Table 1.
Summary of existing classification approaches for PD diagnosis.
Authors | Objectives | Sample Size | Features | Methods | Accuracy |
---|---|---|---|---|---|
Diego et al. (2018) [21] | Classify PD patients and HC subjects | 388 subjects obtained from PPMI database | Morphological features extracted from DaTSCAN images with biomedical tests | SVM classifier with LOO-CV method | 96% |
Nicolas Nicastro et al. (2019) [24] | Distinguish PD patients from other parkinsonian syndromes and HC subjects | 578 subjects (local database) | Semi-quantitative 123-FP-CIT SPECT uptake values | SVM with five-fold CV method | 58.4% |
Yang et al. (2020) [22] | Classify PD patients and HC subjects | 101 subjects taken from PPMI dataset | Multimodel neuroimaging features composed of MRI and DTI with clinical evaluation | SVM, Random Forests, K-nearest Neighbors, Artificial Neural Network and Logistic Regression with ten-fold CV method | 96.88% |
Dotinga et al. (2021) [23] | Distinguish PD patients from non-PD subjects | 210 subjects | SBR values computed from I-123 FP-CIT SPECT, age and gender | SVM with ten-fold CV method | 95% |
Lavanya Madhuri Bollipo et al. (2021) [25] | Classify early PD patients and HC subjects | 600 subjects obtained from PPMI dataset | Clinical scores, SBRs values and demographic information | Incremental SVM with LOO-CV method |
98.3% |
Lavanya Madhuri Bollipo et al. (2021) [26] | Distinguish early PD patients from HC subjects | 634 subjects taken from PPMI dataset | Motor, cognitive symptom scores and SBR values computed from DaTSCAN | SVR | 96.73% |
Diego Castillo-Barnes et al. (2021) [27] | Distinguish PD patients from HC subjects | 386 samples selected from PPMI database | Morphological features computed from 123I-FP-CIT SPECT | SVM, Naive Bayesian and MLP with ten-fold CV method | 97.04% |