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心血管-肾脏-代谢综合征中的炎症:关键作用及潜在机制——综述

Inflammation in cardiovascular-kidney-metabolic syndrome: key roles and underlying mechanisms-a comprehensive review.

作者信息

Xu Zhen, Yang Shuo, Tan Yuan, Zhang Qian, Wang He, Tao Jingjin, Liu Qi, Wang Qingchen, Feng Weimin, Li Zhongxin, Wang Chong, Cui Liyan

机构信息

Peking University Third Hospital, Beijing, China.

出版信息

Mol Cell Biochem. 2025 Sep 10. doi: 10.1007/s11010-025-05379-9.

Abstract

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.

摘要

心血管-肾脏-代谢(CKM)综合征是一种新定义的全身性疾病,其特征是糖尿病、慢性肾脏病(CKD)和心血管疾病(CVD)之间存在病理相互作用。最近的研究表明,慢性炎症不仅是CKM综合征病理进展的核心介质,也是驱动多个器官系统协同损伤的关键分子枢纽。机制研究表明,诸如核因子κB(NF-κB)、Wnt、磷脂酰肌醇-3激酶-蛋白激酶B(PI3K-AKT)、Janus激酶-信号转导和转录激活因子(JAK-STAT)以及过氧化物酶体增殖物激活受体(PPAR)等信号通路的异常激活构成了一个复杂的炎症调节网络。值得注意的是,这些信号通路促进器官间的炎症串扰,在心脏、肾脏和代谢组织之间建立正反馈回路。这反过来又以级联方式放大氧化应激、内皮功能障碍和纤维化等病理过程。本综述系统地阐述了CKM综合征的多维病理生理机制,特别强调了关键信号通路介导的器官间炎症调节。此外,我们根据最新临床证据探讨了针对炎性细胞因子(如白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α)的治疗策略的转化潜力,旨在为打破CKM综合征的恶性循环提供理论框架和新的视角。

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