Evidence map›Paper›PMID 41526383›Full record

ArticleNPJ Parkinson's disease2026

Data-driven subtyping of early Parkinson's disease via mutual cross-attention fusion of EEG and dual-task gait features.

Deyu Wang, Yu Shi, Jun Pang, Xiaodong Zhu, Lin Meng, Dong Ming

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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3 · Its place in the literature

Who cites it

3 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

6 authors.

Deyu WangAcademy of Medical Engineering and Translational Medicine, Medical School, Faculty of Medicine, Tianjin University, Tianjin, China.
Yu ShiAcademy of Medical Engineering and Translational Medicine, Medical School, Faculty of Medicine, Tianjin University, Tianjin, China.
Jun PangAcademy of Medical Engineering and Translational Medicine, Medical School, Faculty of Medicine, Tianjin University, Tianjin, China.
Xiaodong ZhuDepartment of Neurology, Tianjin Medical University General Hospital, Tianjin, China.
Lin MengAcademy of Medical Engineering and Translational Medicine, Medical School, Faculty of Medicine, Tianjin University, Tianjin, China. linmeng@tju.edu.cn.ORCID http://orcid.org/0000-0001-9787-9936
Dong MingAcademy of Medical Engineering and Translational Medicine, Medical School, Faculty of Medicine, Tianjin University, Tianjin, China.

Funding

National Natural Science Foundation of China 82372083
6 · The paper itself

Abstract

Parkinson's disease (PD) exhibits marked clinical heterogeneity, which poses challenges for diagnosis, prognosis, and therapeutic precision, especially for early-stage PD patients. Existing subtyping approaches often rely on subjective clinical scales and single-modality data, which limits their sensitivity in capturing subtle but clinically relevant differences across patients. To reveal clinically meaningful PD subtypes, we propose a data-driven multimodal framework that integrates resting-state electroencephalography (EEG) and dual-task gait features using mutual cross-attention (MCA) fusion. Forty idiopathic early-stage PD patients were enrolled in a prospective study. EEG biomarkers were encoded via a convolutional neural network for the prediction of motor severity (MDS-UPDRS-III), while dual-task gait features were derived to capture subtle motor dysfunctions. The MCA enabled bidirectional attention-guided integration of EEG and gait features, which were then clustered using an unsupervised method. The analysis revealed three distinct subtypes, with dual-task-based fusion providing superior clinical separation. Subtype I was characterized by pronounced motor deficits; Subtype II showed moderate symptoms with relatively preserved quality of life; and Subtype III presented mild motor impairments but exhibited poorer cognitive and psychosocial outcomes. Feature contribution analyses highlighted central beta and theta EEG activity, along with dual-task gait metrics (e.g., stride length during turning), as key drivers of subtype differentiation. Longitudinal follow-up demonstrated subtype-specific rehabilitation responses, with Subtype II showing an insufficient response compared to other subtypes. In conclusion, this study enables digital phenotyping of PD with prognostic implications for personalized rehabilitation strategies and accelerates precision medicine.

Identifiers

PMID41526383
PMCPMC12905180

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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.