Cargando…

Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia

BACKGROUND: ALL is the most common childhood malignancy. The children with ALL are treated with methotrexate (MTX) based chemotherapy protocols. MTX causes unpredictable serious hepatic and renal side effects. Silymarin has antioxidant and anti-inflammatory activities and stimulates tissue regenerat...

Descripción completa

Detalles Bibliográficos
Autores principales: Hagag, Adel A., Elgamsy, Mohamed A., El-Asy, Hassan M., Mabrouk, Maaly M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Università Cattolica del Sacro Cuore 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016017/
https://www.ncbi.nlm.nih.gov/pubmed/27648206
http://dx.doi.org/10.4084/MJHID.2016.043
_version_ 1782452530639273984
author Hagag, Adel A.
Elgamsy, Mohamed A.
El-Asy, Hassan M.
Mabrouk, Maaly M.
author_facet Hagag, Adel A.
Elgamsy, Mohamed A.
El-Asy, Hassan M.
Mabrouk, Maaly M.
author_sort Hagag, Adel A.
collection PubMed
description BACKGROUND: ALL is the most common childhood malignancy. The children with ALL are treated with methotrexate (MTX) based chemotherapy protocols. MTX causes unpredictable serious hepatic and renal side effects. Silymarin has antioxidant and anti-inflammatory activities and stimulates tissue regeneration. This study aims to evaluate the protective effects of Silymarin on MTX-based chemotherapy-induced Hepatic and renal toxicity in children with ALL. PATIENTS AND METHODS: 80 children with newly diagnosed ALL were enrolled in the study. They were randomly divided into two groups. Group I included 40 children with ages ranging from 4–13 years and the mean age of 6.85± 2.89 years, who received Silymarin 420 mg/day in 3 divided doses for one week after each MTX dose. Group II included 40 children, with ages ranging from 4–12 years and the mean age of 7.30±2.6 years, who received placebo for one week after MTX therapy. For all patients liver functions including serum bilirubin, total proteins, albumin, globulin and albumin-globulin ratio, alkaline phosphatase, ALT and AST, prothrombin time and activity and renal functions including blood urea and serum creatinine, serum cystatin C and urinary N-acetyl-beta-D-glucosaminidase were done to assess hepatic and renal toxicity before and after chemotherapy. RESULTS: There were no significant differences between group I and II as regard liver and renal functions before chemotherapy. After chemotherapy, there were significantly higher values of ALT and AST and alkaline phosphatase, and significantly lower Prothrombin activity in group II compared with group I. No significant differences between group I and II were found in total bilirubin, serum protein, and albumin levels. There was significantly lower blood urea, serum creatinine, and cystatin C and urinary N-acetyl-beta-D-glucosaminidase in group I compared with group II. CONCLUSION: Silymarin improved some hepatic and renal functions in children with ALL who received MTX-based chemotherapy protocols. Recommendations: Extensive multicenter studies could be recommended to prove the hepatic and renal protective effects of Silymarin in patients with ALL who received MTX-based chemotherapy protocols.
format Online
Article
Text
id pubmed-5016017
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Università Cattolica del Sacro Cuore
record_format MEDLINE/PubMed
spelling pubmed-50160172016-09-19 Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia Hagag, Adel A. Elgamsy, Mohamed A. El-Asy, Hassan M. Mabrouk, Maaly M. Mediterr J Hematol Infect Dis Original Article BACKGROUND: ALL is the most common childhood malignancy. The children with ALL are treated with methotrexate (MTX) based chemotherapy protocols. MTX causes unpredictable serious hepatic and renal side effects. Silymarin has antioxidant and anti-inflammatory activities and stimulates tissue regeneration. This study aims to evaluate the protective effects of Silymarin on MTX-based chemotherapy-induced Hepatic and renal toxicity in children with ALL. PATIENTS AND METHODS: 80 children with newly diagnosed ALL were enrolled in the study. They were randomly divided into two groups. Group I included 40 children with ages ranging from 4–13 years and the mean age of 6.85± 2.89 years, who received Silymarin 420 mg/day in 3 divided doses for one week after each MTX dose. Group II included 40 children, with ages ranging from 4–12 years and the mean age of 7.30±2.6 years, who received placebo for one week after MTX therapy. For all patients liver functions including serum bilirubin, total proteins, albumin, globulin and albumin-globulin ratio, alkaline phosphatase, ALT and AST, prothrombin time and activity and renal functions including blood urea and serum creatinine, serum cystatin C and urinary N-acetyl-beta-D-glucosaminidase were done to assess hepatic and renal toxicity before and after chemotherapy. RESULTS: There were no significant differences between group I and II as regard liver and renal functions before chemotherapy. After chemotherapy, there were significantly higher values of ALT and AST and alkaline phosphatase, and significantly lower Prothrombin activity in group II compared with group I. No significant differences between group I and II were found in total bilirubin, serum protein, and albumin levels. There was significantly lower blood urea, serum creatinine, and cystatin C and urinary N-acetyl-beta-D-glucosaminidase in group I compared with group II. CONCLUSION: Silymarin improved some hepatic and renal functions in children with ALL who received MTX-based chemotherapy protocols. Recommendations: Extensive multicenter studies could be recommended to prove the hepatic and renal protective effects of Silymarin in patients with ALL who received MTX-based chemotherapy protocols. Università Cattolica del Sacro Cuore 2016-09-01 /pmc/articles/PMC5016017/ /pubmed/27648206 http://dx.doi.org/10.4084/MJHID.2016.043 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hagag, Adel A.
Elgamsy, Mohamed A.
El-Asy, Hassan M.
Mabrouk, Maaly M.
Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia
title Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia
title_full Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia
title_fullStr Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia
title_full_unstemmed Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia
title_short Protective Role of Silymarin on Hepatic and Renal Toxicity Induced by MTX Based Chemotherapy in Children with Acute Lymphoblastic Leukemia
title_sort protective role of silymarin on hepatic and renal toxicity induced by mtx based chemotherapy in children with acute lymphoblastic leukemia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016017/
https://www.ncbi.nlm.nih.gov/pubmed/27648206
http://dx.doi.org/10.4084/MJHID.2016.043
work_keys_str_mv AT hagagadela protectiveroleofsilymarinonhepaticandrenaltoxicityinducedbymtxbasedchemotherapyinchildrenwithacutelymphoblasticleukemia
AT elgamsymohameda protectiveroleofsilymarinonhepaticandrenaltoxicityinducedbymtxbasedchemotherapyinchildrenwithacutelymphoblasticleukemia
AT elasyhassanm protectiveroleofsilymarinonhepaticandrenaltoxicityinducedbymtxbasedchemotherapyinchildrenwithacutelymphoblasticleukemia
AT mabroukmaalym protectiveroleofsilymarinonhepaticandrenaltoxicityinducedbymtxbasedchemotherapyinchildrenwithacutelymphoblasticleukemia