» Articles » PMID: 33262986

Integrated Genetics and Micronutrient Data to Inform the Causal Association Between Serum Calcium Levels and Ischemic Stroke

Overview
Specialty Cell Biology
Date 2020 Dec 2
PMID 33262986
Citations 2
Authors
Affiliations
Soon will be listed here.
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 = 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 = 0.005. Meanwhile, the estimates from other MR methods are also consistent with the above findings.

Citing Articles

Altered serum calcium homeostasis independently predicts mortality in patients with acute coronary syndrome: a retrospective observational cohort study.

Su W, Zhu J, Zhao X, Chen H, Li W, Li H BMJ Open. 2021; 11(11):e049957.

PMID: 34848511 PMC: 8634212. DOI: 10.1136/bmjopen-2021-049957.


An Updated Mendelian Randomization Analysis of the Association Between Serum Calcium Levels and the Risk of Alzheimer's Disease.

Shi Y, Liu R, Guo Y, Li Q, Zhou H, Yu S Front Genet. 2021; 12:731391.

PMID: 34567081 PMC: 8457382. DOI: 10.3389/fgene.2021.731391.

References
1.
Emdin C, Khera A, Natarajan P, Klarin D, Zekavat S, Hsiao A . Genetic Association of Waist-to-Hip Ratio With Cardiometabolic Traits, Type 2 Diabetes, and Coronary Heart Disease. JAMA. 2017; 317(6):626-634. PMC: 5571980. DOI: 10.1001/jama.2016.21042. View

2.
Anderson J, Kruszka B, Delaney J, He K, Burke G, Alonso A . Calcium Intake From Diet and Supplements and the Risk of Coronary Artery Calcification and its Progression Among Older Adults: 10-Year Follow-up of the Multi-Ethnic Study of Atherosclerosis (MESA). J Am Heart Assoc. 2016; 5(10). PMC: 5121484. DOI: 10.1161/JAHA.116.003815. View

3.
OSeaghdha C, Yang Q, Glazer N, Leak T, Dehghan A, Smith A . Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. Hum Mol Genet. 2010; 19(21):4296-303. PMC: 2951868. DOI: 10.1093/hmg/ddq342. View

4.
Puccetti L . Calcium supplementation: Confounders were ignored. BMJ. 2008; 336(7641):403-4. PMC: 2249641. DOI: 10.1136/bmj.39493.418704.1F. View

5.
Zhuang H, Han J, Cheng L, Liu S . A Positive Causal Influence of IL-18 Levels on the Risk of T2DM: A Mendelian Randomization Study. Front Genet. 2019; 10:295. PMC: 6459887. DOI: 10.3389/fgene.2019.00295. View