Related Experiment Video
Updated: May 20, 2026

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data
Published on: December 9, 2015
Randomized controlled trial of cholecalciferol supplementation in chronic kidney disease patients with
Peter Marckmann1, Hanne Agerskov, Sasikala Thineshkumar
1Clinical Research Unit, Department of Nephrology, Odense University Hospital, Odense, Denmark. peter.marckmann@dadlnet.dk
Insights
Vitamin D (25-hydroxyvitamin D) replenishment effectively raised levels in chronic kidney disease (CKD) patients. Non-dialysis CKD patients showed improved vitamin D metabolism and reduced parathyroid hormone, but hypercalcemia risk necessitates monitoring.
Area of Science:
- Nephrology
- Endocrinology
- Nutritional Science
Background:
- Hypovitaminosis D is prevalent in chronic kidney disease (CKD) patients.
- The impact of 25-hydroxyvitamin D (25-OHD) repletion in CKD requires further elucidation.
Purpose of the Study:
- To assess the efficacy of cholecalciferol supplementation for 25-OHD replenishment in CKD patients.
- To investigate the effects of 25-OHD replenishment on vitamin D metabolites, parathyroid hormone (PTH), fibroblast growth factor 23 (FGF-23), and cardiovascular biomarkers.
Main Methods:
- An 8-week, randomized, placebo-controlled, double-blind study in hemodialysis (HD) and non-HD CKD patients.
- Weekly oral cholecalciferol (40,000 IU) administration.
- Analysis of 25-OHD, 1,25-dihydroxyvitamin D (1,25-diOHD), PTH, FGF-23, calcium, phosphate, cardiovascular biomarkers, and health outcomes.
Main Results:
- Cholecalciferol significantly increased 25-OHD levels to a median of 155 nmol/L.
- Non-HD patients experienced increased 1,25-diOHD and decreased PTH.
- Increased serum calcium and FGF-23 were observed in supplemented patients.
Conclusions:
- Weekly cholecalciferol effectively replenishes 25-OHD in CKD patients.
- Favorable effects on 1,25-diOHD and PTH were noted in non-HD patients.
- Monitoring for hypercalcemia is crucial; no significant pleiotropic effects were identified.
Background:
Hypovitaminosis D is common in chronic kidney disease (CKD). Effects of 25-hydroxyvitamin D replenishment in CKD are not well described.
Methods:
An 8-week randomized, placebo-controlled, double-blind parallel intervention study was conducted in haemodialysis (HD) and non-HD CKD patients. Treatment consisted of 40,000 IU of cholecalciferol orally per week. Plasma 25-hydroxyvitamin D (25-OHD), plasma 1,25-dihydroxyvitamin D (1,25-diOHD), plasma parathyroid hormone (PTH), serum phosphate, ionized serum calcium and serum fibroblast growth factor 23 (FGF-23) were analysed. We also investigated biomarkers related to cardiovascular disease (plasma D-dimer, plasma fibrinogen, plasma von Willebrand factor antigen and activity, plasma interleukin 6, plasma C-reactive protein, blood pressure, aortic augmentation index, aortic pulse wave velocity and 24-h urinary protein loss). Objective and subjective health variables were assessed (muscle function tests, visual analogue scores and Health Assessment Questionnaire).
Results:
Fifty-two CKD patients with 25-OHD <50 nmol/L at screening were included. Cholecalciferol supplementation led to a significant increase to a median of 155 nmol/L 25-OHD (interquartile range 137-173 nmol/L) in treated patients (n = 25, P < 0.001). In non-HD patients, we saw a significant increase in 1,25-diOHD (n = 13, P < 0.01) and a lowering of PTH (n = 13, P < 0.001). This was not observed in HD patients. Cholecalciferol supplementation caused a significant increase in serum calcium and FGF-23.
Conclusions:
25-OHD replenishment was effectively obtained with the employed cholecalciferol dosing. In non-HD patients, it had favourable effects on 1,25-diOHD and PTH. Vitamin D-supplemented patients must be monitored for hypercalcaemia. The present study could not identify significant pleiotropic effects of 25-OHD replenishment.
Related Concept Videos
Chronic Kidney Disease III: Interprofessional Care
Chronic Kidney Disease II: Clinical Manifestations
Role of Skin in Vitamin D Synthesis
The solar UV B rays (290-315 nm) are absorbed by the skin, and 7-dehydrocholesterol (provitamin D3) photolyzes it to previtamin D3, which undergoes a rapid transformation to vitamin D3(cholecalciferol).
Chronic Kidney Disease I: Introduction
Chronic Kidney Disease IV: Nursing Management
Bioavailability Study Design: Healthy Subjects Versus Patients
