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The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients

BACKGROUND: Vitamin A has different functions in the body and after being converted to acid form; it can play many roles in immune system regulation. Therefore, this vitamin can be used as a supplement in the treatment of diseases, such as cancer and autoimmune diseases. Vitamin A is a fat-soluble c...

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Autores principales: Jafarirad, Sima, Siassi, Fereydoon, Harirchian, Mohammad-Hossein, Amani, Reza, Bitarafan, Sama, Saboor-Yaraghi, Aliakbar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745746/
https://www.ncbi.nlm.nih.gov/pubmed/23983997
http://dx.doi.org/10.5812/ircmj.3480
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author Jafarirad, Sima
Siassi, Fereydoon
Harirchian, Mohammad-Hossein
Amani, Reza
Bitarafan, Sama
Saboor-Yaraghi, Aliakbar
author_facet Jafarirad, Sima
Siassi, Fereydoon
Harirchian, Mohammad-Hossein
Amani, Reza
Bitarafan, Sama
Saboor-Yaraghi, Aliakbar
author_sort Jafarirad, Sima
collection PubMed
description BACKGROUND: Vitamin A has different functions in the body and after being converted to acid form; it can play many roles in immune system regulation. Therefore, this vitamin can be used as a supplement in the treatment of diseases, such as cancer and autoimmune diseases. Vitamin A is a fat-soluble compound and its long-term consumption in high doses can have some adverse effects. OBJECTIVE: The current study aimed to investigate the possible complications and find solutions to minimize the adverse effects. PATIENTS AND METHODS: This study was a double blind randomized clinical trial. In the main study, vitamin A (as retinyl palmitate) was given to 35 multiple sclerosis (MS) patients in order to regulate their immune system with a dose of 25000 IU/day for a period of six months. To investigate the possible biochemical complications, lipid profiles, fasting blood sugar (FBS), liver enzymes, and C-reactive protein (CRP) were tested. RESULTS: Vitamin A did not have a significant difference in lipid profiles, FBS and liver enzymes between the two groups receiving vitamin A and the placebo, but CRP increased in patients who were taking vitamin A, 1.65±0.43 (mg/L) and 2.88±0.67, (Mean±SEM), before and after the intervention respectively (P=0.029), and statistical analysis showed significant differences with the group receiving placebo (P=0.011) and CRP level in vitamin A group was 1.3 mg/L more than those of the placebo group after intervention (P=0.011). CONCLUSIONS: Considering that no significant difference was found in the proven vitamin A side effects, due to the increase in CRP, frequent clinical and biochemical controls are required along with vitamin A supplementation.
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spelling pubmed-37457462013-08-27 The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients Jafarirad, Sima Siassi, Fereydoon Harirchian, Mohammad-Hossein Amani, Reza Bitarafan, Sama Saboor-Yaraghi, Aliakbar Iran Red Crescent Med J Research Article BACKGROUND: Vitamin A has different functions in the body and after being converted to acid form; it can play many roles in immune system regulation. Therefore, this vitamin can be used as a supplement in the treatment of diseases, such as cancer and autoimmune diseases. Vitamin A is a fat-soluble compound and its long-term consumption in high doses can have some adverse effects. OBJECTIVE: The current study aimed to investigate the possible complications and find solutions to minimize the adverse effects. PATIENTS AND METHODS: This study was a double blind randomized clinical trial. In the main study, vitamin A (as retinyl palmitate) was given to 35 multiple sclerosis (MS) patients in order to regulate their immune system with a dose of 25000 IU/day for a period of six months. To investigate the possible biochemical complications, lipid profiles, fasting blood sugar (FBS), liver enzymes, and C-reactive protein (CRP) were tested. RESULTS: Vitamin A did not have a significant difference in lipid profiles, FBS and liver enzymes between the two groups receiving vitamin A and the placebo, but CRP increased in patients who were taking vitamin A, 1.65±0.43 (mg/L) and 2.88±0.67, (Mean±SEM), before and after the intervention respectively (P=0.029), and statistical analysis showed significant differences with the group receiving placebo (P=0.011) and CRP level in vitamin A group was 1.3 mg/L more than those of the placebo group after intervention (P=0.011). CONCLUSIONS: Considering that no significant difference was found in the proven vitamin A side effects, due to the increase in CRP, frequent clinical and biochemical controls are required along with vitamin A supplementation. Kowsar 2013-03-05 2013-03 /pmc/articles/PMC3745746/ /pubmed/23983997 http://dx.doi.org/10.5812/ircmj.3480 Text en Copyright © 2013, Iranian Red Crescent Medical Journal http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jafarirad, Sima
Siassi, Fereydoon
Harirchian, Mohammad-Hossein
Amani, Reza
Bitarafan, Sama
Saboor-Yaraghi, Aliakbar
The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients
title The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients
title_full The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients
title_fullStr The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients
title_full_unstemmed The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients
title_short The Effect of Vitamin A Supplementation on Biochemical Parameters in Multiple Sclerosis Patients
title_sort effect of vitamin a supplementation on biochemical parameters in multiple sclerosis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745746/
https://www.ncbi.nlm.nih.gov/pubmed/23983997
http://dx.doi.org/10.5812/ircmj.3480
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