At-home wearable-based monitoring predicts clinical measures and biological biomarkers of disease severity in Friedreich’s Ataxia

IF 5.4 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Communications medicine Pub Date : 2024-10-29 DOI:10.1038/s43856-024-00653-1
Ram Kinker Mishra, Adonay S. Nunes, Ana Enriquez, Victoria R. Profeta, McKenzie Wells, David R. Lynch, Ashkan Vaziri
{"title":"At-home wearable-based monitoring predicts clinical measures and biological biomarkers of disease severity in Friedreich’s Ataxia","authors":"Ram Kinker Mishra, Adonay S. Nunes, Ana Enriquez, Victoria R. Profeta, McKenzie Wells, David R. Lynch, Ashkan Vaziri","doi":"10.1038/s43856-024-00653-1","DOIUrl":null,"url":null,"abstract":"Friedreich ataxia (FRDA) results in progressive impairment in gait, upper extremity coordination, and speech. Currently, these symptoms are assessed through expert examination at clinical visits. Such in-clinic assessments are time-consuming, subjective, of limited sensitivity, and provide only a limited perspective of the daily disability of patients. In this study, we recruited 39 FRDA patients and remotely monitored their physical activity and upper extremity function using a set of wearable sensors for 7 consecutive days. We compared the sensor-derived metrics of lower and upper extremity function as measured during activities of daily living with FRDA clinical measures (e.g., mFARS and FA-ADL) and biological biomarkers of disease severity (guanine-adenine-adenine (GAA) and frataxin (FXN) levels), using Spearman correlation analyses. The results show significant correlations with moderate to high effect sizes between multiple sensor-derived metrics and the FRDA clinical and biological outcomes. In addition, we develop multiple machine learning-based models to predict disease severity in FRDA using demographic, biological, and sensor-derived metrics. When sensor-derived metrics are included, the model performance enhances 1.5-fold and 2-fold in terms of explained variance, R², for predicting FRDA clinical measures and biological biomarkers of disease severity, respectively. Our results establish the initial clinical validity of using wearable sensors in assessing disease severity and monitoring motor dysfunction in FRDA. Friedreich ataxia (FRDA) is a condition that impairs movement and coordination. Current clinical assessments are subjective, highlighting the need for better ways to monitor disease severity. By using wearable devices to track symptoms in everyday life, we can gain better insights into how patients function outside the clinical environment, offering a more comprehensive understanding of the disease’s impact. In this study, 39 patients were observed using wearable sensors for a week to track their physical activity and arm movements. The data collected was compared with traditional clinical tests and biological markers of the disease. The findings demonstrate that wearable sensors can accurately predict disease severity, offering continuous real-world monitoring that could enhance patient care and treatment outcomes. Mishra, Nunes et al. monitor the physical activity and upper limb function of 39 people with Friedreich ataxia (FRDA) using wearable sensors over 7 days. The results demonstrate that incorporating sensor data significantly enhances predictive models of disease severity, offering a comprehensive approach to assessing and monitoring FRDA.","PeriodicalId":72646,"journal":{"name":"Communications medicine","volume":" ","pages":"1-9"},"PeriodicalIF":5.4000,"publicationDate":"2024-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11519636/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.nature.com/articles/s43856-024-00653-1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
引用次数: 0

Abstract

Friedreich ataxia (FRDA) results in progressive impairment in gait, upper extremity coordination, and speech. Currently, these symptoms are assessed through expert examination at clinical visits. Such in-clinic assessments are time-consuming, subjective, of limited sensitivity, and provide only a limited perspective of the daily disability of patients. In this study, we recruited 39 FRDA patients and remotely monitored their physical activity and upper extremity function using a set of wearable sensors for 7 consecutive days. We compared the sensor-derived metrics of lower and upper extremity function as measured during activities of daily living with FRDA clinical measures (e.g., mFARS and FA-ADL) and biological biomarkers of disease severity (guanine-adenine-adenine (GAA) and frataxin (FXN) levels), using Spearman correlation analyses. The results show significant correlations with moderate to high effect sizes between multiple sensor-derived metrics and the FRDA clinical and biological outcomes. In addition, we develop multiple machine learning-based models to predict disease severity in FRDA using demographic, biological, and sensor-derived metrics. When sensor-derived metrics are included, the model performance enhances 1.5-fold and 2-fold in terms of explained variance, R², for predicting FRDA clinical measures and biological biomarkers of disease severity, respectively. Our results establish the initial clinical validity of using wearable sensors in assessing disease severity and monitoring motor dysfunction in FRDA. Friedreich ataxia (FRDA) is a condition that impairs movement and coordination. Current clinical assessments are subjective, highlighting the need for better ways to monitor disease severity. By using wearable devices to track symptoms in everyday life, we can gain better insights into how patients function outside the clinical environment, offering a more comprehensive understanding of the disease’s impact. In this study, 39 patients were observed using wearable sensors for a week to track their physical activity and arm movements. The data collected was compared with traditional clinical tests and biological markers of the disease. The findings demonstrate that wearable sensors can accurately predict disease severity, offering continuous real-world monitoring that could enhance patient care and treatment outcomes. Mishra, Nunes et al. monitor the physical activity and upper limb function of 39 people with Friedreich ataxia (FRDA) using wearable sensors over 7 days. The results demonstrate that incorporating sensor data significantly enhances predictive models of disease severity, offering a comprehensive approach to assessing and monitoring FRDA.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
基于可穿戴设备的居家监测可预测弗里德里希共济失调症的临床症状和疾病严重程度的生物标志物。
背景:弗里德里希共济失调症(FRDA)会导致步态、上肢协调能力和语言能力逐渐受损。目前,这些症状是在临床就诊时通过专家检查进行评估的。这种临床评估耗时长、主观性强、灵敏度有限,而且只能从有限的角度反映患者的日常残疾情况:在这项研究中,我们招募了 39 名 FRDA 患者,使用一套可穿戴传感器连续 7 天远程监测他们的体力活动和上肢功能。我们使用斯皮尔曼相关性分析比较了日常生活活动中测量的下肢和上肢功能的传感器衍生指标与 FRDA 临床指标(如 mFARS 和 FA-ADL)和疾病严重程度的生物标志物(鸟嘌呤腺嘌呤腺嘌呤 (GAA) 和 frataxin (FXN) 水平):结果:结果表明,多个传感器衍生指标与 FRDA 临床和生物学结果之间存在明显的相关性,且具有中等到较高的效应大小。此外,我们还开发了多种基于机器学习的模型,利用人口统计学、生物学和传感器衍生指标预测 FRDA 的疾病严重程度。当包括传感器衍生指标时,预测 FRDA 临床指标和疾病严重程度生物标志物的模型性能在解释方差、R² 方面分别提高了 1.5 倍和 2 倍:我们的研究结果初步确定了使用可穿戴传感器评估 FRDA 疾病严重程度和监测运动功能障碍的临床有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Inferring the regional distribution of Visceral Leishmaniasis incidence from data at different spatial scales. Underestimated risk of secondary complications in pathogenic and glucose-elevating GCK variant carriers with type 2 diabetes. Ursodeoxycholic acid and severe COVID-19 outcomes in a cohort study using the OpenSAFELY platform. Using UK Biobank data to establish population-specific atlases from whole body MRI. Predicting individual patient and hospital-level discharge using machine learning.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1