# Development of a clinical prediction model for inflammatory biomarkers and enlarged basal ganglia perivascular spaces using SHAP analysis: feature selection and model interpretation

**Authors:** Jiayu Lv, Dewang Gao, Wen Yong, Wenlong Yu, Lu Wang, Shangjia Ma, Hua Li, Shuaiqiang Zhang, Zi Guo, Hao Yan, Zhipeng Ju, Yiming Liu, Lie Wu, Xia Guo

PMC · DOI: 10.3389/fneur.2025.1665841 · Frontiers in Neurology · 2026-01-02

## TL;DR

This study develops a model to predict enlarged perivascular spaces in the brain using cognitive and inflammatory markers, showing their clinical value for early disease detection.

## Contribution

A novel predictive model integrating cognitive and inflammatory biomarkers for assessing BG-EPVS burden using SHAP analysis for interpretation.

## Key findings

- Age, hypertension, and SIRI were positively correlated with BG-EPVS burden.
- MoCA score and education duration were negatively correlated with BG-EPVS burden.
- The model combining MoCA and inflammatory biomarkers accurately predicts BG-EPVS burden.

## Abstract

Enlarged perivascular spaces (EPVS) may lead to dysfunction of the cerebral lymphatic system, which may be associated with cerebrovascular diseases, cognitive dysfunction, and other neurological diseases. However, the association between cognitive function and systemic inflammation has not been systematically elucidated. This study aimed to develop a predictive model integrating the Montreal Cognitive Assessment (MoCA) and complete blood count-derived inflammatory markers to analyze the relationship between multidimensional indicators and BG-EPVS burden.

We consecutively enrolled patients with cerebral small vessel disease (CSVD) admitted to the Department of Neurology, First Affiliated Hospital of Baotou Medical College, between 2023 and 2024. BG-EPVS severity was evaluated using MRI, and statistical analyses were conducted on clinical variables. Univariate and multivariate logistic regression analyses were conducted to identify independent predictors of BG-EPVS severity. Model performance and clinical utility were evaluated using receiver operating characteristic curves (ROC-AUC), calibration plots, decision curve analysis (DCA), and clinical impact curves (CIC). Model interpretability was assessed using SHapley Additive exPlanations (SHAP).

Multivariate logistic regression identified MoCA score, age, hypertension, SIRI and education independent predictors of BG-EPVS burden.

These findings demonstrate that age, hypertension and SIRI were positively correlated with high BG-EPVS burden, while MoCA score and education duration were negatively correlated. The integrated model combining MoCA and inflammatory biomarkers accurately predicts BG-EPVS burden, demonstrating their clinical value in early disease screening and dynamic monitoring.

## Full-text entities

- **Diseases:** inflammation (MESH:D007249), lymphatic system (MESH:D008206), cognitive dysfunction (MESH:D003072), CSVD (MESH:D059345), neurological diseases (MESH:D020271), hypertension (MESH:D006973), cerebrovascular diseases (MESH:D002561)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12807889/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12807889/full.md

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Source: https://tomesphere.com/paper/PMC12807889