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Animals : an open access journal from MDPI2026; 16(16); 2514; doi: 10.3390/ani16162514

Serum Osteocalcin and CTX-I in Fit-to-Race Thoroughbred Racehorses: Reference Intervals and Associations with Demographic, Training, and Lameness-Related Factors.

Abstract: Musculoskeletal injury remains a major welfare and performance concern in Thoroughbred racing, and biomarkers for early risk stratification are of scientific interest. This multicentre observational cohort study characterised serum concentrations of two bone turnover markers, osteocalcin/BGLAP (OC) and C-terminal telopeptide of type I collagen (CTX-I), in 1359 fit-to-race Thoroughbred racehorses sampled across New South Wales, Victoria, and Western Australia. Biomarker distributions, population-wide percentile ranges, demographic and training-related associations, and short-term soundness outcomes were evaluated using nonparametric methods. Both markers were positively skewed, with population-wide percentile ranges (2.5-97.5 percentile) of 0.13-9.44 ng/mL for CTX-I and 0.02-7.25 ng/mL for OC; CTX-I varied substantially by jurisdiction, so this pooled range should not be interpreted as a clinical reference interval for individual horses. CTX-I varied significantly by age, jurisdiction, venue, and training surface, with markedly higher concentrations in New South Wales horses and lower concentrations associated with polytrack training, but did not predict lameness outcomes. OC concentrations were significantly higher in horses classified as lame at sampling and showed modest discriminatory ability for subsequent lameness in univariate analysis, with the strongest performance for persistent lameness at both 7 and 28 days; this association attenuated after adjustment for age, sex, state, and training surface. At an unadjusted operational threshold of approximately 1.24 ng/mL, OC achieved high negative predictive value for persistent lameness. These findings suggest OC may have scientific value as a potential rule-out screening marker for short-term soundness, warranting further investigation, while CTX-I appears more informative for characterising population-level skeletal turnover variation.
Publication Date: 2026-08-12 PubMed ID: 42651921DOI: 10.3390/ani16162514Google Scholar: Lookup
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  • Journal Article

Summary

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Overview

  • This study examined two blood biomarkers related to bone turnover in Thoroughbred racehorses to establish reference values and investigate how these markers relate to factors like age, training, and lameness.
  • The goal was to assess whether these markers could help predict short-term soundness issues (lameness) in racehorses to improve animal welfare and performance management.

Background and Purpose

  • Musculoskeletal injuries are a significant welfare concern in Thoroughbred horse racing.
  • Early identification of horses at risk for injury could improve management and performance outcomes.
  • Biomarkers measurable in the blood, specifically markers indicating bone turnover, may help with early risk stratification.
  • The two biomarkers studied are:
    • Osteocalcin (OC or BGLAP), a protein linked with bone formation.
    • C-terminal telopeptide of type I collagen (CTX-I), a marker of bone resorption (breakdown).
  • The study intended to establish reference ranges for these markers in fit-to-race Thoroughbreds and to explore how demographic factors, training conditions, and lameness relate to biomarker levels.

Study Design and Population

  • This was a multicenter observational cohort study involving 1,359 fit-to-race Thoroughbred racehorses.
  • Horses were sampled from three Australian states: New South Wales (NSW), Victoria, and Western Australia.
  • Sampling focused on horses considered healthy enough to race, aiming to establish baseline biomarker levels and detect any relationships to specific factors.

Key Findings: Distribution and Reference Intervals

  • Both OC and CTX-I biomarker levels in serum showed positive skew (more low values with a tail toward higher values).
  • Population-wide percentile ranges (from 2.5th to 97.5th percentile) were:
    • CTX-I: 0.13 to 9.44 ng/mL
    • OC: 0.02 to 7.25 ng/mL
  • CTX-I levels varied substantially depending on geographical location (jurisdiction), indicating environmental or management differences.
  • Because of this variation, the combined population reference range for CTX-I should not be used as a clinical reference for individual horses without considering location.

Associations of Biomarkers with Demographic and Training Variables

  • CTX-I:
    • Varied significantly by age, with older or younger horses showing different CTX-I levels.
    • Varied by jurisdiction (with notably higher levels in NSW horses).
    • Varied by racing venue and training surface; training on polytrack surfaces was associated with lower CTX-I levels.
  • OCs:
    • Higher in horses that were lame at the time of sampling.
    • Showed some ability to discriminate/preempt which horses would develop lameness later, especially persistent lameness at 7 and 28 days.
    • This predictive ability was modest and weakened after adjusting for age, sex, location, and training surface.

Predictive Value for Lameness Outcomes

  • OC, at an unadjusted threshold around 1.24 ng/mL, showed a high negative predictive value for persistent lameness—meaning horses with OC levels below this cutoff were unlikely to develop long-term lameness.
  • This suggests OC might be useful as a “rule-out” biomarker in screening fit racehorses to identify those unlikely to develop short-term lameness.
  • CTX-I did not predict lameness outcomes effectively, indicating it may be better suited to understanding population-level bone turnover rather than individual clinical risk.

Implications and Future Directions

  • OC could be valuable in clinical or training environments to screen horses for soundness and possibly prevent injury by early identification of risk.
  • More research is needed to validate OC as a screening tool, particularly addressing how adjustments for demographic and training factors affect its predictive performance.
  • CTX-I may serve more as a research tool to characterize overall population skeletal turnover influenced by environment and management rather than as a clinical marker.
  • The findings underscore the importance of considering location, age, and training surface when interpreting bone turnover markers in racehorses.

Cite This Article

APA
Tually P, Meadows J, Hathway M, Currie G. (2026). Serum Osteocalcin and CTX-I in Fit-to-Race Thoroughbred Racehorses: Reference Intervals and Associations with Demographic, Training, and Lameness-Related Factors. Animals (Basel), 16(16), 2514. https://doi.org/10.3390/ani16162514

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 16
Issue: 16
PII: 2514

Researcher Affiliations

Tually, Peter
  • Department of Nuclear Medicine, TeleMedVET, 44 Epsom Ave, Ascot, WA 6104, Australia.
  • School of Dentistry and Medical Sciences, Charles Sturt University, Wagga Wagga, NSW 2678, Australia.
Meadows, Jack
  • Department of Nuclear Medicine, TeleMedVET, 44 Epsom Ave, Ascot, WA 6104, Australia.
Hathway, Matilda
  • School of Veterinary Nursing, AVT, 39 Epsom Avenue, Ascot, WA 6104, Australia.
Currie, Geoffrey
  • School of Dentistry and Medical Sciences, Charles Sturt University, Wagga Wagga, NSW 2678, Australia.

Grant Funding

  • Racing Australia

Citations

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