Imu-based kinematic analysis to enhance upper limb motor function assessment in neuromuscular diseases.

IF 5.2 2区 医学 Q1 ENGINEERING, BIOMEDICAL
Alessandra Favata, Roger Gallart-Agut, Luc van Noort, Jesica Exposito-Escudero, Julita Medina-Cantillo, Carme Torras, Daniel Natera-de Benito, Josep M Font-Llagunes, Rosa Pàmies-Vilà
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Abstract

Duchenne muscular dystrophy (DMD) and spinal muscular atrophy (SMA) are neuromuscular diseases that lead to progressive muscle degeneration and weakness. Recent therapeutic advances for DMD and SMA highlight the need for accurate clinical evaluation. Traditionally, motor function of the upper limbs is assessed using motor function scales. However, these scales are influenced by clinician's interpretation and may lack accuracy. For this reason, clinicians are becoming interested in finding alternative solutions. In this context, Inertial Measurement Units (IMUs) have gained popularity, offering the possibility to quantitatively and objectively analyze motor function of patients to support clinicians' assessments. We analyzed upper limb kinematics of two groups of children with neuromuscular diseases, seventeen DMD patients and fifteen SMA patients, while performing the corresponding clinical assessment. These two groups were further subdivided into two categories (Category A and Category B), according to disease severity (Brooke scores 2 and Brooke scores > 2 , respectively). The results were compared against a group of ten healthy children. The metrics showing the strongest correlation with the clinical score were the workspace area in the frontal and transverse plane (DMD: ρ = 0.94 and ρ = 0.90; SMA: ρ = 0.78 and ρ = 0.81) and the workspace volume (DMD: ρ = 0.92; SMA ρ = 0.81). Additionally, statistically significant differences were found not only between healthy children and those with neuromuscular disease, but also across severity levels within the patient group. These results represent a first step toward validating IMU-based systems to helping clinicians to accurately quantify the motor status of children with neuromuscular diseases. Furthermore, data collected with inertial sensors can provide clinicians with additional information not available through subjective observation.

基于imu的运动学分析增强神经肌肉疾病患者上肢运动功能评估。
杜氏肌营养不良症(DMD)和脊髓性肌萎缩症(SMA)是导致进行性肌肉变性和无力的神经肌肉疾病。DMD和SMA的最新治疗进展强调了准确临床评估的必要性。传统上,上肢的运动功能是用运动功能量表来评估的。然而,这些量表受到临床医生解释的影响,可能缺乏准确性。因此,临床医生对寻找替代解决方案越来越感兴趣。在这种背景下,惯性测量单元(imu)已经得到普及,提供了定量和客观分析患者运动功能的可能性,以支持临床医生的评估。我们分析了两组神经肌肉疾病患儿(17例DMD患者和15例SMA患者)的上肢运动学,并进行了相应的临床评估。根据疾病严重程度(Brooke评分≤2分,Brooke评分> 2分)将两组进一步细分为A类和B类。研究结果与一组10名健康儿童进行了比较。与临床评分相关性最强的指标是额骨面和横切面的工作区域(DMD: ρ = 0.94和ρ = 0.90;SMA: ρ = 0.78和ρ = 0.81)和工作空间体积(DMD: ρ = 0.92;ρ = 0.81)。此外,不仅在健康儿童和患有神经肌肉疾病的儿童之间发现了统计学上的显著差异,而且在患者组内的严重程度之间也发现了显著差异。这些结果代表了验证基于imu的系统的第一步,以帮助临床医生准确量化患有神经肌肉疾病的儿童的运动状态。此外,惯性传感器收集的数据可以为临床医生提供通过主观观察无法获得的额外信息。
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来源期刊
Journal of NeuroEngineering and Rehabilitation
Journal of NeuroEngineering and Rehabilitation 工程技术-工程:生物医学
CiteScore
9.60
自引率
3.90%
发文量
122
审稿时长
24 months
期刊介绍: Journal of NeuroEngineering and Rehabilitation considers manuscripts on all aspects of research that result from cross-fertilization of the fields of neuroscience, biomedical engineering, and physical medicine & rehabilitation.
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