Outcomes of Phentermine-Topiramate in Children Living with Duchenne Muscular Dystrophy.

IF 3.8 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Li-Min Chen, Po-Chih Shen, Philip Zeitler
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引用次数: 0

Abstract

Introduction: Duchenne muscular dystrophy (DMD) is a progressive neuromuscular disorder associated with obesity due to low energy expenditure and high-dose corticosteroid treatment. Obesity significantly impacts quality of life in individuals with DMD and is consistently identified as a top family concern. Despite FDA approval of weight-loss medications for adolescents, including phentermine/topiramate (PHEN/TPM), there is limited evidence for their use in children with DMD, particularly regarding potential cardiac complications in a population already at elevated risk.

Method: Individuals with a genetic diagnosis of DMD, who were prescribed PHEN/TPM from January 1, 2015, to April 25, 2025, were identified from the electronic medical record system of Children's Hospital Colorado (CHCO). A final cohort of six individuals treated for at least 6 months had clinic-obtained weights documented and were included in the analysis.

Results: All patients were aged 9.9-16.9 years, with baseline weight 45-108.2 kg and BMI 29.5-39.7 kg/m2. Treatment duration ranged from 0.6 to 4.2 years. In the first year of therapy, median BMI decreased by 3.75 kg/m2 (interquartile ranges [IQRs]: -5.5 to -2.6), BMI standard deviation (SD) by 0.57 (IQR: -0.99 to -0.31), and weight SD by 0.73 (IQR: -1.17 to -0.59). Over the full treatment course (0.6-4.2 years), median annualized changes were BMI -1.73 kg/m2 (IQR: -2.93 to 0.17), BMI SD -0.31 (IQR: -0.44 to -0.15), and weight SD -0.30 (IQR: -0.70 to -0.11). Longitudinal analysis revealed significant nonlinear trends for BMI and BMI SD, with nadir effect by year two. Cardiac parameters showed initial transient heart rate increase (HR, median +13.5 bpm at 0.5 years) but no significant changes in longitudinal follow-up of HR, systolic blood pressure, diastolic blood pressure, or left ventricular ejection fraction. Two individuals developed kidney stones; other adverse events were mild to moderate.

Conclusion: Treatment with PHEN/TPM in a small group of children with DMD and obesity was associated with clinically relevant reductions in measures of obesity and was generally well-tolerated with no significant adverse cardiac effects observed during extended follow-up. These findings support the potential use of PHEN/TPM as a weight management option in carefully selected individuals with DMD, though larger prospective studies are warranted.

芬特明-托吡酯治疗儿童杜氏肌营养不良的疗效。
杜氏肌营养不良症(DMD)是一种进行性神经肌肉疾病,与肥胖相关,由于低能量消耗和高剂量皮质类固醇治疗。肥胖严重影响DMD患者的生活质量,一直被认为是家庭最关心的问题。尽管FDA批准了包括芬特明/托吡酯(phentermine/topiramate, PHEN/TPM)在内的青少年减肥药,但它们在患有DMD的儿童中使用的证据有限,特别是在已经处于高危人群的潜在心脏并发症方面。我们报告了2015年1月至2025年4月在科罗拉多州儿童医院接受PHEN/TPM治疗的6名患有DMD的男孩(年龄9.9-16.9岁),体重指数(BMI)为29.5 - 39.7 kg/m2。在治疗的第一年,BMI中位数下降了3.75 kg/m²(IQR: -5.5至-2.6),BMI标准差(SD)下降了0.57 (IQR: -0.99至-0.31),体重SD下降了0.59 (IQR: -1.17至-0.59)。在整个治疗过程(0.6至4.2年)中,年化变化中位数为BMI -1.73 kg/m²(IQR: -2.93至0.17),BMI SD -0.31 (IQR:-0.44至-0.15),体重SD -0.30 (IQR:-0.70至-0.11)。纵向分析显示BMI和BMI标准差呈显著的非线性趋势,在第2年达到最低点。心脏参数显示初始瞬态心率升高(HR, 0.5年时中位数+13.5 bpm),但HR、收缩压、舒张压或左心室射血分数的纵向随访无显著变化。2人患上肾结石;其他不良事件为轻度至中度。结论:在一小群患有DMD和肥胖的儿童中,PHEN/TPM治疗与临床相关的肥胖测量减少有关,并且在延长随访期间通常耐受性良好,未观察到明显的心脏不良反应。这些发现支持PHEN/TPM在精心挑选的DMD患者中作为体重管理选择的潜在用途,尽管需要更大规模的前瞻性研究。
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来源期刊
Hormone Research in Paediatrics
Hormone Research in Paediatrics ENDOCRINOLOGY & METABOLISM-PEDIATRICS
CiteScore
4.90
自引率
6.20%
发文量
88
审稿时长
4-8 weeks
期刊介绍: The mission of ''Hormone Research in Paediatrics'' is to improve the care of children with endocrine disorders by promoting basic and clinical knowledge. The journal facilitates the dissemination of information through original papers, mini reviews, clinical guidelines and papers on novel insights from clinical practice. Periodic editorials from outstanding paediatric endocrinologists address the main published novelties by critically reviewing the major strengths and weaknesses of the studies.
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