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Original Article | Open Access

Dopamine Transporter Imaging‐Based Radiomics for Predicting 4‐Year Motor Progression (Unified Parkinson's Disease Rating Scale Part Ⅲ) in Parkinson's Disease

Xiaoxuan Fan1Yanghan Chen1Junfeng Lin1Zenwen Han1,2,3Jianqiang Ye1,2,3Lili Lin1,2,3Hong Zhang4,5,6,7,8 Ang Li1,2,3( )Han Jiang1,2,3 ( )
PET Center, Fujian Medical University Union Hospital, Fuzhou, China
Fujian Key Laboratory of Intelligent Imaging and Precision Radiotherapy for Tumors, Fujian Medical University, Fuzhou, China
Clinical Research Center for Radiology and Radiotherapy of Fujian Province (Digestive, Hematological and Breast Malignancies), Fuzhou, China
Department of Nuclear Medicine, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine, Chinese Academy of Sciences, Hangzhou, China
Institute of Nuclear Medicine and Molecular Imaging of Zhejiang University, Hangzhou, China
Key Laboratory of Medical Molecular Imaging of Zhejiang Province, Hangzhou, China
Key Laboratory for Biomedical Engineering of Ministry of Education, Zhejiang University, Hangzhou, China
College of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, China
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Abstract

Background

Parkinson's disease (PD) shows substantial heterogeneity in motor progression, and reliable early prediction remains challenging. Dopamine transporter (DAT) imaging reflects presynaptic dopaminergic degeneration but is typically analyzed using simplified metrics that may not capture spatial heterogeneity. This study aims to evaluate whether magnetic resonance imaging (MRI)‐guided DAT radiomics combined with machine learning can predict 4‐year motor progression in PD.

Methods

In this retrospective study, 120 patients from the Parkinson's Progression Markers Initiative were included. Motor progression was defined using the 4‐year change in Movement Disorder Society–Unified Parkinson's Disease Rating Scale part Ⅲ (UPDRS‐Ⅲ) score. Bilateral caudate nuclei and putamina were manually delineated on T1‐weighted MRI and transferred to co‐registered DAT images. Radiomics features were extracted using PyRadiomics. Twenty base models were constructed by combining two feature‐selection methods with 10 classifiers, and Top‐2 voting fusion models were developed. Clinical‐variable, levodopa equivalent daily dose (LEDD)‐adjusted, and clinical‐radiomics models were also evaluated.

Results

The best‐performing base model achieved a mean area under the receiver operating characteristic curve (AUROC) of 0.736. Fusion models improved discrimination, with the best soft‐voting model achieving an AUROC of 0.920 and balanced accuracy (BACC) of 0.734. A more balanced fusion model achieved an AUROC of 0.902 with higher sensitivity (0.818). The clinical‐radiomics model showed only a slight AUROC increase over the clinical‐only model, and adding Year‐4 LEDD did not materially alter radiomics performance. Stable radiomics features were predominantly texture‐based, particularly gray‐level co‐occurrence matrix (GLCM) and gray‐level run‐length matrix (GLRLM) features derived from original and wavelet‐filtered images.

Conclusions

MRI‐guided DAT radiomics combined with ensemble learning may provide prognostically relevant information for predicting 4‐year motor progression in PD. Fusion strategies improved discrimination, and stable texture features may reflect striatal dopaminergic heterogeneity.

Graphical Abstract

References

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iRADIOLOGY
Pages 246-260

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Cite this article:
Fan X, Chen Y, Lin J, et al. Dopamine Transporter Imaging‐Based Radiomics for Predicting 4‐Year Motor Progression (Unified Parkinson's Disease Rating Scale Part Ⅲ) in Parkinson's Disease. iRADIOLOGY, 2026, 4(3): 246-260. https://doi.org/10.1002/ird3.70079

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Received: 03 April 2026
Revised: 20 May 2026
Accepted: 26 May 2026
Published: 08 June 2026
© 2026 The Author(s). Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.