Height, weight, and body mass index trajectories and their correlation with functional outcome assessments in boys with Duchenne muscular dystrophy.

IF 4.3 2区 医学 Q1 CLINICAL NEUROLOGY
Marianela Schiava, Utkarsh J Dang, Claire Wood, Sze Choong Wong, Leanne M Ward, Robert Muni Lofra, Anna Mayhew, William B Martens, Stephanie Gregory, Robert C Griggs, Michela Guglieri
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引用次数: 0

Abstract

Aim: To examine the factors influencing height, weight, and body mass index (BMI) z-scores, and the relationship between them and motor performance, in boys with Duchenne muscular dystrophy (DMD).

Method: This was a randomized, double-blind, parallel group trial involving 32 study sites across five countries. Height, weight, BMI z-scores, and clinical outcome assessments (COAs)-rise from supine velocity, 10-m walk/run velocity, NorthStar Ambulatory Assessment, and 6-minute walk test-were analysed in 4-year-old to 7-year-old boys with DMD randomized to 0.75 mg/kg/day prednisone, 0.75 mg/kg/day intermittent prednisone, or 0.90 mg/kg/day deflazacort in the FOR-DMD study. Trajectories were modelled using a linear mixed-effects model and correlations were explored through Spearman's partial correlations.

Results: In 194 boys with DMD, higher height at glucocorticoid initiation was associated with slower growth (p < 0.001) and older age was associated with increased weight gain (p = 0.001). Glucocorticoid type and regimen influenced height and weight trajectories but not BMI. Changes in height and weight z-scores were negatively correlated with COAs (p < 0.05 in all cases). Correlations were weak 3 years after glucocorticoid initiation and moderate after 5 years (closer to the age of loss of ambulation).

Interpretation: Changes in anthropometric measures after glucocorticoid initiation are associated with COA performance and larger correlations closer to the age of loss of ambulation. This emphasizes the need for weight management strategies and discussions that support treatment.

杜氏肌营养不良男孩的身高、体重和体重指数轨迹及其与功能结局评估的相关性
目的:探讨Duchenne型肌营养不良症(DMD)男孩身高、体重、身体质量指数(BMI) z分数的影响因素及其与运动表现的关系。方法:这是一项随机、双盲、平行组试验,涉及5个国家的32个研究点。在FOR-DMD研究中,我们分析了4- 7岁DMD男孩的身高、体重、BMI z评分和临床结果评估(COAs)——仰位上升速度、10米步行/跑步速度、NorthStar动态评估和6分钟步行测试。这些DMD男孩被随机分为0.75 mg/kg/天强的松组、0.75 mg/kg/天间歇性强的松组或0.90 mg/kg/天地扎克特组。轨迹使用线性混合效应模型建模,并通过Spearman的偏相关性来探索相关性。结果:在194名患有DMD的男孩中,糖皮质激素开始使用时身高越高,生长速度越慢(p)。解释:糖皮质激素开始使用后人体测量值的变化与COA表现有关,且与失去行走能力年龄的相关性越大。这强调了体重管理策略和支持治疗的讨论的必要性。
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来源期刊
CiteScore
7.80
自引率
13.20%
发文量
338
审稿时长
3-6 weeks
期刊介绍: Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA). For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.
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