Table 1.
Parameters |
Healthy control |
Naïve |
SOF + SIM |
SOF + DAC |
SOF + DAC + RBV |
Relapsed |
(n = 20) | (n = 30) | (n = 30) | (n = 20) | (n = 20) | (n = 30) | |
Age (yr) | 40.2 ± 5 | 44.3 ± 6.9 | 42.2 ± 6.7 | 42.8 ± 7.2 | 39.7 ± 5.1 | 44.1 ± 6.5 |
Gender (M/F) | 16/4 | 26/4 | 27/3 | 19/1 | 19/1 | 25/5 |
ALT (IU/L) | 9.2 ± 6.2 | 37.2 ± 25b | 18.7 ± 8.2ad | 17.6 ± 5.6ad | 26.7 ± 2.4adeg | 23.7 ± 6.9d |
AST (IU/L) | 10.3 ± 4.2 | 34.4 ± 16.4b | 27.4 ± 13.7bc | 26.9 ± 6.9bc | 32.7 ± 5.2b | 23.3 ± 6.3d |
Albumin (g/dL) | 3.8 ± 0.27 | 2.7 ± 0.43b | 3.2 ± 0.5bd | 3.9 ± 0.3dh | 4 ± 0.4adh | 3 ± 0.4d |
ALP (IU/L) | 53.7 ± 6.8 | 130.6 ± 21b | 86.1 ± 16bd | 78.4 ± 16bd | 81.2 ± 12.4bd | 99.4 ± 11.2bf |
Bilirubin (mg/dL) | 0.9 ± 0.1 | 1.1 ± 0.4a | 1.2 ± 0.5b | 1.1 ± 0.4 | 0.9 ± 0.3ce | 1.2 ± 0.4 |
INR | 1.06 ± 0.07 | 1.4 ± 0.25b | 1.5 ± 0.25b | 1.3 ± 0.19b | 1.2 ± 0.22adfh | 1.4 ± 0.27 |
AFP (ng/mL) | 7.6 ± 1.3 | 15 ± 8.6b | 7.3 ± 0.8d | 7 ± 1d | 6.9 ± 1d | 32 ± 9.6bf |
PT | 11.7 ± 0.5 | 14.8 ± 2b | 13.7 ± 1.4bd | 13.1 ± 1.2bd | 12.6 ± 1.5de | 14.1 ± 1.1 |
Viral load (log copies/mL) | 0 | 6.47 ± 0.7c | 0d | 0d | 0d | 6.38 ± 0.39f |
P < 0.05,
P < 0.01, vs control group;
P < 0.05,
P < 0.01, vs naïve group;
P < 0.05,
P < 0.01, vs SOF + SIM group;
P < 0.05,
P < 0.01, vs SOF + DAC group. The data are expressed as the mean ± SD. The data were analysed by one-way ANOVA followed by Tukey HSD multiple comparison test. Naïve: Hepatitis C virus naïve patients without any treatment; SOF + SIM: Hepatitis C virus-infected patients treated with sovaldi and simeprevir; SOF + DAC: Hepatitis C virus-infected patients treated with combined therapy sovaldi and daclatasvir; SOF + DAC + RBV: Hepatitis C virus-infected patients treated with triplet therapy sovaldi, daclatasvir and ribavirin; Relapsed: Relapsed HCV patients from SOF + SIM treatment; ALT: Alanine aminotransferases; AST: Aspartate aminotransferases; ALP: Alkaline phosphatase; INR: International normalized ratio AFP: Alfa fetoprotein; PT: Prothrombin time.