Liver disease in adult transfusion-dependent beta-thalassaemic patients: investigating the role of iron overload and chronic HCV infection

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3161122 12 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Liver disease in adult transfusion-dependent beta-thalassaemic patients:
investigating the role of iron overload and chronic HCV infection
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
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.
Έτος δημοσίευσης:
2013
Συγγραφείς:
Kountouras, Dimitrios
Tsagarakis, Nikolaos J.
Fatourou,
Evangelia
Dalagiorgos, Efthimios
Chrysanthos, Nikolaos and
Berdoussi, Helen
Vgontza, Niki
Karagiorga, Markissia and
Lagiandreou, Athanasios
Kaligeros, Konstantinos
Voskaridou, Ersi
and Roussou, Paraskevi
Diamanti-Kandarakis, Evanthia
Koskinas,
John
Περιοδικό:
Liver International
Εκδότης:
Wiley
Τόμος:
33
Αριθμός / τεύχος:
3
Σελίδες:
420-427
Λέξεις-κλειδιά:
HCV; iron; liver fibrosis; thalassaemia
Επίσημο URL (Εκδότης):
DOI:
10.1111/liv.12095
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.