Université Bourgogne, LNC UMR1231, Dijon, France.
INSERM, UMR1231, Dijon, France.
Cardiovasc Diabetol. 2023 Sep 14;22(1):248. doi: 10.1186/s12933-023-01979-1.
Type 2 diabetes mellitus (T2DM) is a major global health issue and a significant risk factor for atherosclerosis. Atherosclerosis in T2DM patients has been associated with inflammation, insulin resistance, hyperglycemia, dyslipidemia, and oxidative stress. Identifying molecular features of atherosclerotic plaques in T2DM patients could provide valuable insights into the pathogenesis of the disease.
The MASCADI (Arachidonic Acid Metabolism in Carotid Stenosis Plaque in Diabetic Patients) study aimed to investigate the increase of 2-arachidonoyl-lysophatidylcholine (2-AA-LPC) in carotid plaques from T2DM and control patients and to explore its association with plaque vulnerability as well as with blood and intra-plaque biomarkers altered during diabetes.
In a population of elderly, polymedicated patients with advanced stage of atherosclerosis, we found that T2DM patients had higher systemic inflammation markers, such as high-sensitivity C-reactive protein (hsCRP) and IL-1β, higher levels of oxysterols, increased triglyceride levels, and decreased HDL levels as compared to control patients. Furthermore, 2-AA-LPC was significantly enriched in plaques from diabetic patients, suggesting its potential role in diabetic atherosclerosis. Interestingly, 2-AA-LPC was not associated with systemic markers related to diabetes, such as hsCRP, triglycerides, or HDL cholesterol. However, it was significantly correlated with the levels of inflammatory markers within the plaques such as lysophospholipids and 25-hydroxycholesterol, strengthening the link between local inflammation, arachidonic acid metabolism and diabetes.
Our study is in line with a key role for inflammation in the pathogenesis of diabetic atherosclerosis and highlights the involvement of 2-AA-LPC. Further research is needed to better understand the local processes involved in the alteration of plaque composition in T2DM and to identify potential therapeutic targets.
The MASCADI was registered on ClinicalTrials.gov (clinical registration number: NCT03202823).
2 型糖尿病(T2DM)是一个全球性的健康问题,也是动脉粥样硬化的重要危险因素。T2DM 患者的动脉粥样硬化与炎症、胰岛素抵抗、高血糖、血脂异常和氧化应激有关。鉴定 T2DM 患者动脉粥样硬化斑块的分子特征可以为疾病的发病机制提供有价值的见解。
MASCADI(糖尿病患者颈动脉狭窄斑块中花生四烯酸代谢研究)旨在研究 T2DM 和对照组患者颈动脉斑块中 2-花生四烯酰基-溶血磷脂酰胆碱(2-AA-LPC)的增加,并探讨其与斑块易损性的关系,以及与糖尿病期间血液和斑块内生物标志物的改变的关系。
在一个老年、多药治疗、动脉粥样硬化晚期的人群中,我们发现 T2DM 患者的全身炎症标志物,如高敏 C 反应蛋白(hsCRP)和白细胞介素-1β(IL-1β)水平较高,氧化固醇水平较高,甘油三酯水平升高,高密度脂蛋白(HDL)水平降低,与对照组患者相比。此外,2-AA-LPC 在糖尿病患者的斑块中明显富集,提示其在糖尿病动脉粥样硬化中的潜在作用。有趣的是,2-AA-LPC 与与糖尿病相关的系统性标志物,如 hsCRP、甘油三酯或 HDL 胆固醇无关。然而,它与斑块内炎症标志物的水平呈显著相关,如溶血磷脂和 25-羟胆固醇,这加强了局部炎症、花生四烯酸代谢和糖尿病之间的联系。
我们的研究支持炎症在糖尿病性动脉粥样硬化发病机制中的关键作用,并强调了 2-AA-LPC 的作用。需要进一步研究以更好地了解 T2DM 中斑块成分改变涉及的局部过程,并确定潜在的治疗靶点。
MASCADI 在 ClinicalTrials.gov 上注册(临床注册号:NCT03202823)。