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Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients

OBJECTIVES: To check the amount of cellular damage caused by serial transfusions of blood in thalassemia patients. METHODS: A cross-sectional study was conducted in the University of Lahore, Lahore, Pakistan between August 2012 and December 2012. A total of 43 thalassemia patients underwent at least...

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Autores principales: Rasool, Mahmood, Malik, Arif, Jabbar, Uzma, Begum, Irshad, Qazi, Mahmood H., Asif, Muhammad, Naseer, Muhammad I., Ansari, Shakeel A., Jarullah, Jummanah, Haque, Absarul, Jamal, Mohammad S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Saudi Medical Journal 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303802/
https://www.ncbi.nlm.nih.gov/pubmed/27761563
http://dx.doi.org/10.15537/smj.2016.11.16242
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author Rasool, Mahmood
Malik, Arif
Jabbar, Uzma
Begum, Irshad
Qazi, Mahmood H.
Asif, Muhammad
Naseer, Muhammad I.
Ansari, Shakeel A.
Jarullah, Jummanah
Haque, Absarul
Jamal, Mohammad S.
author_facet Rasool, Mahmood
Malik, Arif
Jabbar, Uzma
Begum, Irshad
Qazi, Mahmood H.
Asif, Muhammad
Naseer, Muhammad I.
Ansari, Shakeel A.
Jarullah, Jummanah
Haque, Absarul
Jamal, Mohammad S.
author_sort Rasool, Mahmood
collection PubMed
description OBJECTIVES: To check the amount of cellular damage caused by serial transfusions of blood in thalassemia patients. METHODS: A cross-sectional study was conducted in the University of Lahore, Lahore, Pakistan between August 2012 and December 2012. A total of 43 thalassemia patients underwent at least 10 blood transfusions. Comprehensive biochemical analysis of blood was performed to record the levels of creatinine, urea, uric acid, albumin, liver function tests, malondialdehyde (MDA), and ferritin. RESULTS: Serum creatinine (0.732±0.23mg/dl) and uric acid (6.7±0.94mg/dl, p<0.05) were significantly higher in patient groups as compared with the control. Ferritin levels were significantly higher in patients as compared with the control (3103.9±1747.4, p<0.05). Hemoglobin levels were observed in controls 14±1.3g/dl and in patients 7.1±1.03g/dl. No clear relationship exists between age and hematological parameters of thalassemic patients. Serum ferritin level is positively related with serum alanine transaminase, aspartate aminotransferase, and alkaline phosphatase and MDA (p<0.05). CONCLUSION: Serum MDA and serum ferritin of patients (r=0.593, p<0.05) reflects that both are crucial parameters estimating the cellular damage in patients suffering from thalassemia.
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spelling pubmed-53038022017-02-16 Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients Rasool, Mahmood Malik, Arif Jabbar, Uzma Begum, Irshad Qazi, Mahmood H. Asif, Muhammad Naseer, Muhammad I. Ansari, Shakeel A. Jarullah, Jummanah Haque, Absarul Jamal, Mohammad S. Saudi Med J Original Article OBJECTIVES: To check the amount of cellular damage caused by serial transfusions of blood in thalassemia patients. METHODS: A cross-sectional study was conducted in the University of Lahore, Lahore, Pakistan between August 2012 and December 2012. A total of 43 thalassemia patients underwent at least 10 blood transfusions. Comprehensive biochemical analysis of blood was performed to record the levels of creatinine, urea, uric acid, albumin, liver function tests, malondialdehyde (MDA), and ferritin. RESULTS: Serum creatinine (0.732±0.23mg/dl) and uric acid (6.7±0.94mg/dl, p<0.05) were significantly higher in patient groups as compared with the control. Ferritin levels were significantly higher in patients as compared with the control (3103.9±1747.4, p<0.05). Hemoglobin levels were observed in controls 14±1.3g/dl and in patients 7.1±1.03g/dl. No clear relationship exists between age and hematological parameters of thalassemic patients. Serum ferritin level is positively related with serum alanine transaminase, aspartate aminotransferase, and alkaline phosphatase and MDA (p<0.05). CONCLUSION: Serum MDA and serum ferritin of patients (r=0.593, p<0.05) reflects that both are crucial parameters estimating the cellular damage in patients suffering from thalassemia. Saudi Medical Journal 2016-11 /pmc/articles/PMC5303802/ /pubmed/27761563 http://dx.doi.org/10.15537/smj.2016.11.16242 Text en Copyright: © Saudi Medical Journal http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Rasool, Mahmood
Malik, Arif
Jabbar, Uzma
Begum, Irshad
Qazi, Mahmood H.
Asif, Muhammad
Naseer, Muhammad I.
Ansari, Shakeel A.
Jarullah, Jummanah
Haque, Absarul
Jamal, Mohammad S.
Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients
title Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients
title_full Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients
title_fullStr Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients
title_full_unstemmed Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients
title_short Effect of iron overload on renal functions and oxidative stress in beta thalassemia patients
title_sort effect of iron overload on renal functions and oxidative stress in beta thalassemia patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5303802/
https://www.ncbi.nlm.nih.gov/pubmed/27761563
http://dx.doi.org/10.15537/smj.2016.11.16242
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