Evidence map›Paper›PMID 40990032›Full record

ArticleFrontiers in neurology2025

Development of a radiomics-based model for diagnosis of multiple system atrophy using multimodal MRI.

Zhichao Li, Wei Zhang, Ran Yang, Dong Chen, Xin Li, Kun Wang, Lei Cheng, Heng Yang, Yili Deng

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Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Zhichao Li *Department of Radiology, Chongqing Western Hospital, Chongqing, China.
Wei Zhang *Department of Radiology, Chongqing Western Hospital, Chongqing, China.
Ran YangDepartment of Radiology, Chongqing Western Hospital, Chongqing, China.
Dong ChenDepartment of Radiology, Second People's Hospital of Jiulongpo District, Chongqing, China.
Xin LiDepartment of Radiology, Second People's Hospital of Jiulongpo District, Chongqing, China.
Kun WangDepartment of Radiology, Second People's Hospital of Jiulongpo District, Chongqing, China.
Lei ChengDepartment of Internal Medicine, Second People's Hospital of Jiulongpo District, Chongqing, China.
Heng YangDepartment of Internal Medicine, Second People's Hospital of Jiulongpo District, Chongqing, China.
Yili DengDepartment of Internal Medicine, Second People's Hospital of Jiulongpo District, Chongqing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Multiple system atrophy (MSA) is a rapidly progressive neuro-degenerative disorder characterized by autonomic dysfunction, levodopa- unresponsive parkinsonism, cerebellar ataxia, and corticospinal tract involvement. Early diagnosis remains challenging due to overlapping clinical manifestations and the absence of reliable biomarkers. This study aimed to develop a radiomics-based diagnostic model using multimodal MRI to improve MSA detection. Methods: A retrospective cohort of 62 clinically probable MSA patients (per the 2022 Movement Disorder Society criteria), and 73 matched healthy controls underwent 3.0-T MRI (T1WI, T2WI, FLAIR, DWI). Seven brain regions (bilateral cerebellar hemispheres, middle cerebellar peduncles, putamen, and pons) were manually segmented. A total of 1,502 radiomics features were extracted per region, using PyRadiomics (IBSI-compliant). Features with an intraclass correlation coefficient (ICC) ≥ 0.75 were retained, and the least absolute shrinkage and selection operator (LASSO) regression identified the top discriminative features to construct region-specific radiomics scores (Rad-scores). A logistic regression (LR) model integrated Rad-scores from all regions. Model performance was evaluated via precision, recall, and F1-score in training, testing, and validation cohorts (split ratio 6:2:2), and compared with visual assessments by two radiologists. Results: The LR model achieved high performance: accuracy was 0.98 in the training cohort, 0.97 in the testing cohort, and 0.95 in the validation cohort. Notably, classification precision for MSA reached 1.0 (indicating no false positives) across all cohorts. SHapley Additive exPlanations (SHAP) analysis revealed that the left putamen Rad-score as the most influential predictor. The model significantly outperformed radiologists' visual assessments (radiologist AUCs: 0.559 and 0.535; Conclusion: Multimodal MRI radiomics accurately differentiates MSA from healthy controls, even in the absence of conventional MRI markers. The Rad-score model demonstrates high sensitivity (89% recall in the validation cohort) and perfect specificity (100% precision), providing a clinically actionable tool for early MSA diagnosis.

Indexed as

diagnostic modelmachine learningmagnetic resonance imaging (MRI)multiple system atrophyneurodegenerative disordersradiomics

Identifiers

PMID40990032
PMCPMC12450663

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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.