Abstract
Background: Parkinson's disease (PD) is a neurodegenerative disease in which the neostriatum, including the caudate nucleus (CN) and putamen (PU), has an important role in the pathophysiology. However, conventional magnetic resonance imaging (MRI) lacks sufficient specificity to diagnose PD. Therefore, the study's aim was to investigate the feasibility of using a radiomics approach to distinguish PD patients from healthy controls on T2-weighted images of the neostriatum and provide a basis for the clinical diagnosis of PD.Methods: T2-weighted images from 69 PD patients and 69 age- and sex-matched healthy controls were obtained on the same 3.0T MRI scanner. Regions of interest (ROIs) were manually placed at the CN and PU on the slices showing the largest respective sizes of the CN and PU. We extracted 274 texture features from each ROI and then used the least absolute shrinkage and selection operator regression to perform feature selection and radiomics signature building to identify the CN and PU radiomics signatures consisting of optimal features. We used a receiver operating characteristic curve analysis to assess the diagnostic performance of two radiomics signatures in a training group and estimate the generalization performance in the test group.Results: There were no significant differences in the demographic and clinical characteristics between the PD patients and healthy controls. The CN and PU radiomics signatures were built using 12 and 7 optimal features, respectively. The performance of the two radiomics signatures to distinguish PD patients from healthy controls was good. In the training and test groups, the AUCs of the CN radiomics signatures were 0.9410 (95% confidence interval [CI]: 0.8986–0.9833) and 0.7732 (95% CI: 0.6292–0.9173), respectively, and the AUCs of the PU radiomics signature were 0.8767 (95% CI: 0.8066–0.9469) and 0.7143 (95% CI: 0.5540–0.8746), respectively. Vertl_GlevNonU_R appeared simultaneously in both the CN and PU radiomics signatures as an optimal feature. A t-test analysis revealed significantly higher levels of texture values of the CN and PU in the PD patients than healthy controls (P < 0.05).Conclusion: Neostriatum radiomics signatures achieved good diagnostic performance for PD and potentially could serve as a basis for the clinical diagnosis of PD.
Highlights
Parkinson’s disease (PD) is a progressive neurodegenerative disease characterized by rigidity, tremor, slowed movements, and other non-motor symptoms
In the training and test groups, the AUCs of the caudate nucleus (CN) radiomics signatures were 0.9410 (95% confidence interval [CI]: 0.8986–0.9833) and 0.7732, respectively, and the AUCs of the PU radiomics signature were 0.8767 and 0.7143, respectively
We developed two T2-weighted imaging (T2WI)-based radiomics signatures, each consisting of optimal features for either CN or PU, and estimated the generalization performance in the test group by using receiver operating characteristic (ROC) analysis
Summary
Parkinson’s disease (PD) is a progressive neurodegenerative disease characterized by rigidity, tremor, slowed movements, and other non-motor symptoms. As part of the nigrostriatal system, the neostriatum includes both the caudate nucleus (CN) and putamen (PU) [3]. Iron deposition in the brain, including the neostriatum, has been proposed as having an important role in the pathophysiology of PD [5, 6]. Parkinson’s disease (PD) is a neurodegenerative disease in which the neostriatum, including the caudate nucleus (CN) and putamen (PU), has an important role in the pathophysiology. Conventional magnetic resonance imaging (MRI) lacks sufficient specificity to diagnose PD. The study’s aim was to investigate the feasibility of using a radiomics approach to distinguish PD patients from healthy controls on T2-weighted images of the neostriatum and provide a basis for the clinical diagnosis of PD
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