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Updated: Jun 20, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Effects of bone and mineral metabolism on arterial elasticity in chronic renal failure
Eva Kis1, Orsolya Cseprekál, Edina Bíró
1First Department of Pediatrics, Semmelweis University, Budapest Bókay János u. 53-54, 1083, Hungary.
Insights
Mineral and bone metabolism significantly impact arterial stiffness (Ast) in children with kidney disease. Increased bone turnover and calcification potential correlate with higher Ast in dialyzed children, suggesting kidney transplantation may improve outcomes.
Area of Science:
- Pediatric Nephrology
- Cardiovascular Health
- Mineral and Bone Disorders
Background:
- Arterial stiffness (Ast) is a predictor of cardiovascular mortality, often exacerbated by vascular calcification.
- Pulse wave velocity (PWV) is a key indicator of Ast.
- Mineral and bone metabolism disturbances are common in children with chronic kidney disease.
Purpose of the Study:
- To investigate the influence of mineral and bone metabolism on arterial stiffness in pediatric patients undergoing dialysis (D) and kidney transplantation (Tx).
- To assess the roles of fetuin-A, calcium (Ca), phosphate (P), and bone markers in arterial stiffness.
- To explore the relationship between calcification potential (Ca x P/fetuin-A ratio) and Ast.
Main Methods:
- Measured normalized pulse wave velocity/height (PWV/h) in 11 dialyzed and 17 transplanted children using applanation tonometry.
- Analyzed serum levels of Ca, P, fetuin-A, bone-specific alkaline phosphatase (BALP), and beta-CrossLaps (beta).
- Calculated the Ca x P/fetuin-A ratio and assessed cumulative calcitriol dosage.
Main Results:
- Fetuin-A levels were lower in dialyzed and transplanted children compared to controls.
- Dialyzed children exhibited higher bone markers and Ca x P/fetuin-A ratios than transplanted children and controls.
- In dialyzed patients, PWV/h correlated significantly with Ca x P/fetuin-A and BALP. In transplanted patients, prior calcitriol dose correlated with PWV/h.
Conclusions:
- Increased bone turnover and calcification potential are linked to arterial stiffness in pediatric kidney disease patients.
- Kidney transplantation may offer benefits for arterial stiffness compared to dialysis, though further research is warranted.
- Disturbed mineral and bone metabolism plays a crucial role in the development of arterial stiffness in this population.
Abstract:
Arterial stiffness (Ast) individually predicts cardiovascular (CV) mortality. Ast increases via vascular calcification and can be characterized by pulse wave velocity (PWV). We assessed the influence of mineral and bone metabolism on Ast in dialyzed (D) and renal transplanted (Tx) children by measuring fetuin-A and bone markers [bone-specific alkaline phosphatase (BALP); beta-CrossLaps (beta)]. Normalized PWV/height (PWV/h) of 11 D and 17 Tx patients was measured by applanation tonometry. Levels of calcium (Ca), phosphate (P), fetuin-A, and bone markers were analyzed. Ca x P/fetuin-A ratio was calculated to characterize the balance of calcification and inhibition. Cumulative dose of calcitriol was also assessed. Fetuin-A was lower in D and Tx compared with healthy controls. Bone markers and Ca x P/ fetuin-A of D were significantly higher than those of Tx and controls. In D PWV/h correlated with Ca x P/fetuin-A and BALP (r=0.8; p=0.005, r=0.6, p=0.05, respectively); BALP correlated with Ca x P/fetuin-A (r=0.7, p=0.01). In Tx, there was a correlation between calcitriol administered before transplantation and PWV/h (r=0.5, p=0.04). Increased bone turnover was coupled with an increased potential of calcium-phosphate precipitation, as shown by the increased Ca x P/fetuin-A. It might explain the connection between disturbed mineral and bone metabolism and Ast. Tx might be beneficial on Ast, though follow-up studies are needed.
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