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Updated: May 31, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Serum fetuin-A and vitamin D in children with mild-to-severe chronic kidney disease: a cross-sectional study
Jan Schaible1, Marianne Wigger, Hagen Staude
1Department of Paediatrics, University of Rostock, Rostock, Germany.
Insights
Serum fetuin-A levels are reduced in children with chronic kidney disease (CKD) on dialysis, but not in those with moderate CKD or after transplantation. Vitamin D intake, not just status, influences fetuin-A levels in pediatric CKD patients.
Area of Science:
- Pediatric Nephrology
- Biochemistry
- Cardiovascular Health
Background:
- Fetuin-A and vitamin D are linked to cardiovascular issues in pediatric chronic kidney disease (CKD).
- The relationship between serum fetuin-A and vitamin D status or treatment in these patients remains unclear.
Purpose of the Study:
- To investigate the association between serum fetuin-A levels and vitamin D status/treatment in pediatric CKD patients.
- To identify factors influencing fetuin-A concentrations in this population.
Main Methods:
- Cross-sectional study of 112 pediatric CKD patients (Stages 1-5) and post-transplant patients.
- Measured serum fetuin-A, 25-hydroxyvitamin D3 (25OHD), and 1,25-dihydroxyvitamin D3 (calcitriol).
- Assessed vitamin D supplementation and treatment in 64% of patients.
Main Results:
- Fetuin-A was reduced in dialysis patients, comparable to controls in moderate CKD and post-transplant.
- Despite vitamin D treatment, many patients remained deficient in 25OHD and calcitriol.
- Fetuin-A correlated with serum calcium and cumulative 25OHD dosage, with dialysis and 25OHD dosage predicting fetuin-A levels.
Conclusions:
- Fetuin-A levels are significantly reduced in pediatric dialysis patients.
- Cumulative vitamin D intake (25OHD and calcitriol) and microinflammation influence fetuin-A levels.
- Vitamin D treatment's effect on fetuin-A may be partly mediated by serum calcium levels.
Background:
Fetuin-A and vitamin D are significant correlates of cardiovascular morbidity in paediatric chronic kidney disease (CKD) patients. It is thus far unknown, whether or not serum fetuin-A is affected by the vitamin D status or treatment with vitamin D preparations in these patients.
Methods:
In a cross-sectional study, serum concentrations of fetuin-A, 25-hydroxyvitamin D(3) (25OHD) and 1,25-dihydroxyvitamin D(3) (calcitriol) levels were determined in 112 paediatric patients with mild-to-severe CKD (Stages 1-5) and after renal transplantation. A25OHD supplementation and/or calcitriol treatment were given in 64% of the patients.
Results:
Fetuin-A levels were clearly reduced in dialysis patients but were comparable to healthy controls in those with moderate CKD and after transplantation. Although 64 and 46% of all patients received 25OHD and/or calcitriol treatment, 48 and 20% of patients were 25OHD and/or calcitriol deficient, respectively. Within the whole patient cohort, fetuin-A correlated with serum calcium and yearly weight-related 25OHD dosage (each P < 0.01) but not with the vitamin D status per se. Multiple regression analysis revealed the need for dialysis treatment and cumulative 25OHD dosage as independent predictors of fetuin-A concentrations (model r(2) = 0.17). In dialysis patients, fetuin-A was inversely correlated with serum C-reactive protein but positively correlated with cumulative calcitriol dosage and serum parathormone (each P < 0.01).
Conclusions:
Fetuin-A levels are clearly reduced in children on dialysis but not in those with moderate CKD and after transplantation. Besides the degree of microinflammation, the cumulative intake of 25OHD and calcitriol are significantly correlated to fetuin-A in these patients. The impact of vitamin D treatment appears to be at least partly mediated by serum calcium.
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