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Journal of veterinary internal medicine2015; 29(3); 940-945; doi: 10.1111/jvim.12587

Acute phase proteins in racehorses with inflammatory airway disease.

Abstract: Systemic inflammation is observed in horses with heaves and could also be present in horses with a lesser degree of pulmonary inflammation. Objective: It was hypothesized that racehorses with inflammatory airway disease (IAD) have increased concentration of circulating acute phase proteins. The objective of this study was to compare serum acute phase proteins of racehorses with and without lower airway inflammation. Methods: Serum from 21 client-owned Standardbred racehorses with exercise intolerance and lower airway inflammation and serum from 10 client-owned Standardbred racehorses with exercise intolerance without lower airway inflammation. Methods: In a case-control study, serum samples from previously characterized horses presented for exercise intolerance with or without lower airway inflammation based on bronchoalveolar lavage fluid cytology were analyzed for serum amyloid A protein (SAA), C-reactive protein (CRP), and haptoglobin using commercial ELISAs. Results: There was no significant differences between groups for SAA (non-IAD versus IAD, median (range): 3.47 (0.06-34.94) versus 6.33 (0.06-80) μg/mL, P = .49), CRP (10.87 (2.05-29.03) versus 4.63 (0.02-31.81) μg/mL, P = .23) or haptoglobin (900.36 (607.99-2018.84) versus 749.54 (530.81-1076.95) μg/mL, P = .09). Conclusions: In this population of poorly performing racehorses in training, serum SAA, CRP, and haptoglobin were not helpful in distinguishing between horses with IAD from horses with exercise intolerance from other causes.
Publication Date: 2015-04-09 PubMed ID: 25857218PubMed Central: PMC4895423DOI: 10.1111/jvim.12587Google Scholar: Lookup
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  • Journal Article

Summary

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The research explores the levels of acute phase proteins in racehorses suffering from inflammatory airway disease (IAD). It concludes that these protein levels were not significantly different in horses with and without the disease, so these markers may not be used to distinguish between horses with IAD and those experiencing exercise intolerance due to other reasons.

Objective and Hypothesis

  • The researchers hypothesized that racehorses with IAD have higher concentration of circulating acute phase proteins.
  • The study aimed to establish if specific acute phase proteins could be used as reliable indicators of IAD.

Methods

  • The study compared the serum acute phase proteins (SAA, CRP, and haptoglobin) of two groups of horses: one with lower airway inflammation (21 horses) and the other (10 horses) without it.
  • All tested horses were Standardbred racehorses with exercise intolerance.
  • A case-control study was performed and serum samples from horses with distinct performance characteristics were analyzed using commercial ELISA kits.
  • The presence of airway inflammation in the horses was identified through bronchoalveolar lavage fluid cytology.

Findings

  • No significant difference was found in the concentrations of SAA, CRP, and haptoglobin between two groups of horses.
  • The median values for SAA, CRP, and haptoglobin were found to be comparable for both groups, and the differences were not statistically significant (p > 0.05).

Conclusion

  • The serum levels of SAA, CRP, and haptoglobin, which are considered as indicators of systemic inflammation, did not prove useful for distinguishing between horses with IAD and those experiencing performance issues due to other causes.
  • The findings suggest that other novel indicators need to be explored for accurate diagnosis of IAD in horses.

Cite This Article

APA
Leclere M, Lavoie-Lamoureux A, Lavoie JP. (2015). Acute phase proteins in racehorses with inflammatory airway disease. J Vet Intern Med, 29(3), 940-945. https://doi.org/10.1111/jvim.12587

Publication

ISSN: 1939-1676
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 29
Issue: 3
Pages: 940-945

Researcher Affiliations

Leclere, M
  • Faculty of Veterinary Medicine, Clinical Sciences Department, Université de Montréal, Saint-Hyacinthe, QC, Canada.
Lavoie-Lamoureux, A
  • Faculty of Veterinary Medicine, Clinical Sciences Department, Université de Montréal, Saint-Hyacinthe, QC, Canada.
Lavoie, J-P
  • Faculty of Veterinary Medicine, Clinical Sciences Department, Université de Montréal, Saint-Hyacinthe, QC, Canada.

MeSH Terms

  • Acute-Phase Proteins / analysis
  • Animals
  • Bronchoalveolar Lavage Fluid / cytology
  • C-Reactive Protein / analysis
  • Case-Control Studies
  • Enzyme-Linked Immunosorbent Assay / veterinary
  • Female
  • Haptoglobins / analysis
  • Horse Diseases / blood
  • Horses
  • Inflammation / blood
  • Inflammation / veterinary
  • Male
  • Respiratory Tract Diseases / blood
  • Respiratory Tract Diseases / veterinary
  • Serum Amyloid A Protein / analysis

References

This article includes 23 references
  1. Lavoie JP, Cesarini C, Lavoie‐Lamoureux A. Bronchoalveolar lavage fluid cytology and cytokine messenger ribonucleic Acid expression of racehorses with exercise intolerance and lower airway inflammation. J Vet Intern Med 2011;25:322–329.
    pubmed: 21281348
  2. Jain S, Gautam V, Naseem S. Acute‐phase proteins: As diagnostic tool. J Pharm Bioallied Sci 2011;3:118–127.
    pmc: PMC3053509pubmed: 21430962
  3. Crisman MV, Scarratt WK, Zimmerman KL. Blood proteins and inflammation in the horse. Vet Clin North Am Equine Pract 2008;24:285–297, vi.
    pubmed: 18652956
  4. Jacobsen S, Andersen PH. The acute phase protein serum amyloid A (SAA) as a marker of inflammation in horses. Equine Vet Educ 2007;19:38–46.
  5. Upragarin N, Landman WJ, Gaastra W. Extrahepatic production of acute phase serum amyloid A. Histol Histopathol 2005;20:1295–1307.
    pubmed: 16136510
  6. Yang F, Friedrichs WE, Navarijo‐Ashbaugh AL. Cell type‐specific and inflammatory‐induced expression of haptoglobin gene in lung. Lab Invest 1995;73:433–440.
    pubmed: 7564277
  7. Ramage L, Proudfoot L, Guy K. Expression of C‐reactive protein in human lung epithelial cells and upregulation by cytokines and carbon particles. Inhal Toxicol 2004;16:607–613.
    pubmed: 16036753
  8. Lavoie‐Lamoureux A, Leclere M, Lemos K. Markers of systemic inflammation in horses with heaves. J Vet Intern Med 2012;26:1419–1426.
    pubmed: 22925172
  9. Couetil LL, Hoffman AM, Hodgson J. Inflammatory airway disease of horses. J Vet Intern Med 2007;21:356–361.
    pubmed: 17427403
  10. Pollock PJ, Prendergast M, Schumacher J. Effects of surgery on the acute phase response in clinically normal and diseased horses. Vet Rec 2005;156:538–542.
    pubmed: 15849343
  11. Hulten C, Sandgren B, Skioldebrand E. The acute phase protein serum amyloid A (SAA) as an inflammatory marker in equine influenza virus infection. Acta Vet Scand 1999;40:323–333.
    pmc: PMC8043133pubmed: 10918902
  12. Hulten C, Demmers S. Serum amyloid A (SAA) as an aid in the management of infectious disease in the foal: Comparison with total leucocyte count, neutrophil count and fibrinogen. Equine Vet J 2002;34:693–698.
    pubmed: 12455840
  13. Hobo S, Niwa H, Anzai T. Evaluation of serum amyloid A and surfactant protein D in sera for identification of the clinical condition of horses with bacterial pneumonia. J Vet Med Sci 2007;69:827–830.
    pubmed: 17827889
  14. Takiguchi M, Fujinaga T, Naiki M. Isolation, characterization, and quantitative analysis of C‐reactive protein from horses. Am J Vet Res 1990;51:1215–1220.
    pubmed: 2117410
  15. Kusano K, Hobo S, Ode H. Tracheal endoscopic and cytological findings and blood examination results in thoroughbred racehorses suspected to have lower respiratory tract disease. J Equine Sci 2008;19:97–102.
    pmc: PMC4013951pubmed: 24833960
  16. Kristensen L, Buhl R, Nostell K. Acute exercise does not induce an acute phase response (APR) in Standardbred trotters. Can J Vet Res 2014;78:97–102.
    pmc: PMC3962284pubmed: 24688170
  17. Cywinska A, Witkowski L, Szarska E. Serum amyloid A (SAA) concentration after training sessions in Arabian race and endurance horses. BMC Vet Res 2013;9:91.
    pmc: PMC3655847pubmed: 23634727
  18. Cywinska A, Szarska E, Gorecka R. Acute phase protein concentrations after limited distance and long distance endurance rides in horses. Res Vet Sci 2012;93:1402–1406.
    pubmed: 22390917
  19. Fazio F, Assenza A, Tosto F. Modifications of some acute phase proteins and the white blood cell count in thoroughbreds during training. Vet Rec 2010;167:370–373.
    pubmed: 20817897
  20. Richard EA, Pitel PH, Christmann U. Serum concentration of surfactant protein D in horses with lower airway inflammation. Equine Vet J 2012;44:277–281.
    pubmed: 21696440
  21. Malle E, De Beer FC. Human serum amyloid A (SAA) protein: A prominent acute‐phase reactant for clinical practice. Eur J Clin Invest 1996;26:427–435.
    pubmed: 8817153
  22. Nunokawa Y, Fujinaga T, Taira T. Evaluation of serum amyloid A protein as an acute‐phase reactive protein in horses. J Vet Med Sci 1993;55:1011–1016.
    pubmed: 7509640
  23. Wood LG, Baines KJ, Fu J. The neutrophilic inflammatory phenotype is associated with systemic inflammation in asthma. Chest 2012;142:86–93.
    pubmed: 22345378

Citations

This article has been cited 13 times.
  1. Craven A, Todd-Donato A, Stokol T, Liepman R, Glasberg I, Wilkins P, Luethy D, Wong D, Schoster A, van den Brom-Spierenburg AJ, Tomlinson JE. Clinical findings and outcome predictors for multinodular pulmonary fibrosis in horses: 46 cases (2009-2019). J Vet Intern Med 2024 May-Jun;38(3):1842-1857.
    doi: 10.1111/jvim.17084pubmed: 38619130google scholar: lookup
  2. Peixoto Rabelo I, Barroco de Paula V, Carvalho Bustamante C, Santana AM, Gomes da Silva D, Baldassi AC, Canola PA, Araújo Valadão CA. Acute phase proteins levels in horses, after a single carbohydrate overload, associated with cecal alkalinization. Front Vet Sci 2023;10:1043656.
    doi: 10.3389/fvets.2023.1043656pubmed: 36816195google scholar: lookup
  3. Mihelić K, Vrbanac Z, Bojanić K, Kostanjšak T, Ljubić BB, Gotić J, Vnuk D, Bottegaro NB. Changes in Acute Phase Response Biomarkers in Racing Endurance Horses. Animals (Basel) 2022 Oct 31;12(21).
    doi: 10.3390/ani12212993pubmed: 36359117google scholar: lookup
  4. Janssen P, Tosi I, Hego A, Maréchal P, Marichal T, Radermecker C. Neutrophil Extracellular Traps Are Found in Bronchoalveolar Lavage Fluids of Horses With Severe Asthma and Correlate With Asthma Severity. Front Immunol 2022;13:921077.
    doi: 10.3389/fimmu.2022.921077pubmed: 35911691google scholar: lookup
  5. Minamijima Y, Niwa H, Uchida E, Yamamoto K. Comparison of the proteomes in sera between healthy Thoroughbreds and Thoroughbreds with respiratory disease associated with transport using mass spectrometry-based proteomics. J Equine Sci 2021 Mar;32(1):11-15.
    doi: 10.1294/jes.32.11pubmed: 33776535google scholar: lookup
  6. Perez-Ecija A, Buzon-Cuevas A, Aguilera-Aguilera R, Gonzalez-De Cara C, Mendoza Garcia FJ. Reference intervals of acute phase proteins in healthy Andalusian donkeys and response to experimentally induced endotoxemia. J Vet Intern Med 2021 Jan;35(1):580-589.
    doi: 10.1111/jvim.16015pubmed: 33336874google scholar: lookup
  7. Couetil L, Cardwell JM, Leguillette R, Mazan M, Richard E, Bienzle D, Bullone M, Gerber V, Ivester K, Lavoie JP, Martin J, Moran G, Niedźwiedź A, Pusterla N, Swiderski C. Equine Asthma: Current Understanding and Future Directions. Front Vet Sci 2020;7:450.
    doi: 10.3389/fvets.2020.00450pubmed: 32903600google scholar: lookup
  8. Kinnison T, Cardwell JM. Conflict Between Direct Experience and Research-Based Evidence Is a Key Challenge to Evidence-Based Respiratory Medicine on British Racing Yards. Front Vet Sci 2020;7:266.
    doi: 10.3389/fvets.2020.00266pubmed: 32537459google scholar: lookup
  9. Long A, Nolen-Walston R. Equine Inflammatory Markers in the Twenty-First Century: A Focus on Serum Amyloid A. Vet Clin North Am Equine Pract 2020 Apr;36(1):147-160.
    doi: 10.1016/j.cveq.2019.12.005pubmed: 32007299google scholar: lookup
  10. Gy C, Leclere M, Vargas A, Grimes C, Lavoie JP. Investigation of blood biomarkers for the diagnosis of mild to moderate asthma in horses. J Vet Intern Med 2019 Jul;33(4):1789-1795.
    doi: 10.1111/jvim.15505pubmed: 31099114google scholar: lookup
  11. Witkowska-Piłaszewicz OD, Żmigrodzka M, Winnicka A, Miśkiewicz A, Strzelec K, Cywińska A. Serum amyloid A in equine health and disease. Equine Vet J 2019 May;51(3):293-298.
    doi: 10.1111/evj.13062pubmed: 30565319google scholar: lookup
  12. Couëtil LL, Cardwell JM, Gerber V, Lavoie JP, Léguillette R, Richard EA. Inflammatory Airway Disease of Horses--Revised Consensus Statement. J Vet Intern Med 2016 Mar-Apr;30(2):503-15.
    doi: 10.1111/jvim.13824pubmed: 26806374google scholar: lookup
  13. Bullone M, de Lagarde M, Vargas A, Lavoie JP. Serum Surfactant Protein D and Haptoglobin as Potential Biomarkers for Inflammatory Airway Disease in Horses. J Vet Intern Med 2015 Nov-Dec;29(6):1707-11.
    doi: 10.1111/jvim.13602pubmed: 26289543google scholar: lookup