发育正常儿童下肢肌肉尺寸和力量的人体测量相关百分位曲线

Ines Vandekerckhove, Britta Hanssen, Nicky Peeters, Tijl Dewit, Nathalie De Beukelaer, Marleen Van den Hauwe, Liesbeth De Waele, Anja Van Campenhout, Friedl De Groote, Kaat Desloovere
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摘要

摘要:目的:在一组典型发育(TD)儿童中建立与人体测量相关的肌肉尺寸和力量百分位曲线,并通过在脑瘫(CP)和杜氏肌营养不良症(DMD)儿童中的应用来证明其用途。方法:通过三维徒手超声波(四块肌肉,n=154,♂/♀=82/72,年龄范围:0y7mo-17y10mo)和固定测力法(七组肌肉,n=153,♂/♀=108/45,年龄范围:4y6mo-16y1mo)分别对TD儿童的下肢肌肉大小和力量进行评估。使用位置、尺度和形状的广义加法模型估算人体测量相关指标,即体重和身高、TD 百分位曲线,并将个别 CP 和 DMD 患者的结果转换为 z 分数。研究结果随着人体测量值的增加,肌肉大小和力量及其受试者之间的差异也随之增加。个别患者的 z 值为负值,表明与 TD 同龄人相比,他们的肌肉尺寸和力量存在缺陷。解释:在一组 TD 儿童中建立的与人体测量相关的肌肉尺寸和力量百分位曲线可成功用于表达患者与 TD 相关的结果。这有助于解释运动障碍儿童的肌肉大小和薄弱情况,并可评估成长过程中的疾病进展和治疗效果。
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Anthropometric-related percentile curves for muscle size and strength of lower limb muscles of typically developing children
Abstract Aims: To establish anthropometric-related percentile curves for muscle size and strength in a cohort of typically developing (TD) children and to demonstrate their use through applications in children with cerebral palsy (CP) and Duchenne muscular dystrophy (DMD). Methods: Lower limb muscle size and strength were assessed in a large cross-sectional cohort of TD children with 3D freehand ultrasound (four muscles, n=154, ♂/♀=82/72, age range: 0y7mo-17y10mo) and fixed dynamometry (seven muscle groups, n=153, ♂/♀=108/45, age range: 4y6mo-16y1mo), respectively. Generalized additive models for location, scale and shape were used to estimate anthropometric-related, i.e. body mass and height, TD percentile curves and to convert outcomes of individual patients with CP and DMD into z-scores. Results: Muscle size and strength, as well as their inter-subject variation, increased with increasing anthropometric values. Individual patients exhibited negative z-scores, indicating muscle size and strength deficits in reference to TD peers. Interpretation: The established anthropometric-related percentile curves for muscle size and strength in a cohort of TD children can successfully be used to express patient outcomes in reference to TD. This facilitates the interpretation of muscle size and weakness in children with a motor disability and allows for the evaluation of the disease progression and treatment impact during growth.
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