The role of nutritional vitamin D in chronic kidney disease–mineral and bone disorder in children and adults with chronic kidney disease, on dialysis, and after kidney transplantation—a European consensus statement
ERA · 2025 · Europe
Source and licence
- Authors
- Hanne Skou Jørgensen, Marc Vervloet, Etienne Cavalier et al.
- Title
- The role of nutritional vitamin D in chronic kidney disease–mineral and bone disorder in children and adults with chronic kidney disease, on dialysis, and after kidney transplantation—a European consensus statement
- Journal
- Nephrology Dialysis Transplantation, 2025
- Licence
- CC BY 4.0
- Changes
- Verbatim excerpts; formatting adapted
Full text retrieved 2026-10-27 from Europe PMC · PMC11960744
Licence statement of the original publication
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
This page reproduces excerpts of the original publication; the original is authoritative. It has not been reviewed by a physician, does not state a recommendation of Medelix and does not replace medical advice. The guideline may have been updated since.
Open the original publication →Full text on Europe PMC
Recommendations
Verbatim, with grade of recommendation or strength of consensus where given.
Clinical practice points
- We recommend supplementing vitamin D to >75 nmol/l (>30 ng/ml) in adults and children with CKD G2–5D to delay the onset, or improve the control, of secondary hyperparathyroidism, recognizing that the effect in CKD G5–5D is uncertain.
- We suggest replenishing vitamin D before using an active vitamin D compound in CKD G2–3 and before or concomitantly with an active vitamin D compound in CKD G4–5D.
- We suggest supplementing vitamin D to >75 nmol/l (>30 ng/ml) in kidney transplant recipients to reduce the risk of bone loss and fractures.
- We suggest using oral cholecalciferol to increase and maintain serum 25(OH)D concentration in the target range. If cholecalciferol is unavailable, oral ergocalciferol may be used in an equivalent dose.
- We suggest using oral cholecalciferol with once-daily, weekly, fortnightly, or monthly dosing schedules, adjusting the dose for baseline 25(OH)D levels and body size.
- We suggest avoiding exceeding doses of 100 000 IU given as a single dose.
Abstract
Vitamin D deficiency is common in patients with chronic kidney disease (CKD) and associates with poor outcomes. Current clinical practice guidelines recommend supplementation with nutritional vitamin D as for the general population. However, recent large-scale clinical trials in the general population failed to demonstrate a benefit of vitamin D supplementation on skeletal or non-skeletal outcomes, fueling a debate on the rationale for screening for and correcting vitamin D deficiency, both in non-CKD and CKD populations. In a collaboration between the European Renal Osteodystrophy initiative of the European Renal Association (ERA) and the European Society for Paediatric Nephrology (ESPN), an expert panel performed an extensive literature review and formulated clinical practice points on vitamin D supplementation in children and adults with CKD and after kidney transplantation. These were reviewed by a Delphi panel of members from relevant working groups of the ERA and ESPN. Key clinical practice points include recommendations to monitor for, and correct, vitamin D deficiency in children and adults with CKD and after kidney transplantation, targeting 25-hydroxyvitamin D levels >75 nmol/l (>30 ng/ml). Although vitamin D supplementation appears well-tolerated and safe, it is recommended to avoid mega-doses (≥100 000 IU) and very high levels of 25 hydroxyvitamin D (>150–200 nmol/l, or 60–80 ng/ml) to reduce the risk of toxicity. Future clinical trials should investigate the benefit of vitamin D supplementation on patient-relevant outcomes in the setting of vitamin D deficiency across different stages of CKD.
Contents of the original publication
The section headings of the original.
- INTRODUCTION
- METHODS
- Developing the PICO questions
- Literature search
- Framing advice
- Q1: What are the current recommendations for vitamin D supplementation in the general population?
- 1.1 Vitamin D metabolism in health
- Nutritional vitamin D targets and supplementation guidelines in the general population
- Vitamin D metabolism in CKD
- Vitamin D metabolism in incident kidney transplant recipients
- Q2: What are the (pre)-analytical issues of vitamin D measurements and monitoring?
- Analytical considerations
- Monitoring strategy
- Q3: Is there evidence for benefit of vitamin D supplementation on bone and mineral metabolism in CKD?
- Vitamin D supplementation and PTH control in CKD
- Vitamin D supplementation and bone outcomes in CKD
- Vitamin D metabolism, PTH control, and bone outcomes in kidney transplant recipients
- Q4: Is there evidence for benefit of vitamin D supplementation on cardiovascular outcomes and all-cause mortality in CKD?
- Vitamin D supplementation and cardiovascular outcomes and mortality in CKD
- Q5: What is the approach to the management and prevention of vitamin D deficiency in patients with CKD?
- Pharmaceutical considerations
- Recommended dosage regimens in CKD
- Use of (extended release) calcifediol in CKD
- Safety considerations
- RESULTS OF THE DELPHI SURVEY
- RESEARCH RECOMMENDATIONS
- CONCLUDING REMARKS
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