Effect of Simple Oral Dental Extraction on Systemic Serum Amyloid A Concentrations in Horses.
Abstract: The translocation of gingival commensals resulting in measurable systemic inflammation has been described in humans and non-equine veterinary species with dental disorders, particularly periodontal disease. Routine odontoplasty does not result in increased serum amyloid A (SAA) concentration in horses, but a measurable increase in SAA concentration in horses undergoing dental extractions could suggest that local inflammation resulting from more severe dental disease has potential for wider, systemic consequences that warrants further study. To determine whether SAA increases in horses undergoing simple, oral extraction of non-fractured cheek teeth with and without periodontal disease. Prospective cohort study. SAA was measured using a stall-side test in horses undergoing simple oral extraction of cheek teeth with intact clinical crowns at baseline (T = 0), 24 h (T = 24) and 48 h (T = 48) post-extraction. Eight horses and 4 ponies aged between 4 and 23 years underwent cheek tooth extraction. A statistically significant difference in SAA concentration was noted between groups with and without periodontal disease at both 24 h (p = 0.004) and 48 h (p = 0.043). At 24 h, the median SAA concentration was 135 mg/L (range: 0-260 mg/L; IQR: 77.5-174 mg/L) in horses with periodontal disease and 27.5 mg/L (range: 0-47 mg/L; IQR: 4.8-43.5 mg/L) in horses without periodontal disease. At 48 h, median SAA concentration was 264 mg/L (range: 236-440 mg/L; IQR: 245.5-300.5 mg/L) in horses with periodontal disease and 0 mg/L (range = 0-41 mg/L; IQR: 0-21.8 mg/L) in horses without periodontal disease. Small sample group. Horses undergoing extraction of fractured cheek teeth were not included. Extraction of non-fractured cheek teeth does not result in a remarkable increase in SAA, except in horses with periodontal disease. These results suggest that periodontal disease in horses is associated with a local inflammatory response, which in turn drives the development of systemic inflammation, resulting in detectable increases in inflammatory markers when diseased periodontal tissues are disturbed.
© 2024 The Author(s). Veterinary Medicine and Science published by John Wiley & Sons Ltd.
Publication Date: 2024-11-13 PubMed ID: 39508719PubMed Central: PMC11542291DOI: 10.1002/vms3.70104Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.
This research article discusses the impact of simple oral tooth extraction on the systemic serum amyloid A (SAA) protein levels in horses, thus shedding light on the possibility of more severe dental issues causing wider inflammation. The findings suggest that horses with periodontal disease, a severe dental disorder, see a significant rise in their SAA levels post-extraction, indicating that systemic inflammation may result from the local inflammation triggered by the dental health condition.
Objective and Methods
- The study aimed to examine whether SAA levels increase in horses undergoing straightforward oral extraction of non-fractured cheek teeth, with or without periodontal disease.
- This was a prospective cohort study in which SAA levels were measured at baseline (T = 0), at 24 hours (T = 24), and at 48 hours (T = 48) post-extraction.
- SAA is an acute phase protein that indicates inflammation in the body, and its concentration was measured using a stall-side test.
- A total of eight horses and four ponies aged between 4 and 23 years were included in the study who required cheek tooth extraction. The sample did not include horses undergoing extraction of fractured teeth.
Results
- The findings showed a significant difference in SAA concentration between the groups of horses with and without periodontal disease 24 and 48 hours after extraction.
- The horses with periodontal disease were found to have a higher median SAA concentration at both intervals. At 24 hours, the SAA concentration median was 135 mg/L, at 48 hours post-extraction, the median concentration was 264 mg/L.
- In contrast, in horses without periodontal disease, the median SAA concentration at 24 hours was 27.5 mg/L and at 48 hours post-extraction, was 0 mg/L.
Conclusion
- Despite the small sample size used in the study, the results indicate that the extraction of non-fractured cheek teeth does not trigger a notable increase in SAA in horses, except in those with pre-existing periodontal disease.
- This suggests that periodontal disease may lead to a local inflammatory response in horses and when these inflamed periodontal tissues get disturbed, it can lead to a systemic inflammatory response that can be determined by a detectable increase in inflammatory markers.
- The findings underscore the potential systemic consequences of severe dental disease in horses and warrant further study to better understand these effects.
Cite This Article
APA
Sidwell AE, Duz M, Khan A, Bodnàr R, Hole SL.
(2024).
Effect of Simple Oral Dental Extraction on Systemic Serum Amyloid A Concentrations in Horses.
Vet Med Sci, 10(6), e70104.
https://doi.org/10.1002/vms3.70104 Publication
Researcher Affiliations
- School of Veterinary Medicine and Science, University of Nottingham, Nottingham, UK.
- Pool House Equine Hospital, IVC Evidensia, Lichfield, UK.
- School of Veterinary Medicine and Science, University of Nottingham, Nottingham, UK.
- School of Veterinary Medicine and Science, University of Nottingham, Nottingham, UK.
- Pool House Equine Hospital, IVC Evidensia, Lichfield, UK.
- Pool House Equine Hospital, IVC Evidensia, Lichfield, UK.
MeSH Terms
- Animals
- Horses
- Serum Amyloid A Protein / analysis
- Serum Amyloid A Protein / metabolism
- Horse Diseases / surgery
- Horse Diseases / blood
- Tooth Extraction / veterinary
- Prospective Studies
- Female
- Male
- Periodontal Diseases / veterinary
- Periodontal Diseases / surgery
- Cohort Studies
Conflict of Interest Statement
The authors declare no conflicts of interest.
References
This article includes 49 references
- Arias Z, Nizami MZ I, Chen X. Recent Advances in Apical Periodontitis Treatment: A Narrative Review. Bioengineering 10: 488.
- Belgrave RL, Dickey MM, Arheart KL, Cray C. Assessment of Serum Amyloid A Testing of Horses and Its Clinical Application in a Specialized Equine Practice. Journal of the American Veterinary Medical Association 243: 113–119.
- Bienert A, Bartmann CP, Verspohl J, Deegen E. Bacteriological Findings for Endodontical and Apical Molar Dental Diseases in the Horse. Dtsch Tierarztl Wochenschr 110, no. 9: 358–361.
- Birmingham SSW, Mason RM. The Effect of Sedation, Oral Examination, and Odontoplasty on Systemic Inflammation as Measured by Serum Amyloid A in the Adult Performance Horse. Journal of Veterinary Dentistry 36: 198–201.
- Borkent D, Kennedy R. Chapter 8 – Equine Oral Microbiology. In Equine Dentistry and Maxillofacial Surgery. 1st edn, 122–139. Cambridge Scholars Publishing.
- Busk P, Jacobsen S, Martinussen T. Administration of Perioperative Penicillin Reduces Postoperative Serum Amyloid A Response in Horses Being Castrated Standing: Perioperative Penicillin Reduces Postoperative Serum Amyloid A Response. Veterinary Surgery 39: 638–643.
- Collins NM, Dixon PM. Diagnosis and Management of Equine Diastemata. Clinical Techniques in Equine Practice 4: 148–154.
- Cox A, Dixon P, Smith S. Histopathological Lesions Associated With Equine Periodontal Disease. Veterinary Journal 194: 386–391.
- Cray C, Zaias J, Altman NH. Acute Phase Response in Animals: A Review. Comparative Medicine 59: 517–526.
- D'Aiuto F, Parkar M, Andreou G. Periodontitis and Systemic Inflammation: Control of the Local Infection Is Associated With a Reduction in Serum Inflammatory Markers. Journal of Dental Research 83: 156–160.
- Dixon DR, Bainbridge BW, Darveau RP. Modulation of the Innate Immune Response Within the Periodontium. Periodontology 2000 35: 53–74.
- Dixon PM, Dacre I, Dacre K, Tremaine WH, McCANN J, Barakzai S. Standing Oral Extraction of Cheek Teeth in 100 Horses (1998–2003). Equine Veterinary Journal 37: 105–112.
- DeBowes LJ, Mosier D, Logan E, Harvey CE, Lowry S, Richardson DC. Association of Periodontal Disease and Histologic Lesions in Multiple Organs from 45 Dogs. Journal of Veterinary Dentistry 13, no. 2: 57–60.
- Earley ET, Rawlinson JE, Baratt RM. Complications Associated With Cheek Tooth Extraction in the Horse. Journal of Veterinary Dentistry 30: 220–235.
- Galler KM, Weber M, Korkmaz Y, Widbiller M, Feuerer M. Inflammatory Response Mechanisms of the Dentine‐Pulp Complex and the Periapical Tissues. International Journal of Molecular Sciences 22, no. 3: 1480.
- Graziani F, D'Aiuto F, Gennai S. Systemic Inflammation After Third Molar Removal: A Case‐Control Study. Journal of Dental Research 96: 1505–1512.
- Guentsch A, Kramesberger M, Sroka A, Pfister W, Potempa J, Eick S. Comparison of Gingival Crevicular Fluid Sampling Methods in Patients With Severe Chronic Periodontitis. Journal of Periodontology 82: 1051–1060.
- Haltmayer E, Schwendenwein I, Licka TF. Course of Serum Amyloid A (SAA) Plasma Concentrations in Horses Undergoing Surgery for Injuries Penetrating Synovial Structures, an Observational Clinical Study. BMC Veterinary Research 13: 137.
- Hirai K, Furusho H, Kawashima N. Serum Amyloid A Contributes to Chronic Apical Periodontitis via TLR2 and TLR4. Journal of Dental Research 98: 117–125.
- Hoeberg E, Sånge A, Saegerman C. Serum Amyloid A as a Marker to Detect Sepsis and Predict Outcome in Hospitalized Neonatal Foals. Journal of Veterinary Internal Medicine 36: 2245–2253.
- Jacobsen S, Nielsen JV, Kjelgaard‐Hansen M. Acute Phase Response to Surgery of Varying Intensity in Horses: A Preliminary Study. Veterinary Surgery 38, no. 6: 762–769.
- Jacobsen S, Andersen PH. The Acute Phase Protein Serum Amyloid A (SAA) as a Marker of Inflammation in Horses. Equine Veterinary Education 19: 38–46.
- Kennedy R, Lappin DF, Dixon PM. The Microbiome Associated With Equine Periodontitis and Oral Health. Veterinary Research 47: 49.
- Kern I, Bartmann CP, Verspohl J, Rohde J, Bienert‐Zeit A. Bacteraemia Before, During and After Tooth Extraction in Horses in the Absence of Antimicrobial Administration. Equine Veterinary Journal 49: 178–182.
- Kiemle J, Hindenberg S, Bauer N, Roecken M. Comparison of a Point‐of‐Care Serum Amyloid A Analyzer Frequently Used in Equine Practice With 2 Turbidimetric Immunoassays Used in Human and Veterinary Medicine. Journal of Veterinary Diagnostic Investigation 34: 42–53.
- Kim AR, Lim YK, Kook J-K, Bak EJ, Yoo Y-J. Lipopolysaccharides of Fusobacterium nucleatum and Porphyromonas gingivalis Increase RANKL‐Expressing Neutrophils in Air Pouches of Mice. Laboratory Animal Research 37: 5.
- Klugh DO. Equine Periodontal Disease. Clinical Techniques in Equine Practice 4: 135–147.
- Li Q, Ouyang X, Lin J. The Impact of Periodontitis on Vascular Endothelial Dysfunction. Frontiers in Cellular and Infection Microbiology 12: 998313.
- Liuti T, Smith S, Dixon PM. A Comparison of Computed Tomographic, Radiographic, Gross and Histological, Dental, and Alveolar Findings in 30 Abnormal Cheek Teeth From Equine Cadavers. Frontiers in Veterinary Science 4: 236.
- Lockhart PB, Chu V, Zhao J. Oral Hygiene and Infective Endocarditis: A Case Control Study. Oral Surgery, Oral Medicine, Oral Pathology, and Oral Radiology 136: 333–342.
- Marsh PD. Dental Plaque as a Biofilm and a Microbial Community—Implications for Health and Disease. BMC Oral Health 6: S14.
- Martínez‐García M, Hernández‐Lemus E. Periodontal Inflammation and Systemic Diseases: An Overview. Frontiers in Physiology 12: 709438.
- Martins CC, Lockhart PB, Firmino RT. Bacteremia Following Different Oral Procedures: Systematic Review and Meta‐Analysis. Oral Diseases 30, no. 3: 846–854.
- Murray DA, Wilton JMA. Lipopolysaccharide From the Periodontal Pathogen Porphyromonas gingivalis Prevents Apoptosis of HL60‐Derived Neutrophils In Vitro. Infection and Immunity 71: 7232–7235.
- O'Neill DG, Church DB, McGreevy PD, Thomson PC, Brodbelt DC. Prevalence of Disorders Recorded in Cats Attending Primary‐Care Veterinary Practices in England. Veterinary Journal 202: 286–291.
- O'Neill DG, Mitchell CE, Humphrey J, Church DB, Brodbelt DC, Pegram C. Epidemiology of Periodontal Disease in Dogs in the uk Primary‐Care Veterinary Setting. Journal of Small Animal Practice 62: 1051–1061.
- Page RC. The Role of Inflammatory Mediators in the Pathogenesis of Periodontal Disease. Journal of Periodontal Research 26: 230–242.
- Peeran SW, Elhassan A, Zameer M, Basheer SN, Mustafa M, Thiruneervannan M. Role of Serum Amyloid A (SAA) Protein in Various Diseases With Special Reference to Periodontal and Periapical Inflammation‐A Review. Journal of Clinical and Diagnostic Research 14: ZE01–ZE05.
- Petersen HH, Nielsen JP, Heegaard PMH. Application of Acute Phase Protein Measurements in Veterinary Clinical Chemistry. Veterinary Research 35: 163–187.
- Pollock PJ, Prendergast M, Schumacher J, Bellenger CR. Effects of Surgery on the Acute Phase Response in Clinically Normal and Diseased Horses. The Veterinary Record 156: 538–542.
- Rechenberg D-K, Galicia JC, Peters OA. Biological Markers for Pulpal Inflammation: A Systematic Review. PLoS ONE 11: e0167289.
- Reis C, Da Costa AV, Guimarães JT. Clinical Improvement Following Therapy for Periodontitis: Association With a Decrease in IL‐1 and IL‐6. Experimental and Therapeutic Medicine 8: 323–327.
- Rice MK. Regional Nerve Blocks for Equine Dentistry. Journal of Veterinary Dentistry 34: 106–109.
- Rowley KJ, Townsend NB, Chang YR, Fiske-Jackson AR. A Computed Tomographic Study of Endodontic and Apical Changes in 81 Equine Cheek Teeth with Sagittal Fractures. Equine Veterinary Journal 54: 541–548.
- Takai S, Kuriyama T, Yanagisawa M, Nakagawa K, Karasawa T. Incidence and Bacteriology of Bacteremia Associated With Various Oral and Maxillofacial Surgical Procedures. Oral Surgery, Oral Medicine, Oral Pathology, and Oral Radiology 99: 292–298.
- Townsend NB, Hawkes CS, Rex R, Boden LA, Barakzai SZ. Investigation of the Sensitivity and Specificity of Radiological Signs for Diagnosis of Periapical Infection of Equine Cheek Teeth: Equine CT. Equine Veterinary Journal 43: 170–178.
- Tremaine H. Local Analgesia Techniques for Dental and Head Procedures in Horses. In Practice 41: 165–176.
- Wallis C, Holcombe LJ. A Review of the Frequency and Impact of Periodontal Disease in Dogs. Journal of Small Animal Practice 61: 529–540.
- Watanabe R, Doodnaught G, Proulx C. A Multidisciplinary Study of Pain in Cats Undergoing Dental Extractions: A Prospective, Blinded, Clinical Trial. PLoS ONE 14: e0213195.
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists