炎症
调解人
机制(生物学)
疾病
纤维化
生物信息学
病态的
肾脏疾病
自噬
医学
生物
信号转导
神经科学
炎症介质
免疫学
系统生物学
病理生理学
促炎细胞因子
计算生物学
氧化应激
发病机制
细胞信号
小RNA
评论文章
细胞因子
复杂疾病
转化研究
心力衰竭
作者
Zhen Xu,Shuo Yang,Yuan Tan,Qian Zhang,He Wang,Jingjin Tao,Qi Liu,Qingchen Wang,Weimin Feng,Zhongxin Li,Chong Wang,Liyan Cui
标识
DOI:10.1007/s11010-025-05379-9
摘要
Cardiovascular-Kidney-Metabolic (CKM) syndrome, a newly defined systemic disorder, is characterized by the pathological interplay among diabetes, chronic kidney disease (CKD), and cardiovascular disease (CVD). Recent studies have identified chronic inflammation not only as a central mediator in the pathological progression of CKM syndrome but also as a pivotal molecular hub that drives coordinated damage across multiple organ systems. Mechanistic investigations have revealed that aberrant activation of signaling pathways such as NF-κB, Wnt, PI3K-AKT, JAK-STAT, and PPAR constitutes a complex inflammatory regulatory network. Notably, these pathways facilitate inter-organ inflammatory crosstalk, establishing positive feedback loops among the heart, kidneys, and metabolic tissues. This, in turn, amplifies pathological processes such as oxidative stress, endothelial dysfunction, and fibrosis in a cascading manner.This review systematically delineates the multidimensional pathophysiological mechanisms of CKM syndrome, with particular emphasis on the inter-organ inflammatory regulation mediated by key signaling pathways. Furthermore, we explore the translational potential of therapeutic strategies targeting inflammatory cytokines (e.g., IL-1β, IL-6, and TNF-α) based on the latest clinical evidence, aiming to provide a theoretical framework and novel perspectives for disrupting the vicious cycle of CKM syndrome.
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