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Causal association between basal metabolic rate and risk of cardiovascular diseases: a univariable and multivariable
Yihua Li1, Huiqi Zhai1, Liang Kang1
1The First Clinical Medical College of Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Insights
Higher basal metabolic rate (BMR) causally increases the risk of aortic aneurysm and atrial fibrillation but decreases myocardial infarction risk. This Mendelian randomization study clarifies BMR
Area of Science:
- Genetics and Cardiovascular Epidemiology
- Metabolic Health and Disease
- Biomarkers and Disease Risk Assessment
Background:
- Basal metabolic rate (BMR) is linked to cardiovascular health, but its direct causal impact on cardiovascular diseases (CVDs) is not well-established.
- Understanding the causal relationship between BMR and specific CVDs is crucial for developing targeted prevention strategies.
- Previous observational studies suggest associations, but confounding factors limit causal inference.
Purpose of the Study:
- To investigate the potential causal relationship between genetically predicted basal metabolic rate (BMR) and the risk of common cardiovascular diseases (CVDs).
- To examine the causal effects of BMR on aortic aneurysm (AA), atrial fibrillation and flutter (AFF), calcific aortic valvular stenosis (CAVS), heart failure (HF), and myocardial infarction (MI).
- To differentiate direct BMR effects from those mediated by common cardiovascular risk factors using multivariable Mendelian randomization.
Main Methods:
- Employed Mendelian randomization (MR) analysis, a robust method for inferring causality from genetic variants.
- Utilized the inverse variance weighted (IVW) model as the primary univariable MR method for effect estimation.
- Conducted multivariable MR analysis to adjust for potential confounding factors, including common cardiovascular risk factors.
Main Results:
- Genetically predicted higher BMR was causally associated with increased risk of AA, AFF, and HF.
- Higher BMR was causally associated with a decreased risk of MI.
- Multivariable MR confirmed direct causal effects of BMR on increased risk of AA and AFF, decreased risk of MI, and an attenuated effect on HF.
Conclusions:
- This Mendelian randomization study provides significant evidence for a causal relationship between basal metabolic rate and the risk of aortic aneurysm, atrial fibrillation, heart failure, and myocardial infarction.
- The findings highlight BMR as a potential causal factor in the development of specific cardiovascular diseases.
- Further research may explore therapeutic targets related to BMR modulation for cardiovascular disease prevention.
Abstract:
Basal metabolic rate (BMR) is associated with cardiovascular health; however, the causal relationship between BMR and the risk of cardiovascular diseases (CVDs) remains unclear. This study aimed to investigate the potential causal relationship of BMR on common CVDs including aortic aneurysm (AA), atrial fibrillation and flutter (AFF), calcific aortic valvular stenosis (CAVS), heart failure (HF), and myocardial infarction (MI) by Mendelian randomization (MR). The univariable MR analysis using inverse variance weighted (IVW) model as the primary analysis method revealed that genetically predicted higher BMR causally increased the risk of AA [IVW odds ratio (OR) = 1.34, 95% confidence interval CI 1.09-1.65, p = 0.00527], AFF (IVW OR = 1.87, 95% CI 1.65-2.12, p = 1.697 × E-22), and HF (IVW OR = 1.35, 95% CI 1.20-1.51, p = 2.364 × E-07), while causally decreasing the risk of MI (IVW OR = 0.83, 95% CI 0.73-0.93, p = 0.00255). In the multivariable MR analysis, which controlled for common cardiovascular risk factors, direct effects of BMR on an increased risk of AA and AFF, as well as a decreased risk of MI, but an attenuated causal effect on HF, were observed. In conclusion, the current MR study provides evidence for a causal relationship between BMR and the risk of AA, AFF, HF, and MI.
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