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Минеральные и костные нарушения при хронической болезни почек: согласительная конференция инициативы по улучшению глобальных исходов при болезнях почек (KDIGO)

Translated title of the contribution: Chronic kidney disease-mineral and bone disorder: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Сonference
  • 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
  • , Conference Participants
  • *Corresponding author for this work
  • Robert Bosch Foundation
  • KU Leuven
  • Queen's University Kingston
  • Northwestern University
  • Aalborg University
  • Aarhus University
  • Tokai University
  • Washington University St. Louis
  • Northern Care Alliance NHS Foundation Trust
  • University of Manchester
  • Radboud University Nijmegen
  • KDIGO
  • New York University
  • Université catholique de Louvain
  • Universidade de São Paulo

Research output: Contribution to journalArticleAcademicpeer-review

17 Downloads (Pure)

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 (CKDMBD). 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.
Translated title of the contributionChronic kidney disease-mineral and bone disorder: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Сonference
Original languageRussian
Pages (from-to)20-37
Number of pages18
JournalNephrology and Dialysis
Volume27
Issue number1
DOIs
Publication statusPublished - 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

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

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