Osteoporosis and CKD-metabolic bone disease under the same umbrella: insights from a joint scientific symposium
Osteoporosis and CKD-metabolic bone disease under the same umbrella: insights from a joint scientific symposium
Osteoporosis and chronic kidney disease (CKD)-metabolic bone disease (MBD) (CKD-MBD) are increasingly recognized as overlapping conditions, particularly in the aging population. Declining renal function and skeletal fragility often coexist, because CKD-MBD may develop in a skeleton already compromised by preexisting osteoporosis. Adynamic bone, often resulting from excessive suppression of parathyroid hormone (PTH) and now a common form of renal osteodystrophy (ROD), may histologically resemble low-turnover osteoporosis; distinguishing between the 2 under light microscopy remains difficult, and reliable differentiation often depends on clinical context. Nevertheless, nephrologists and nonnephrologist bone specialists frequently work in parallel rather than in collaboration.This separation has contributed to persistent diagnostic gaps and fragmented management, especially in patients with advanced CKD. Advances in imaging, biochemical markers, and bone histomorphometry have improved insight into disease mechanisms; however, limitations in current diagnostic approaches remain. Osteoporosis therapies are frequently underused in CKD, despite growing evidence supporting efficacy and safety across a broader range of kidney function than previously assumed. Despite efforts to refine the definition of osteoporosis beyond bone mineral density (BMD) alone, clinical misclassification continues.Beyond skeletal health, vascular calcification (VC)-driven by disordered calcium-phosphate homeostasis-remains insufficiently prioritized in clinical decision-making, despite its strong association with cardiovascular morbidity and mortality in CKD. Emerging concepts, such as intermittent PTH administration, an established treatment in osteoporosis, illustrate the potential for interventions that may restore mineral balance and improve skeletal integrity in selected CKD populations. Whether such strategies can also favorably influence cardiovascular risk remains uncertain and warrant investigation. This integrated framework may improve interdisciplinary care.
CKD-MBD, osteoporosis, renal osteodystrophy, vascular calcification
Dempster, David W.
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Evenepoel, Pieter
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Nickolas, Thomas L.
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Massy, Ziad A.
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Mazzaferro, Sandro
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Harvey, Nicholas C.
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Miller, Paul D.
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Pazianas, Michael
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10 March 2026
Dempster, David W.
060fe34f-77f9-4a60-a83c-05ff78638116
Evenepoel, Pieter
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Nickolas, Thomas L.
928065d5-47bb-4cf7-8084-8d33fccde988
Massy, Ziad A.
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Mazzaferro, Sandro
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Harvey, Nicholas C.
ce487fb4-d360-4aac-9d17-9466d6cba145
Miller, Paul D.
d08ce2e7-dc60-4511-b065-70da5b36158c
Pazianas, Michael
dcba1270-21c4-4b16-b0ca-4ec9ad12eecc
Dempster, David W., Evenepoel, Pieter, Nickolas, Thomas L., Massy, Ziad A., Mazzaferro, Sandro, Harvey, Nicholas C., Miller, Paul D. and Pazianas, Michael
(2026)
Osteoporosis and CKD-metabolic bone disease under the same umbrella: insights from a joint scientific symposium.
Kidney International Reports, 11 (5), [106362].
(doi:10.1016/j.ekir.2026.106362).
Abstract
Osteoporosis and chronic kidney disease (CKD)-metabolic bone disease (MBD) (CKD-MBD) are increasingly recognized as overlapping conditions, particularly in the aging population. Declining renal function and skeletal fragility often coexist, because CKD-MBD may develop in a skeleton already compromised by preexisting osteoporosis. Adynamic bone, often resulting from excessive suppression of parathyroid hormone (PTH) and now a common form of renal osteodystrophy (ROD), may histologically resemble low-turnover osteoporosis; distinguishing between the 2 under light microscopy remains difficult, and reliable differentiation often depends on clinical context. Nevertheless, nephrologists and nonnephrologist bone specialists frequently work in parallel rather than in collaboration.This separation has contributed to persistent diagnostic gaps and fragmented management, especially in patients with advanced CKD. Advances in imaging, biochemical markers, and bone histomorphometry have improved insight into disease mechanisms; however, limitations in current diagnostic approaches remain. Osteoporosis therapies are frequently underused in CKD, despite growing evidence supporting efficacy and safety across a broader range of kidney function than previously assumed. Despite efforts to refine the definition of osteoporosis beyond bone mineral density (BMD) alone, clinical misclassification continues.Beyond skeletal health, vascular calcification (VC)-driven by disordered calcium-phosphate homeostasis-remains insufficiently prioritized in clinical decision-making, despite its strong association with cardiovascular morbidity and mortality in CKD. Emerging concepts, such as intermittent PTH administration, an established treatment in osteoporosis, illustrate the potential for interventions that may restore mineral balance and improve skeletal integrity in selected CKD populations. Whether such strategies can also favorably influence cardiovascular risk remains uncertain and warrant investigation. This integrated framework may improve interdisciplinary care.
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Accepted/In Press date: 9 February 2026
e-pub ahead of print date: 17 February 2026
Published date: 10 March 2026
Keywords:
CKD-MBD, osteoporosis, renal osteodystrophy, vascular calcification
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Local EPrints ID: 511269
URI: http://eprints.soton.ac.uk/id/eprint/511269
ISSN: 2468-0249
PURE UUID: 0a10a1f0-b540-4aa0-9a41-4ddf46a86881
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Date deposited: 11 May 2026 16:40
Last modified: 12 May 2026 01:41
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Author:
David W. Dempster
Author:
Pieter Evenepoel
Author:
Thomas L. Nickolas
Author:
Ziad A. Massy
Author:
Sandro Mazzaferro
Author:
Paul D. Miller
Author:
Michael Pazianas
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