Prospective Study
Copyright ©The Author(s) 2018.
World J Gastroenterol. Mar 21, 2018; 24(11): 1269-1277
Published online Mar 21, 2018. doi: 10.3748/wjg.v24.i11.1269
Table 1 Demographic and clinical characteristics of the chronic hepatitis C patients prior to direct-acting antivirals treatment and after achieving sustained virological response 12 n (%)
Prior to DAA treatment (baseline)Post-SVR 12P1 value
Demographics
Male49 (48)49 (48)NS
Age (yr, mean ± SD)60.3 ± 10.760.3 ± 10.7NS
White37 (37)37 (37)NS
Hispanic26 (26)26 (26)NS
African American13 (13)13 (13)NS
Asian7 (7)7 (7)NS
Other2 (2)2 (2)NS
Declined16 (15)16 (15)NS
Clinical
Hypertension45 (43)45 (43)NS
Type 2 diabetes13 (12.3)13 (12.3)NS
Dyslipidemia8 (7.5)8 (7.5)NS
Anthropometric (mean ± SD)
Body mass index (kg/m2)27.6 ± 6.927.5 ± 6.9NS
Weight (Lbs.)174.9 ± 46.9172.7 ± 44.5NS
Laboratory panel (mean ± SD)
HCV vial load log10 IU/mL6.2 ± 0.90.0 ± 0.0< 0.0001
HCV genotype
Genotype 186 (85)
Genotype 215 (14)
Genotype 41 (1)
AST (U/L)51.8 ± 41.121.5 ± 8.0< 0.0001
ALT (U/L)63.1 ± 62.617.8 ± 12.3< 0.0001
Alkaline phosphatase (U/L)77.5 ± 34.071.0 ± 24.30.004
Albumin (g/dL)4.3 ± 0.44.4 ± 0.4NS
Bilirubin, total (mg/dL)0.6 ± 0.20.6 ± 0.3NS
Fasting glucose (mg/dL)99.1 ± 30.1102.1 ± 23.5NS
FibroScan (mean ± SD)
Fibrosis Score (kPa)7.4 ± 1.96.1 ± 3.60.013
IQR (%)12.6 ± 4.912.3 ± 5.5NS
Table 2 Characteristics of chronic hepatitis C patients after achieving sustained virological response 12 comparing those with and without steatosis n (%)
Patients without steatosis(CAP < 248 dB/m) (n = 53)Patients with steatosis(CAP ≥ 248 dB/m) (n = 48)P1 value
Demographics
Male25 (47)27 (56)NS
Age (yr, mean ± SD)59.4 ± 11.660.9 ± 9.4NS
White18 (34)18 (38)NS
Hispanic14 (26)12 (25)NS
Clinical
Hypertension25 (47.2)20 (41.7)NS
Dyslipidemia3 (5.7)5 (10.4)0.048
Type 2 diabetes4 (7.5)9 (18.7)0.04
Anthropometric (mean ± SD)
Body mass index (kg/m2)26.1 ± 6.928.9 ± 6.60.049
Weight (Lbs.)161.0 ± 33.4172.7 ± 44.50.005
Hepatology and viral hepatitis panel (mean ± SD)
AST (U/L)20.2 ± 5.422.9 ± 9.8NS
ALT (U/L)15.3 ± 5.520.4 ± 16.50.048
Alkaline phosphatase (U/L)70.7 ± 28.271.3 ± 19.4NS
Albumin (g/dL)4.3 ± 0.24.5 ± 0.6NS
Bilirubin, total (mg/dL)0.6 ± 0.30.6 ± 0.2NS
Other laboratory studies (mean ± SD)
Total cholesterol (mg/dL)184.8 ± 35.1179 ± 37.2NS
HDL cholesterol (mg/dL)57.6 ± 18.650.8 ± 17.0NS
LDL cholesterol (mg/dL)102.6 ± 33.2100.7 ± 31.5NS
Triglycerides (mg/dL)109.7 ± 63.9138.9 ± 77.90.05
HbA1c (%)5.7 ± 0.66.0 ± 0.9NS
Fasting serum glucose (mg/dL)96.5 ± 11.1107.8 ± 30.50.023
FibroScan (mean ±SD)
Fibrosis Score (kPa)5.3 ± 1.67.0 ± 4.80.0013
CAP (dB/m)212.4 ± 29.0296.3 ± 37.4< 0.0001
% of patient with fibrosis score of (≥ 7 kPa)0%6.25%0.066
Table 3 Comparison of pre-treatment vs post-sustained virological response characteristics in patients with and without post-sustained virological response steatosis
Patients without steatosis n = 53
Patients with steatosis n = 48
PretreatmentPost SVRP valuePretreatmentPost SVRP value
Body mass index (kg/m2)25.5 ± 4.026.1 ± 6.9NS30.0 ± 8.529.0 ± 6.6NS
Weight (Lbs.)161.9 ± 32.6161.0 ± 33.4NS187.3 ± 55.8186.1 ± 51.3NS
Laboratory panel (mean ± SD)
HCV vial load log10 IU/mL6.1 ± 1.00.0 ± 0.0< 0.00016.3 ± 0.80.0 ± 0.0< 0.0001
AST (U/L)43.3 ± 35.620.2 ± 5.4< 0.000161.3 ± 44.722.9 ± 9.8< 0.0001
ALT (U/L)55.6 ± 60.915.3 ± 5.5< 0.000168.78 ± 52.820.4 ± 16.5< 0.0001
Alkaline phosphatase (U/L)78.5 ± 43.170.8 ± 28.80.0175.5 ± 21.871.3 ± 19.40.04
Albumin (g/dL)4.2 ± 0.54.4 ± 0.30.0064.3 ± 0.24.5 ± 0.60.006
Bilirubin total (mg/dL)0.6 ± 0.20.6 ± 0.3NS0.6 ± 0.30.6 ± 0.2NS
Fasting glucose (mg/dL)95.6 ± 31.996.6 ± 11.1NS103.0 ± 27.5107.8 ± 30.5NS
FibroScan (mean ± SD)
Fibrosis score (kPa)7.1 ± 2.15.3 ± 1.5< 0.00017.7 ± 1.77.0 ± 4.80.0037