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Published on: February 20, 2019
Causal Relationship Between Serum Uric Acid and Atherosclerotic Disease: A Mendelian Randomization and Transcriptomic
Shitao Wang1,2, Shuai Mei1,2, Xiaozhu Ma1,2
1Division of Cardiology, Departments of Internal Medicine, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
Insights
High serum uric acid levels causally link to coronary heart disease (CHD). This relationship is partly mediated by blood pressure and triglycerides, suggesting urate control may benefit CHD patients.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Metabolic Disease
Background:
- Elevated serum uric acid is linked to coronary heart disease (CHD) occurrence, development, and adverse events.
- The direct pathogenic role of uric acid in CHD and the mediating influence of risk factors remain unclear.
Purpose of the Study:
- To evaluate the potential causal association between serum uric acid and CHD.
- To investigate the mediating roles of CHD risk factors in the uric acid-CHD relationship.
Main Methods:
- Mendelian randomization (MR) analysis to assess causality.
- Bayesian colocalization to analyze genetic tool pleiotropy.
- Two-step MR to identify mediating risk factors.
- Transcriptomic analysis to explore mechanisms.
Main Results:
- MR analysis confirmed a significant causal relationship between serum uric acid and coronary artery disease, stable angina, and myocardial infarction.
- Diastolic blood pressure, mean arterial pressure, and serum triglycerides partially mediate this causal link.
- Transcriptomic data suggest uric acid may directly promote atherosclerosis by altering macrophage gene expression.
Conclusions:
- Serum urate concentration control may be essential for long-term CHD patient management.
- Further clinical trials and research are needed to confirm cardiovascular benefits of urate reduction.
Abstract:
Background/Objectives: Elevated serum uric acid levels are associated with the occurrence, development, and adverse events of coronary heart disease (CHD) and CHD risk factors. However, the extent of any pathogenic effect of the serum uric acid on CHD and whether CHD risk factors play a confounding or mediating role are still unclear. Methods: The potential causal associations of serum uric acid with CHD were evaluated via cross-trait linkage disequilibrium score regression analysis and Mendelian randomization. The pleiotropy of genetic tools was analyzed via a Bayesian colocalization approach. Moreover, we utilized two-step MR to identify risk factors mediating the relationship between uric acid and CHD. Results: Mendelian randomization results derived from two genetic instrument selection strategies support that serum uric acid levels have a significant causal relationship with coronary artery disease, stable angina pectoris, and myocardial infarction. This causal relationship was partially mediated by diastolic blood pressure, mean arterial pressure, and serum triglycerides. Transcriptomic analysis revealed that serum uric acid may directly contribute to the development of atherosclerosis by inducing transcriptomic changes in macrophages. Conclusions: Our findings highlight that the control of serum urate concentration in the long-term management of CHD patients may be necessary. Well-designed clinical trials and foundational research are presently required to furnish conclusive proof regarding the specific clinical scenarios in which adequate reduction in urate concentrations can confer cardiovascular advantages.
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