Interferon-Based Hepatitis C Antiviral Treatment Outcomes May Be Predicted by Alanine Aminotransferase Levels
Author(s) -
Erin Kelly,
Sarah Blach,
Homie Razavi,
Curtis Cooper
Publication year - 2015
Publication title -
canadian journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.921
H-Index - 65
eISSN - 2291-2797
pISSN - 2291-2789
DOI - 10.1155/2015/897035
Subject(s) - medicine , alanine aminotransferase , alanine transaminase , interferon , virology , hepatitis c , immunology , antiviral treatment , alanine , chronic hepatitis , virus , biochemistry , chemistry , amino acid
To the Editor: On-therapy decline or normalization of liver enzyme levels is often observed following initiation of interferon-based hepatitis C virus (HCV) antiviral treatment and may reflect response to therapy and decreasing HCV RNA levels (1,2). On-treatment alanine aminotransferase (ALT) level elevation may be associated with persistent viremia (3-5). The value of enzymatic response in predicting sustained virological response (SVR) and relapse is unclear. We evaluated the role of baseline and week 4 ALT and aspartate aminotransferase (AST) levels in predicting HCV response to interferon-based antiviral therapy. A retrospective database analysis of 434 adults with HCV initiating therapy at The Ottawa Hospital Viral Hepatitis Clinic (Ottawa, Ontario) between January 1, 2000 and December 31, 2009 was conducted (Research Ethics Board number 2004-196). Patients were predominately Caucasian (81%) and male (72%), with a mean (± SD) age of 44.3± 9.1 years. HCV risk factors included intravenous drug use history (56%) and contaminated blood product exposure (26%). Nine percent were HIV coinfected. The population was predominantly infected with HCV genotype 1 (56.1%), genotype 3 (22.4%) and genotype 2 (15.8%). Advanced fibrosis (F3 to F4) was identified in 35% of patients. Thirty-nine percent had normal ALT (<63 U/L) and 26% had normal AST (<37 U/L) levels at baseline. At week 4, 83% of patients had normal ALT levels and 57% had normal AST levels. Fifty-two patients (62%) achieved rapid virological response, 182 (88%) early virological response and 154 (68%) SVR. Twenty-four (11%) patients relapsed post-treatment. Baseline ALT and AST levels were higher in patients not achieving SVR. According to multivariate analysis, baseline AST (OR 0.99 [95% CI 0.98 to 0.99]) was a predictor of SVR. A ROC curve of this model generated an area under the curve (AUC) of 0.739. In a model including week 4 variables, baseline ALT and normal ALT levels at week 4 predicted SVR. The ROC AUC for this model was 0.627. Among the subset of patients with elevated ALT levels at baseline, genotype (2/3), low baseline viral load (<800,000 U/L) and baseline platelet levels were associated with SVR. The ROC AUC for this model was 0.531. In a model considering week 4 variables, normalized ALT levels at week 4 resulted in an AUC of 0.734 (OR 17.04 [95% CI 6.17 to 47.09]). In an evaluation of the entire population, ALT levels at week 4 (above/below normal) yielded a 77% positive predictive value and a 77% negative predictive value for SVR (Figure 1). This suggests
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