Chen Yongming, Wu Xiaoying, Long Tianxin, Jiang Yuxiao, Wang Miao, Lv Zhengtong, Hou Huimin, Li Ziang, Liu Ming
Beijing Hospital, National Center of Gerontology Institute of Geriatric Medicine, Chinese Academy of Medical Sciences & Peking Union Medical College, Peking University Fifth School of Clinical Medicine, Beijing, China.
State Key Laboratory of Cardiovascular Disease, Department of Cardiology, Fuwai Hospital, National Center for Cardiovascular Disease, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
JACC Adv. 2025 Jun;4(6 Pt 2):101843. doi: 10.1016/j.jacadv.2025.101843.
The cardiovascular-kidney-metabolic (CKM) syndrome, introduced by the American Heart Association, underscores the interplay among metabolic, renal, and cardiovascular dysfunctions.
This study aimed to evaluate the prevalence and mortality risk across CKM syndrome stages in the UK population.
This prospective cohort study included 110,933 participants from the UK Biobank. The primary outcome was all-cause mortality, with cardiovascular disease (CVD)-specific mortality as a secondary outcome. Kaplan-Meier and Cox proportional hazards models were used to estimate survival and mortality risks.
Among the 110,933 participants, 9.16% were classified as CKM stage 0, 13.53% as stage 1, 44.15% as stage 2, 26.25% as stage 3, and 6.91% as stage 4. Over a median follow-up of 14.7 years, 13,012 all-cause deaths and 1,613 CVD-specific deaths were recorded. All-cause mortality rates increased progressively across CKM stages: 6.32% (stage 0), 7.47% (stage 1), 10.12% (stage 2), 13.67% (stage 3), and 30.09% (stage 4). Similarly, CVD-specific mortality rates increased from 0.43% to 5.43%. Compared to stage 0, the adjusted HRs for all-cause mortality were 1.14 for stage 2, 1.25 for stage 3, and 2.13 for stage 4. For CVD-specific mortality, the adjusted HRs were 1.48 for stage 2, 1.99 for stage 3, and 3.46 for stage 4.
Nearly 80% of individuals were classified into poor CKM stages (stages 2-4), which were strongly associated with significantly elevated risks of both all-cause and CVD-specific mortality. These findings emphasize the urgent need for early detection and targeted interventions in high-risk cardiometabolic populations.
美国心脏协会提出的心血管-肾脏-代谢(CKM)综合征强调了代谢、肾脏和心血管功能障碍之间的相互作用。
本研究旨在评估英国人群中CKM综合征各阶段的患病率和死亡风险。
这项前瞻性队列研究纳入了英国生物银行的110933名参与者。主要结局是全因死亡率,心血管疾病(CVD)特异性死亡率作为次要结局。采用Kaplan-Meier和Cox比例风险模型来估计生存和死亡风险。
在110933名参与者中,9.16%被分类为CKM 0期,13.53%为1期,44.15%为2期,26.25%为3期,6.91%为4期。在中位随访14.7年期间,记录了13012例全因死亡和1613例CVD特异性死亡。全因死亡率在CKM各阶段逐渐升高:6.32%(0期)、7.47%(1期)、10.12%(2期)、13.67%(3期)和30.09%(4期)。同样,CVD特异性死亡率从0.43%升至5.43%。与0期相比,2期全因死亡的调整后风险比为1.14,3期为1.25,4期为2.13。对于CVD特异性死亡,2期调整后风险比为1.48,3期为1.99,4期为3.46。
近80%的个体被分类为CKM不良阶段(2-4期),这些阶段与全因死亡和CVD特异性死亡风险显著升高密切相关。这些发现强调了对高危心脏代谢人群进行早期检测和针对性干预的迫切需求。