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Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study

OBJECTIVE: To determine whether serum magnesium and calcium concentrations are causally associated with ischemic stroke or any of its subtypes using the mendelian randomization approach. METHODS: Analyses were conducted using summary statistics data for 13 single-nucleotide polymorphisms robustly as...

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Autores principales: Larsson, Susanna C., Traylor, Matthew, Burgess, Stephen, Boncoraglio, Giorgio B., Jern, Christina, Michaëlsson, Karl, Markus, Hugh S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404465/
https://www.ncbi.nlm.nih.gov/pubmed/30804065
http://dx.doi.org/10.1212/WNL.0000000000007001
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author Larsson, Susanna C.
Traylor, Matthew
Burgess, Stephen
Boncoraglio, Giorgio B.
Jern, Christina
Michaëlsson, Karl
Markus, Hugh S.
author_facet Larsson, Susanna C.
Traylor, Matthew
Burgess, Stephen
Boncoraglio, Giorgio B.
Jern, Christina
Michaëlsson, Karl
Markus, Hugh S.
author_sort Larsson, Susanna C.
collection PubMed
description OBJECTIVE: To determine whether serum magnesium and calcium concentrations are causally associated with ischemic stroke or any of its subtypes using the mendelian randomization approach. METHODS: Analyses were conducted using summary statistics data for 13 single-nucleotide polymorphisms robustly associated with serum magnesium (n = 6) or serum calcium (n = 7) concentrations. The corresponding data for ischemic stroke were obtained from the MEGASTROKE consortium (34,217 cases and 404,630 noncases). RESULTS: In standard mendelian randomization analysis, the odds ratios for each 0.1 mmol/L (about 1 SD) increase in genetically predicted serum magnesium concentrations were 0.78 (95% confidence interval [CI] 0.69–0.89; p = 1.3 × 10(−4)) for all ischemic stroke, 0.63 (95% CI 0.50–0.80; p = 1.6 × 10(−4)) for cardioembolic stroke, and 0.60 (95% CI 0.44–0.82; p = 0.001) for large artery stroke; there was no association with small vessel stroke (odds ratio 0.90, 95% CI 0.67–1.20; p = 0.46). Only the association with cardioembolic stroke was robust in sensitivity analyses. There was no association of genetically predicted serum calcium concentrations with all ischemic stroke (per 0.5 mg/dL [about 1 SD] increase in serum calcium: odds ratio 1.03, 95% CI 0.88–1.21) or with any subtype. CONCLUSIONS: This study found that genetically higher serum magnesium concentrations are associated with a reduced risk of cardioembolic stroke but found no significant association of genetically higher serum calcium concentrations with any ischemic stroke subtype.
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spelling pubmed-64044652019-03-16 Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study Larsson, Susanna C. Traylor, Matthew Burgess, Stephen Boncoraglio, Giorgio B. Jern, Christina Michaëlsson, Karl Markus, Hugh S. Neurology Article OBJECTIVE: To determine whether serum magnesium and calcium concentrations are causally associated with ischemic stroke or any of its subtypes using the mendelian randomization approach. METHODS: Analyses were conducted using summary statistics data for 13 single-nucleotide polymorphisms robustly associated with serum magnesium (n = 6) or serum calcium (n = 7) concentrations. The corresponding data for ischemic stroke were obtained from the MEGASTROKE consortium (34,217 cases and 404,630 noncases). RESULTS: In standard mendelian randomization analysis, the odds ratios for each 0.1 mmol/L (about 1 SD) increase in genetically predicted serum magnesium concentrations were 0.78 (95% confidence interval [CI] 0.69–0.89; p = 1.3 × 10(−4)) for all ischemic stroke, 0.63 (95% CI 0.50–0.80; p = 1.6 × 10(−4)) for cardioembolic stroke, and 0.60 (95% CI 0.44–0.82; p = 0.001) for large artery stroke; there was no association with small vessel stroke (odds ratio 0.90, 95% CI 0.67–1.20; p = 0.46). Only the association with cardioembolic stroke was robust in sensitivity analyses. There was no association of genetically predicted serum calcium concentrations with all ischemic stroke (per 0.5 mg/dL [about 1 SD] increase in serum calcium: odds ratio 1.03, 95% CI 0.88–1.21) or with any subtype. CONCLUSIONS: This study found that genetically higher serum magnesium concentrations are associated with a reduced risk of cardioembolic stroke but found no significant association of genetically higher serum calcium concentrations with any ischemic stroke subtype. Lippincott Williams & Wilkins 2019-02-26 /pmc/articles/PMC6404465/ /pubmed/30804065 http://dx.doi.org/10.1212/WNL.0000000000007001 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Larsson, Susanna C.
Traylor, Matthew
Burgess, Stephen
Boncoraglio, Giorgio B.
Jern, Christina
Michaëlsson, Karl
Markus, Hugh S.
Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study
title Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study
title_full Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study
title_fullStr Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study
title_full_unstemmed Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study
title_short Serum magnesium and calcium levels in relation to ischemic stroke: Mendelian randomization study
title_sort serum magnesium and calcium levels in relation to ischemic stroke: mendelian randomization study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404465/
https://www.ncbi.nlm.nih.gov/pubmed/30804065
http://dx.doi.org/10.1212/WNL.0000000000007001
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