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

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.

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Publication Details

Journal
Nephrology and Dialysis
Published
2025-03-22
DOI
https://doi.org/10.28996/2618-9801-2025-1-20-37
Citations
1
Primary Topic
Renal function and acid-base balance
Type
article
Field-Weighted Citation Impact
1.43
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article

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

Tamara Isakova, Rosa Maria Affonso Moysés, Hanne Skou Jørgensen, R. M. Holden et al.
1 citations
Nephrology and Dialysis
Renal function and acid-base balance
1.43
article

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

Tamara Isakova, Rosa Maria Affonso Moysés, Hanne Skou Jørgensen, R. M. Holden, Morgan E. Grams, Michel Jadoul, Marc Vervloet, Jennifer King, Markus Ketteler, Michael Cheung, Thomas L. Nickolas, Smeeta Sinha, Hirotaka Komaba, Pieter Evenepoel, Participants Conference
article en
1 citations

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.

Nephrology and DialysisVol. 27(1)
Tokai University (JP), Cliniques Universitaires Saint-Luc (BE), Radboud University Nijmegen (NL), Queen's University (CA), Aalborg University Hospital (DK), Aarhus University Hospital (DK), Health Sciences Centre (CA), Robert Bosch Hospital (DE), University Medical Center (US), Radboud University Medical Center (NL), Northern Health and Social Care Trust (GB), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (BR), New York University (US), UCLouvain (BE), KU Leuven (BE)
Good health and well-being
Openalex Percentile: Top 22%
Renal function and acid-base balance
1.43
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