@article{3161122, title = "Liver disease in adult transfusion-dependent beta-thalassaemic patients: investigating the role of iron overload and chronic HCV infection", author = "Kountouras, Dimitrios and Tsagarakis, Nikolaos J. and Fatourou, and Evangelia and Dalagiorgos, Efthimios and Chrysanthos, Nikolaos and and Berdoussi, Helen and Vgontza, Niki and Karagiorga, Markissia and and Lagiandreou, Athanasios and Kaligeros, Konstantinos and Voskaridou, Ersi and and Roussou, Paraskevi and Diamanti-Kandarakis, Evanthia and Koskinas, and John", journal = "Liver International", year = "2013", volume = "33", number = "3", pages = "420-427", publisher = "Wiley", issn = "1478-3223, 1478-3231", doi = "10.1111/liv.12095", keywords = "HCV; iron; liver fibrosis; thalassaemia", abstract = "Background Iron overload and hepatitis-C virus (HCV) infection, have been implicated in the evolution of liver disease, in patients with transfusion-dependent beta-thalassaemia major (BTM). However, the impact of these factors in late stages of liver disease in adults with BTM, has not been extensively studied. Aims To investigate serum indices of iron overload, HCV infection and liver disease, in a cohort of 211 adult Greek patients with BTM, in relation with the findings from liver biopsies. Methods In this cross-sectional study, 211 patients with BTM were enrolled and studied, in relation with HCV infection, ferritin, transaminases, chelation treatment and antiviral treatment. Based on 109 patients biopsied, we correlated liver fibrosis, haemosiderosis and inflammation, with serum indices and HCV status Results Among all patients, 74.4% were anti-HCV positive (HCV+). Ferritin was positively correlated with transaminases and negatively correlated with age, while it was not significantly different among HCV+ and HCV patients. Among the HCV+ patients, 55.4% reported antiviral treatment, while genotype 1 predominated. In a subfraction of 109 patients, in which liver biopsy was performed, 89% were HCV+ and 11% HCV. Fibrosis was significantly correlated with age (P=0.046), AST (P=0.004), ALT (P=0.044) and inflammation (P<0.001). Advanced fibrosis was present with even minimal haemosiderosis, independently of ferritin values or HCV history. Conclusions These data suggest that in the late stages of liver disease in BTM patients, iron overload may be the critical determinant, since fibrosis is related to the minimal haemosiderosis, independently of HCV history." }