Mury Pauline, Dagher Olina, Fortier Annik, Diaz Ariel, Lamarche Yoan, Noly Pierre-Emmanuel, Ibrahim Marina, Pagé Pierre, Demers Philippe, Bouchard Denis, Bernier Pierre-Luc, Poirier Nancy, Moss Emmanuel, Durrleman Nicolas, Jeanmart Hughes, Pellerin Michel, Lettre Guillaume, Thorin-Trescases Nathalie, Carrier Michel, Thorin Eric
Montreal Heart Institute, Research Center, Université de Montréal, Montréal, Québec, Canada.
Department of Pharmacology & Physiology, Faculty of Medicine, Université de Montréal, Montréal, Québec, Canada.
Aging Cell. 2025 Aug;24(8):e70108. doi: 10.1111/acel.70108. Epub 2025 May 15.
Recent studies suggest that vascular senescence and its associated inflammation fuel the inflammaging to favor atherogenesis; whether these pathways can be therapeutically targeted in coronary artery disease (CAD) patients remains unknown. In a randomized, double-blind trial, 97 patients (78 men) undergoing coronary artery bypass graft surgery were treated with either quercetin (500 mg twice daily, 47 patients) or placebo (50 patients) for two days pre-surgery through hospital discharge. Primary outcomes were reduced inflammation and improved endothelial function ex vivo. Exploratory analyses included plasma proteomics and single-nuclei RNA sequencing of internal thoracic artery (ITA) samples. Quercetin treatment showed a trend toward reduced C-reactive protein at discharge (p = 0.073) and differentially modulated circulating inflammatory protein expression between men and women, with a pro-inflammatory effect of quercetin in females. Endothelial acetylcholine-induced relaxation improved significantly with quercetin (p = 0.049), with effects in men (p = 0.043) but not in women (p = 0.852). ITA transcriptomics revealed the overexpression of senescence and inflammaging pathways in male vascular cells, which quercetin reversed. In female cells, quercetin had minimal endothelial benefit and increased inflammaging in fibroblasts. In male cells, a candidate target of quercetin involves interactions between the receptor PLAUR and its ligands PLAU and SERPINE1. Post-operative atrial fibrillation incidence was significantly lower with quercetin, representing 4% of the patients compared to 18% in the placebo group (p = 0.033). In conclusion, short-term quercetin treatment effectively targeted vascular senescence in male CAD patients, improving inflammatory and functional outcomes. However, these benefits were not observed in female patients. Trial Registration: https://clinicaltrials.gov, NCT04907253.
近期研究表明,血管衰老及其相关炎症推动了炎症衰老,促进动脉粥样硬化的发生;这些途径是否能成为冠状动脉疾病(CAD)患者的治疗靶点仍不清楚。在一项随机双盲试验中,97例接受冠状动脉搭桥手术的患者(78例男性)在术前两天至出院期间,分别接受槲皮素治疗(每日两次,每次500毫克,共47例患者)或安慰剂治疗(50例患者)。主要结局是体外炎症减轻和内皮功能改善。探索性分析包括血浆蛋白质组学和胸内动脉(ITA)样本的单核RNA测序。槲皮素治疗在出院时显示出C反应蛋白降低的趋势(p = 0.073),并且对男性和女性循环炎症蛋白表达的调节存在差异,槲皮素对女性有促炎作用。槲皮素使内皮乙酰胆碱诱导的舒张功能显著改善(p = 0.049),对男性有作用(p = 0.043),但对女性无作用(p = 0.852)。ITA转录组学显示男性血管细胞中衰老和炎症衰老途径的过表达,而槲皮素可使其逆转。在女性细胞中,槲皮素对内皮的益处极小,且会增加成纤维细胞中的炎症衰老。在男性细胞中,槲皮素的一个候选靶点涉及受体PLAUR与其配体PLAU和SERPINE1之间的相互作用。槲皮素治疗组术后房颤发生率显著更低,为4%,而安慰剂组为18%(p = 0.033)。总之,短期槲皮素治疗有效靶向男性CAD患者的血管衰老,改善炎症和功能结局。然而,在女性患者中未观察到这些益处。试验注册:https://clinicaltrials.gov,NCT04907253。