دورية أكاديمية

Vitamin B12 supplementation improves rates of sustained viral response in patients chronically infected with hepatitis C virus.

التفاصيل البيبلوغرافية
العنوان: Vitamin B12 supplementation improves rates of sustained viral response in patients chronically infected with hepatitis C virus.
المؤلفون: Rocco, Alba, Compare, Debora, Coccoli, Pietro, Esposito, Ciro, Spirito, Antimo Di, Barbato, Antonio, Strazzullo, Pasquale, Nardone, Gerardo
المصدر: Gut; May2013, Vol. 62 Issue 5, p766-773, 8p, 1 Diagram, 6 Charts, 2 Graphs
مصطلحات موضوعية: VITAMIN B12 metabolism, HEPATITIS C virus, HEALTH risk assessment, ANTIVIRAL agents, GENETIC polymorphisms, INTERLEUKINS, PATIENTS
مستخلص: 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 naïve to antiviral therapy. Methods Ninety-four patients with chronic HCV hepatitis were randomly assigned to receive pegylated interferon a plus ribavirin (standard-of-care; SOC) or SOC plus vitamin B12 (SOC+B12). Viral responsednamely, 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-oftreatment 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 naïve to antiviral therapy. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:00175749
DOI:10.1136/gutjnl-2012-302344