Department of Nephrology, Dialysis and Transplant, San Bortolo Hospital, Vicenza, Italy,
IRRIV-International Renal Research Institute, Vicenza, Italy,
Cardiorenal Med. 2019;9(4):201-211. doi: 10.1159/000497748. Epub 2019 Apr 2.
Cardiorenal syndromes (CRS) include a scenario of clinical interactions characterized by the heart and kidney dysfunction. The crosstalk between cardiac and renal systems is clearly evidenced but not completely understood. Multi-factorial mechanisms leading to CRS do not involve only hemodynamic parameters. In fact, in recent works on organ crosstalk endothelial injury, the alteration of normal immunologic balance, cell death, inflammatory cascades, cell adhesion molecules, cytokine and chemokine overexpression, neutrophil migration, leukocyte trafficking, caspase-mediated induction of apoptotic mechanisms and oxidative stress has been demonstrated to induce distant organ dysfunction. Furthermore, new alternative mechanisms using the multi-omics approach may be implicated in the pathogenesis of cardiorenal crosstalk. The study of "omics" modifications in the setting of cardiovascular and renal disease represents an emerging area of research. Over the last years, indeed, many studies have elucidated the exact mechanisms involved in gene expression and regulation, cellular communication and organ crosstalk. In this review, we analyze epigenetics, gene expression, small non-coding RNAs, extracellular vesicles, proteomics, and metabolomics in the setting of CRS.
心肾综合征(CRS)包括一种以心脏和肾脏功能障碍为特征的临床相互作用情况。心脏和肾脏系统之间的相互作用是明确的,但尚未完全理解。导致 CRS 的多因素机制不仅涉及血流动力学参数。事实上,在最近关于器官相互作用内皮损伤的研究中,已经证明正常免疫平衡、细胞死亡、炎症级联、细胞黏附分子、细胞因子和趋化因子过度表达、中性粒细胞迁移、白细胞迁移、半胱天冬酶介导的诱导细胞凋亡机制和氧化应激的改变会导致远处器官功能障碍。此外,使用多组学方法的新替代机制可能与心肾相互作用的发病机制有关。在心血管和肾脏疾病背景下研究“组学”修饰是一个新兴的研究领域。事实上,在过去的几年中,许多研究已经阐明了涉及基因表达和调控、细胞通讯和器官相互作用的确切机制。在这篇综述中,我们分析了 CRS 背景下的表观遗传学、基因表达、小非编码 RNA、细胞外囊泡、蛋白质组学和代谢组学。