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Update on the role of bone turnover markers in the diagnosis and management of osteoporosis: a consensus paper from The European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO), International Osteoporosis Foundation (IOF), and International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)

Update on the role of bone turnover markers in the diagnosis and management of osteoporosis: a consensus paper from The European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO), International Osteoporosis Foundation (IOF), and International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)
Update on the role of bone turnover markers in the diagnosis and management of osteoporosis: a consensus paper from The European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO), International Osteoporosis Foundation (IOF), and International Federation of Clinical Chemistry and Laboratory Medicine (IFCC)

Purpose: the International Osteoporosis Foundation (IOF) and the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) have proposed procollagen type I N propeptide (PINP) and β isomerized C-terminal telopeptide of type I collagen (β-CTX-I) as reference bone turnover markers (BTMs) for osteoporosis. This report examines the published literature since the 2011 IOF-IFCC position paper in order to determine the clinical potential of the reference BTMs and newer markers for the prediction of fracture risk and monitoring the treatment of osteoporosis.

Methods: evidence for the relationship between BTMs and subsequent fractures was gathered from prospective studies through literature review of the Medline database from years 2011 to May 2024. The impact of treatment on BTMs was also studied by examining publications in that period. Studies of the accuracy of BTMs in the assessment of bone turnover in the setting of advanced chronic kidney disease were also examined.

Results: increased BTM concentrations are associated with higher fracture risk in postmenopausal women. PINP and β-CTX-I measured in blood are associated with fracture risk but their interaction with other risk factors has not been sufficiently studied limiting their incorporation into fracture risk algorithms. Treatment-induced changes in PINP and β-CTX-I account for a substantial proportion of fracture risk reduction and are useful for improving adherence; they are recommended for inclusion in studies to examine adherence in individual patients. However, total PINP (tPINP) and β-CTX-I may be elevated in CKD due to renal retention. Bone alkaline phosphatase (BALP), intact PINP (iPINP), and tartrate resistant acid phosphatase 5b (TRACP5b) show the most promise in discriminating high and low turnover bone diseases in patients with advanced CKD and for predicting fracture risk, monitoring treatment response, and assessing the risk of treatment-related complications.

Conclusion: we re-affirm the use of serum/plasma tPINP and plasma β-CTX-I as reference BTMs with appropriate patient preparation and sample handling and measurement by standardized/harmonized assays in clinical studies to accumulate further data, and for monitoring treatment of osteoporosis in the setting of normal renal function in clinical practice. BALP and TRACP5b, measured by standardized assays, are recommended as reference BTMs for CKD-associated osteoporosis and should be included in observational and intervention studies to ascertain their utility for risk-evaluation, treatment initiation, and assessment of treatment response in CKD-associated osteoporosis.

BALP, Bone status indices, Bone turnover markers, PINP, TRACP5b, β-CTX-I
0937-941X
579-608
Bhattoa, Harjit Pal
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Vasikaran, Samuel
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Trifonidi, Ioulia
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Kapoula, Georgia
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Lombardi, Giovanni
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Jørgensen, Niklas Rye
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Pikner, Richard
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Miura, Masakazu
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Chapurlat, Roland
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Hiligsmann, Mickael
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Haarhaus, Mathias
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Evenepoel, Pieter
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Jørgensen, Hanne Skou
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Herrmann, Markus
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Clark, Patricia
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Tuzun, Şansın
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Al-Daghri, Nasser
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Silverman, Stuart
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Alokail, Majed S.
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Ormarsdóttir, Sif
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Yerro, María Concepción Prieto
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Matijevic, Radmila
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Laslop, Andrea
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da Silva Rosa, Mario Miguel Coelho
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Zakraoui, Leith
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Burlet, Nansa
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Kanis, John A.
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Rizzoli, René
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Makris, Konstantinos
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et al.
Bhattoa, Harjit Pal
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Vasikaran, Samuel
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Trifonidi, Ioulia
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Kapoula, Georgia
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Lombardi, Giovanni
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Miura, Masakazu
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Haarhaus, Mathias
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Evenepoel, Pieter
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Jørgensen, Hanne Skou
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Herrmann, Markus
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Kaufman, Jean-Marc
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Clark, Patricia
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Tuzun, Şansın
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Al-Daghri, Nasser
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Silverman, Stuart
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da Silva Rosa, Mario Miguel Coelho
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Zakraoui, Leith
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Burlet, Nansa
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Harvey, Nicholas C.
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Fusaro, Maria
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Torre, Carla
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Kanis, John A.
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Rizzoli, René
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Reginster, Jean-Yves
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Makris, Konstantinos
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Bhattoa, Harjit Pal, Vasikaran, Samuel and Trifonidi, Ioulia , et al. (2025) Update on the role of bone turnover markers in the diagnosis and management of osteoporosis: a consensus paper from The European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO), International Osteoporosis Foundation (IOF), and International Federation of Clinical Chemistry and Laboratory Medicine (IFCC). Osteoporosis International, 36 (4), 579-608, [513925]. (doi:10.1007/s00198-025-07422-3).

Record type: Article

Abstract

Purpose: the International Osteoporosis Foundation (IOF) and the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) have proposed procollagen type I N propeptide (PINP) and β isomerized C-terminal telopeptide of type I collagen (β-CTX-I) as reference bone turnover markers (BTMs) for osteoporosis. This report examines the published literature since the 2011 IOF-IFCC position paper in order to determine the clinical potential of the reference BTMs and newer markers for the prediction of fracture risk and monitoring the treatment of osteoporosis.

Methods: evidence for the relationship between BTMs and subsequent fractures was gathered from prospective studies through literature review of the Medline database from years 2011 to May 2024. The impact of treatment on BTMs was also studied by examining publications in that period. Studies of the accuracy of BTMs in the assessment of bone turnover in the setting of advanced chronic kidney disease were also examined.

Results: increased BTM concentrations are associated with higher fracture risk in postmenopausal women. PINP and β-CTX-I measured in blood are associated with fracture risk but their interaction with other risk factors has not been sufficiently studied limiting their incorporation into fracture risk algorithms. Treatment-induced changes in PINP and β-CTX-I account for a substantial proportion of fracture risk reduction and are useful for improving adherence; they are recommended for inclusion in studies to examine adherence in individual patients. However, total PINP (tPINP) and β-CTX-I may be elevated in CKD due to renal retention. Bone alkaline phosphatase (BALP), intact PINP (iPINP), and tartrate resistant acid phosphatase 5b (TRACP5b) show the most promise in discriminating high and low turnover bone diseases in patients with advanced CKD and for predicting fracture risk, monitoring treatment response, and assessing the risk of treatment-related complications.

Conclusion: we re-affirm the use of serum/plasma tPINP and plasma β-CTX-I as reference BTMs with appropriate patient preparation and sample handling and measurement by standardized/harmonized assays in clinical studies to accumulate further data, and for monitoring treatment of osteoporosis in the setting of normal renal function in clinical practice. BALP and TRACP5b, measured by standardized assays, are recommended as reference BTMs for CKD-associated osteoporosis and should be included in observational and intervention studies to ascertain their utility for risk-evaluation, treatment initiation, and assessment of treatment response in CKD-associated osteoporosis.

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s00198-025-07422-3 - Version of Record
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Accepted/In Press date: 3 February 2025
e-pub ahead of print date: 28 March 2025
Published date: April 2025
Keywords: BALP, Bone status indices, Bone turnover markers, PINP, TRACP5b, β-CTX-I

Identifiers

Local EPrints ID: 500644
URI: http://eprints.soton.ac.uk/id/eprint/500644
ISSN: 0937-941X
PURE UUID: 27022c58-69b8-4ee1-b338-d189f2206410
ORCID for Nicholas C. Harvey: ORCID iD orcid.org/0000-0002-8194-2512

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Date deposited: 07 May 2025 16:53
Last modified: 28 Aug 2025 01:43

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Contributors

Author: Harjit Pal Bhattoa
Author: Samuel Vasikaran
Author: Ioulia Trifonidi
Author: Georgia Kapoula
Author: Giovanni Lombardi
Author: Niklas Rye Jørgensen
Author: Richard Pikner
Author: Masakazu Miura
Author: Roland Chapurlat
Author: Mickael Hiligsmann
Author: Mathias Haarhaus
Author: Pieter Evenepoel
Author: Hanne Skou Jørgensen
Author: Markus Herrmann
Author: Jean-Marc Kaufman
Author: Patricia Clark
Author: Şansın Tuzun
Author: Nasser Al-Daghri
Author: Stuart Silverman
Author: Majed S. Alokail
Author: Sif Ormarsdóttir
Author: María Concepción Prieto Yerro
Author: Radmila Matijevic
Author: Andrea Laslop
Author: Mario Miguel Coelho da Silva Rosa
Author: Leith Zakraoui
Author: Nansa Burlet
Author: Eugene McCloskey
Author: Regis P. Radermecker
Author: Maria Fusaro
Author: Carla Torre
Author: John A. Kanis
Author: René Rizzoli
Author: Jean-Yves Reginster
Author: Konstantinos Makris
Author: Etienne Cavalier
Corporate Author: et al.

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