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A randomized double‐blind, placebo‐controlled study of therapeutic effects of silymarin in β‐thalassemia major patients receiving desferrioxamine
Author(s) -
Moayedi Behjat,
Gharagozloo Marjan,
Esmaeil Nafiseh,
Maracy Mohammad R.,
Hoorfar Hamid,
Jalaeikar Mohsen
Publication year - 2013
Publication title -
european journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0902-4441
DOI - 10.1111/ejh.12061
Subject(s) - medicine , placebo , soluble transferrin receptor , gastroenterology , chelation therapy , hepcidin , thalassemia , anemia , ferritin , serum iron , transferrin , pharmacology , liver function , iron deficiency , pathology , iron status , alternative medicine
Objective Thalassemia is one of the most common genetic disorders worldwide. Chronic blood transfusions treat the underlying anemia but may lead to iron toxicity. Effective iron chelation remains one of the main targets of clinical management of thalassemia major. In this study, iron‐chelating activity of silymarin, a flavonolignan isolated from silybum marianum, was examined in β‐thalassemia major. Methods Patients were treated with the combination of desferrioxamine and silymarin ( L egalon ® ; n = 49) or desferrioxamine plus placebo ( n = 48) for 9 months. The serum levels of ferritin, iron, total iron‐binding capacity ( TIBC ), soluble transferrin receptor, and hepcidin were determined at the baseline and after 9‐month therapy. Liver function test was performed before and after treatment in both groups. Results Serum ferritin levels decreased significantly from the beginning to the end of silymarin treatment (3028.8 ± 2002.6 vs. 1972.2 ± 1250.6 ng/mL); however, no significant change in serum ferritin was observed in the patients receiving placebo (2249.0 ± 1304.2 vs. 2015.6 ± 1146.8). Moreover, serum iron and TIBC levels were significantly reduced in silymarin group compared with placebo. Patients on silymarin therapy also exhibited a significant decrease in serum levels of hepcidin and soluble transferrin receptor after 9‐month treatment period. A significant improvement in liver function test was observed in silymarin group in comparison with placebo. Conclusion This study shows that silymarin is effective at reducing iron overload in patients when used in conjunction with desferrioxamine. Therapeutic effects of silymarin on a background of desferrioxamine suggest the potential effectiveness of silymarin alone in reducing body iron burden.