Andreini Daniele, Melotti Eleonora, Vavassori Chiara, Chiesa Mattia, Piacentini Luca, Conte Edoardo, Mushtaq Saima, Manzoni Martina, Cipriani Eleonora, Ravagnani Paolo M, Bartorelli Antonio L, Colombo Gualtiero I
Centro Cardiologico Monzino IRCCS, 20138 Milan, Italy.
Department of Biomedical and Clinical Science "Luigi Sacco", University of Milan, 20121 Milan, Italy.
Biomedicines. 2022 Jun 2;10(6):1309. doi: 10.3390/biomedicines10061309.
Existing tools to estimate cardiovascular (CV) risk have sub-optimal predictive capacities. In this setting, non-invasive imaging techniques and omics biomarkers could improve risk-prediction models for CV events. This study aimed to identify gene expression patterns in whole blood that could differentiate patients with severe coronary atherosclerosis from subjects with a complete absence of detectable coronary artery disease and to assess associations of gene expression patterns with plaque features in coronary CT angiography (CCTA). Patients undergoing CCTA for suspected coronary artery disease (CAD) were enrolled. Coronary stenosis was quantified and CCTA plaque features were assessed. The whole-blood transcriptome was analyzed with RNA sequencing. We detected highly significant differences in the circulating transcriptome between patients with high-degree coronary stenosis (≥70%) in the CCTA and subjects with an absence of coronary plaque. Notably, regression analysis revealed expression signatures associated with the Leaman score, the segment involved score, the segment stenosis score, and plaque volume with density <150 HU at CCTA. This pilot study shows that patients with significant coronary stenosis are characterized by whole-blood transcriptome profiles that may discriminate them from patients without CAD. Furthermore, our results suggest that whole-blood transcriptional profiles may predict plaque characteristics.
现有的评估心血管(CV)风险的工具预测能力欠佳。在此背景下,非侵入性成像技术和组学生物标志物可改善CV事件的风险预测模型。本研究旨在识别全血中的基因表达模式,以区分患有严重冠状动脉粥样硬化的患者与完全没有可检测到的冠状动脉疾病的受试者,并评估基因表达模式与冠状动脉CT血管造影(CCTA)中斑块特征的相关性。纳入因疑似冠状动脉疾病(CAD)而接受CCTA检查的患者。对冠状动脉狭窄进行定量分析,并评估CCTA斑块特征。采用RNA测序分析全血转录组。我们检测到CCTA中冠状动脉高度狭窄(≥70%)的患者与无冠状动脉斑块的受试者之间循环转录组存在高度显著差异。值得注意的是,回归分析揭示了与CCTA时的利曼评分、受累节段评分、节段狭窄评分以及密度<150 HU的斑块体积相关的表达特征。这项初步研究表明,冠状动脉严重狭窄的患者具有全血转录组特征,这可能使他们与无CAD的患者区分开来。此外,我们的结果表明全血转录谱可能预测斑块特征。