Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy.
Institute of Clinical Physiology, National Research Council, 56124 Pisa, Italy.
Int J Mol Sci. 2022 Oct 18;23(20):12449. doi: 10.3390/ijms232012449.
Carotid atherosclerosis represents a relevant healthcare problem, since unstable plaques are responsible for approximately 15% of neurologic events, namely transient ischemic attack and stroke. Although statins treatment has proven effective in reducing LDL-cholesterol and the onset of acute clinical events, a residual risk may persist suggesting the need for the detection of reliable molecular markers useful for the identification of patients at higher risk regardless of optimal medical therapy. In this regard, several lines of evidence show a relationship among specific biologically active plasma lipids, atherosclerosis, and acute clinical events. We performed a Selected Reaction Monitoring-based High Performance Liquid Chromatography-tandem Mass Spectrometry (SRM-based HPLC-MS/MS) analysis on plasma HDL, LDL, and VLDL fractions purified, by isopycnic salt gradient ultracentrifugation, from twenty-eight patients undergoing carotid endarterectomy, having either a "hard" or a "soft" plaque, with the aim of characterizing the specific lipidomic patterns associated with features of carotid plaque instability. One hundred and thirty lipid species encompassing different lipid (sub)classes were monitored. Supervised multivariate analysis showed that lipids belonging to phosphatidylethanolamine (PE), sphingomyelin (SM), and diacylglycerol (DG) classes mostly contribute to discrimination within each lipoprotein fraction according to the plaque typology. Differential analysis evidenced a significant dysregulation of LDL PE (38:6), SM (32:1), and SM (32:2) between the two groups of patients (adj. -value threshold = 0.05 and logFC ≥ |0.58|). Using this approach, some LDL-associated markers of plaque vulnerability have been identified, in line with the current knowledge of the key roles of these phospholipids in lipoprotein metabolism and cardiovascular disease. This proof-of-concept study reports promising results, showing that lipoprotein lipidomics may present a valuable approach for identifying new biomarkers of potential clinical relevance.
颈动脉粥样硬化是一个重要的医疗保健问题,因为不稳定斑块约占 15%的神经事件,即短暂性脑缺血发作和中风。尽管他汀类药物治疗已被证明能有效降低 LDL 胆固醇和急性临床事件的发生,但仍可能存在残余风险,这表明需要检测可靠的分子标志物,以识别无论接受最佳药物治疗的患者的更高风险。在这方面,有几条证据表明特定的生物活性血浆脂质、动脉粥样硬化和急性临床事件之间存在关联。我们对通过等密度盐梯度超速离心从 28 名接受颈动脉内膜切除术的患者中纯化的血浆 HDL、LDL 和 VLDL 级分进行了基于选择反应监测的高效液相色谱-串联质谱(SRM 基于 HPLC-MS/MS)分析,目的是表征与颈动脉斑块不稳定性特征相关的特定脂质组学模式。监测了涵盖不同脂质(亚)类别的 130 种脂质。有监督的多元分析表明,属于磷脂酰乙醇胺(PE)、神经鞘磷脂(SM)和二酰基甘油(DG)类的脂质根据斑块类型在每种脂蛋白级分中最有助于区分。差异分析表明,两组患者之间 LDL PE(38:6)、SM(32:1)和 SM(32:2)存在显著失调(调整后的 - 值阈值=0.05 和 logFC≥|0.58|)。使用这种方法,已经确定了一些 LDL 相关的斑块脆弱性标志物,这与这些磷脂在脂蛋白代谢和心血管疾病中的关键作用的现有知识一致。这项概念验证研究报告了有希望的结果,表明脂蛋白脂质组学可能是一种有价值的方法,可以识别具有潜在临床相关性的新生物标志物。