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Leandro, G., Mangia, A., Hui, J., Fabris, P., Rubbia-Brandt, L., Colloredo, G., Adinolfi, L.E., et al. (2006) HCV Meta-Analysis (on) Individual Patients’ Data Study Group. Relationship between steatosis, inflammation, and fibrosis in chronic hepatitis C: A meta-analysis of individual patient data. Gastroenterology, 130, 1636-1642.
http://dx.doi.org/10.1053/j.gastro.2006.03.014

has been cited by the following article:

• TITLE: Polymorphisms in methylenetetrahydrofolate reductase gene: Their impact on liver steatosis and fibrosis of chronic hepatitis c patients

  AUTHORS: Engin Altintas, Zuhal Mert Altintas, Orhan Sezgin, Enver Ucbilek, Erdinc Nayir, Mehmet Emin Erdal, Ayse Polat, Gulhan Orekeci

  KEYWORDS: Fibrosis; Hepatitis C; Gene Polymorphism; Methylenetetrahydrofolate Reductase; Steatosis

  JOURNAL NAME: Open Journal of Gastroenterology, Vol.4 No.2, February 14, 2014

  ABSTRACT: Aim & Background: The mechanism of steatosis in Hepatitis C virus infection is multifactorial; therefore, it is complex and unclear. The aim of this study was to investigate the effects of methylentetrahydrofolate reductase (MTHFR) gene polymorphisms on the course of chronic hepatitis C virus infection and the development of steatosis due to hepatitis C virus. Methods: This study included 109 patients with chronic hepatitis C virus infection. Necroinflammatory activity, degrees of fibrosis and steatosis and MTHFR gene polymorphisms were investigated. Polymerase chain reaction-restriction fragment length polymorphism was used to determine MTHFR C677T and A1298C polymorphisms. Results: Fibrosis was correlated with age (r = 0.336, p = 0.002), platelet (r = ?0.448, p was a relation between MTHFR C677T and the degree of fibrosis but not A1298C (p = 0.014, p = 0.187 respectively). Conclusion: We found that MTHFR C677T polymorphism contributed to the development of fibrosis in patients with chronic hepatitis C virus infection.