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慢性肾脏病-矿物质和骨异常:来自改善全球肾脏病预后组织(KDIGO)争议会议的结论

Chronic kidney disease-mineral and bone disorder: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.

作者信息

Ketteler Markus, Evenepoel Pieter, Holden Rachel M, Isakova Tamara, Jørgensen Hanne Skou, Komaba Hirotaka, Nickolas Thomas L, Sinha Smeeta, Vervloet Marc G, Cheung Michael, King Jennifer M, Grams Morgan E, Jadoul Michel, Moysés Rosa M A

机构信息

Department of General Internal Medicine and Nephrology, Robert-Bosch-Hospital, Stuttgart, Germany.

Department of Microbiology, Immunology and Transplantation, Nephrology and Renal Transplantation Research Group, Katholieke Universiteit Leuven, Leuven, Belgium; Department of Nephrology and Renal Transplantation, University Hospitals Leuven, Leuven, Belgium.

出版信息

Kidney Int. 2025 Mar;107(3):405-423. doi: 10.1016/j.kint.2024.11.013. Epub 2025 Jan 24.

Abstract

In 2017, Kidney Disease: Improving Global Outcomes (KDIGO) published a Clinical Practice Guideline Update for the Diagnosis, Evaluation, Prevention, and Treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD). Since then, new lines of evidence have been published related to evaluating disordered mineral metabolism and bone quality and turnover, identifying and inhibiting vascular calcification, targeting vitamin D levels, and regulating parathyroid hormone. For an in-depth consideration of the new insights, in October 2023, KDIGO held a Controversies Conference on CKD-MBD: Progress and Knowledge Gaps Toward Personalizing Care. Participants concluded that the recommendations in the 2017 CKD-MBD guideline remained largely consistent with the available evidence. However, the framework of the 2017 Guideline, with 3 major sections-biochemical abnormalities in mineral metabolism; bone disease; and vascular calcification-may no longer best reflect currently available evidence related to diagnosis and treatment. Instead, future guideline efforts could consider mineral homeostasis and deranged endocrine systems in adults within a context of 2 clinical syndromes: CKD-associated osteoporosis, encompassing increased fracture risk in patients with CKD; and CKD-associated cardiovascular disease, including vascular calcification and structural abnormalities, such as valvular calcification and left ventricular hypertrophy. Participants emphasized that the complexity of bone and cardiovascular manifestations of CKD-MBD necessitates personalized approaches to management.

摘要

2017年,改善全球肾脏病预后组织(KDIGO)发布了《慢性肾脏病-矿物质和骨异常(CKD-MBD)诊断、评估、预防及治疗临床实践指南更新》。自那时起,已发表了一系列新的证据,涉及评估矿物质代谢紊乱、骨质量和骨转换、识别和抑制血管钙化、调整维生素D水平以及调节甲状旁腺激素。为深入探讨这些新见解,2023年10月,KDIGO召开了CKD-MBD争议会议:个性化治疗的进展与知识空白。与会者得出结论,2017年CKD-MBD指南中的建议在很大程度上仍与现有证据一致。然而,2017年指南的框架,分为矿物质代谢生化异常、骨病和血管钙化这三个主要部分,可能不再最能反映目前与诊断和治疗相关的现有证据。相反,未来的指南制定工作可以在两种临床综合征的背景下考虑成人的矿物质稳态和内分泌系统紊乱:CKD相关骨质疏松症,包括CKD患者骨折风险增加;以及CKD相关心血管疾病,包括血管钙化和结构异常,如瓣膜钙化和左心室肥厚。与会者强调,CKD-MBD的骨骼和心血管表现的复杂性需要个性化的管理方法。

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