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The Veterinary clinics of North America. Equine practice2026; S0749-0739(26)00024-6; doi: 10.1016/j.cveq.2026.04.009

Syndrome of High Gamma-Glutamyl Transferase in Racehorses.

Abstract: Horses in racing and race training can develop high gamma-glutamyl transferase (GGT) syndrome (HGS), or increased GGT without overt evidence of primary liver disease. Current evidence points toward overtraining and a response to oxidative stress, but the etiology is incompletely understood. Evidence for an association of HGS with poor performance is mixed. Without a clear understanding of the etiology, the only evidence-based treatment option is rest or reduced training intensity. More research is needed to determine whether HGS is a physiologic adaptation, perhaps indicative of overtraining but not requiring direct intervention, versus a pathologic response that should be treated.
Publication Date: 2026-06-05 PubMed ID: 42248792DOI: 10.1016/j.cveq.2026.04.009Google Scholar: Lookup
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Summary

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Overview

  • This study discusses the occurrence of high gamma-glutamyl transferase (GGT) syndrome (HGS) in racehorses, characterized by elevated GGT levels without clear liver disease.
  • It explores current theories about its cause, its potential impact on racehorse performance, and highlights the need for further research to guide treatment strategies.

Background on High Gamma-Glutamyl Transferase Syndrome (HGS) in Racehorses

  • HGS is defined by an elevated level of the enzyme gamma-glutamyl transferase (GGT) found in the blood of racehorses.
  • Unlike typical liver diseases where GGT is increased due to liver damage, horses with HGS show high GGT without obvious signs of primary liver disease.
  • This makes HGS a unique syndrome whose underlying causes are not fully understood.

Current Understanding of Etiology

  • One leading hypothesis is that HGS is related to overtraining in racehorses.
  • Increased GGT may be a response to oxidative stress caused by intense and prolonged exercise.
  • Oxidative stress involves the accumulation of free radicals which can impact cellular functions, potentially elevating GGT as a protective or stress-related marker.
  • Other causes or contributing factors to the elevated GGT have not been clearly identified, underscoring the complexity of the syndrome.

Association with Performance

  • Research so far offers mixed evidence about whether HGS negatively affects a horse’s racing performance.
  • Some studies suggest a correlation between high GGT levels and poorer performance, while others find no clear relationship.
  • This inconsistency limits the ability to use GGT levels as a straightforward predictor or diagnostic marker for performance issues.

Treatment and Management

  • Due to incomplete understanding of the syndrome’s cause, treatment options remain limited.
  • Currently, the only evidence-based approach involves rest or reducing the intensity of training to allow recovery.
  • No pharmaceutical or specific intervention treatments have been established as effective for HGS at this time.
  • Decisions about treatment are often empirical and guided by clinical judgment and monitoring of GGT levels and performance.

Implications and Future Research Needs

  • The key open question is whether HGS represents a normal physiological adaptation to training stress or a harmful pathological condition.
  • If HGS is an adaptive response, it might not require treatment beyond normal management adjustments.
  • If it is pathologic, more aggressive interventions may be needed to prevent long-term damage or performance decline.
  • Future research should focus on:
    • Clarifying the biological mechanisms that cause elevated GGT in racehorses
    • Determining the impact of HGS on overall health and racing outcomes
    • Identifying potential biomarkers or diagnostic criteria for monitoring HGS
    • Developing targeted treatments or preventative strategies

Cite This Article

APA
Haughan J, Cathcart J, Tomlinson JE. (2026). Syndrome of High Gamma-Glutamyl Transferase in Racehorses. Vet Clin North Am Equine Pract, S0749-0739(26)00024-6. https://doi.org/10.1016/j.cveq.2026.04.009

Publication

ISSN: 1558-4224
NlmUniqueID: 8511904
Country: United States
Language: English
PII: S0749-0739(26)00024-6

Researcher Affiliations

Haughan, Joanne
  • Equine Pharmacology Laboratory, New Bolton Center, University of Pennsylvania School of Veterinary Medicine, Kennett Square, PA, USA.
Cathcart, Jessica
  • Department of Clinical Studies, New Bolton Center, University of Pennsylvania School of Veterinary Medicine, Kennett Square, PA, USA.
Tomlinson, Joy E
  • Department of Clinical Studies, New Bolton Center, University of Pennsylvania School of Veterinary Medicine, Kennett Square, PA, USA. Electronic address: joytom@vet.upenn.edu.

Conflict of Interest Statement

Disclosures No conflict of interest or other disclosures to report.

Citations

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