There Is No Direct Causal Relationship Between Coronary Artery Disease and Alzheimer Disease: A Bidirectional
Aifang Zhong1, Yejun Tan2, Yaqiong Liu3
1Department of Emergency Medicine, The Second Xiangya Hospital Central South University Changsha Hunan China.
Insights
This study found no genetic evidence linking Alzheimer disease (AD) and coronary artery disease (CAD). Managing these conditions separately may be more effective for patient care.
Area of Science:
- Neuroscience
- Cardiovascular Science
- Genetics
Background:
- Inconsistent findings exist regarding the link between cardiovascular health and cognitive decline.
- Investigating causal relationships between Alzheimer disease (AD), total-tau levels, and coronary artery disease (CAD) is crucial.
Purpose of the Study:
- To utilize Mendelian randomization (MR) to explore the potential causal links between AD, total-tau, and CAD.
- To determine if genetic predisposition to AD influences CAD risk, or vice versa.
Main Methods:
- Mendelian randomization (MR) analysis was the primary methodology.
- Inverse-variance weighted (IVW) method was employed for primary analysis.
- MR-Egger regression and the Q statistic were used to assess pleiotropy and heterogeneity.
Main Results:
- No significant causal effect of AD on various forms of CAD (heart failure, myocardial infarction, ischemic heart disease, coronary heart disease, coronary atherosclerosis) was detected.
- Reverse MR analysis showed no significant causal effect of CAD on AD.
- CAD did not affect circulating total-tau levels, and total-tau did not increase CAD risk.
Conclusions:
- There is no direct genetic causal relationship established between AD and CAD.
- Independent and targeted management strategies for AD and CAD are recommended.
- Further investigation into the shared mechanisms may not be beneficial for current treatment advancements.
Background:
The association between poor cardiovascular health and cognitive decline as well as dementia progression has been inconsistent across studies. This study used Mendelian randomization (MR) to investigate the causal relationship between Alzheimer disease (AD), circulating levels of total-tau, and coronary artery disease (CAD).
Methods And Results:
This study used MR to investigate the causal relationship between AD or circulating levels of total-tau and CAD, including ischemic heart disease, myocardial infarction, coronary heart disease, coronary atherosclerosis, and heart failure. The primary analysis used the inverse-variance weighted method, with pleiotropy and heterogeneity assessed using MR-Egger regression and the Q statistic. The overall results of the MR analysis indicated that AD did not exhibit a causal effect on heart failure (odds ratio [OR], 0.969 [95% CI, 0.921-1.018]; P=0.209), myocardial infarction (OR, 0.972 [95% CI, 0.915-1.033]; P=0.359), ischemic heart disease (OR, 1.013 [95% CI, 0.949-1.082]; P=0.700), coronary heart disease (OR, 1.005 [95% CI, 0.937-1.078]; P=0.881), or coronary atherosclerosis (OR, 0.987 [95% CI, 0.926-1.052]; P=0.690). No significant causal effect of CAD was observed on AD in the reverse MR analysis. Additionally, our findings revealed that CAD did not influence circulating levels of total-tau, nor did circulating levels of total-tau increase the risk of CAD. Sensitivity analysis and assessment of horizontal pleiotropy suggested that these factors did not distort the causal estimates.
Conclusions:
The findings of this study indicate the absence of a direct causal relationship between AD and CAD from a genetic perspective. Therefore, managing the 2 diseases should be more independent and targeted. Concurrently, investigating the mechanism underlying their comorbidity may not yield meaningful insights for advancing treatment strategies.
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