Title of article :
Evaluating Protective Effects of Silymarin on Liver and Cardiac Side Effects of Chemotherapy Drugs in Childhood Acute Lymphoblastic Leukemia
Author/Authors :
Ghaderian, Mehdi Isfahan University of Medical Sciences, Isfahan , Reisi, Nahid Isfahan University of Medical Sciences, Isfahan , Moafi, Alireza Isfahan University of Medical Sciences, Isfahan , Farasat, Safora Isfahan University of Medical Sciences, Isfahan
Abstract :
Background: The protective effects of silymarin on liver and heart have been investigated and identified by
many researchers. This study evaluates the protective effects of this substance on hepatotoxicity and
cardiotoxcity of chemotherapy drugs in leukemic children.
Materials and Methods: In this study, 71 children, aging 2-14 years old, going through the maintenance phase
of acute lymphoblastic leukemia (ALL) treatment at Children's Cancer Center of Isfahan University of Medical
Sciences (Iran) in 2015 were studied. Two patients died and the remaining patients were divided into
intervention and control groups. Intervention group received Mercaptopurin and Methotrexate plus Silymarin
140mg/day and control group were taking only Mercaptopurin and Methotrexate. Liver enzymes, Coagulation
tests, Creatine kinase- Muscle and Brain (CK-MB), Ejection fraction and Systolic function (SF) were measured
at the first, and 3 and 6 months’ intervals from the commencement of study. The Data was analyzed by using
SPSS and P ≤ 0.05 was considered as statistically significant. Associations between variables were analyzed
using independent t-test, chi square, and repeated measures ANOVA test.
Results: Mean levels of Alanine aminotransferase in both groups increased significantly at 6 months interval
(P=0.01, 0.01, for control and intervention groups respectively). Although increment was more among controls,
there were no significant differences between the two groups (P= 0.85). Furthermore, Aspartate
aminotransferase and Alkaline phosphatase increased in both groups and the increment was significant in the
controls (P=0.001, 0.05, for control and intervention groups respectively). Coagulation tests prolonged in the
first 3 months in both groups and the prolongation was more in control group. Changes in CK-MB were not
significant in intervention and controls (P=0.07, 0.10, respectively) but ejection fraction and SF decreased in
both groups, especially among controls.
Conclusion: It seems that Silymarin can be useful in prevention of hepatotoxicity and cardiotoxcity of
chemotherapy drugs for ALL children.
Keywords :
Acute lymphoblastic leukemia , Cardiotoxity , Hepatotoxicity , Silymarin
Journal title :
Astroparticle Physics