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Development and Multicenter External Validation of a Real-Time Artificial Intelligence Diagnostic System for Diabetic Peripheral Neuropathy Based on Wearable Devices

医学 逻辑回归 物理医学与康复 可穿戴计算机 步态 周围神经病变 一致性 队列 机器学习 随机森林 跨步 无症状的 糖尿病神经病变 物理疗法 可穿戴技术 科恩卡帕 人工智能 糖尿病足 队列研究 假阳性悖论 手腕 前脚 糖尿病 疾病严重程度
作者
Junlin Ran,Pengcheng Huang,Min He,Liling Deng,Qingqing Chen,Yiwen Qin,David J. Armstrong,Bijan Najafi,Edward Jude,Yanzhong Wang,Wuquan Deng,Chenzhen Du
出处
期刊:Gerontology [Karger Publishers]
卷期号:: 1-17
标识
DOI:10.1159/000551704
摘要

INTRODUCTION: Diabetic peripheral neuropathy (DPN) is a frequent diabetes complication, affecting over half of patients and causing pain, falls, ulcers, and amputations if undetected. Traditional methods like electromyography are resource-intensive and inaccessible. This study developed and validated STRIDE, a machine learning model using wearable gait and balance data for real-time DPN classification. METHODS: In this study conducted across multiple centers, 206 participants from Chongqing hospitals were categorized as follows: healthy controls (n = 32), diabetics without DPN (n = 47), asymptomatic DPN (n = 48), and symptomatic DPN (n = 79). A separate group of 42 was used for validation. During a one-minute walk and modified balance test, LEG-Sys/BalanSens sensors produced 68 features. STRIDE used random forest and logistic regression with cross-validation. The metrics used were area under the receiver operating characteristic curve (AUROC), accuracy, sensitivity, specificity, F1-score, and SHAP for interpretability, with a scoring system allowing for real-time evaluation. RESULTS: Random forest achieved AUROC 0.80 (95% CI: 0.64-0.92); logistic regression 0.79 (95% CI: 0.62-0.95). Key SHAP features: stride length variability (weight = 0.61) and double-support time. External validation: initial accuracy 78.6%, recall 86.5%, precision 88.9%; three of four false positives developed DPN within 1 year, yielding 89.3% adjusted concordance. STRIDE outperformed other parameters in mid-term prediction, unaffected by anemia for up to 4 years. CONCLUSION: STRIDE provides a scalable, interpretable tool for DPN classification, supporting early intervention and improved outcomes. Larger longitudinal studies are needed for clinical integration.
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