Abstract

There has been an increased interest for observational studies or randomized controlled trials exploring the impact of calcium intake on cardiovascular diseases (CVD) including coronary artery disease (CAD) and ischemic stroke (IS). However, a direct relationship between total calcium intake and CVD has not been well established and remains controversial. Mendelian randomization (MR) studies have been performed to evaluate the causal association between serum calcium levels and CAD risk and found that increased serum calcium levels could increase the risk of CAD. However, MR analysis found no significant association between genetically higher serum calcium levels and IS as well as its subtypes. Hence, three MR studies reported inconsistent effects of serum calcium levels on CAD and IS. Here, we performed an updated MR study to investigate the association of serum calcium levels with the risk of IS using large-scale genome-wide association study (GWAS) datasets. We selected 14 independent genetic variants as the potential instrumental variables from a large-scale serum calcium GWAS dataset and extracted summary statistics corresponding to the 14 serum calcium genetic variants from the MEGASTROKE Consortium IS GWAS dataset. Interestingly, we found a significant association between serum calcium levels and IS risk using the robust inverse-variance weighted (IVW) and penalized robust IVW methods, with β = 0.243 and P = 0.002. Importantly, the MR results from the robust MR-Egger and penalized robust MR-Egger methods further supported the causal association between serum calcium levels and IS risk, with β = 0.256 and P = 0.005. Meanwhile, the estimates from other MR methods are also consistent with the above findings.

Highlights

  • In recent years, there has been an increased interest for observational studies or randomized controlled trials exploring the impact of calcium intake on cardiovascular diseases (CVD) including coronary artery disease (CAD) and ischemic stroke (IS; Heaney et al, 2012; Anderson et al, 2016; Tankeu et al, 2017)

  • In the IS genome-wide association study (GWAS) dataset from the MEGASTROKE Consortium, we extracted the summary statistics corresponding to the 14 serum calcium genetic variants

  • Mendelian randomization (MR) studies have been performed to evaluate the causal effects of high serum calcium levels on the risk of CAD and IS

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Summary

Introduction

There has been an increased interest for observational studies or randomized controlled trials exploring the impact of calcium intake on cardiovascular diseases (CVD) including coronary artery disease (CAD) and ischemic stroke (IS; Heaney et al, 2012; Anderson et al, 2016; Tankeu et al, 2017). Xu et al (2017) selected four independent variants for the main analysis and 13 correlated variants for a sensitivity analysis as the included instrumental variables All these genetic variants could influence the serum calcium levels, with the genome-wide significance (P < 5.00E-08) from a recent genome-wide association study (GWAS) including 20,611 individuals of European ancestry (O’Seaghdha et al, 2010). Larsson et al (2017a) selected seven independent genetic variants influencing serum calcium levels, with the genomewide significance (P < 5.00E-08) from a recent GWAS including 61,079 individuals of European ancestry (O’Seaghdha et al, 2013), as the instrumental variables. Both Xu et al (2017) and Larsson et al (2017a) identified that increased serum calcium levels could increase the risk of CAD

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