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Updated: Oct 17, 2025

A Semi-Automated and Reproducible Biological-Based Method to Quantify Calcium Deposition In Vitro
Published on: June 2, 2022
Low bone turnover is associated with plain X-ray vascular calcification in predialysis patients
Ricardo Neto1,2,3, Luciano Pereira1,2,3, Juliana Magalhães1
1Institute for Innovation and Health Research (I3S), Institute of Biomedical Engineering (INEB), Nephrology and Infectious Diseases Research Group, University of Porto, Porto, Portugal.
Insights
Vascular calcification is common in chronic kidney disease (CKD) patients before dialysis. Low bone formation rate is linked to vascular calcification, suggesting it
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Bone Biology
Background:
- Vascular calcification (VC) is prevalent in chronic kidney disease (CKD), predicting cardiovascular events.
- VC is associated with mineral metabolism disorders and bone changes in CKD.
- Limited data exists on VC in predialysis CKD patients.
Purpose of the Study:
- To investigate the prevalence and risk factors of vascular calcification in predialysis CKD patients.
- To examine the relationship between vascular calcification and bone histomorphometry in this population.
Main Methods:
- Cross-sectional study of 56 predialysis CKD patients.
- Transiliac bone biopsy with histomorphometric evaluation.
- Vascular calcification assessed using Kauppila and Adragão scores.
Main Results:
- Vascular calcification detected in two-thirds of patients.
- VC patients were more likely male, diabetic, with higher sclerostin and osteoprotegerin levels.
- Lower bone formation rate observed in patients with VC, independently associated with VC presence.
Conclusions:
- Vascular calcification is highly prevalent in predialysis CKD, particularly in diabetics.
- An independent association exists between low bone formation rate and VC.
- Low bone turnover may be a non-traditional cardiovascular risk factor in predialysis CKD.
Background:
Vascular calcification (VC) is a common finding in chronic kidney disease (CKD) patients and predicts subsequent cardiovascular morbidity and mortality in this population. Vascular calcification is linked to disordered mineral metabolism and has been associated with bone histomorphometry changes in CKD. However, data on predialysis patients is scarce.
Methods:
A cross-sectional study was conducted on a cohort of 56 CKD patients not yet on dialysis, who underwent a transiliac bone biopsy for histomorphometric evaluation after double tetracycline labeling. Patients had no previous exposure to calcium salts, vitamin D agents, steroids or bisphosphonates. Vascular calcification was assessed at the time of biopsy, using Kauppila (plain X-ray of the lateral lumbar spine) and Adragão (plain X-ray of the pelvis and hands) scores.
Results:
Vascular calcification was seen in two-thirds of the cohort. Subjects with VC were more likely to be male and have diabetes, and had significantly higher sclerostin and osteoprotegerin circulating levels than those without VC. The histomorphometric analysis showed that bone formation rate was significantly lower in VC compared to non-VC patients. In the multivariable logistic regression analysis, bone formation rate was independently associated with the presence of VC.
Conclusions:
Vascular calcification is highly prevalent in predialysis patients, especially in those with diabetes. The independent association between bone formation rate and VC provides evidence of an important interaction between bone and vessel in CKD. Our results suggest that low bone turnover is a non-traditional risk factor for cardiovascular disease in predialysis patients.
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