Center for Interdisciplinary Cardiovascular Sciences, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Center for Excellence in Vascular Biology, Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Nat Rev Cardiol. 2019 May;16(5):261-274. doi: 10.1038/s41569-018-0123-8.
Cardiovascular calcification is a health disorder with increasing prevalence and high morbidity and mortality. The only available therapeutic options for calcific vascular and valvular heart disease are invasive transcatheter procedures or surgeries that do not fully address the wide spectrum of these conditions; therefore, an urgent need exists for medical options. Cardiovascular calcification is an active process, which provides a potential opportunity for effective therapeutic targeting. Numerous biological processes are involved in calcific disease, including matrix remodelling, transcriptional regulation, mitochondrial dysfunction, oxidative stress, calcium and phosphate signalling, endoplasmic reticulum stress, lipid and mineral metabolism, autophagy, inflammation, apoptosis, loss of mineralization inhibition, impaired mineral resorption, cellular senescence and extracellular vesicles that act as precursors of microcalcification. Advances in molecular imaging and big data technology, including in multiomics and network medicine, and the integration of these approaches are helping to provide a more comprehensive map of human disease. In this Review, we discuss ectopic calcification processes in the cardiovascular system, with an emphasis on emerging mechanistic knowledge obtained through patient data and advances in imaging methods, experimental models and multiomics-generated big data. We also highlight the potential and challenges of artificial intelligence, machine learning and deep learning to integrate imaging and mechanistic data for drug discovery.
心血管钙化是一种患病率不断增加、发病率和死亡率均较高的健康紊乱。治疗血管钙化和心脏瓣膜病的唯一可用方法是有创的经导管程序或手术,但这些方法并不能完全解决这些疾病的广泛谱;因此,迫切需要有医疗选择。心血管钙化是一个活跃的过程,为有效的治疗靶向提供了潜在的机会。许多生物过程参与了钙化疾病,包括基质重塑、转录调控、线粒体功能障碍、氧化应激、钙和磷酸盐信号、内质网应激、脂质和矿物质代谢、自噬、炎症、细胞凋亡、矿化抑制丧失、矿物质吸收减少、细胞衰老和细胞外囊泡,这些都可作为微钙化的前体。分子成像和大数据技术的进步,包括多组学和网络医学,以及这些方法的整合,正在帮助提供更全面的人类疾病图谱。在这篇综述中,我们讨论了心血管系统中的异位钙化过程,重点介绍了通过患者数据和成像方法、实验模型和多组学生成的大数据方面的进展而获得的新兴机制知识。我们还强调了人工智能、机器学习和深度学习在整合成像和机制数据以进行药物发现方面的潜力和挑战。
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