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Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women

BACKGROUND: This study aimed to investigate whether magnesium supplementation might affect serum magnesium, high sensitive C-reactive protein (hs-CRP), plasma fibrinogen, and interleukin 6 (IL-6) levels in healthy middle-aged overweight women. The relationships, if any, between serum magnesium and t...

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Autores principales: Moslehi, Nazanin, Vafa, Mohammadreza, Rahimi-Foroushani, Abbas, Golestan, Banafsheh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685774/
https://www.ncbi.nlm.nih.gov/pubmed/23798918
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author Moslehi, Nazanin
Vafa, Mohammadreza
Rahimi-Foroushani, Abbas
Golestan, Banafsheh
author_facet Moslehi, Nazanin
Vafa, Mohammadreza
Rahimi-Foroushani, Abbas
Golestan, Banafsheh
author_sort Moslehi, Nazanin
collection PubMed
description BACKGROUND: This study aimed to investigate whether magnesium supplementation might affect serum magnesium, high sensitive C-reactive protein (hs-CRP), plasma fibrinogen, and interleukin 6 (IL-6) levels in healthy middle-aged overweight women. The relationships, if any, between serum magnesium and the inflammatory markers were also examined cross-sectionally in the entire participants at the beginning of the study. MATERIALS AND METHODS: This double-blinded, placebo-controlled, randomized trial included 74 middle-aged overweight women. Participants were randomly assigned to receive either 250 mg magnesium as magnesium oxide or placebo daily for 8 weeks. Serum magnesium, hs-CRP, fibrinogen and IL-6 concentrations were measured before and after the intervention. RESULTS: Serum magnesium was found to be inversely correlated with hs-CRP (r(s) =−0.22, P=0.05) in the entire participants at baseline. Serum hs-CRP declined significantly in both groups as compared with baseline values (median change=0.8 mg/L; P(Magnesium)= 0.03, P(Placebo) < 0.001). Plasma fibrinogen decreased significantly, by 9%, in the magnesium group at the end of week 8 compared to baseline (P=0.001). Mean concentration of IL-6 was significantly increased in the magnesium group comparing the baseline value(P=0.001). However hs-CRP, fibrinogen and IL-6 levels at week 8 or any changes during the study were not statistically different between the two groups. Serum magnesium showed no significant changes in any groups. CONCLUSIONS: Serum magnesium had a significant inverse correlation with hs-CRP. In the present study, magnesium as magnesium oxide, 250 mg/day, for 8 weeks did not significantly attenuate inflammatory markers in the magnesium group as compared to the placebo.
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spelling pubmed-36857742013-06-24 Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women Moslehi, Nazanin Vafa, Mohammadreza Rahimi-Foroushani, Abbas Golestan, Banafsheh J Res Med Sci Original Article BACKGROUND: This study aimed to investigate whether magnesium supplementation might affect serum magnesium, high sensitive C-reactive protein (hs-CRP), plasma fibrinogen, and interleukin 6 (IL-6) levels in healthy middle-aged overweight women. The relationships, if any, between serum magnesium and the inflammatory markers were also examined cross-sectionally in the entire participants at the beginning of the study. MATERIALS AND METHODS: This double-blinded, placebo-controlled, randomized trial included 74 middle-aged overweight women. Participants were randomly assigned to receive either 250 mg magnesium as magnesium oxide or placebo daily for 8 weeks. Serum magnesium, hs-CRP, fibrinogen and IL-6 concentrations were measured before and after the intervention. RESULTS: Serum magnesium was found to be inversely correlated with hs-CRP (r(s) =−0.22, P=0.05) in the entire participants at baseline. Serum hs-CRP declined significantly in both groups as compared with baseline values (median change=0.8 mg/L; P(Magnesium)= 0.03, P(Placebo) < 0.001). Plasma fibrinogen decreased significantly, by 9%, in the magnesium group at the end of week 8 compared to baseline (P=0.001). Mean concentration of IL-6 was significantly increased in the magnesium group comparing the baseline value(P=0.001). However hs-CRP, fibrinogen and IL-6 levels at week 8 or any changes during the study were not statistically different between the two groups. Serum magnesium showed no significant changes in any groups. CONCLUSIONS: Serum magnesium had a significant inverse correlation with hs-CRP. In the present study, magnesium as magnesium oxide, 250 mg/day, for 8 weeks did not significantly attenuate inflammatory markers in the magnesium group as compared to the placebo. Medknow Publications & Media Pvt Ltd 2012-07 /pmc/articles/PMC3685774/ /pubmed/23798918 Text en Copyright: © Journal of Research in Medical Sciences 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
Moslehi, Nazanin
Vafa, Mohammadreza
Rahimi-Foroushani, Abbas
Golestan, Banafsheh
Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women
title Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women
title_full Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women
title_fullStr Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women
title_full_unstemmed Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women
title_short Effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women
title_sort effects of oral magnesium supplementation on inflammatory markers in middle-aged overweight women
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3685774/
https://www.ncbi.nlm.nih.gov/pubmed/23798918
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