Cardiovascular-kidney-metabolic syndrome and all-cause and cardiovascular mortality: A retrospective cohort study
Min-Kuang Tsai1,2, Juliana Tze-Wah Kao1,2,3,4, Chung-Shun Wong5,6
1Division of Nephrology, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Insights
Cardiovascular-kidney-metabolic (CKM) syndrome prevalence is high, increasing mortality risks from all causes and cardiovascular disease (CVD). Integrated CKM care is crucial for prevention and treatment.
Area of Science:
- Cardiology
- Nephrology
- Metabolic Health
Background:
- The American Heart Association introduced Cardiovascular-Kidney-Metabolic (CKM) syndrome to promote multidisciplinary care.
- This study investigates CKM syndrome prevalence and mortality risks in an Asian population.
Purpose of the Study:
- To assess the prevalence of CKM syndrome stages.
- To evaluate the mortality risks associated with CKM syndrome and its components (hypertension, diabetes, CKD, metabolic syndrome, hyperlipidemia).
Main Methods:
- Retrospective cohort analysis of 515,602 Taiwanese adults screened between 1996-2017.
- Follow-up for a median of 16.5 years, assessing all-cause, CVD, and cause-specific mortality.
- Multivariate Cox proportional hazards models and life table methods were used.
Main Results:
- 71.5% of participants met CKM syndrome criteria; stages 1-4 prevalence was 19.5%, 46.3%, 1.9%, 3.8%.
- CKM syndrome significantly increased risks for all-cause mortality (HR: 1.33), CVD mortality (HR: 2.81), and end-stage kidney disease (ESKD) (HR: 10.15).
- Each additional CKM component raised all-cause mortality risk by 22% and CVD mortality risk by 37%, reducing life expectancy by 3 years.
Conclusions:
- CKM syndrome and its components are prevalent and significantly associated with increased mortality and ESKD risk.
- Findings underscore the clinical necessity for integrated care approaches in CKM health.
- Failure to include CKD in CKM assessment may lead to underestimation of CVD mortality risks.
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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