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Updated: Feb 19, 2026

Calcification of Vascular Smooth Muscle Cells and Imaging of Aortic Calcification and Inflammation
Published on: May 31, 2016
Correlation between complement C3 level and abdominal aortic calcification in non-dialysis chronic kidney disease
Chenfei Fu1, Wen Li1, Weijia Xu2
1Department of Nephrology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Insights
Serum complement C3 is linked to vascular calcification in non-dialysis-dependent chronic kidney disease patients. Higher C3 levels correlate with increased calcification risk, highlighting C3 as a potential biomarker for cardiovascular disease progression.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Immunology
Background:
- Previous research links complement activation to cardiovascular disease in dialysis patients.
- This study focuses on non-dialysis-dependent chronic kidney disease (NDD-CKD) patients.
- Investigates the specific role of complement C3 in vascular calcification (VC) within this population.
Purpose of the Study:
- To examine the association between serum complement C3 levels and vascular calcification (VC).
- To identify potential biomarkers for cardiovascular risk in NDD-CKD patients.
- To explore the relationship between C3 and VC in a cohort of NDD-CKD patients.
Main Methods:
- Enrolled 456 NDD-CKD patients between 2019-2022.
- Measured serum C3 using immunoscattering turbidimetry and assessed VC via CT imaging.
- Employed restricted cubic spline (RCS) and logistic regression for association analysis, with ROC analysis for prediction assessment.
Main Results:
- The highest tertile of C3 (0.95-1.63 g/L) showed a significant correlation with VC (OR=2.06, p=0.020).
- Older age, hypertension, and hyperlipidemia were identified as independent risk factors for VC.
- C3 demonstrated good predictive value for VC with an AUC of 0.849 (sensitivity 79.4%, specificity 76.7%).
Conclusions:
- Serum C3 exhibits a J-shaped, non-linear relationship with vascular calcification in NDD-CKD patients.
- Confirms older age, hypertension, and hyperlipidemia as independent risk factors for VC.
- Suggests C3 may serve as a valuable biomarker for predicting VC in NDD-CKD.
Background:
Previous studies have shown that complement activation is associated with an increased risk of cardiovascular disease in patients with chronic kidney disease (CKD) on dialysis. This study aims to investigate the relationship between complement 3 (C3) and vascular calcification (VC) in non-dialysis-dependent CKD (NDD-CKD) patients.
Methods:
Four hundred and fifty six NDD-CKD patients were enrolled from 2019 to 2022. C3 was measured by immunoscattering turbidimetry. According to the results of CT imaging, the patients were divided into the aorta vascular calcification group and the non-aortic vascular calcification group. Restricted cubic spline (RCS) analysis and logistic regression model were used to explore the association between C3 and VC in NDD-CKD patients. To assess how it predicted, a receiver operating characteristic (ROC) analysis was undertaken.
Results:
In NDD-CKD patients, the third tertile of C3 (0.95-1.63 g/L) was significantly correlated with VC (OR = 2.06, 95% CI: 1.13-3.83, p = 0.020). Older age and history of underlying diseases (hypertension, hyperlipidemia) are independent risk factors for VC in NDD-CKD patients. The area under the curve (AUC) of C3 for predicting VC was 0.849 g/L (sensitivity, 79.4%; specificity, 76.7%).
Conclusion:
In patients with NDD-CKD, serum complement C3 exhibits a J-shaped relationship with vascular calcification, indicating a complex, non-linear association. Additionally, older age, hypertension, and hyperlipidemia were confirmed as independent risk factors.
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