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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Effect of calcitriol on serum hepcidin in individuals with chronic kidney disease: a randomized controlled trial
Bhupesh Panwar1, Diane McCann2, Gordana Olbina2
1Departments of Medicine, University of Alabama at Birmingham, ZRB 522, 1720 2nd AVE S, Birmingham, AL, 35294-0006, USA. bpanwar@uabmc.edu.
Insights
Vitamin D (calcitriol) did not lower hepcidin levels in patients with chronic kidney disease (CKD). Further research is needed to explore other forms of vitamin D for treating anemia in CKD.
Area of Science:
- Nephrology
- Endocrinology
- Hematology
Background:
- Anemia is common in chronic kidney disease (CKD).
- Elevated hepcidin levels disrupt iron metabolism in CKD.
- Vitamin D may reduce hepcidin in healthy individuals.
Purpose of the Study:
- To investigate if calcitriol reduces serum hepcidin in CKD patients.
- To assess calcitriol's effect on iron parameters and hemoglobin in CKD.
Main Methods:
- 40 participants with stage 3-4 CKD were randomized.
- Intervention: Oral calcitriol (0.5 mcg/day) or placebo for 6 weeks.
- Primary outcome: Change in serum hepcidin; secondary outcomes: iron, calcium, phosphorus, PTH, hemoglobin.
Main Results:
- No significant difference in hepcidin, iron, or hemoglobin changes between groups.
- Calcitriol increased calcium and phosphorus, and decreased PTH.
- No significant changes in these parameters in the placebo group.
Conclusions:
- Calcitriol did not reduce serum hepcidin in mild to moderate CKD.
- Further studies on nutritional vitamin D forms for hepcidin in CKD are warranted.
Background:
Anemia is highly prevalent in chronic kidney disease (CKD). Elevated hepcidin concentrations are an important mediator of disordered iron metabolism, a key mechanism underlying anemia of CKD. Vitamin D was recently shown to reduce serum hepcidin concentrations in healthy individuals. We examined whether treatment with calcitriol reduces serum hepcidin in individuals with CKD.
Methods:
A total of 40 participants with stage 3 or 4 CKD (eGFR 15-60 ml/min/1.73m2) were randomized to receive either oral calcitriol 0.5 mcg daily or identically-matched placebo for 6 weeks. The primary outcome variable was change in serum hepcidin concentrations. Secondary outcomes variables included the change in iron parameters, calcium, phosphorus, intact parathyroid hormone and hemoglobin concentrations. Study samples were drawn at baseline, 3 days, 1 week, 4 weeks and 6 weeks after randomization. Repeated measures analysis was used to examine differences in outcome variables over time in the two groups.
Results:
There were no significant differences in the baseline characteristics between the placebo and calcitriol arms. Over 6 weeks of follow-up there were no significant differences in the change in serum hepcidin, iron parameters, or hemoglobin between the two groups. Serum calcium and phosphorus significantly increased and PTH significantly decreased after 6 weeks in calcitriol group whereas these analytes did not change in the placebo group.
Conclusion:
Calcitriol did not reduce serum hepcidin concentrations among individuals with mild to moderate CKD. Future studies are needed to assess if nutritional forms of vitamin D affect hepcidin concentrations in CKD.
Trial Registration:
ClinicalTrials.gov Identifier: NCT01988116 . Registered: November 4, 2013.
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