Department of Cardiovascular Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Bioinformatics and Biostatistics, SJTU-Yale Joint Center for Biostatistics and Data Science, College of Life Science and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
DNA Cell Biol. 2022 Nov;41(11):966-980. doi: 10.1089/dna.2022.0200. Epub 2022 Oct 17.
Chronic kidney disease (CKD) accelerates atherosclerosis. The mechanism of CKD-related atherosclerosis is complex, and CKD-specific risk factors may contribute to this process in addition to traditional risk factors such as hypertension, diabetes, and hypercholesterolemia. In the present study, to discover CKD-specific atherosclerosis risk factors, a total of 62 patients with different stages of kidney function were enrolled. All patients underwent coronary angiographies and the severity of coronary atherosclerosis was defined by the SYNTAX score. Patients were divided into different groups according to their kidney function levels and coronary atherosclerosis severity. Data-independent acquisition mass spectrometry was used to identify differentially expressed proteins (DEPs) in the plasma samples, and weighted correlation network analysis (WGCNA) was employed to identify significant protein modules and hub proteins related to CKD-specific atherosclerosis. The results showed that 10 DEPs associated with atherosclerosis were found in the comparative groups with modest and severe CKD. Through WGCNA, 1768 proteins were identified and 8 protein modules were established. Enrichment analyses of protein modules revealed functional clusters mainly associated with inflammation and the complement and coagulation cascade as atherosclerosis developed under CKD conditions. The results may help to better understand the mechanisms of CKD-related atherosclerosis and guide future research on developing treatments for CKD-related atherosclerosis.
慢性肾脏病(CKD)会加速动脉粥样硬化。CKD 相关动脉粥样硬化的机制很复杂,除了高血压、糖尿病和高脂血症等传统危险因素外,CKD 特有的危险因素也可能促成这一过程。在本研究中,为了发现 CKD 特有的动脉粥样硬化危险因素,共纳入了 62 名肾功能不同阶段的患者。所有患者均进行了冠状动脉造影检查,并通过 SYNTAX 评分定义了冠状动脉粥样硬化的严重程度。根据患者的肾功能水平和冠状动脉粥样硬化严重程度将其分为不同组。采用无依赖数据采集质谱技术鉴定血浆样本中的差异表达蛋白(DEPs),并采用加权相关网络分析(WGCNA)鉴定与 CKD 特异性动脉粥样硬化相关的显著蛋白模块和枢纽蛋白。结果显示,在肾功能轻度和重度 CKD 的对比组中发现了 10 个与动脉粥样硬化相关的 DEP。通过 WGCNA 鉴定出 1768 个蛋白质,并建立了 8 个蛋白质模块。对蛋白质模块的富集分析显示,随着 CKD 条件下动脉粥样硬化的发展,功能簇主要与炎症和补体及凝血级联相关。这些结果可能有助于更好地理解 CKD 相关动脉粥样硬化的机制,并为开发 CKD 相关动脉粥样硬化的治疗方法提供指导。