据患者在开始服用 SGA 时的特征,可以预测 CSWG 的风险。这一观点强调了在实际工作中对经历过持续 CSWG 的高危人群进行个性化监测和及时干预策略的重要性。
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来源期刊
CiteScore
3.60
自引率
5.30%
发文量
61
审稿时长
>12 weeks
期刊介绍: Journal of Child and Adolescent Psychopharmacology (JCAP) is the premier peer-reviewed journal covering the clinical aspects of treating this patient population with psychotropic medications including side effects and interactions, standard doses, and research on new and existing medications. The Journal includes information on related areas of medical sciences such as advances in developmental pharmacokinetics, developmental neuroscience, metabolism, nutrition, molecular genetics, and more. Journal of Child and Adolescent Psychopharmacology coverage includes: New drugs and treatment strategies including the use of psycho-stimulants, selective serotonin reuptake inhibitors, mood stabilizers, and atypical antipsychotics New developments in the diagnosis and treatment of ADHD, anxiety disorders, schizophrenia, autism spectrum disorders, bipolar disorder, eating disorders, along with other disorders Reports of common and rare Treatment Emergent Adverse Events (TEAEs) including: hyperprolactinemia, galactorrhea, weight gain/loss, metabolic syndrome, dyslipidemia, switching phenomena, sudden death, and the potential increase of suicide. Outcomes research.
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