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Updated: Aug 30, 2025

A Semi-Automated and Reproducible Biological-Based Method to Quantify Calcium Deposition In Vitro
Published on: June 2, 2022
Mendelian randomization study of the effect of coronary artery calcification on atherosclerotic cardiovascular
Wichanon Sae-Jie1, Tarinee Tangcharoen2, Prin Vathesatogkit2
1Department of Mathematics, Faculty of Science, Mahidol University, Bangkok, Thailand.
Insights
Calcium calcification in arteries (CAC) causally increases myocardial infarction (MI) risk, particularly inferior wall MI. This suggests calcification
Area of Science:
- Cardiovascular Science
- Genetics
- Epidemiology
Background:
- Artery calcification (CAC) is linked to atherosclerosis and myocardial infarction (MI).
- The causal role of CAC in various atherosclerotic cardiovascular diseases remains unclear.
Purpose of the Study:
- To investigate the causal role of CAC in a wide range of atherosclerotic cardiovascular diseases using Mendelian randomization.
- Specifically examine the association between CAC and different types of MI.
Main Methods:
- Employed a two-sample Mendelian randomization (MR) approach.
- Utilized data from the UK Biobank and other sources.
- Applied three MR models (inverse variance weighted, weighted-median, weighted-mode) with eight single nucleotide polymorphisms (SNPs) as instrumental variables for CAC.
Main Results:
- Confirmed a causal effect of CAC on overall MI across all MR models.
- Demonstrated a consistent causal association between CAC and inferior wall MI.
- Did not find a consistent causal effect of CAC on anterior wall MI.
Conclusions:
- CAC causally contributes to myocardial infarction, particularly affecting the inferior wall.
- The findings suggest that artery calcification may play a more significant role in inferior wall MI, potentially due to prolonged calcification processes.
- Anterior wall MI might be influenced by non-calcified plaque or other mechanisms in advanced atherosclerosis.
Abstract:
Calcium calcification in the wall of arteries (CAC) leads to a higher risk of atherosclerosis related outcomes, especially myocardial infarction (MI). Nevertheless, the causal role of CAC on other related outcomes is unclear. In this study, we used Mendelian randomization (MR) to systematically investigate the causal role of CAC across a broad range of atherosclerotic cardiovascular diseases including coronary heart disease, angina, MI, ischemic heart disease, stroke, and peripheral vascular disease. Publicly available data from the UK biobank and other data sources were used. Using the two-sample Mendelian randomization (MR) approach, we applied 3 MR models including the inverse variance weighted, the weighted-median, and the weighted-mode methods. Eight SNPs associated with CAC were selected as instrumental variables. We observed causal evidence of CAC on MI consistently across all MR models (PIVW = 1.0 × 10-4, PW-Median = 1.1 × 10-4, PW-Mode = 3.8 × 10-2) and this causation is shown in an acute transmural MI of inferior wall (PIVW = 1.5 × 10-4, PW-Median = 4.8 × 10-5, PW-Mode = 3.2 × 10-2) but not consistently observed in an anterior wall. As each site of acute MI was suggested to have relatively specific mechanisms, our finding suggested that the causal role of CAC on MI is in an inferior wall possibly as a consequence of large calcification from a prolonged process, whereas non-calcified artery plaque or other underlying mechanisms may predominantly play role in an anterior infarction during an advanced atherosclerotic process.
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