Fishman Sarah Louise, Sonmez Halis, Basman Craig, Singh Varinder, Poretsky Leonid
Division of Endocrinology, Department of Medicine, Lenox Hill Hospital, Northwell Health, 110 East 59th St #8B, New York, NY, 10022, USA.
Center for Diabetes and Endocrinology, 111 Salem Tpke, Norwich, CT, 06360, USA.
Mol Med. 2018 Nov 23;24(1):59. doi: 10.1186/s10020-018-0060-3.
Traditional risk factors are insufficient to explain all cases of coronary artery disease (CAD) in patients with diabetes mellitus (DM). Advanced glycation end-products (AGEs) and their receptors may play important roles in the development and progression of CAD. BODY: Hyperglycemia is the hallmark feature of DM. An increase in the incidence of both micro-and macrovascular complications of diabetes has been observed with increased duration of hyperglycemia. This association persists even after glycemic control has been achieved, suggesting an innate mechanism of "metabolic memory." AGEs are glycated proteins that may serve as mediators of metabolic memory due to their increased production in the setting of hyperglycemia and generally slow turnover. Elevated AGE levels can lead to abnormal cross linking of extracellular and intracellular proteins disrupting their normal structure and function. Furthermore, activation of AGE receptors can induce complex signaling pathways leading to increased inflammation, oxidative stress, enhanced calcium deposition, and increased vascular smooth muscle apoptosis, contributing to the development of atherosclerosis. Through these mechanisms, AGEs may be important mediators of the development of CAD. However, clinical studies regarding the role of AGEs and their receptors in advancing CAD are limited, with contradictory results.
AGEs and their receptors may be useful biomarkers for the presence and severity of CAD. Further studies are needed to evaluate the utility of circulating and tissue AGE levels in identifying asymptomatic patients at risk for CAD or to identify patients who may benefit from invasive intervention.
传统危险因素不足以解释糖尿病(DM)患者中所有的冠状动脉疾病(CAD)病例。晚期糖基化终产物(AGEs)及其受体可能在CAD的发生和发展中起重要作用。
高血糖是DM的标志性特征。随着高血糖持续时间的增加,糖尿病微血管和大血管并发症的发生率均有所上升。即使在实现血糖控制后,这种关联仍然存在,提示存在“代谢记忆”的内在机制。AGEs是糖基化蛋白质,由于其在高血糖环境中产量增加且周转通常较慢,可能作为代谢记忆的介质。AGE水平升高可导致细胞外和细胞内蛋白质异常交联,破坏其正常结构和功能。此外,AGE受体的激活可诱导复杂的信号通路,导致炎症增加、氧化应激、钙沉积增强和血管平滑肌细胞凋亡增加,促进动脉粥样硬化的发展。通过这些机制,AGEs可能是CAD发生发展的重要介质。然而,关于AGEs及其受体在CAD进展中作用的临床研究有限,结果相互矛盾。
AGEs及其受体可能是CAD存在和严重程度的有用生物标志物。需要进一步研究来评估循环和组织AGE水平在识别有CAD风险的无症状患者或识别可能从侵入性干预中获益的患者方面的效用。