The Role of Hyperuricemia in Cardiac Diseases: Evidence, Controversies, and Therapeutic Strategies.
Yue ZhengZhirui ChenJinya YangJing ZhengXiaorong ShuiYiguang YanShian HuangZheng LiangWei LeiYuan HePublished in: Biomolecules (2024)
Hyperuricemia (HUA) may lead to myocardial cell damage, thereby promoting the occurrence and adverse outcomes of heart diseases. In this review, we discuss the latest clinical research progress, and explore the impact of HUA on myocardial damage-related diseases such as myocardial infarction, arrhythmias, and heart failure. We also combined recent findings from basic research to analyze potential mechanisms linking HUA with myocardial injury. In different pathological models (such as direct action of high uric acid on myocardial cells or combined with myocardial ischemia-reperfusion model), HUA may cause damage by activating the NOD-like receptor protein 3 inflammasome-induced inflammatory response, interfering with cardiac cell energy metabolism, affecting antioxidant defense systems, and stimulating reactive oxygen species production to enhance the oxidative stress response, ultimately resulting in decreased cardiac function. Additionally, we discuss the impact of lowering uric acid intervention therapy and potential safety issues that may arise. However, as the mechanism underlying HUA-induced myocardial injury is poorly defined, further research is warranted to aid in the development novel therapeutic strategies for HUA-related cardiovascular diseases.
Keyphrases
- uric acid
- left ventricular
- heart failure
- metabolic syndrome
- oxidative stress
- inflammatory response
- diabetic rats
- cardiac resynchronization therapy
- cardiovascular disease
- high glucose
- single cell
- reactive oxygen species
- cell therapy
- induced apoptosis
- drug induced
- randomized controlled trial
- risk assessment
- signaling pathway
- atrial fibrillation
- endothelial cells
- immune response
- protein protein
- stem cells
- toll like receptor
- coronary artery disease
- amino acid
- cell cycle arrest
- bone marrow
- smoking cessation
- lps induced
- cardiovascular events
- cardiovascular risk factors
- innate immune
- endoplasmic reticulum stress
- climate change