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© Veterinary Business Development Ltd 2026

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18 Aug 2026

Understanding syndrome’s risks

Nicola Menzies-Gow MA, VetMB, PhD, DipECEIM, CertEM(IntMed),FHEA, FRCVS discusses the differing risk factors for each form of this common and painful condition of the horse foot

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Nicola Menzies-Gow

Job Title



Understanding syndrome’s risks

Image: fotorauschen / Adobe Stock

  • When and where at BEVA Congress 2026?
  • Thursday 10 September 1:30pm, Hall 1

Laminitis is a common, painful condition of the equine foot that is now defined as a clinical syndrome associated with systemic disease (sepsis or systemic inflammatory response syndrome [SIRS] or endocrine disease) or altered weight bearing rather than being a discrete disease entity.

The three forms of laminitis are:

  • Sepsis-associated laminitis, which occurs secondary to SIRS and/or sepsis and so occurs in animals with, for example, severe gastrointestinal disease, pleuropneumonia and septic metritis following retention of fetal membranes.
  • Hyperinsulinaemia-associated laminitis (HAL), which is the most common form of laminitis, accounting for up to 90% of cases of laminitis in some studies1. It encompasses laminitis associated with insulin dysregulation (ID), as occurs in equine metabolic syndrome (EMS) and in a subset of animals with pituitary pars intermedia dysfunction (PPID), as well as corticosteroid-associated laminitis.
  • Supporting-limb laminitis, which is a major contributor to treatment failure in painful limb conditions such as fractures and refractory cases of synovial sepsis as laminitis develops in the contralateral limb due to reduced limb cycling and consequent reduced perfusion.

Risk factors for sepsis-associated laminitis

Several studies have investigated risk factors for sepsis-associated laminitis. In one study, laminitis developed in 28.4% of animals with duodenitis/proximal enteritis2. Increased risk of laminitis was associated with bodyweight (horses weighing more than 550kg were twice as likely to develop laminitis as those below 550kg), haemorrhagic reflux observed at admission and not receiving heparin as laminitis prophylaxis.

In another study that included all horses presenting to a single hospital across an eight-year period, only endotoxaemia was significantly associated with the development of acute laminitis3. In a study of horses with infectious colitis, 20% developed laminitis during hospitalisation. Horses with neorickettsiosis were more likely to develop laminitis than coronavirus cases and admission heart rate, total solids, band neutrophils and bicarbonate concentration were predictive of laminitis development4.

Finally, administration of low molecular weight heparin appeared to be effective in reducing the risk of laminitis following colic surgery5, while digital cryotherapy reduced the risk of laminitis in horses with colitis6.

Risk factors for hyperinsulinaemia-associated laminitis

Early studies that evaluated risk factors for laminitis did not necessarily distinguish the three types of laminitis, and the results related to signalment, height, bodyweight, health parameters, weather and seasonality were inconsistent7. It is now clear that HAL occurs in association with ID, which is a feature of all animals with EMS and a subset (25% to 50%) of animals with PPID. EMS is associated with an increased risk of laminitis and those animals with PPID that have ID are at the greatest risk of developing laminitis. Thus, the risk factors for HAL are the risk factors for ID/EMS/PPID.

Initial experimental studies suggested that a circulating insulin concentration of 200mIU/ml was the threshold above which laminitis was induced8. A cohort study determined that an increased risk of future laminitis was associated with basal serum insulin concentration greater than 21.6µIU/ml and plasma adiponectin lower than 2.5mg/ml 9.

A second cohort study determined the risk could be stratified according to basal serum insulin concentrations with low (lower than 21.6µIU/ml), medium (21.6µIU/ml to 45.2µIU/ml) and high-risk (greater than 45.2µIU/ml) categories that had estimated four-year laminitis incidences (95% confidence index) of 6% (2-9), 22% (10-33) and 69% (48-82) respectively10.

Animals could similarly be stratified according to their insulin response to an oral sugar test with low (lower than 53.4µIU/ml), medium (53.4µIU/ml to 153µIU/ml) and high-risk (greater to or equal to 153µIU/ml) categories that had estimated four-year laminitis incidences (95% confidence index) of 3% (0-6), 20% (10-29) and 73% (52-84) respectively. The risk could not be estimated from any owner-reported or physically apparent data11.

With respect to the development of ID in animals with EMS, evidence supports a role for genetics, epigenetics, obesity, diet, the gastrointestinal microbiome and endocrine-disrupting chemicals as risk factors. The development of ID in animals with PPID is postulated to be associated with the production of pars intermedia products that antagonise insulin, but their exact identity and the reasons why this only occurs in a subset of animals with PPID remains unclear. The main risk factor for PPID itself is increasing age12, and Morgan horses and ponies are thought to be at a higher risk13.

HAL appears to be triggered by the consumption of pasture, and it is likely that this is associated with the insulinaemic response to ingestion of non-structural carbohydrate (NSC). The NSC content of pasture is influenced by various weather factors including temperature, rainfall and sunshine. Thus, these are indirectly risk factors for HAL.

Corticosteroid-associated laminitis is also included within HAL. No evidence suggests corticosteroid administration is associated with laminitis in adult horses without underlying endocrine or severe systemic disease14. However, there is weak evidence of an association between administration of multiple doses of systemic corticosteroid and the onset of laminitis in adult horses/ponies with underlying endocrine disorders or severe systemic disease.

Two horses in a paddock. Image: Margarita Borodina/ Adobe Stock
Image: Margarita Borodina/ Adobe Stock

Risk factors for supporting limb laminitis

While overall the prevalence of supporting limb laminitis (SLL) is low (0.02% in a study at a large UK hospital)15,it is a relatively common complication in horses being treated for severe orthopaedic problems such as fractures and synovial sepsis. For example, 12% of horses that had a limb cast fitted across a nine-year period in one North American hospital developed SLL16. However, it has also been described as being associated with osteoarthritis and neurologic conditions that affect weight bearing.

Limited epidemiologic data is available for SLL, making risk factor identification difficult. Although severe and prolonged lameness is anecdotally considered to predispose horses to the development of SLL, only the duration of lameness17, duration of cast application and bodyweight16 have been identified as significant risk factors.

Other factors including age, breed, limb affected, heart rate and temperature at admission, clinicopathological test results, or whether a cast was applied, were not significantly associated with a greater risk. Thus, SLL can be difficult to predict, and some horses will develop SLL despite apparently mild lameness, and others with severe lameness for prolonged periods will not. Accurate prediction of SLL may require more sensitive and objective means of monitoring changes in limb weight-bearing patterns and/or perfusion than are currently available.

Conclusion

The risk factors for each form of laminitis are very different. Sepsis-associated laminitis risk factors include bodyweight above 550kg, haemorrhagic reflux observed at admission, heart rate, total solids, band neutrophils and bicarbonate concentration all at admission, endotoxemia and underlying disease.

Prophylactic heparin therapy and digital cryotherapy reduce the risk. HAL risk factors are the risk factors for EMS and PPID. Those for EMS include genetics, epigenetics, diet, and obesity, while the risk factors for PPID include increasing age.

HAL appears to be triggered by the consumption of pasture, and it is likely that this is associated with the insulinaemic response to ingestion of NSC.

The NSC content of pasture is influenced by various weather factors, including temperature, rainfall and sunshine. Thus, these are indirectly risk factors for HAL in animals with EMS and PPID. Corticosteroid-associated laminitis is also included within HAL, and an underlying endocrine disorder or severe systemic disease appear to be risk factors. Finally, supporting limb laminitis risk factors include the duration of lameness, duration of cast application and bodyweight.

  • This article appeared in Vet Times Equine (18 August 2026), Volume 12, Issue 3, Pages 9-10 (supplement with Vet Times 56(33).

Nicola Menzies-Gow qualified from the University of Cambridge in 1997 and, after three years in first opinion equine practice in Essex, joined the RVC, where she completed a residency in equine medicine and a PhD. Now a senior lecturer in equine medicine, Nicola’s clinical interests focus on endocrinology, cardiology and general medicine.

References

  • 1. Karikoski NP, Horn I, McGowan TW et al (2011). The prevalence of endocrinopathic laminitis among horses presented for laminitis at a first-opinion/referral equine hospital, Domest Anim Endocrinol 41(3): 111-117.
  • 2. Cohen ND, Parson EM, Seahorn TL et al (1994). Prevalence and factors associated with development of laminitis in horses with duodenitis/proximal jejunitis: 33 cases (1985-1991), J Am Vet Med Assoc 204(2): 250-254.
  • 3. Parsons CS, Orsini JA, Krafty R et al (2007). Risk factors for development of acute laminitis in horses during hospitalization: 73 cases (1997-2004), J Am Vet Med Assoc 230(6): 885-889.
  • 4. Luethy D, Feldman R, Stefanovski D et al (2021). Risk factors for laminitis and nonsurvival in acute colitis: Retrospective study of 85 hospitalized horses (2011-2019), J Vet Intern Med 35(5): 2,019-2,025.
  • 5. de la Rebière de Pouyade G, Grulke S, Detilleux J et al (2009). Evaluation of low-molecular-weight heparin for the prevention of equine laminitis after colic surgery, J Vet Emerg Crit Care (San Antonio) 19(1): 113-119.
  • 6. Kullmann A, Holcombe SJ, Hurcombe SD et al (2014). Prophylactic digital cryotherapy is associated with decreased incidence of laminitis in horses diagnosed with colitis, Equine Vet J 46(5): 554-559.
  • 7. Wylie CE, Collins SN, Verheyen KL et al (2012). Risk factors for equine laminitis: a systematic review with quality appraisal of published evidence, Vet J 193(1): 58-66.
  • 8. de Laat MA, Sillence MN, McGowan CM et al (2012). Continuous intravenous infusion of glucose induces endogenous hyperinsulinaemia and lamellar histopathology in Standardbred horses, Vet J 191(3): 317-322.
  • 9. Menzies-Gow NJ, Harris PA and Elliott J (2017). Prospective cohort study evaluating risk factors for the development of pasture-associated laminitis in the United Kingdom, Equine Vet J 49(3): 300-306.
  • 10. Knowles EJ, Elliott J, Harris PA et al (2023). Predictors of laminitis development in a cohort of nonlaminitic ponies, Equine Vet J 55(1): 12-23.
  • 11. Knowles EJ, Harris PA, Elliott J et al (2024). Factors associated with insulin responses to oral sugars in a mixed-breed cohort of ponies, Equine Vet J 56(2): 253-263.
  • 12. McGowan TW, Pinchbeck GP and McGowan CM (2013). Prevalence, risk factors and clinical signs predictive for equine pituitary pars intermedia dysfunction in aged horses, Equine Vet J 45(1): 74-79.
  • 13. Schott HC, 2nd (2002). Pituitary pars intermedia dysfunction: equine Cushing's disease, Vet Clin North Am Equine Pract 18(2): 237-270.
  • 14. McGowan CM, Cooper D and Ireland JL (2016). No evidence that therapeutic systemic corticosteroid administration is associated with laminitis in adult horses without underlying endocrine or severe systemic disease, Vet Evidence 1(1).
  • 15. Wylie CE, Newton JR, Bathe AP et al (2015). Prevalence of supporting limb laminitis in a UK equine practice and referral hospital setting between 2005 and 2013: implications for future epidemiological studies, Vet Rec 176(3): 72.
  • 16. Virgin JE, Goodrich LR, Baxter GM et al (2011). Incidence of support limb laminitis in horses treated with half limb, full limb or transfixation pin casts: a retrospective study of 113 horses (2000-2009), Equine Vet J Suppl Nov(40): 7-11.
  • 17. Peloso JG, Cohen ND, Walker MA et al (1996). Case-control study of risk factors for the development of laminitis in the contralateral limb in Equidae with unilateral lameness, J Am Vet Med Assoc 209(10): 1,746-1,749.