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

  • Markus Ketteler
  • , Pieter Evenepoel
  • , Rachel M. Holden
  • , Tamara Isakova
  • , Hanne Skou Jørgensen
  • , Hirotaka Komaba
  • , Thomas L. Nickolas
  • , Smeeta Sinha
  • , Marc G. Vervloet
  • , Michael Cheung
  • , Jennifer M. King
  • , Morgan E. Grams
  • , Michel Jadoul
  • , Rosa M. A. Moysés*
  • , Conference Participants
  • *Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

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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.

Original languageEnglish
JournalKidney International
Volume107
Issue number3
Pages (from-to)405-423
Number of pages19
ISSN0085-2538
DOIs
Publication statusPublished - Mar 2025

Bibliographical note

Copyright © 2024 Kidney Disease: Improving Global Outcomes (KDIGO). Published by Elsevier Inc. All rights reserved.

Keywords

  • CKD-MBD
  • calcium
  • parathyroid hormone
  • phosphate
  • renal osteodystrophy
  • vitamin D

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