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Equine veterinary journal2026; doi: 10.1002/evj.70328

Serum osteocalcin is associated with scintigraphic abnormalities in lame and clinically sound racehorses.

Abstract: Musculoskeletal injury is a major welfare and economic challenge in racehorses, with stress-related bone injury contributing to training interruption and catastrophic failure. Advanced imaging modalities can detect early skeletal pathology but remain limited in routine screening environments. Circulating biomarkers of bone turnover may provide complementary indicators of skeletal remodelling but require validation against objective imaging findings. Objective: Evaluate whether osteocalcin (OC) and C-terminal telopeptide of type I collagen (CTX), or the CTX/OC ratio, are associated with scintigraphic abnormalities and lameness status in racehorses and explore relationships with short-term adverse musculoskeletal outcomes. Methods: Prospective, observational case-control study. Methods: Ninety-six racehorses were enrolled, including 48 lame horses referred for scintigraphy and 48 clinically sound controls. Serum OC and CTX concentrations were measured by ELISA at the time of scintigraphic examination. Scintigraphic scans were classified as no abnormality detected (NAD), moderately positive (mPOS) or strongly positive (sPOS). Associations were assessed using non-parametric tests, logistic regression and receiver operating characteristic analysis. Clinically sound horses were followed for 28 days to record adverse musculoskeletal outcomes. Results: OC concentrations were higher in lame horses than in controls (mean difference 0.68 ng/mL, 95% CI 0.19-1.17) and differed across scintigraphic categories, with OC concentrations lower in NAD horses than in mPOS horses (mean difference 1.61 ng/mL, 95% CI 0.35-2.87). In the exploratory pooled injury analysis, higher OC concentrations were associated with musculoskeletal injury status (OR 9.75, 95% CI 2.82-49.38; AUC 0.75). In clinically sound horses, CTX and the CTX/OC ratio were not significantly associated with 28-day adverse musculoskeletal outcome. Conclusions: Short follow-up duration, limited outcome events and potential workload-related confounding at sampling. Conclusions: Serum OC concentrations were associated with lameness status and scintigraphic severity. Bone turnover markers may provide complementary biological information alongside imaging but require validation in larger longitudinal studies.
Publication Date: 2026-09-22 PubMed ID: 42770892DOI: 10.1002/evj.70328Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study investigated whether blood levels of bone turnover markers, specifically osteocalcin (OC) and C-terminal telopeptide of type I collagen (CTX), are linked to bone abnormalities seen on scintigraphy and to lameness in racehorses.
  • It also explored whether these markers could predict short-term musculoskeletal injuries, aiming to find less invasive methods to detect bone problems early in racehorses.

Background and Purpose

  • Musculoskeletal injuries, especially stress-related bone injuries, pose serious welfare issues and economic challenges for racehorses by causing interruptions in training or catastrophic breakdowns.
  • Advanced imaging, like scintigraphy, can detect early bone pathology but is not always practical for routine screening due to cost and accessibility.
  • Blood biomarkers that reflect bone remodeling could potentially serve as complementary or screening tools, but their clinical relevance needs validation comparing to imaging results.
  • The study focused on two blood markers: osteocalcin (OC), indicative of bone formation, and CTX, a marker of bone resorption, as well as the ratio between them.

Study Design and Methods

  • This was a prospective, observational case-control study involving 96 Thoroughbred racehorses.
  • The study group consisted of 48 lame horses referred for scintigraphic imaging and 48 clinically sound controls matched for comparison.
  • At the time of scintigraphy, serum OC and CTX concentrations were measured using ELISA tests.
  • Scintigraphic scans were classified into three categories based on detected bone abnormalities:
    • No abnormality detected (NAD)
    • Moderately positive (mPOS)
    • Strongly positive (sPOS)
  • Statistical methods included non-parametric tests to assess differences, logistic regression to estimate odds ratios, and receiver operating characteristic (ROC) analysis to evaluate predictive performance.
  • Clinically sound horses were monitored for 28 days post-examination to observe any adverse musculoskeletal outcomes.

Key Findings

  • Serum osteocalcin concentrations were significantly higher in lame horses compared to the clinically sound controls.
  • OC levels differed between scintigraphic groups, being lowest in horses with no detected abnormalities and increased with more severe scintigraphic abnormalities (mPOS > NAD).
  • Higher OC concentrations were strongly associated with an increased likelihood of musculoskeletal injury when considering pooled data (both lame and control horses), with an odds ratio around 9.75 and acceptable predictive accuracy (AUC 0.75).
  • CTX levels and the ratio of CTX to OC did not show a significant association with short-term (28-day) adverse musculoskeletal outcomes in clinically sound horses.

Conclusions and Implications

  • Serum osteocalcin appears to be a promising biomarker reflective of bone turnover changes linked with both lameness and bone abnormalities detected by scintigraphy.
  • Bone turnover markers like OC may add valuable biological information alongside imaging findings, potentially aiding early detection of bone pathology in racehorses.
  • The lack of association of CTX and CTX/OC ratio with short-term injury risk suggests these markers may be less useful in predicting imminent musculoskeletal problems.
  • Limitations include:
    • Short duration of follow-up (28 days) for detecting adverse outcomes in sound horses.
    • Relatively small number of injury events, affecting statistical power.
    • Potential confounding due to differing workloads or training status at the time of sampling.
  • Future research with larger longitudinal studies is necessary to validate these findings and establish clinical utility for routine monitoring and early injury detection.

Cite This Article

APA
Tually P, Blache D, Meadows J, Tagore S, O'Callaghan P, Hathway M, Fulton I, Currie G. (2026). Serum osteocalcin is associated with scintigraphic abnormalities in lame and clinically sound racehorses. Equine Vet J. https://doi.org/10.1002/evj.70328

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English

Researcher Affiliations

Tually, Peter
  • Department of Nuclear Medicine, TeleMedVET, Ascot, Western Australia, Australia.
  • School of Dentistry and Medical Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.
Blache, Dominique
  • School of Agriculture and Environment, University of Western Australia, Perth, Western Australia, Australia.
Meadows, Jack
  • Department of Nuclear Medicine, TeleMedVET, Ascot, Western Australia, Australia.
Tagore, Shiphrah
  • Department of Nuclear Medicine, TeleMedVET, Ascot, Western Australia, Australia.
  • School of Dentistry and Medical Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.
O'Callaghan, Paul
  • Perth Equine Hospital, Ascot, Western Australia, Australia.
Hathway, Matilda
  • Department of Nuclear Medicine, TeleMedVET, Ascot, Western Australia, Australia.
  • School of Veterinary Nursing, AVT, Ascot, Western Australia, Australia.
Fulton, Ian
  • Fulton Equine Consulting, Miners Rest, Victoria, Australia.
Currie, Geoffrey
  • School of Dentistry and Medical Sciences, Charles Sturt University, Wagga Wagga, New South Wales, Australia.

Grant Funding

  • C001840 / Racing and Wagering Western Australia

References

This article includes 36 references
  1. Davies M, Jackson KA, Mackinnon AL, Turner A, Kuznik K, Hill J. Epidemiology of race day injury in young professional jockeys in Great Britain from 2007 to 2018: a retrospective cohort study. BMJ Open 2021;11(8):e044075.
  2. Crawford K. The epidemiology of musculoskeletal injuries, fatalities and retirements in Thoroughbred racehorses in Queensland, Australia. PhD Thesis. School of Veterinary Science, The University of Queensland 2021.
    doi: 10.14264/16df24agoogle scholar: lookup
  3. Wright I, Minshall G, Young N, Riggs C. Fractures in Thoroughbred racing and the potential for pre‐race identification of horses at risk. Equine Vet J 2024;56(3):424–436.
  4. Morrice‐West AV, Thomas M, Wong AS, Flash M, Whitton RC, Hitchens PL. Linkage of jockey falls and injuries with racehorse injuries and fatalities in Thoroughbred flat racing in Victoria, Australia. Front Vet Sci 2025;11:1481016.
  5. Jackson B, Dyson P, Lonnell C, Verheyen K, Pfeiffer D, Price J. Bone biomarkers and risk of fracture in two‐and three‐year‐old Thoroughbreds. Equine Vet J 2009;41(4):410–413.
  6. Nielsen BD. A review of three decades of research dedicated to making equine bones stronger: implications for horses and humans. Animals 2023;13(5):789.
  7. Irandoust S, O'Neil LM, Stevenson CM, Franseen FM, Ramzan PHL, Powell SE. Comparison of radiography and computed tomography for identification of third metacarpal structural change and associated assessment of condylar stress fracture risk in Thoroughbred racehorses. Equine Vet J 2025;57(3):723–736.
  8. Spriet M, Vandenberghe F. Equine nuclear medicine in 2024: use and value of scintigraphy and PET in equine lameness diagnosis. Animals 2024;14(17):2499.
  9. Adugani S, Bannimath G, Sastry P. A review on biomarkers in clinical osteoporosis‐significance of hydroxyproline. Biomed Biotechnol Res J 2021;5(3):245–251.
  10. Garnero P. Biomarkers for osteoporosis management: utility in diagnosis, fracture risk prediction and therapy monitoring. Mol Diagn Ther 2008;12:157–170.
  11. Turlo AJ, Cywinska A, Frisbie DD. Revisiting predictive biomarkers of musculoskeletal injury in thoroughbred racehorses: longitudinal study in polish population. BMC Vet Res 2019;15(1):66.
  12. Lee S, Baker ME, Clinton M, Taylor SE. Use of omics data in fracture prediction; a scoping and systematic review in horses and humans. Animals 2021;11(4):959.
  13. Kacprzyk M, Dąbrowska I, Grzędzicka J, Milczek‐Haduch D, Kiełbik P, Gołębiewski M. Training and race‐induced coordination of oxidative stress markers in racehorses: insights from multivariate and univariate analyses. J Vet Intern Med 2026;40(1):aalaf085.
    doi: 10.1093/jvimsj/aalaf085google scholar: lookup
  14. McIlwraith CW, Clegg PD. Science in brief: report on the Havemeyer Foundation workshop on equine musculoskeletal biomarkers—current knowledge and future needs. Equine Vet J 2014;46(6):651–653.
  15. Garnero P, Ferreras M, Karsdal MA, Nicamhlaoibh R, Risteli J, Borel O. The type I collagen fragments ICTP and CTX reveal distinct enzymatic pathways of bone collagen degradation. J Bone Miner Res 2003;18(5):859–867.
  16. Bailey S, Poundarik AA, Sroga GE, Vashishth D. Structural role of osteocalcin and its modification in bone fracture.. Appl Phys Rev 2023;10(1):011410.
  17. Pool RR, Meagher DM. Pathologic findings and pathogenesis of racetrack injuries.. Vet Clin N Am Equine Pract 1990;6(1):1–30.
  18. Costa da Silva RG, Sun TC, Mishra AP, Boyde A, Doube M, Riggs CM. Intracortical remodelling increases in highly loaded bone after exercise cessation.. J Anat 2024;244(3):424–437.
  19. Tually P, Currie G, Blache D, Meadows J, Gray C, Hemmings L. Concurrent measurement of serum and radiomic biomarkers in the clinical investigation of equine musculoskeletal injuries: a prospective pilot study.. Vet Radiol Ultrasound 2023;64(3):484–491.
  20. Stover SM. The epidemiology of thoroughbred racehorse injuries.. Clin Tech Equine Pract 2003;2(4):312–322.
  21. Frost HM. Bone “mass” and the “mechanostat”: a proposal.. Anat Rec 1987;219(1):1–9.
  22. Verheyen KL, Wood JL. Descriptive epidemiology of fractures occurring in British thoroughbred racehorses in training.. Equine Vet J 2004;36(2):167–173.
  23. Parkin TD, Clegg PD, French NP, Parkin TDH, Riggs CM, Morgan KL. Risk of fatal distal limb fractures among Thoroughbreds involved in the five types of racing in the United Kingdom.. Vet Rec 2004;154(16):493–497.
  24. Parfitt A. The bone remodeling compartment: a circulatory function for bone lining cells.. J Bone Miner Res 2001;16(9):1583–1585.
  25. Ma C, Du T, Niu X, Fan Y. Biomechanics and mechanobiology of the bone matrix.. Bone Res 2022;10(1):59.
  26. Martin TJ, Seeman E. Bone remodelling: its local regulation and the emergence of bone fragility.. Best Pract Res Clin Endocrinol Metab 2008;22(5):701–722.
  27. Seeman E, Delmas PD. Bone quality—the material and structural basis of bone strength and fragility.. New Engl J Med 2006;354(21):2250–2261.
  28. McManus P. Animal‐based entertainment industries, animal death and Social Licence to Operate (SLO): an analysis of ‘The Final Race’ and the 2019 Melbourne Cup.. Soc Cult Geogr 2023;24(7):1242–1261.
  29. Stover S, Uzal FA. Autopsies are required for all racehorses at most US racetracks.. J Vet Diagn Invest 2022;34(6):925–926.
  30. Whitton RC, Ayodele BA, Hitchens PL, Mackie EJ. Subchondral bone microdamage accumulation in distal metacarpus of Thoroughbred racehorses.. Equine Vet J 2018;50(6):766–773.
  31. Shieh A, Han W, Ishii S, Greendale GA, Crandall CJ, Karlamangla AS. Quantifying the balance between total bone formation and total bone resorption: an index of net bone formation.. J Clin Endocrinol Metabol 2016;101(7):2802–2809.
  32. Yoon JH, Lee H, Kwon D, Lee D, Lee S, Cho E. Integrative approach of omics and imaging data to discover new insights for understanding brain diseases.. Brain Commun 2024;6(4):fcae265.
  33. Pullamsetti SS, Vanderpool RR, de Man F, de Jesus Perez VA, Hemnes AR, Mukherjee M. Advanced molecular, metabolic, and imaging approaches to characterizing right ventricular failure: a scientific statement from the American Heart Association.. Circulation 2026;153(19):e1304–e1322.
  34. Wassberg C, Lubberink M, Sörensen J, Johansson S. Repeatability of quantitative parameters of 18F‐fluoride PET/CT and biochemical tumour and specific bone remodelling markers in prostate cancer bone metastases.. EJNMMI Res 2017;7(1):42.
  35. Karpinski MJ, Hüsing J, Claassen K, Möller L, Kajüter H, Oesterling F. Combining PSMA‐PET and PROMISE to re‐define disease stage and risk in patients with prostate cancer: a multicentre retrospective study.. Lancet Oncol 2024;25(9):1188–1201.
  36. Zhou Y, Li C, Jiang S, Niu F, Cui F, Zhao Y. Diagnosis of SPECT/CT bone imaging combined with two serum examinations in patients with bone metastases from pulmonary cancer.. Clin Transl Oncol 2024;26(1):147–154.

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