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Serum magnesium levels and risk of coronary artery disease: Mendelian randomisation study.

Published version
Peer-reviewed

Type

Article

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Abstract

Background. Observational studies have shown that serum magnesium levels are inversely associated risk of cardiovascular disease, but whether this association is causal is unknown. We conducted a Mendelian randomization study to investigate whether serum magnesium levels may be causally associated with coronary artery disease (CAD).

Methods: This Mendelian randomization analysis is based on summary-level data from the CARDIoGRAMplusC4D consortium’s 1000 Genomes-based genome-wide association meta-analysis of 48 studies with a total 60,801 CAD cases and 123,504 non-cases. Six single nucleotide polymorphisms (SNPs) associated with serum magnesium levels at genome-wide significance were used as instrumental variables.

Results: A genetic predisposition to higher serum magnesium levels was inversely associated with CAD. In conventional Mendelian randomization analysis, the odds ratio of CAD was 0.88 (95% confidence interval [CI]: 0.78 to 0.99; P = 0.03) per 0.1 mmol/L (about 1 standard deviation) increase in genetically predicted serum magnesium levels. Results were consistent in sensitivity analyses using the weighted median and heterogeneity-penalized model averaging methods, with odds ratios of 0.84 (95% CI: 0.72 to 0.98; P = 0.03) and 0.83 (95% CI: 0.71 to 0.96; P = 0.02), respectively.

Conclusions: This study based on genetics provides evidence that serum magnesium levels are inversely associated with risk of CAD. Randomized controlled trials elucidating whether magnesium supplementation lowers the risk of CAD, preferably in a setting at higher risk of hypomagnesemia, are warranted.

Description

Keywords

Humans, Genetic Predisposition to Disease, Magnesium, Female, Male, Coronary Artery Disease, Genome-Wide Association Study, Mendelian Randomization Analysis

Journal Title

BMC medicine

Conference Name

Journal ISSN

1741-7015
1741-7015

Volume Title

16

Publisher

BioMed Central
Sponsorship
Wellcome Trust (204623/Z/16/Z)
MRC (MR/L003120/1)
British Heart Foundation (RG/13/13/30194)
Medical Research Council (MC_UU_00002/7)