LGSep 10, 2022

Shape Analysis for Pediatric Upper Body Motor Function Assessment

arXiv:2209.04710v11 citationsh-index: 35
Originality Incremental advance
AI Analysis

It addresses the challenge of tracking incremental motor function changes in children with disorders like SMA and DMD, offering a more objective assessment method, though it is incremental as it builds on existing shape analysis techniques.

This paper tackles the problem of quantitatively assessing upper body motor function in children with neuromuscular disorders by using curve registration and shape analysis to align motion trajectories and extract a mean reference shape, resulting in a metric that shows statistically significant differences between patient and control populations (p=0.0213) and correlates with clinical scores like Brooke's score (p=0.00063).

Neuromuscular disorders, such as Spinal Muscular Atrophy (SMA) and Duchenne Muscular Dystrophy (DMD), cause progressive muscular degeneration and loss of motor function for 1 in 6,000 children. Traditional upper limb motor function assessments do not quantitatively measure patient-performed motions, which makes it difficult to track progress for incremental changes. Assessing motor function in children with neuromuscular disorders is particularly challenging because they can be nervous or excited during experiments, or simply be too young to follow precise instructions. These challenges translate to confounding factors such as performing different parts of the arm curl slower or faster (phase variability) which affects the assessed motion quality. This paper uses curve registration and shape analysis to temporally align trajectories while simultaneously extracting a mean reference shape. Distances from this mean shape are used to assess the quality of motion. The proposed metric is invariant to confounding factors, such as phase variability, while suggesting several clinically relevant insights. First, there are statistically significant differences between functional scores for the control and patient populations (p$=$0.0213$\le$0.05). Next, several patients in the patient cohort are able to perform motion on par with the healthy cohort and vice versa. Our metric, which is computed based on wearables, is related to the Brooke's score ((p$=$0.00063$\le$0.05)), as well as motor function assessments based on dynamometry ((p$=$0.0006$\le$0.05)). These results show promise towards ubiquitous motion quality assessment in daily life.

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