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Sustained virologic response and other potential genotype-specific roles of statins among patients with hepatitis C-related chronic liver diseases

Authors :
Prashant Pandya
Fadi Rzouq
Olurinde Oni
Source :
Clinics and Research in Hepatology and Gastroenterology. 39:555-565
Publication Year :
2015
Publisher :
Elsevier BV, 2015.

Abstract

Summary Background While statins have shown antiviral effects in different studies, few data are available about their effect among different HCV genotypes. Aim To evaluate the effect of concomitant statin use on sustained virologic response (SVR) and other treatment outcomes among patients with HCV genotypes 1–3. Method Using US Department of Veterans Affairs database, multivariate (MV), propensity score matched (PSM) and repeated measures mixed model analyses were performed on patients who received combination therapy with Peg–IFN and Ribavirin for treatment of HCV genotypes 1–3 between October 2001–December 2011. Concomitant statin users were matched with non-users in each genotype and SVR rates were compared. Changes in serum ALT during treatment was assessed. Results Of 37,611 treated patients, 236 genotype 1 (GT1), 78 genotype 2 (GT2) and 23 genotype 3 (GT3) statin users and non-users were used for PSM. SVR among GT1 patients was 22.8% (overall), significantly higher among statin users (26.3% vs. 19.5% P P = 0.02 from MV). No significant impact of statin use was observed among GT2 (overall SVR – 55.8%, statin users vs. non-users – 53.9% vs. 57.7%, P = 0.32), and GT3 (overall SVR – 58.7%, statin users vs. non-users – 60.9% vs. 56.2%, P = 0.39) patients. Higher baseline LDL was positively associated with SVR while statin use reduced ALT during treatment in GT1 patients. Conclusion In view of additional benefits of statins, and the prohibitive cost of newer HCV therapies, statins could be a potential assist for hard-to-treat GT1 patients especially in resource-poor settings.

Details

ISSN :
22107401
Volume :
39
Database :
OpenAIRE
Journal :
Clinics and Research in Hepatology and Gastroenterology
Accession number :
edsair.doi.dedup.....453182ef17b133152dad5bc0802d50e5
Full Text :
https://doi.org/10.1016/j.clinre.2015.02.005