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Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study

To examine the association between serum magnesium and incident heart failure (HF) in older men and investigate potential pathways including cardiac function, inflammation and lung function. Prospective study of 3523 men aged 60–79 years with no prevalent HF or myocardial infarction followed up for...

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Autores principales: Wannamethee, Sasiwarang Goya, Papacosta, Olia, Lennon, Lucy, Whincup, Peter H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133024/
https://www.ncbi.nlm.nih.gov/pubmed/29663176
http://dx.doi.org/10.1007/s10654-018-0388-6
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author Wannamethee, Sasiwarang Goya
Papacosta, Olia
Lennon, Lucy
Whincup, Peter H.
author_facet Wannamethee, Sasiwarang Goya
Papacosta, Olia
Lennon, Lucy
Whincup, Peter H.
author_sort Wannamethee, Sasiwarang Goya
collection PubMed
description To examine the association between serum magnesium and incident heart failure (HF) in older men and investigate potential pathways including cardiac function, inflammation and lung function. Prospective study of 3523 men aged 60–79 years with no prevalent HF or myocardial infarction followed up for a mean period of 15 years, during which 268 incident HF cases were ascertained. Serum magnesium was inversely associated with many CVD risk factors including prevalent atrial fibrillation, lung function (FEV(1)) and markers of inflammation (IL-6), endothelial dysfunction (vWF) and cardiac dysfunction [NT-proBNP and cardiac troponin T (cTnT)]. Serum magnesium was inversely related to risk of incident HF after adjustment for conventional CVD risk factors and incident MI. The adjusted hazard ratios (HRs) for HF in the 5 quintiles of magnesium groups were 1.00, 0.72 (0.50, 1.05), 0.85 (0.59, 1.26), 0.76 (0.52, 1.11) and 0.56 (0.36, 0.86) respectively [p (trend) = 0.04]. Further adjustment for atrial fibrillation, IL-6, vWF and FEV(1) attenuated the association but risk remained significantly reduced in the top quintile (≥ 0.87 mmol/l) compared with the lowest quintile [HR 0.62 (0.40, 0.97)]. Adjustment for NT-proBNP and cTnT attenuated the association further [HR 0.70 (0.44, 1.10)]. The benefit of high serum magnesium on HF risk was most evident in men with ECG evidence of ischaemia [HR 0.29 (0.13, 0.68)]. The potential beneficial effect of high serum magnesium was partially explained by its favourable association with CVD risk factors. Further studies are needed to investigate whether serum magnesium supplementation in older adults may protect from the development of HF.
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spelling pubmed-61330242018-09-18 Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study Wannamethee, Sasiwarang Goya Papacosta, Olia Lennon, Lucy Whincup, Peter H. Eur J Epidemiol Cardiovascular Disease To examine the association between serum magnesium and incident heart failure (HF) in older men and investigate potential pathways including cardiac function, inflammation and lung function. Prospective study of 3523 men aged 60–79 years with no prevalent HF or myocardial infarction followed up for a mean period of 15 years, during which 268 incident HF cases were ascertained. Serum magnesium was inversely associated with many CVD risk factors including prevalent atrial fibrillation, lung function (FEV(1)) and markers of inflammation (IL-6), endothelial dysfunction (vWF) and cardiac dysfunction [NT-proBNP and cardiac troponin T (cTnT)]. Serum magnesium was inversely related to risk of incident HF after adjustment for conventional CVD risk factors and incident MI. The adjusted hazard ratios (HRs) for HF in the 5 quintiles of magnesium groups were 1.00, 0.72 (0.50, 1.05), 0.85 (0.59, 1.26), 0.76 (0.52, 1.11) and 0.56 (0.36, 0.86) respectively [p (trend) = 0.04]. Further adjustment for atrial fibrillation, IL-6, vWF and FEV(1) attenuated the association but risk remained significantly reduced in the top quintile (≥ 0.87 mmol/l) compared with the lowest quintile [HR 0.62 (0.40, 0.97)]. Adjustment for NT-proBNP and cTnT attenuated the association further [HR 0.70 (0.44, 1.10)]. The benefit of high serum magnesium on HF risk was most evident in men with ECG evidence of ischaemia [HR 0.29 (0.13, 0.68)]. The potential beneficial effect of high serum magnesium was partially explained by its favourable association with CVD risk factors. Further studies are needed to investigate whether serum magnesium supplementation in older adults may protect from the development of HF. Springer Netherlands 2018-04-17 2018 /pmc/articles/PMC6133024/ /pubmed/29663176 http://dx.doi.org/10.1007/s10654-018-0388-6 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Cardiovascular Disease
Wannamethee, Sasiwarang Goya
Papacosta, Olia
Lennon, Lucy
Whincup, Peter H.
Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study
title Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study
title_full Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study
title_fullStr Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study
title_full_unstemmed Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study
title_short Serum magnesium and risk of incident heart failure in older men: The British Regional Heart Study
title_sort serum magnesium and risk of incident heart failure in older men: the british regional heart study
topic Cardiovascular Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133024/
https://www.ncbi.nlm.nih.gov/pubmed/29663176
http://dx.doi.org/10.1007/s10654-018-0388-6
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