Evidence map›Paper›PMID 40457336›Full record

ArticleJournal of neuroengineering and rehabilitation2025

Using machine learning to identify Parkinson's disease severity subtypes with multimodal data.

Hwayoung Park, Changhong Youm, Sang-Myung Cheon, Bohyun Kim, Hyejin Choi, Juseon Hwang, Minsoo Kim

Abstract read
In one paragraph

Article in Journal of neuroengineering and rehabilitation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Hwayoung ParkBiomechanics Laboratory, Department of Healthcare and Science, College of Health Sciences, Dong-A University, 37 Nakdong‑daero, 550 Beon‑gil, Hadan 2-Dong, Saha-gu, Busan, 49315, Republic of Korea.
Changhong YoumBiomechanics Laboratory, Department of Healthcare and Science, College of Health Sciences, Dong-A University, 37 Nakdong‑daero, 550 Beon‑gil, Hadan 2-Dong, Saha-gu, Busan, 49315, Republic of Korea. chyoum@dau.ac.kr.
Sang-Myung CheonDepartment of Neurology, School of Medicine, Dong-A University, 26 Daesingongwon-ro, Seo-gu, Busan, 49201, Republic of Korea. smcheon@dau.ac.kr.
Bohyun KimBiomechanics Laboratory, Department of Healthcare and Science, College of Health Sciences, Dong-A University, 37 Nakdong‑daero, 550 Beon‑gil, Hadan 2-Dong, Saha-gu, Busan, 49315, Republic of Korea.
Hyejin ChoiBiomechanics Laboratory, Department of Healthcare and Science, College of Health Sciences, Dong-A University, 37 Nakdong‑daero, 550 Beon‑gil, Hadan 2-Dong, Saha-gu, Busan, 49315, Republic of Korea.
Juseon HwangBiomechanics Laboratory, Department of Healthcare and Science, College of Health Sciences, Dong-A University, 37 Nakdong‑daero, 550 Beon‑gil, Hadan 2-Dong, Saha-gu, Busan, 49315, Republic of Korea.
Minsoo KimBiomechanics Laboratory, Department of Healthcare and Science, College of Health Sciences, Dong-A University, 37 Nakdong‑daero, 550 Beon‑gil, Hadan 2-Dong, Saha-gu, Busan, 49315, Republic of Korea.

Funding

Basic Science Research Program through the NRF 2022R1A6A3A0108756411Ministry of Education of the Republic of Korea and the NRF 2024S1A5B5A16021673National Research Foundation of Korea 2022R1A2C100933711
6 · The paper itself

Abstract

backgroundClassifying and predicting Parkinson's disease (PD) is challenging because of its diverse subtypes based on severity levels. Currently, identifying objective biomarkers associated with disease severity that can distinguish PD subtypes in clinical trials is necessary. This study aims to address the clinical applicability and heterogeneity of PD using PD severity subtypes classification and digital biomarker development by combining objective multimodal data with machine learning (ML) approaches.

methodsWe analyzed datasets that combine clinical characteristics, physical function and lifestyle data, gait parameters in motion analysis systems, and wearable sensors collected from persons with PD (n = 102) to perform clustering for subtype classification.

resultsWe identified three PD severity subtypes, each exhibiting different patterns of clinical severity, with the severity increasing as it progressed from clusters 1 to 3. We found significant mutual information between all/single modalities and the unified PD rating scale scores, identifying potential modalities with high feature importance using ML. Among all modalities, the principal components of gait parameters derived from wearable sensors were identified as the most associated indicators of PD severity. A model utilizing the first principal component of the left and right ankle achieved perfect classification with an area under the curve of 1.0, accurately distinguishing clinically severe subtypes from mild subtypes of PD. These findings suggest that gait features in both ankles can reflect asymmetry factors associated with PD severity subtypes, which contributes to high classification performance.

conclusionsDigital biomarkers obtained from wearable sensors attached bilaterally to body segments demonstrate potential for classifying PD severity subtypes and tracking disease progression. Our findings emphasized the clinical value of sensor-based gait analysis in PD management, which suggested its integration into personalized monitoring systems and therapeutic interventions for persons with PD.

Indexed as

Machine LearningParkinson DiseaseSeverity of Illness IndexAgedBiomarkersFemaleGaitHumansMaleMiddle AgedWearable Electronic DevicesBiomarkersClusteringDigital biomarkerMachine learningMultimodal dataParkinson's diseaseSeverity subtype

Identifiers

PMID40457336
PMCPMC12131740

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.