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Cardiovascular Disease in CKD: Ethnic and Regional Differences in Risk and Phenotype
Jwa-Kyung Kim1, Yong-Joon Lee2, Jung-Sun Kim2
1Division of Nephrology, Department of Internal Medicine, Hallym University Sacred Heart Hospital, Anyang-si, South Korea.
Insights
Cardiovascular disease (CVD) in chronic kidney disease (CKD) varies globally. Focusing on phenotypes and exposures, not race, can improve cardiovascular risk assessment and prevention for diverse CKD populations worldwide.
Area of Science:
- Nephrology
- Cardiology
- Epidemiology
Background:
- Cardiovascular disease (CVD) is the primary cause of death in chronic kidney disease (CKD) patients.
- Global variations in CVD burden and outcomes exist among CKD populations.
- Differences attributed to race may reflect underlying cardiometabolic risk, inflammation, environment, and healthcare access.
Purpose of the Study:
- To review global patterns of cardiovascular burden and outcomes in CKD.
- To compare cardiorenal phenotypes across major international CKD cohorts.
- To advocate for phenotype- and exposure-informed cardiovascular risk assessment in CKD.
Main Methods:
- Synthesis of evidence from major international CKD cohorts (CRIC, GCKD, CRISIS, EQUAL, CKD-JAC, C-STRIDE, KNOW-CKD).
- Examination of cardiovascular burden, phenotypes, and clinical outcomes.
- Comparison of findings between North American/European and East Asian cohorts.
Main Results:
- North American/European CKD cohorts exhibit higher inflammatory burden, coronary artery calcification, and left ventricular hypertrophy, leading to a CVD-dominant trajectory.
- East Asian CKD cohorts show fewer atherosclerotic and cardiac structural issues, with a kidney-dominant trajectory.
- Significant global variations in cardiorenal phenotypes are observed.
Conclusions:
- Cardiorenal phenotypes in CKD differ substantially across global populations.
- Moving beyond race-based descriptions to phenotype- and exposure-informed approaches is crucial.
- Integrating imaging, inflammatory biomarkers, and cardiometabolic profiles can enhance precision and equity in CKD cardiovascular prevention.
Abstract:
Cardiovascular disease (CVD) is the leading cause of morbidity and mortality in patients with CKD. Although the association between CKD and CVD is well established, the overall CVD burden, dominant cardiovascular phenotypes, and clinical outcomes vary substantially across populations. These differences are often described using racial or ethnic categories, yet emerging evidence suggests that they more closely reflect variation in cardiometabolic risk, inflammatory burden, environmental exposures, and health care access than race itself. This review synthesizes evidence from major CKD cohorts, including Chronic Renal Insufficiency Cohort (United States), German CKD, Chronic Renal Insufficiency Standards Implementation Study, and European Quality Study (Europe) and CKD Japan Cohort (Japan), Chinese Cohort Study of CKD (China), and KoreaN Cohort Study for Outcomes in Patients With CKD (Korea), to examine global patterns of cardiovascular burden and outcomes in CKD. North American and European CKD cohorts are characterized by greater inflammatory burden, more severe coronary artery calcification, and more pronounced left ventricular hypertrophy, corresponding to a clinical trajectory more heavily dominated by cardiovascular events and mortality. By contrast, East Asian cohorts show fewer overt atherosclerotic and cardiac structural abnormalities and a more kidney-dominant trajectory, in which kidney outcomes are more prominent relative to cardiovascular events. Genetic, environmental, and lifestyle-related modifiers likely contribute to these divergent cardiorenal phenotypes. Collectively, current evidence supports moving beyond race-based descriptions toward phenotype-informed and exposure-informed approaches to cardiovascular risk assessment in CKD, in which integration of imaging markers, inflammatory biomarkers, and cardiometabolic profiles may improve the precision and equity of cardiovascular prevention strategies across diverse CKD populations.
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