4.4 Article

Parkinson's disease: deep learning with a parameter-weighted structural connectome matrix for diagnosis and neural circuit disorder investigation

期刊

NEURORADIOLOGY
卷 63, 期 9, 页码 1451-1462

出版社

SPRINGER
DOI: 10.1007/s00234-021-02648-4

关键词

Parkinson disease; Connectome; Magnetic resonance imaging; Deep learning; Artificial intelligence

资金

  1. Brain/MINDS Beyond program from Japan Agency for Medical Research and Development [JP19dm0307024, JP19dm0307101]
  2. Japan Society for the Promotion of Science KAKENHI [19K17244]
  3. Grants-in-Aid for Scientific Research [19K17244] Funding Source: KAKEN

向作者/读者索取更多资源

Deep learning techniques applied to parameter-weighted structural matrices can differentiate patients with Parkinson's disease from healthy controls. Neural circuit disorders, such as alterations in connections between the basal ganglia and cerebellum, can be visualized using gradient-weighted class activation mapping.
Purpose To investigate whether Parkinson's disease (PD) can be differentiated from healthy controls and to identify neural circuit disorders in PD by applying a deep learning technique to parameter-weighted and number of streamlines (NOS)-based structural connectome matrices calculated from diffusion-weighted MRI. Methods In this prospective study, 115 PD patients and 115 healthy controls were enrolled. NOS-based and parameter-weighted connectome matrices were calculated from MRI images obtained with a 3-T MRI unit. With 5-fold cross-validation, diagnostic performance of convolutional neural network (CNN) models using those connectome matrices in differentiating patients with PD from healthy controls was evaluated. To identify the important brain connections for diagnosing PD, gradient-weighted class activation mapping (Grad-CAM) was applied to the trained CNN models. Results CNN models based on some parameter-weighted structural matrices (diffusion kurtosis imaging (DKI)-weighted, neurite orientation dispersion and density imaging (NODDI)-weighted, and g-ratio-weighted connectome matrices) showed moderate performance (areas under the receiver operating characteristic curve (AUCs) = 0.895, 0.801, and 0.836, respectively) in discriminating PD patients from healthy controls. The DKI-weighted connectome matrix performed significantly better than the conventional NOS-based matrix (AUC = 0.761) (DeLong's test, p < 0.0001). Alterations of neural connections between the basal ganglia and cerebellum were indicated by applying Grad-CAM to the NODDI- and g-ratio-weighted matrices. Conclusion Patients with PD can be differentiated from healthy controls by applying the deep learning technique to the parameter-weighted connectome matrices, and neural circuit disorders including those between the basal ganglia on one side and the cerebellum on the contralateral side were visualized.

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