炎症
串扰
调解人
代谢综合征
疾病
纤维化
生物信息学
PI3K/AKT/mTOR通路
病态的
肾脏疾病
肾
医学
生物
信号转导
糖尿病
神经科学
免疫学
病理
内科学
细胞生物学
内分泌学
光学
物理
作者
Zhen Xu,Shuo Yang,Yuan Tan,Qian Zhang,He Wang,J. C. 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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