心血管-肾代谢综合征与全因死亡率和心血管死亡率:一项回顾性队列研究。

IF 15.8 1区 医学 Q1 Medicine
PLoS Medicine Pub Date : 2025-06-26 eCollection Date: 2025-06-01 DOI:10.1371/journal.pmed.1004629
Min-Kuang Tsai, Juliana Tze-Wah Kao, Chung-Shun Wong, Chia-Te Liao, Wei-Cheng Lo, Kuo-Liong Chien, Chi-Pang Wen, Mai-Szu Wu, Mei-Yi Wu
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引用次数: 0

摘要

背景:美国心脏协会最近发布了指南,介绍了心血管-肾脏代谢综合征(CKM)的概念,以强调多学科方法预防、风险分层和治疗这些疾病的重要性。本研究在一个大型亚洲队列中评估了CKM综合征分期的患病率及其组成部分的死亡风险。方法和研究结果:我们分析了1996年至2017年在台湾进行的健康筛查项目中年龄≥20岁的515,602名参与者的回顾性队列。我们评估了全因死亡率、心血管疾病(CVD)死亡率和病因特异性死亡率与CKM分期及其组成部分(高血压、糖尿病、慢性肾病(CKD)、代谢综合征和高脂血症)的关系。所有参与者的随访时间中位数为16.5年(四分位数间距:11.5年,21.2年)。采用多变量Cox比例风险模型,对年龄、性别、教育水平、吸烟状况、饮酒状况和体力活动组进行校正,计算风险比(hr)。我们使用蒋的生命表方法来估计由于每个CKM成分而损失的寿命年数。在所有参与者中,女性为257,535人(49.9%)。大多数参与者(n = 368,578名参与者,(71.5%))符合CKM综合征的标准,第1、2、3和4期的患病率分别为19.5%、46.3%、1.9%和3.8%。CKM综合征与较高的全因死亡率相关(HR: 1.33;95%可信区间(CI: 1.28, 1.39),心血管疾病死亡率(HR: 2.81;95% CI: 2.45, 3.22)和终末期肾病(ESKD)的发生率(HR: 10.15;95% ci: 7.54, 13.67)。每增加一个CKM成分,全因死亡风险增加22% (HR: 1.22;95% CI: 1.21, 1.23),心血管疾病死亡风险增加37% (HR: 1.37;95% CI: 1.35, 1.40)。此外,每增加一个部件,平均预期寿命就会减少3年。CKM综合征的人群归因部分在全因死亡率中为18.7% (95% CI: 15.8, 21.7),在CVD死亡率中为55.0% (95% CI: 49.0, 60.4)。我们估计,未将CKD纳入CKM综合征可能导致11%的CVD死亡的遗漏归因。主要的限制是我们的分析只依赖于基线测量,没有考虑纵向变化。结论:在这项大型队列研究中,CKM综合征及其组成部分的患病率与全因死亡率、CVD死亡率和ESKD的风险相关。这些发现强调了在慢性慢性疾病健康中进行综合护理的临床需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cardiovascular-kidney-metabolic syndrome and all-cause and cardiovascular mortality: A retrospective cohort study.

Background: The American Heart Association recently issued guidelines introducing the concept of cardiovascular-kidney-metabolic (CKM) syndrome to emphasize the importance of multidisciplinary approaches to prevention, risk stratification, and treatment for these diseases. This study assessed the prevalence of CKM syndrome stages and the mortality risk associated with its components in a large Asian cohort.

Methods and findings: We analyzed a retrospective cohort of 515,602 participants aged ≥20 years from a health screening program conducted between 1996 and 2017 in Taiwan. We assessed the associations of all-cause mortality, cardiovascular disease (CVD) mortality, and cause-specific mortality with CKM stages and its components-hypertension, diabetes mellitus, chronic kidney disease (CKD), metabolic syndrome, and hyperlipidemia. All participants were followed for a median of 16.5 years (interquartile range: 11.5, 21.2 years). Multivariate Cox proportional hazards models, adjusted for age, sex, educational level, smoking status, alcohol drinking status, and physical activity groups, were used to calculate hazard ratios (HRs). We used Chiang's life table method to estimate years of life lost due to each CKM component. Among all participants, 257,535 (49.9%) were female. The majority of participants (n = 368,578 participants, (71.5%)) met criteria for CKM syndrome, with prevalence rates of 19.5%, 46.3%, 1.9%, and 3.8% for stages 1, 2, 3, and 4, respectively. CKM syndrome was associated with higher risks of all-cause mortality (HR: 1.33; 95% confidence interval, CI: 1.28, 1.39), CVD mortality (HR: 2.81; 95% CI: 2.45, 3.22), and incident end-stage kidney disease (ESKD) (HR: 10.15; 95% CI: 7.54, 13.67). Each additional CKM component was associated with a 22% increase in the risk of all-cause mortality (HR: 1.22; 95% CI: 1.21, 1.23), a 37% increase in the risk of CVD mortality (HR: 1.37; 95% CI: 1.35, 1.40) compared with those without any CKM components. In addition, each additional component reduced average life expectancy by 3 years. The population-attributable fractions of CKM syndrome were 18.7% (95% CI: 15.8, 21.7) for all-cause mortality and 55.0% (95% CI: 49.0, 60.4) for CVD mortality. We estimated that failing to include CKD in CKM syndrome could result in the missed attribution of 11% of CVD deaths. The primary limitation is that our analysis relied on baseline measurements only, without accounting for longitudinal changes.

Conclusions: In the large cohort study, the prevalence of CKM syndrome and its components were associated with risks of all-cause mortality, CVD mortality, and ESKD. These findings highlight the clinical need for integrated care within CKM health.

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来源期刊
PLoS Medicine
PLoS Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
17.60
自引率
0.60%
发文量
227
审稿时长
4-8 weeks
期刊介绍: PLOS Medicine is a prominent platform for discussing and researching global health challenges. The journal covers a wide range of topics, including biomedical, environmental, social, and political factors affecting health. It prioritizes articles that contribute to clinical practice, health policy, or a better understanding of pathophysiology, ultimately aiming to improve health outcomes across different settings. The journal is unwavering in its commitment to uphold the highest ethical standards in medical publishing. This includes actively managing and disclosing any conflicts of interest related to reporting, reviewing, and publishing. PLOS Medicine promotes transparency in the entire review and publication process. The journal also encourages data sharing and encourages the reuse of published work. Additionally, authors retain copyright for their work, and the publication is made accessible through Open Access with no restrictions on availability and dissemination. PLOS Medicine takes measures to avoid conflicts of interest associated with advertising drugs and medical devices or engaging in the exclusive sale of reprints.
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