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Equine veterinary journal2025; doi: 10.1111/evj.14514

Western performance horses with fetlock lameness demonstrate radiographic evidence of chronic exercise remodelling.

Abstract: Pathological changes of the fetlock joint are well documented in Thoroughbreds, but little information is available describing the common radiographic findings in western performance horses with fetlock lameness. Objective: To describe radiographic findings in western performance horses with fetlock lameness. It was hypothesised that the degree of lameness would correlate with the severity of radiographic findings. Methods: Retrospective case series. Methods: Retrospective review (2012-2022) of horses with lameness isolated to the fetlock joint via intra-articular analgesia and corresponding radiographs was included. Signalment, lameness, flexion, and effusion grades were recorded. Radiographs were evaluated for presence, severity, and location of pathology. Subjective radiographic severity scores were assigned. Correlations between outcome parameters were evaluated with Spearman's correlation coefficient. Statistically significant changes in median lameness grades for each radiographic abnormality were determined using the Wilcoxon Rank Sum test. Results: Ninety cases met inclusion criteria. Radiographic lesions were identified in 96.7% of cases. Distal cannon bone sclerosis, periarticular osteophytes, increased soft tissue opacity, proximal phalanx (P1) sclerosis, and subchondral bone (SCB) defects were most common. Horses with SCB cysts (median 3; Interquartile range (IQR) 2.25-3.75; p < 0.05), P1 fissures (median 3; IQR 3-3; p < 0.05), or proximal P1 sclerosis (median 2; IQR 2-3; p < 0.05) had significantly higher median lameness grades. No significant correlation was established between overall radiographic score and lameness grade (r = 0.16, p > 0.05). Conclusions: Outcome parameters were not captured for every horse due to retrospective design. Diagnostic analgesia has inherent limitations with specificity and interpretation of results. Using multiple clinicians may have led to inconsistencies in lameness grade, flexion response, and improvement after diagnostic analgesia. Conclusions: Horses in this study demonstrated changes associated with chronic exercise-induced remodelling and degenerative joint disease. While the degree of lameness did not correlate with the overall radiographic score, certain radiographic findings-P1 sclerosis, SCB cysts, and P1 fissures-were correlated with a higher degree of lameness.
Publication Date: 2025-05-19 PubMed ID: 40384350DOI: 10.1111/evj.14514Google Scholar: Lookup
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  • Journal Article

Summary

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The researchers conducted a retrospective study on western performance horses suffering from fetlock lameness to investigate its radiographic findings and to determine if the severity of lameness correlates with the severity of radiographic findings. The study discovered that while overall radiographic score didn’t correlate with the degree of lameness, specific radiographic indications were associated with a higher level of lameness.

Research Objective and Hypothesis

  • The main objective of this research was to describe the radiographic findings in western performance horses suffering from lameness in the fetlock joint. Fetlock lameness in thoroughbreds is well documented but there is a lack of information regarding its occurrence in western performance horses.
  • The study hypothesized that the level of lameness in a horse would correspond with the radiographic findings, implying a greater level of lameness would be accompanied by more severe radiographic abnormalities.

Methodology

  • The study was a retrospective case series where horses suffering from fetlock lameness between the years 2012-2022 were examined and a review of their corresponding radiographs was conducted.
  • The researchers recorded several factors including lameness, flexion, effusion grades, and signalment (a veterinary term describing a horse’s age, breed, sex, and color).
  • A range of radiographic abnormalities were assessed for presence, severity, and location within the fetlock joint.
  • A statistical analysis was performed to find correlations between lameness severity and radiographic findings and to identify significant changes in median lameness grades corresponding to each radiographic abnormality.

Findings

  • Radiographic abnormalities were found in 96.7% of the 90 cases included in the study. Most commonly identified were distal cannon bone sclerosis, periarticular osteophytes, increased soft tissue opacity, proximal phalanx (P1) sclerosis, and subchondral bone (SCB) defects.
  • Horses with SCB cysts, P1 fissures, or proximal P1 sclerosis had significantly higher median lameness grades.
  • However, the study could not establish a significant correlation between the level of lameness and the overall radiographic findings.

Conclusions

  • The researchers acknowledged certain limitations due to the study’s retrospective design, such as not capturing all outcome parameters for each horse and potential inconsistencies in assessing lameness grade and response after diagnostic analgesia due to multiple clinicians’ involvement.
  • The study concluded that the horses demonstrated changes associated with chronic exercise-induced remodelling and degenerative joint disease. However, the degree of lameness didn’t correlate with the overall radiographic score, even though specific radiographic findings (P1 sclerosis, SCB cysts, and P1 fissures) seemed to be associated with a higher lameness degree.

Cite This Article

APA
Solum G, Acutt E, Johnson SA, Zhou T, Contino EK, Donnell JR, Donnell A, Frisbie DD. (2025). Western performance horses with fetlock lameness demonstrate radiographic evidence of chronic exercise remodelling. Equine Vet J. https://doi.org/10.1111/evj.14514

Publication

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

Researcher Affiliations

Solum, Gabrielle
  • Department of Clinical Sciences, Orthopaedic Research Center, Colorado State University, Fort Collins, Colorado, USA.
Acutt, Elizabeth
  • Department of Clinical Sciences, Orthopaedic Research Center, Colorado State University, Fort Collins, Colorado, USA.
Johnson, Sherry A
  • Equine Sports Medicine, Pilot Point, Texas, USA.
Zhou, Tianjian
  • Department of Clinical Sciences, Orthopaedic Research Center, Colorado State University, Fort Collins, Colorado, USA.
Contino, Erin K
  • Department of Clinical Sciences, Orthopaedic Research Center, Colorado State University, Fort Collins, Colorado, USA.
Donnell, Josh R
  • Equine Sports Medicine, Pilot Point, Texas, USA.
Donnell, Alan
  • Equine Sports Medicine, Pilot Point, Texas, USA.
Frisbie, David D
  • Department of Clinical Sciences, Orthopaedic Research Center, Colorado State University, Fort Collins, Colorado, USA.

References

This article includes 40 references
  1. Bailey CJ, Reid SW, Hodgson DR, Rose RJ. Impact of injuries and disease on a cohort of two‐ and three‐year‐old thoroughbreds in training. Vet Rec 1999;145(17):487–493.
    doi: 10.1136/vr.145.17.487google scholar: lookup
  2. Bertone A. Distal limb: fetlock and pastern. 2014;p. 275–296.
  3. Kawcak CE, Barrett MF. 21 ‐ fetlock. 2016;p. 302–317.
  4. Parkin TDH. Epidemiology of racetrack injuries in racehorses. Vet Clin North Am Equine Pract 2008;24(1):1–19.
  5. Kane AJ, Park RD, McIlwraith CW, Rantanen NW, Morehead JP, Bramlage LR. Radiographic changes in thoroughbred yearlings. Part 1: prevalence at the time of the yearling sales. Equine Vet J 2003;35(4):354–365.
  6. Meagher DM, Bromberek JL, Meagher DT, Gardner IA, Puchalski SM, Stover SM. Prevalence of abnormal radiographic findings in 2‐year‐old thoroughbreds at in‐training sales and associations with racing performance. J Am Vet Med Assoc 2013;242(7):969–976.
    doi: 10.2460/javma.242.7.969google scholar: lookup
  7. Janes JG, Kennedy LA, Garrett KS, Engiles JB. Common lesions of the distal end of the third metacarpal/metatarsal bone in racehorse catastrophic breakdown injuries. J Vet Diagn Invest 2017;29(4):431–436.
    doi: 10.1177/1040638717717948google scholar: lookup
  8. Johnston GCA, Ahern BJ, Palmieri C, Young AC. Imaging and gross pathological appearance of changes in the parasagittal grooves of thoroughbred racehorses. Animals (Basel) 2021;11(12):3366.
    doi: 10.3390/ani11123366google scholar: lookup
  9. Colgate VA, Group TF, Marr CM. Science‐in‐brief: risk assessment for reducing injuries of the fetlock bones in thoroughbred racehorses. Equine Vet J 2020;52(4):482–488.
    doi: 10.1111/evj.13273google scholar: lookup
  10. Powell SE. Low‐field standing magnetic resonance imaging findings of the metacarpo/metatarsophalangeal joint of racing thoroughbreds with lameness localised to the region: a retrospective study of 131 horses. Equine Vet J 2012;44(2):169–177.
  11. Johnson BJ, Stover SM, Daft BM, Kinde H, Read DH, Barr BC. Causes of death in racehorses over a 2 year period. Equine Vet J 1994;26(4):327–330.
  12. Sun TC, Riggs CM, Cogger N, Wright J, Al-Alawneh JI. Noncatastrophic and catastrophic fractures in racing thoroughbreds at the Hong Kong Jockey Club. Equine Vet J 2019;51(1):77–82.
    doi: 10.1111/evj.12953google scholar: lookup
  13. Ayodele BA, Hitchens PL, Wong ASM, Mackie EJ, Whitton RC. Microstructural properties of the proximal sesamoid bones of thoroughbred racehorses in training. Equine Vet J 2021;53(6):1169–1177.
    doi: 10.1111/evj.13394google scholar: lookup
  14. Nagy A, Dyson S. Magnetic resonance imaging, computed tomographic and radiographic findings in the metacarpophalangeal joints of 31 warmblood showjumpers in full work and competing regularly. Animals 2024;14(10):1417.
    doi: 10.3390/ani14101417google scholar: lookup
  15. Dyson SJ, Murray RC. Osseous trauma in the fetlock region of mature sports horses. Proc Am Assoc Equine Practnrs 2006;52:443–456.
  16. Schiavo S, Beccati F, Pokora R, Lin ST, Milmine RC, Bak L. Lesion distribution in the metacarpophalangeal and metatarsophalangeal region of 341 horses using standing magnetic resonance imaging. Animals 2024;14(13):1866.
    doi: 10.3390/ani14131866google scholar: lookup
  17. Contino EK, Park RD, McIlwraith CW. Prevalence of radiographic changes in yearling and 2‐year‐old Quarter Horses intended for cutting. Equine Vet J 2012;44(2):185–195.
  18. Menarim BC, Vasconcelos Machado VM, Cisneros Alvarez LE, Carneiro R, Busch L, Vulcano LC. Radiographic abnormalities in barrel racing horses with lameness referable to the metacarpophalangeal joint. J Equine Vet Sci 2012;32(4):216–221.
  19. Bassage LH, Ross MW. Diagnostic Analgesia. 2011;p. 100–135.
  20. Johnson SA, Donnell JR, Donnell AD, Frisbie DD. Retrospective analysis of lameness localisation in western performance horses: a ten‐year review. Equine Vet J 2021;53(6):1150–1158.
  21. Byam-Cook KL, Singer ER. Is there a relationship between clinical presentation, diagnostic and radiographic findings and outcome in horses with osteoarthritis of the small tarsal joints?. Equine Vet J 2009;41(2):118–123.
    doi: 10.2746/042516408x345107google scholar: lookup
  22. Vargas e Silva NC d O, dos Anjos RL, Santana MMC, Battistella LR, Marcon Alfieri F. Discordance between radiographic findings, pain, and superficial temperature in knee osteoarthritis. Reumatologia 2020;58(6):375–380.
    doi: 10.5114/reum.2020.102002google scholar: lookup
  23. Faulkner JE, Joostens Z, Broeckx BJG, Hauspie S, Mariën T, Vanderperren K. Follow‐up magnetic resonance imaging of sagittal groove disease of the equine proximal phalanx using a classification system in 29 non‐racing sports horses. Animals 2023;14(1):34.
    doi: 10.3390/ani14010034google scholar: lookup
  24. Martig S, Hitchens PL, Lee PVS, Whitton RC. The relationship between microstructure, stiffness and compressive fatigue life of equine subchondral bone. J Mech Behav Biomed Mater 2020;101:103439.
  25. Santschi EM. Articular fetlock injuries in exercising horses. Vet Clin North Am Equine Pract 2008;24(1):117–132.
  26. Smith MRW, Wright IM. Are there radiologically identifiable prodromal changes in thoroughbred racehorses with parasagittal fractures of the proximal phalanx?. Equine Vet J 2014;46(1):88–91.
    doi: 10.1111/evj.12093google scholar: lookup
  27. Ramzan PHL, Powell SE. Clinical and imaging features of suspected prodromal fracture of the proximal phalanx in three thoroughbred racehorses. Equine Vet J 2010;42(2):164–169.
    doi: 10.2746/042516409x478695google scholar: lookup
  28. Cantley CE, Firth EC, Delahunt JW, Pfeiffer DU, Thompson KG. Naturally occurring osteoarthritis in the metacarpophalangeal joints of wild horses. Equine Vet J 1999;31(1):73–81.
  29. Stewart HL, Kawcak CE. The importance of subchondral bone in the pathophysiology of osteoarthritis. Front Vet Sci 2018;5:178.
    doi: 10.3389/fvets.2018.00178google scholar: lookup
  30. Pool R. Pathologic manifestations of joint disease. 1996;p. 49–56.
  31. Davis AM, Fan X, Shen L, Robinson P, Riggs CM. Improved radiological diagnosis of palmar osteochondral disease in the thoroughbred racehorse. Equine Vet J 2017;49(4):454–460.
    doi: 10.1111/evj.12636google scholar: lookup
  32. King JN, Zubrod CJ, Schneider RK, Sampson SN, Roberts G. MRI findings in 232 horses with lameness localized to the metacarpo(tarso)phalangeal region and without a radiographic diagnosis. Vet Radiol Ultrasound 2013;54(1):36–47.
  33. Back W, Schamhardt HC, Hartman W, Barneveld A. Kinematic differences between the distal portions of the forelimbs and hind limbs of horses at the trot. Am J Vet Res 1995;56(11):1522–1528.
  34. Clayton HM, Lanovaz JL, Schamhardt HC, Van Wessum R. The effects of a rider's mass on ground reaction forces and fetlock kinematics at the trot. Equine Vet J 1999;31(S30):218–221.
  35. Kawcak CE, Mcilwraith CW. Proximodorsal first phalanx osteochondral chip fragmentation in 336 horses. Equine Vet J 1994;26(5):392–396.
  36. Harrison SM, Whitton CR, Kawcak CE, Stover SM, Pandy MG. Evaluation of a subject‐specific finite‐element model of the equine metacarpophalangeal joint under physiological load. J Biomech 2014;47(1):65–73.
  37. Juneja P, Munjal A, Hubbard JB. General anatomy and physiology of joints. 2024.
  38. Daniel AJ, Judy CE, Saveraid T. Magnetic resonance imaging of the metacarpo(tarso)phalangeal region in clinically lame horses responding to diagnostic analgesia of the palmar nerves at the base of the proximal sesamoid bones: five cases. Equine Vet Educ 2013;25(5):222–228.
  39. Brommer H, van Weeren PR, Brama PA, Barneveld A. Quantification and age‐related distribution of articular cartilage degeneration in the equine fetlock joint. Equine Vet J 2003;35(7):697–701.
  40. Martig S, Hitchens PL, Stevenson MA, Whitton RC. Subchondral bone morphology in the metacarpus of racehorses in training changes with distance from the articular surface but not with age. J Anat 2018;232(6):919–930.
    doi: 10.1111/joa.12794google scholar: lookup