Jørgensen Hanne Skou, Vervloet Marc, Cavalier Etienne, Bacchetta Justine, de Borst Martin H, Bover Jordi, Cozzolino Mario, Ferreira Ana Carina, Hansen Ditte, Herrmann Markus, de Jongh Renate, Mazzaferro Sandro, Wan Mandy, Shroff Rukshana, Evenepoel Pieter
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Department of Nephrology, Aalborg University Hospital, Aalborg, Denmark.
Nephrol Dial Transplant. 2025 Apr 1;40(4):797-822. doi: 10.1093/ndt/gfae293.
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.
维生素D缺乏在慢性肾脏病(CKD)患者中很常见,且与不良预后相关。目前的临床实践指南建议,CKD患者与普通人群一样补充营养性维生素D。然而,近期针对普通人群的大规模临床试验未能证明补充维生素D对骨骼或非骨骼结局有益,这引发了关于在非CKD人群和CKD人群中筛查和纠正维生素D缺乏的理论依据的争论。在欧洲肾脏协会(ERA)的欧洲肾性骨营养不良倡议与欧洲儿科肾脏病学会(ESPN)的合作中,一个专家小组进行了广泛的文献综述,并制定了关于CKD儿童和成人以及肾移植后维生素D补充的临床实践要点。这些要点由ERA和ESPN相关工作组的成员组成的德尔菲小组进行了审核。关键临床实践要点包括建议监测并纠正CKD儿童和成人以及肾移植后的维生素D缺乏,目标是使25-羟维生素D水平>75 nmol/l(>30 ng/ml)。尽管补充维生素D似乎耐受性良好且安全,但建议避免大剂量(≥100 000 IU)和极高水平的25-羟维生素D(>150 - 200 nmol/l,或60 - 80 ng/ml),以降低中毒风险。未来的临床试验应研究在CKD不同阶段维生素D缺乏情况下补充维生素D对患者相关结局的益处。