物理医学与康复
杜氏肌营养不良
生物标志物
肌营养不良
疾病
日常生活活动
可穿戴计算机
医学
临床试验
心理学
物理疗法
计算机科学
病理
内科学
嵌入式系统
化学
生物化学
作者
Valeria Ricotti,Balasundaram Kadirvelu,Victoria Selby,Richard Festenstein,Eugenio Mercuri,Thomas Voit,A. Aldo Faisal
出处
期刊:Nature Medicine
[Springer Nature]
日期:2023-01-01
卷期号:29 (1): 95-103
被引量:80
标识
DOI:10.1038/s41591-022-02045-1
摘要
Abstract Artificial intelligence has the potential to revolutionize healthcare, yet clinical trials in neurological diseases continue to rely on subjective, semiquantitative and motivation-dependent endpoints for drug development. To overcome this limitation, we collected a digital readout of whole-body movement behavior of patients with Duchenne muscular dystrophy (DMD) ( n = 21) and age-matched controls ( n = 17). Movement behavior was assessed while the participant engaged in everyday activities using a 17-sensor bodysuit during three clinical visits over the course of 12 months. We first defined new movement behavioral fingerprints capable of distinguishing DMD from controls. Then, we used machine learning algorithms that combined the behavioral fingerprints to make cross-sectional and longitudinal disease course predictions, which outperformed predictions derived from currently used clinical assessments. Finally, using Bayesian optimization, we constructed a behavioral biomarker, termed the KineDMD ethomic biomarker, which is derived from daily-life behavioral data and whose value progresses with age in an S-shaped sigmoid curve form. The biomarker developed in this study, derived from digital readouts of daily-life movement behavior, can predict disease progression in patients with muscular dystrophy and can potentially track the response to therapy.
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