Department of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, KU Leuven, Leuven, Belgium.
Department of Medicine, Division of Nephrology, University Hospitals Leuven, Leuven, Belgium.
Nephrol Dial Transplant. 2024 Jan 31;39(2):341-366. doi: 10.1093/ndt/gfad185.
Mineral and bone disorders (MBD) are common in patients with chronic kidney disease (CKD), contributing to significant morbidity and mortality. For several decades, the first-line approach to controlling hyperparathyroidism in CKD was by exogenous calcium loading. Since the turn of the millennium, however, a growing awareness of vascular calcification risk has led to a paradigm shift in management and a move away from calcium-based phosphate binders. As a consequence, contemporary CKD patients may be at risk of a negative calcium balance, which, in turn, may compromise bone health, contributing to renal bone disease and increased fracture risk. A calcium intake below a certain threshold may be as problematic as a high intake, worsening the MBD syndrome of CKD, but is not addressed in current clinical practice guidelines. The CKD-MBD and European Renal Nutrition working groups of the European Renal Association (ERA), together with the CKD-MBD and Dialysis working groups of the European Society for Pediatric Nephrology (ESPN), developed key evidence points and clinical practice points on calcium management in children and adults with CKD across stages of disease. These were reviewed by a Delphi panel consisting of ERA and ESPN working groups members. The main clinical practice points include a suggested total calcium intake from diet and medications of 800-1000 mg/day and not exceeding 1500 mg/day to maintain a neutral calcium balance in adults with CKD. In children with CKD, total calcium intake should be kept within the age-appropriate normal range. These statements provide information and may assist in decision-making, but in the absence of high-level evidence must be carefully considered and adapted to individual patient needs.
矿物质和骨骼疾病(MBD)在慢性肾脏病(CKD)患者中很常见,导致发病率和死亡率显著增加。几十年来,控制 CKD 甲状旁腺功能亢进的一线方法是外源性钙负荷。然而,自本世纪初以来,对血管钙化风险的认识不断提高,导致管理模式发生转变,不再使用基于钙的磷酸盐结合剂。因此,当代 CKD 患者可能存在负钙平衡的风险,这反过来又可能损害骨骼健康,导致肾性骨病和骨折风险增加。钙摄入量低于一定阈值可能与高摄入量一样有问题,会使 CKD 的 MBD 综合征恶化,但目前的临床实践指南并未涉及这一点。欧洲肾脏病协会(ERA)的 CKD-MBD 和欧洲肾脏营养工作组以及欧洲儿科学肾脏病学会(ESPN)的 CKD-MBD 和透析工作组共同制定了 CKD 各期儿童和成人钙管理的关键证据要点和临床实践要点。这些要点由一个由 ERA 和 ESPN 工作组成员组成的 Delphi 小组进行了审查。主要的临床实践要点包括建议 CKD 成人的饮食和药物总钙摄入量为 800-1000mg/天,不超过 1500mg/天,以维持成人的中性钙平衡。CKD 儿童的总钙摄入量应保持在相应的正常范围内。这些陈述提供了信息并可能有助于决策,但由于缺乏高级别证据,必须仔细考虑并适应个体患者的需求。