Table 1.
No.
|
Task
|
Algorithms
|
Sample size (type)
|
Evaluation index
|
Ref.
|
1 | Predicting incidence of hepatitis A | ANN; ARIMA | N/A (CDC data) | ANN: Correlation coefficient 0.71; ARIMA: Correlation coefficient 0.66 | [12] |
2 | Predicting incidence of hepatitis B | ARIMA; ElmanNN | 486983 cases (data from health commission) | ARIMA: RMSE 0.94, MAE 0.81; ElmanNN: RMSE 0.89, MAE 0.70 | [13] |
3 | Forecasting incidence of hepatitis B | Hybrid method (combing GM and BP-ANN) | 10486959 cases (data from health ministry) | R 0.9495, RMSE 4.863 × 103, MAE 3.9704 × 104 | [14] |
4 | Prediction of incidence of hepatitis E | ARIMA; SVM; LSTM | N/A (CDC data) | ARIMA: RMSE 0.022, MAE 0.018; SVM: RMSE 0.0204, MAE 0.0167; LSTM: RMSE 0.01, MAE 0.011 | [15] |
5 | Automated classification of the different stages of hepatitis B | ADHB-ML-MFIS expert system | 52 patients (serological data) | Overall accuracy: 0.922; No hepatitis accuracy: 1; Due to infection accuracy: 0.75; Acute HBV accuracy: 0.95; Chronic HBV accuracy: 0.91 | [16] |
6 | Analyzing HBV infection from normal blood samples | Polynomial function; RBF | 119 serum samples from HBV infected patients (Raman spectroscopy data) | Polynomial kernel (order-2): Quadratic programming/least squares: Accuracy 98%, precision 97%, sensitivity 100%, specificity 95%; RBF kernel (RBF sigma-2): Quadratic programming: accuracy 94%, precision 90%, sensitivity 100%, specificity 87%; RBF kernel (RBF sigma-2): Least squares: Accuracy 95%, precision 92%, sensitivity 100%, specificity 90% | [8] |
7 | Rapidly screening hepatitis B from non-hepatitis B | LSTM | 1134 blood samples (Raman spectroscopy data) | Accuracy 97.32%, sensitivity 97.87%, specificity 96.77%, precision 96.84% | [17] |
8 | Finding undiagnosed patients with hepatitis C infection | Logistic regression; Gradient boosting trees; Gradient boosting trees with temporal variables; Stacked ensemble; Random forest | 9721923 patients (data from the patient’s medical history) | The stacked ensemble had a specificity of 0.99 and precision of 0.97 at a recall level of 0.50 | [19] |
9 | Predicting hepatitis C virus progression among veterans | CS Cox modellongitudinal Cox model; CS boosting modelLongitudinal-boosting model | 72683 CHC individuals (VHA data) | CS Cox model: Concordance 0.746; Longitudinal Cox model: Concordance 0.764; CS boosting model: Concordance 0.758; Longitudinal-boosting model: Concordance 0.774 | [20] |
10 | Forecasting response to IFN plus RIB treatment in HCV patients | ANN | 300 patients (serological data) | The diagnostic accuracy rose from 52% (ANN 2) to 70% (ANN 6) | [21] |
ANN: Artificial neural network; ARIMA: Autoregressive integrated moving average; CDC: Centers for Disease Control; RMSE: Root-mean-square error; MAE: Mean absolute error; GM: Grey model, BP-ANN: Back propagation artificial neural networks; SVM: Supporter vector machine; LSTM: Long-short time memory neural network; ADHB-ML-MFIS: Automated diagnosis of hepatitis B using multilayer Mamdani fuzzy inference; HBV: Hepatitis B virus; RBF: Gaussian radial basic function; CHC: Chronic hepatitis C virus; VHA: National Veterans Health Administration; IFN: Interferon; RIB: Ribavirin, HCV: Hepatitis C virus.