# Similarity Gait Networks with XAI for Parkinson’s Disease Classification: A Pilot Study

**Authors:** Maria Giovanna Bianco, Camilla Calomino, Marianna Crasà, Alessia Cristofaro, Giulia Sgrò, Fabiana Novellino, Salvatore Andrea Pullano, Syed Kamrul Islam, Jolanda Buonocore, Aldo Quattrone, Andrea Quattrone, Rita Nisticò

PMC · DOI: 10.3390/bioengineering13020151 · Bioengineering · 2026-01-28

## TL;DR

This study uses machine learning and sensor data to identify movement patterns that can help detect Parkinson’s disease more objectively.

## Contribution

The novel approach combines kinematic networks with explainable AI to discover digital biomarkers for Parkinson’s disease.

## Key findings

- The model achieved an AUC of 0.87 in distinguishing Parkinson’s patients from healthy controls.
- Key features included increased positional variability and reduced distal limb velocity in Parkinson’s patients.
- Network centrality shifted toward proximal body segments in Parkinson’s disease.

## Abstract

Parkinson’s disease (PD) is characterized by alterations in movement dynamics that are difficult to quantify with conventional clinical assessment. This study proposes an integrated approach combining graph-based kinematic analysis with explainable machine learning to identify digital biomarkers of Parkinsonian motor impairment. Kinematic signals were acquired using Xsens inertial sensors from 51 patients with PD and 53 healthy controls. For each participant, subject-specific kinematic networks were constructed by modeling inter-segment similarities through Jensen–Shannon divergence, from which global and local graph-theoretical metrics were extracted. A machine learning pipeline incorporating voting feature selection, and XGBoost classification was evaluated using a nested cross-validation design. The model achieved robust performance (AUC = 0.87), and explainability analyses using SHAP identified a subset of 13 features capturing alterations in velocity, inter-segment connectivity, and network centrality. PD was characterized by increased positional variability, reduced distal limb velocity, and a redistribution of network centrality towards proximal body segments. These features were associated with clinical severity, confirming their physiological relevance. By integrating graph-theoretical modeling, explainable artificial intelligence, and machine learning methodology, this work provides a method of discovering quantitative biomarkers capturing alterations in motor coordination. These findings highlight the potential of ML and kinematic networks to support objective motor assessment in PD.

## Linked entities

- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** SHROOM4 (shroom family member 4) [NCBI Gene 57477] {aka MRXSSDS, SHAP, shrm4}
- **Diseases:** atrophy (MESH:D001284), ML (MESH:C537366), psychiatric (MESH:D001523), neoplasms (MESH:D009369), HC (MESH:D000067329), PD (MESH:D010300), neurodegenerative disorder (MESH:D019636), injury to (MESH:D014947), XAI (MESH:C538243), multiple system (MESH:D019578), coordination deficits (MESH:D019957), PSP (MESH:D011030), impaired adaptive motor coordination (MESH:D001259), Bradykinesia (MESH:D018476), Tremor (MESH:D014202), postural instability (MESH:D054972), motor abnormalities (MESH:D000014), Movement Disorder (MESH:D009069), dopaminergic motor impairment (MESH:D009422), lacunar infarcts (MESH:D059409), motor dysfunction (MESH:D000068079), hydrocephalus (MESH:D006849), neuromuscular disorders (MESH:D009468), axial rigidity (MESH:D009127), Parkinsonism (MESH:D010302)
- **Chemicals:** lrhol (-), 123I-FP-CIT (MESH:C087552), dopamine (MESH:D004298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12937932/full.md

## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12937932/full.md

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Source: https://tomesphere.com/paper/PMC12937932