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Published on: September 1, 2015
Cystatin C Is Associated with the Extent and Characteristics of Coronary Atherosclerosis in Patients with Preserved
A Král1, T Kovárník1, Z Vaníčková2
12nd Department of Medicine - Department of Cardiovascular Medicine, First Faculty of Medicine, Charles University and General University Hospital in Prague, Czech Republic.
Insights
Elevated Cystatin C (CysC) levels in patients with normal kidney function are linked to more severe coronary artery disease and a higher risk plaque phenotype, indicating increased cardiovascular risk.
Area of Science:
- Cardiology
- Biomarkers
- Vascular Biology
Background:
- Cystatin C (CysC) is a cysteine protease inhibitor and a renal function marker.
- Previous studies suggest CysC is associated with coronary atherosclerosis severity and cardiovascular events.
Purpose of the Study:
- To investigate the relationship between CysC levels and coronary plaque characteristics in patients with preserved renal function.
- To assess plaque volume, composition, and phenotype using intravascular ultrasound and virtual histology.
Main Methods:
- Forty-four patients with coronary artery disease and complete intravascular imaging were analyzed.
- Patients were stratified into tertiles based on CysC levels.
- Intravascular ultrasound and virtual histology were used to assess coronary plaque.
Main Results:
- Higher CysC tertiles showed significantly increased mean plaque burden and a higher number of segments with minimal lumen area < 4 mm2.
- CysC levels positively correlated with mean plaque burden.
- The Liverpool Active Plaque Score was significantly higher in the high CysC tertile.
Conclusions:
- Increased CysC levels are associated with more advanced coronary artery disease in patients with preserved renal function.
- Higher CysC is linked to a higher-risk plaque phenotype, suggesting potential prognostic value.
Abstract:
Cystatin C (CysC), an endogenous inhibitor of cysteine proteases and a sensitive and accurate marker of renal function, is associated with the severity of coronary atherosclerosis assessed by angiography and future cardiovascular events according to previous studies. We aimed to evaluate the association between CysC levels and coronary plaque volume, composition and phenotype assessed by intravascular ultrasound and intravascular ultrasound-derived virtual histology in patients with preserved renal function. Forty-four patients with angiographically documented coronary artery disease and complete intravascular imaging were included in the study. Patients were categorized into tertiles by CysC levels. Subjects in the high CysC tertile had significantly higher mean plaque burden (48.0 % ± 6.9 vs. 42.8 % ± 7.4, P = 0.029), lower mean lumen area (8.1 mm2 ± 1.7 vs. 9.9 mm2 ± 3.1, P = 0.044) and a higher number of 5-mm vessel segments with minimum lumen area < 4 mm2 (17.9 ± 18.9 vs. 6.8 ± 11.7, P = 0.021) compared to patients in the lower tertiles. In addition, CysC levels demonstrated significant positive correlation with the mean plaque burden (r = 0.35, P = 0.021). Neither relative, nor absolute plaque components differed significantly according to CysC tertiles. The Liverpool Active Plaque Score was significantly higher in the high CysC tertile patients (0.91 ± 1.0 vs. 0.18 ± 0.92, P = 0.02). In conclusion, our study demonstrated a significant association of increased CysC levels with more advanced coronary artery disease and higher risk plaque phenotype in patients with preserved renal function.
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