{"title":"Outcomes of Phentermine-Topiramate in Children Living with Duchenne Muscular Dystrophy.","authors":"Li-Min Chen, Po-Chih Shen, Philip Zeitler","doi":"10.1159/000552576","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>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.</p><p><strong>Method: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":13025,"journal":{"name":"Hormone Research in Paediatrics","volume":" ","pages":"1-11"},"PeriodicalIF":3.8000,"publicationDate":"2026-05-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hormone Research in Paediatrics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1159/000552576","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
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.
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.