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Published on: June 16, 2014
Association between the difference in cystatin C and creatinine-based eGFR and risks of multiple cardiovascular
Zhiyu Qiao1, Xinyi Liu1, Hao Liu1
1Department of Cardiovascular Surgery, Beijing Aortic Disease Center, Beijing Anzhen Hospital of Capital Medical University, Beijing, China.
Background:
The difference between cystatin C- and creatinine-based estimated glomerular filtration rate (eGFRdiff) is closely associated with various adverse outcomes. This study aims to comprehensively evaluate the association between eGFRdiff, all-cause mortality, and the risk of multiple cardiovascular-related diseases.
Methods:
This study analyzed data from 297,140 participants in the UK Biobank to assess the association between eGFRdiff, mortality, and the incidence of multiple cardiovascular-related diseases. eGFRdiff was classified into three groups: negative (< -15 mL/min/1.73 m2), intermediate (-15 to 15 mL/min/1.73 m2), and positive (≥ 15 mL/min/1.73 m2). Cox proportional hazards regression models were used to evaluate this association, while various sensitivity analyses were performed to assess its robustness.
Results:
During a mean follow-up of 13.1 years, the positive eGFRdiff group exhibited significantly lower mortality, cardiovascular disease (CVD) incidence, and the occurrence of CVD-related conditions. In the fully adjusted model, participants in the negative eGFRdiff group had a hazard ratio of 1.44 (95% confidence interval [CI], 1.40-1.49) for all-cause mortality, 1.49 (95% CI, 1.41-1.59) for CVD incidence, and 1.25 (95% CI, 1.22-1.27) for CVD mortality. The risk of all 10 CVD-related conditions was also significantly higher in the negative group, whereas the positive group exhibited significantly lower risks. For every 10 mL/min/1.73 m2 increase in eGFRdiff, the incidence of various diseases decreased by approximately 10-19%.
Conclusion:
eGFRdiff is significantly associated with increased risks of mortality, CVD incidence, and multiple CVD-related conditions. These findings underscore the critical need for developing targeted prevention strategies, particularly for populations with reduced eGFRdiff.
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