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MRI-Based Radiomics of Basal Nuclei in Differentiating Idiopathic Parkinson’s Disease From Parkinsonian Variants of Multiple System Atrophy: A Susceptibility-Weighted Imaging Study

OBJECTIVES: To investigate the value of MRI-based radiomic model based on the radiomic features of different basal nuclei in differentiating idiopathic Parkinson’s disease (IPD) from Parkinsonian variants of multiple system atrophy (MSA-P). METHODS: Radiomics was applied to the 3T susceptibility- we...

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Detalles Bibliográficos
Autores principales: Pang, Huize, Yu, Ziyang, Li, Renyuan, Yang, Huaguang, Fan, Guoguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689200/
https://www.ncbi.nlm.nih.gov/pubmed/33281598
http://dx.doi.org/10.3389/fnagi.2020.587250
Descripción
Sumario:OBJECTIVES: To investigate the value of MRI-based radiomic model based on the radiomic features of different basal nuclei in differentiating idiopathic Parkinson’s disease (IPD) from Parkinsonian variants of multiple system atrophy (MSA-P). METHODS: Radiomics was applied to the 3T susceptibility- weighted imaging (SWI) from 102 MSA-P patients and 83 IPD patients (allocated to a training and a testing cohort, 7:3 ratio). The substantia nigra (SN), caudate nucleus (CN), putamen (PUT), globus pallidus (GP), red nucleus (RN), and subthalamic nucleus (STN) were manually segmented, and 396 features were extracted. After feature selection, support vector machine (SVM) was generated, and its predictive performance was calculated in both the training and testing cohorts using the area under receiver operating characteristic curve (AUC). RESULTS: Seven radiomic features were selected from the PUT, by which the SVM classifier achieved the best diagnostic performance with an AUC of 0.867 in the training cohort and an AUC of 0.862 in the testing cohort. Furthermore, the combined model, which incorporating part III of the Parkinson’s Disease Rating Scale (UPDRSIII) scores into radiomic features of the PUT, further improved the diagnostic performance. However, radiomic features extracted from RN, SN, GP, CN, and STN had moderate to poor diagnostic performance, with AUC values that ranged from 0.610 to 0.788 in the training cohort and 0.583 to 0.766 in the testing cohort. CONCLUSION: Radiomic features derived from the PUT had optimal value in differentiating IPD from MSA-P. A combined radiomic model, which contained radiomic features of the PUT and UPDRSIII scores, further improved performance and may represent a promising tool for distinguishing between IPD and MSA-P.