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. 2019 Jun 14;49(10):1114–1120. doi: 10.1111/hepr.13362

Table 3.

Factors associated with non‐sustained virologic response in patients with hepatitis C virus (HCV) genotype 1 after completing antiviral therapy with elbasvir/grazoprevir

Factor Univariate analysis Multivariate analysis
Odds ratio (95% CI) P‐value Odds ratio (95% CI) P‐value
Age 1.069 (0.999–1.162) 0.0538
Sex, male 1.819 (0.511–7.222) 0.3547
History of IFN therapy, yes 6.619 (1.837–26.54) 0.0044 4.25 (0.308–104.5) 0.2706
History of DAA therapy, yes 162.0 (34.49–1199.2) <0.0001 5.293 (0.161–94.86) 0.3070
History of HCC, yes 3.895 (0.811–14.73) 0.0840
Cirrhosis, yes 0.384 (0.021–2.090) 0.3085
NS5A‐L31, mutant 0.000 (0.000–9.593) 0.4845
NS5A‐Y93, mutant 0.000 (0.000–0.000) 0.1041
NS5A‐L31/‐Y93 double mutation, yes 1278 (153.9–31 220) <0.0001 356.3 (23.91–16 940) <.0001
Platelet count 0.954 (0.848–1.048) 0.3689
AST 1.001 (0.978–1.011) 0.9226
ALT 1.001 (0.981–1.011) 0.8975
eGFR 1.013 (0.988–1.043) 0.3371
M2BPGi 0.983 (0.687–1.246) 0.9054
FIB‐4 index 1.047 (0.817–1.257) 0.6777
α‐Fetoprotein 1.001 (0.957–1.015) 0.9029
HCV‐RNA 1.691 (0.735–5.011) 0.2460

Mutation of L31 alone (double mutation with Y93 is excluded).

Mutation of Y93 alone (double mutation with L31 is excluded).

ALT, alanine aminotransferase; AST, aspartate aminotransferase; DAA, direct‐acting antiviral; eGFR, estimated glomerular filtration rate; FIB‐4, Fibrosis‐4; HCC, hepatocellular carcinoma; IFN, interferon; M2BPGi, Mac‐2 binding protein glycosylation isomer; NS5A, non‐structural protein 5A; —, not included