Bone turnover markers in the management of postmenopausal osteoporosis
Abstract
Osteoporosis is the most common cause of fragility fractures. Bone remodelling is essential for repairing damaged areas within bone to preserve bone strength and for assisting in mineral homeostases. In young adults, bone remodelling is usually balanced with approximately as much bone replaced as is removed during each remodelling cycle. However, when remodelling becomes accelerated in combination with an imbalance that favours bone resorption over formation, such as during menopause, precipitous losses in bone mass occur. Bone turnover markers (BTMs) measure the rate of bone remodelling allowing for a dynamic assessment of skeletal status and hold promise in identifying those at highest risk of rapid bone loss and subsequent fracture. Further, the use of BTMs to monitor individuals administered osteoporosis therapy is attractive as monitoring anti-fracture efficacy with bone mineral density has significant limitations. This review details remodelling biology, pre-analytical and analytical sources of variability for BTMs, describes the most commonly used resorption and formation markers, and offers some guidelines for their use and interpretation in the laboratory and the clinic.
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All blood samples were collected in the morning before food intake (fasting >8 h) to control for diurnal variation of CTX and prolactin.
“Since CTX (8) and prolactin (22) are influenced by diurnal variations, all blood samples were collected in the morning before food intake (fasting >8 h).”
International consensus guidelines recommend assessment of two bone turnover markers: PINP and CTX.
“International consensus guidelines recommend assessment of two BTMs: procollagen type I N-terminal propeptide (PINP) (produced by osteoblasts during bone formation), and C-terminal cross-linking telopeptide of type I collagen (CTX) (released by osteoclasts during bone resorption) (8, 9).”
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References 131 · Cited by 204
- Authors
- Brown, J. P., Albert, C., Nassar, B. A., Adachi, J. D., Cole, D., Davison, K. S., Dooley, K. C., Don-Wauchope, A., Douville, P., Hanley, D. A., Jamal, S. A., Josse, R., Kaiser, S., Krahn, J., Krause, R., Kremer, R., Lepage, R., Letendre, E., Morin, S., Ooi, D. S., Papaioaonnou, A., & Ste-Marie, L.-G.
- Affiliations
- Université Laval (CA)
- Université de Montréal (CA)
- Dalhousie University (CA)
- McMaster University (CA)
- University of Toronto (CA)
- University of Calgary (CA)
- University of Saskatchewan (CA)
- McGill University (CA)
- University of Ottawa (CA)
- Corresponding author
- Brown, Jacques P.
- ORCID
- Venue
- Clinical Biochemistry
- Publisher
- Elsevier BV
- Published
- 2009-07
- Volume
- 42
- Issue
- 10-11
- Pages
- 929-942
- ISSN
- 0009-9120 (ISSN-L)
- OpenAlex
- W2034131055
- Cited by
- 204
- References
- 131
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 4 · 2023: 13 · 2022: 11 · 2021: 10 · 2020: 10 · 2019: 13 · 2018: 9 · 2017: 15 · 2016: 17 · 2015: 16 · 2014: 18 · 2013: 17 · 2012: 15
- FWCI
- 2.52
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Osteoporosis Canada
- Topics
- Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
- Health Sciences › Medicine › Oncology › Bone health and treatments
- Keywords
- bone turnover markers, postmenopausal osteoporosis, bone remodeling, bone resorption, bone formation, fragility fractures, bone mineral density, pre-analytical variability, analytical variability, menopause, fracture risk
- MeSH terms
- Bone Resorption, Female, Humans, Osteogenesis, Biomarkers, Osteoporosis, Postmenopausal, Bone Remodeling
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