Roh Jason D, Kitchen Robert R, Guseh J Sawalla, McNeill Jenna N, Aid Malika, Martinot Amanda J, Yu Andy, Platt Colin, Rhee James, Weber Brittany, Trager Lena E, Hastings Margaret H, Ducat Sarah, Xia Peng, Castro Claire, Singh Abhilasha, Atlason Bjarni, Churchill Timothy W, Di Carli Marcelo F, Ellinor Patrick T, Barouch Dan H, Ho Jennifer E, Rosenzweig Anthony
Corrigan Minehan Heart Center, Division of Cardiology, Cardiovascular Research Center, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Division of Pulmonary and Critical Care, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
JACC Basic Transl Sci. 2022 May;7(5):425-441. doi: 10.1016/j.jacbts.2022.01.013. Epub 2022 May 4.
To gain insights into the mechanisms driving cardiovascular complications in COVID-19, we performed a case-control plasma proteomics study in COVID-19 patients. Our results identify the senescence-associated secretory phenotype, a marker of biological aging, as the dominant process associated with disease severity and cardiac involvement. FSTL3, an indicator of senescence-promoting Activin/TGFβ signaling, and ADAMTS13, the von Willebrand Factor-cleaving protease whose loss-of-function causes microvascular thrombosis, were among the proteins most strongly associated with myocardial stress and injury. Findings were validated in a larger COVID-19 patient cohort and the hamster COVID-19 model, providing new insights into the pathophysiology of COVID-19 cardiovascular complications with therapeutic implications.
为深入了解新冠病毒疾病(COVID-19)引发心血管并发症的机制,我们对COVID-19患者进行了一项病例对照血浆蛋白质组学研究。我们的研究结果表明,衰老相关分泌表型(一种生物衰老的标志物)是与疾病严重程度和心脏受累相关的主要过程。FSTL3是促进衰老的激活素/转化生长因子β信号的指标,而ADAMTS13是一种切割血管性血友病因子的蛋白酶,其功能丧失会导致微血管血栓形成,它们是与心肌应激和损伤最密切相关的蛋白质。这些发现已在更大规模的COVID-19患者队列和仓鼠COVID-19模型中得到验证,为COVID-19心血管并发症的病理生理学提供了新的见解,并具有治疗意义。