医学
疾病
重症监护医学
肾脏疾病
代谢综合征
糖尿病
内科学
药物治疗
人口
急性冠脉综合征
多发病率
阶段(地层学)
心脏病学
代谢控制分析
代谢性疾病
心力衰竭
风险评估
终末期肾病
病态的
心脏病
临床实习
队列
冠心病
炎症
血管疾病
复杂疾病
危险分层
失调家庭
药物开发
心脏再同步化治疗
生物信息学
作者
Sophie Gunnarsson,Ortensia Vito,Robert J. Unwin
出处
期刊:American Journal of Physiology-cell Physiology
[American Physical Society]
日期:2025-11-21
标识
DOI:10.1152/ajpcell.00499.2025
摘要
Cardiovascular-Kidney-Metabolic (CKM) syndrome affects approximately 90% of US adults, arising from the convergence of metabolic dysfunction, chronic kidney disease (CKD), and cardiovascular disease (CVD). These conditions create self-reinforcing cycles of multi-organ damage, substantially increasing mortality risk. The American Heart Association's 2023 staging framework stratifies CKM from Stage 0 (no risk factors) through Stage 4 (clinical CVD with persistent metabolic dysfunction), informing stage-specific interventions. This review synthesizes current evidence on CKM epidemiology, pathophysiology, and disease trajectories. Population-based studies reveal that Stage 2 (metabolic risk factors or early CKD) represents the most prevalent category, affecting nearly half of adults in Western cohorts. Progression occurs in 34% of Stage 1 individuals, with each stage transition conferring an incrementally higher cardiovascular mortality risk. We describe the biological cascade linking dysfunctional adiposity, insulin resistance, and endothelial dysfunction to renal and cardiac damage, emphasizing bidirectional organ crosstalk and the emerging role of hepatic pathology (MASLD/MASH) in CKM progression. Finally, we examine stage-specific interventions, from lifestyle modification and weight-loss pharmacotherapy (GLP-1 agonists, dual agonists) in early stages to multi-drug cardio-renal protection (SGLT2 inhibitors, RAAS blockade) in advanced disease. This framework allows targeted risk stratification and evidence-based management to interrupt CKM trajectories and improve population health outcomes.
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