Clinical Practice Study
Copyright ©The Author(s) 2018.
World J Hepatol. Jan 27, 2018; 10(1): 105-115
Published online Jan 27, 2018. doi: 10.4254/wjh.v10.i1.105
Math 1
Math 1 Math(A1).
Figure 1
Figure 1 Partial least squares discriminant analysis metabonomic models to predict significant fibrosis (A, D, G) advanced fibrosis (B, E, H) and cirrhosis (C, F, I) in 69 chronic hepatitis C patients from Pernambuco/Brazil. Three-dimensional score plot (A, B, C). Classification of MM using different numbers of latent components, with accuracy = 1.0/ 1.0/ 0.84, R2 = 0.98/ 0.98/ 0.56 and Q2 = 0.91/ 0.93/ 0.27, using 5 latent components (D, E, F); permutation tests statistics for 1000 permutations with observed statistic at P < 0.001 (G, H, I). MM: Metabonomic models.
Figure 2
Figure 2 Comparison of performance of the linear discriminant analysis metabonomic models, aspartate aminotransferase to platelet ratio index and fibrosis index based on four factors, in 69 chronic hepatitis C patients from Pernambuco/Brazil. A and C: Performance of metabonomic models (MM) and APRI to predict SF and C; B: Performance of MM and FIB-4 to predict advanced fibrosis. APRI: Aspartate aminotransferase to platelet ratio index; FIB-4: Fibrosis index based on four factors.
Figure 3
Figure 3 Comparison of biopsy correctly avoided by metabonomic models, aspartate aminotransferase to platelet ratio index and fibrosis index based on four factors, in 69 chronic hepatitis C patients from Pernambuco/Brazil. APRI: Aspartate aminotransferase to platelet ratio index; FIB-4: Fibrosis index based on four factors.