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. 2019 Sep 5;5(3):215–223. doi: 10.5114/ceh.2019.87634

Table 1.

Clinical and laboratory characteristics of the study group (N = 209)

Number of concomitant medications
0 n = 69 1-5 n = 107 ≥ 5 n = 33
Age, years (±SD) 48.7 (13.1) 53.2 (12.0) 58.0 (8.7)
Gender
 Male, n (%) 33 (47.8) 39 (36.4) 21 (63.4)
 BMI, kg/m2 (±SD) 25.2 (3.9) 26.9 (3.9) 27.1 (3.7)
Treatment history, n (%)
 Naïve 18 (26.1) 23 (21.5) 3 (9.1)
 Partial responder 8 (11.6) 8 (7.5) 1 (3.0)
 Relapser 11 (15.9) 20 (18.7) 6 (18.2)
 Null-responder 26 (37.7) 41 (38.1) 17 (51.5)
 Discontinued 3 (4.3) 8 (7.5) 1 (3.0)
 Unknown 3 (4.3) 7 (6.5) 5 (15.2)
Fibrosis stage, n (%)
 F0 2 (2.9) 0 (0.0) 2 (6.1)
 F1 8 (11.6) 8 (7.5) 5 (15.2)
 F2 11 (15.9) 10 (9.3) 8 (24.2)
 F3 8 (11.6) 20 (18.7) 4 (12.1)
 F4 40 (58.0) 67 (62.6) 12 (36.4)
HCV genotype, n (%)
 1a 9 (13.0) 3 (2.8) 1 (3.0)
 1b 52 (75.4) 92 (86.0) 32 (97.0)
 1 (subgenotyping not available) 3 (4.3) 4 (3.7) 0 (0.0)
 4 4 (5.8) 5 (4.7) 0 (0.0)
HCV RNA level, × 106 IU/ml (SD) 1.3 (2.0) 1.3 (1.8) 2.2 (2.7)
Bilirubin, mg/dl (SD) 2.6 (12.1) 4.0 (16.57) 1.2 (0.84)
ALT, IU/ml (SD) 106.5 (91.3) 105.6 (75.8) 79.6 (44.9)
INR (SD) 1.1 (0.2) 1.1 (0.2) 1.1 (0.2)
Hemoglobin, g/dl (SD) 14.5 (1.6) 14.7 (1.5) 13.7 (1.8)
PLT, × 103 cells/μl (SD) 154.8 (83.3) 123.4 (62.2) 148.8 (72.0)
Albumin, g/dl (SD) 5.5 (11.9) 4.9 (9.5) 4.0 (0.7)
Alpha fetoprotein, μg/l (SD) 14.5 (26.7) 15.8 (28.3) 39.9 (119.8)
Creatinine, mg/dl (SD) 0.8 (0.2) 0.8 (0.2) 1.0 (0.4)
Child-Pugh score, points (SD) 5.2 (0.6) 5.4 (0.8) 5.6 (1.1)
MELD score, points (SD) 8.0 (2.6) 8.3 (2.7) 8.7 (3.2)

ALT – alanine transaminase, BMI – body mass index, HCV RNA – HCV ribonucleic acid, INR – international normalized ratio, MELD – Model for End-Stage Liver Disease, PLT – platelet count, SD – standard deviation