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. 2017 Mar 4;4(1):e000115. doi: 10.1136/bmjgast-2016-000115

Table 1.

Baseline characteristics of patients according to the season of initiating hepatitis C virus treatment

Season A
n=421
Season B
n=509
p Value
Age (years) mean±SD 58.8±9.4 54.4±8.3 0.45
Age >50 years, n (%) 261 (62) 333 (65.4) 0.30
Gender (male), n (%) 277 (65.8) 344 (67.5) 0.57
Body mass index*
 ≤30 kg/m2 119 (78.8) 143 (79) 0.10
 >30 kg/m2 32 (21.2) 38 (21)
Diabetes mellitus, n (%) 65 (12.8) 65 (15.4) 0.25
HCV genotype
 1a, n (%) 89 (21.1) 118 (23.2) 0.68
 1b, n (%) 283 (67.2) 347 (68.2)
 Others, n (%) 49 (11.6) 44 (8.6)
Low viral load (<600 000 UI), n (%) 109 (26.2) 111 (21.9) 0.14
Basal viral load IU, mean±SD 2.459.627±4.553.883 3.383.240±5.406.573 0.006
Log RNA, mean±SD 6.06±0.60 6.18±0.65 0.007
Fibrosis†
 ≤F2, n (%) 67 (12) 66 (13) 0.22
 ≥F3–F4, n (%) 351 (84) 438 (87)
IL28B rs polymorphism CC, n (%)‡ 69 (49.3) 71 (50.7) 0.29
Previous treatment
 Naïve, n (%) 139 (33) 160 (31) 0.62
 Experienced, n (%) 282 (67) 349 (69)
 No response 45 (16) 70 (20.1)
 Early discontinuation 13 (4.6) 17 (4.9)
 Unknown response 47 (16.7) 83 (23.8)
 Relapse 122 (43.3) 120 (34.4)
 Partial response 50 (17.7) 48 (13.8)
 Breakthrough 5 (1.8) 11 (3.2)
AST, UI, mean±SD 78±51 82±54 0.32
ALT, UI, mean±SD 99±67 101±70 0.76
GGT, UI, mean±SD 109±96 101±88 0.19

*In 64% of the patients, body mass index was not calculated.

†In 8 (0.86%) patients, fibrosis degree was not available.

‡In 27% of the patients, ILB28 polymorphism was not available.

ALT, alanine aminotransferase; AST, aspartate aminotransferase; GGT, γ-glutamyltransferase; HCV, hepatitis C virus.