Li Kaiyue, Li Kongwei, Yao Qingmei, Shui Xiaorong, Zheng Jing, He Yuan, Lei Wei
Guangdong Provincial Engineering Technology Research Center for Molecular Diagnosis and Innovative Drugs Translation of Cardiopulmonary Vascular Diseases, University Joint Laboratory of Guangdong Province and Macao Region on Molecular Targets and Intervention of Cardiovascular Diseases, Department of Precision Laboratory, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China.
Cardiovascular Medicine Center, Affiliated Hospital of Guangdong Medical University, Zhanjiang, Guangdong, China.
Heliyon. 2023 May 9;9(5):e16097. doi: 10.1016/j.heliyon.2023.e16097. eCollection 2023 May.
Coronary arterial disease (CAD) is the leading cause of mortality in the world. Hyperuricemia has recently emerged as a novel independent risk factor of CAD, in addition to the traditional risk factors such as hyperlipidemia, smoking, and obesity. Several clinical studies have shown that hyperuricemia is strongly associated with the risk, progression and poor prognosis of CAD, as well as verifying an association with traditional CAD risk factors. Uric acid or enzymes in the uric acid production pathway are associated with inflammation, oxidative stress, regulation of multiple signaling pathways and the renin-angiotensin-aldosterone system (RAAS), and these pathophysiological alterations are currently the main mechanisms of coronary atherosclerosis formation. The risk of death from CAD can be effectively reduced by the uric acid-lowering therapy, but the interventional treatment of uric acid levels in patients with CAD remains controversial due to the diversity of co-morbidities and the complexity of causative factors. In this review, we analyze the association between hyperuricemia and CAD, elucidate the possible mechanisms by which uric acid induces or exacerbates CAD, and discuss the benefits and drawbacks of uric acid-lowering therapy. This review could provide theoretical references for the prevention and management of hyperuricemia-associated CAD.
冠状动脉疾病(CAD)是全球主要的死亡原因。除了高脂血症、吸烟和肥胖等传统危险因素外,高尿酸血症最近已成为CAD新的独立危险因素。多项临床研究表明,高尿酸血症与CAD的风险、进展及不良预后密切相关,同时也证实了其与CAD传统危险因素之间的关联。尿酸或尿酸生成途径中的酶与炎症、氧化应激、多种信号通路的调节以及肾素-血管紧张素-醛固酮系统(RAAS)相关,而这些病理生理改变目前是冠状动脉粥样硬化形成的主要机制。降低尿酸治疗可有效降低CAD的死亡风险,但由于合并症的多样性和致病因素的复杂性,CAD患者尿酸水平的干预治疗仍存在争议。在本综述中,我们分析了高尿酸血症与CAD之间的关联,阐明了尿酸诱发或加重CAD的可能机制,并讨论了降尿酸治疗的利弊。本综述可为高尿酸血症相关CAD的预防和管理提供理论参考。