Vitamin B12 supplementation improves rates of sustained viral response in patients chronically infected with hepatitis C virus.
Rocco, Alba 1; Compare, Debora 1; Coccoli, Pietro 1; Esposito, Ciro 2; Di Spirito, Antimo 2; Barbato, Antonio 3; Strazzullo, Pasquale 3; Nardone, Gerardo 1
[Article]
Gut.
62(5):766-773, May 2013.
(Format: HTML, PDF)
Background: In vitro, vitamin B12 acts as a natural inhibitor of hepatitis C virus (HCV) replication.
Objective: To assess the effect of vitamin B12 on virological response in patients with chronic HCV hepatitis naive to antiviral therapy.
Methods: Ninety-four patients with chronic HCV hepatitis were randomly assigned to receive pegylated interferon [alpha] plus ribavirin (standard-of-care; SOC) or SOC plus vitamin B12 (SOC B12). Viral response-namely, undetectable serum HCV-RNA, was evaluated 4 weeks after starting treatment (rapid viral response), 12 weeks after starting treatment (complete early viral response) and 24 or 48 weeks after starting treatment (end-of-treatment viral response) and 24 weeks after completing treatment (sustained viral response (SVR)). Genotyping for the interleukin (IL)-28B polymorphism was performed a posteriori in a subset (42/64) of HCV genotype 1 carriers.
Results: Overall, rapid viral response did not differ between the two groups, whereas the rates of complete early viral response (p=0.03), end-of-treatment viral response (p=0.03) and SVR (p=0.001) were significantly higher in SOC B12 patients than in SOC patients. In SOC B12 patients, the SVR rate was also significantly higher in carriers of a difficult-to-treat genotype (p=0.002) and in patients with a high baseline viral load (p=0.002). Distribution of genotype IL-28B did not differ between the two groups. At multivariate analysis, only easy-to-treat HCV genotypes (OR=9.00; 95% CI 2.5 to 37.5; p=0.001) and vitamin B12 supplementation (OR=6.9; 95% CI 2.0 to 23.6; p=0.002) were independently associated with SVR.
Conclusion: Vitamin B12 supplementation significantly improves SVR rates in HCV-infected patients naive to antiviral therapy.
(C) 2013 BMJ Publishing Group Ltd and the British Society of Gastroenterology