Analyze Diet
The Veterinary record2017; 181(16); 425; doi: 10.1136/vr.104386

Are serum amyloid A or D-lactate useful to diagnose synovial contamination or sepsis in horses?

Abstract: Synovial sepsis in horses is life threatening and accurate diagnosis allowing prompt treatment is warranted. This study assessed the diagnostic value of serum amyloid A (SAA) and D-lactate in blood and synovial fluid (SF) as diagnostic markers of synovial sepsis in horses and correlated them with total nucleated cell count (TNCC), percentage of neutrophils (%N) and total protein (TP) in SF. Blood and SF SAA and D-lactate concentrations were determined in a case-control observational study including 112 horses (38 with synovial contamination or sepsis (SCS), 66 with non-septic intra-synovial pathology (NSISP) and 8 controls). Blood and SF SAA were significantly higher in SCS than in NSISP and control horses. SAA values were similar in NSISP and control horses. SF SAA was moderately correlated with synovial TNCC, TP and blood SAA. Blood and SF SAA were 82.4 per cent and 80 per cent sensitive and 88.9 per cent and 73 per cent specific for diagnosis of SCS, with cut-off values of 60.7 and 1.14 µg/ml, respectively. Blood and SF D-lactate concentrations were not significantly different between groups. This study shows that blood and SF SAA concentrations can aid to distinguish SCS from non-septic synovial pathology; however, D-lactate was not useful.
Publication Date: 2017-08-01 PubMed ID: 28765498PubMed Central: PMC5738594DOI: 10.1136/vr.104386Google 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
  • Observational Study

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 study examined the efficacy of serum amyloid A (SAA) and D-lactate in diagnosing synovial sepsis in horses, finding that while SAA levels in both blood and synovial fluid can assist in distinguishing sepsis from non-septic conditions, D-lactate wasn’t a useful indicator.

Study Design and Participants

  • The researchers designed a case-control observational study. They considered 112 horses for their research: 38 horses diagnosed with synovial contamination or sepsis (SCS), 66 with non-septic intra-synovial pathology (NSISP) and 8 healthy horses for control.

Measurements Taken

  • The study investigated blood and synovial fluid (SF) concentrations of serum amyloid A (SAA) and D-lactate. SAA and D-lactate are biomarkers found in blood and other body fluids, and their concentrations can indicate the presence of inflammatory or infection conditions.
  • The researchers also determined total nucleated cell count (TNCC), percentage of neutrophils (%N), and total protein (TP) in the SF. These measurements were used to correlate the results.

Findings and Implications

  • The study found significantly higher levels of SAA in blood and SF in SCS horses compared to NSISP and control horses.
  • SAA levels were similar in NSISP and control horses, suggesting the elevated levels in SCS horses directly related to the presence of sepsis or contamination.
  • However, D-lactate concentrations in blood and SF did not significantly differ among the groups, indicating it’s not a useful diagnostic marker for SCS.
  • The sensitivity and specificity of SAA for diagnosing SCS were found to be 82.4% and 80% for blood and SF respectively. This suggests that SAA can be a reliable marker for SCS when using cut-off values of 60.7 and 1.14 µg/ml.
  • The findings of this study might be instrumental in improving the early diagnosis and treatment of synovial sepsis in horses. This could potentially lead to better health outcomes and less mortality in horses suffering from this severe condition.

Cite This Article

APA
Robinson CS, Singer ER, Piviani M, Rubio-Martinez LM. (2017). Are serum amyloid A or D-lactate useful to diagnose synovial contamination or sepsis in horses? Vet Rec, 181(16), 425. https://doi.org/10.1136/vr.104386

Publication

ISSN: 2042-7670
NlmUniqueID: 0031164
Country: England
Language: English
Volume: 181
Issue: 16
Pages: 425

Researcher Affiliations

Robinson, Claire S
  • Department of Equine Clinical Science, Institute of Veterinary Science, University of Liverpool, Wirral, UK.
Singer, Ellen R
  • Department of Equine Clinical Science, Institute of Veterinary Science, University of Liverpool, Wirral, UK.
Piviani, Martina
  • Department of Small Animal Clinical Science, Institute of Veterinary Science, University of Liverpool, Wirral, UK.
Rubio-Martinez, Luis M
  • Department of Equine Clinical Science, Institute of Veterinary Science, University of Liverpool, Wirral, UK.

MeSH Terms

  • Animals
  • Case-Control Studies
  • Female
  • Horse Diseases / blood
  • Horse Diseases / diagnosis
  • Horses
  • Lactate Dehydrogenases / blood
  • Male
  • Sepsis / blood
  • Sepsis / diagnosis
  • Sepsis / veterinary
  • Serum Amyloid A Protein / analysis
  • Synovial Fluid / chemistry

Conflict of Interest Statement

Competing interests: None declared

References

This article includes 31 references
  1. Fraser BS, Bladon BM. Tenoscopic surgery for treatment of lacerations of the digital flexor tendon sheath.. Equine Vet J 2004 Sep;36(6):528-31.
    doi: 10.2746/0425164044877396pubmed: 15460078google scholar: lookup
  2. Wereszka MM, White NA 2nd, Furr MO. Factors associated with outcome following treatment of horses with septic tenosynovitis: 51 cases (1986-2003).. J Am Vet Med Assoc 2007 Apr 15;230(8):1195-200.
    doi: 10.2460/javma.230.8.1195pubmed: 17501662google scholar: lookup
  3. Taylor AH, Mair TS, Smith LJ, Perkins JD. Bacterial culture of septic synovial structures of horses: does a positive bacterial culture influence prognosis?. Equine Vet J 2010 Apr;42(3):213-8.
    doi: 10.2746/042516409X480403pubmed: 20486977google scholar: lookup
  4. Sanchez-Teran AF, Bracamonte JL, Hendrick S, Burguess HJ, Duke-Novakovski T, Schott M, Hoff B, Rubio-Martínez LM. Effect of Arthroscopic Lavage on Systemic and Synovial Fluid Serum Amyloid A in Healthy Horses.. Vet Surg 2016 Feb;45(2):223-30.
    doi: 10.1111/vsu.12439pubmed: 26767549google scholar: lookup
  5. Sanchez-Teran AF, Bracamonte JL, Hendrick S, Riddell L, Musil K, Hoff B, Rubio-Martínez LM. Effect of repeated through-and-through joint lavage on serum amyloid A in synovial fluid from healthy horses.. Vet J 2016 Apr;210:30-3.
    doi: 10.1016/j.tvjl.2016.01.001pubmed: 26831179google scholar: lookup
  6. Sanchez Teran AF, Rubio-Martinez LM, Villarino NF, Sanz MG. Effects of repeated intra-articular administration of amikacin on serum amyloid A, total protein and nucleated cell count in synovial fluid from healthy horses.. Equine Vet J Suppl 2012 Dec;(43):12-6.
  7. Berg LC, Thomsen PD, Andersen PH, Jensen HE, Jacobsen S. Serum amyloid A is expressed in histologically normal tissues from horses and cattle.. Vet Immunol Immunopathol 2011 Nov 15;144(1-2):155-9.
    doi: 10.1016/j.vetimm.2011.06.037pubmed: 21783263google scholar: lookup
  8. Pepys MB, Baltz ML, Tennent GA, Kent J, Ousey J, Rossdale PD. Serum amyloid A protein (SAA) in horses: objective measurement of the acute phase response.. Equine Vet J 1989 Mar;21(2):106-9.
  9. Jacobsen S, Thomsen MH, Nanni S. Concentrations of serum amyloid A in serum and synovial fluid from healthy horses and horses with joint disease.. Am J Vet Res 2006 Oct;67(10):1738-42.
    doi: 10.2460/ajvr.67.10.1738pubmed: 17014325google scholar: lookup
  10. Ludwig EK, Brandon Wiese R, Graham MR, Tyler AJ, Settlage JM, Werre SR, Petersson-Wolfe CS, Kanevsky-Mullarky I, Dahlgren LA. Serum and Synovial Fluid Serum Amyloid A Response in Equine Models of Synovitis and Septic Arthritis.. Vet Surg 2016 Oct;45(7):859-867.
    doi: 10.1111/vsu.12531pubmed: 27580707google scholar: lookup
  11. Drury DR. Chemistry and metabolism of L(+) and D(-0 lactic acids.. Ann N Y Acad Sci 1965 Jul 31;119(3):1061-9.
  12. Smith SM, Eng RH, Buccini F. Use of D-lactic acid measurements in the diagnosis of bacterial infections.. J Infect Dis 1986 Oct;154(4):658-64.
    doi: 10.1093/infdis/154.4.658pubmed: 3528318google scholar: lookup
  13. Smith SM, Eng RH, Campos JM, Chmel H. D-lactic acid measurements in the diagnosis of bacterial infections.. J Clin Microbiol 1989 Mar;27(3):385-8.
    pmc: PMC267326pubmed: 2715313doi: 10.1128/jcm.27.3.385-388.1989google scholar: lookup
  14. Gratacós J, Vila J, Moyá F, Marcos MA, Collado A, Sanmartí R, Brancós MA, Jimenez de Anta MT, Muñoz-Gómez J. D-lactic acid in synovial fluid. A rapid diagnostic test for bacterial synovitis.. J Rheumatol 1995 Aug;22(8):1504-8.
    pubmed: 7473474
  15. Yamout SZ, Nieto JE, Beldomenico PM, Dechant JE, leJeune S, Snyder JR. Peritoneal and plasma D-lactate concentrations in horses with colic.. Vet Surg 2011 Oct;40(7):817-24.
  16. Findley JA, Pinchbeck GL, Milner PI, Bladon BM, Boswell J, Mair TS, Suthers JM, Singer ER. Outcome of horses with synovial structure involvement following solar foot penetrations in four UK veterinary hospitals: 95 cases.. Equine Vet J 2014 May;46(3):352-7.
    doi: 10.1111/evj.12124pubmed: 23789739google scholar: lookup
  17. Milner PI, Bardell DA, Warner L, Packer MJ, Senior JM, Singer ER, Archer DC. Factors associated with survival to hospital discharge following endoscopic treatment for synovial sepsis in 214 horses.. Equine Vet J 2014 Nov;46(6):701-5.
    doi: 10.1111/evj.12212pubmed: 24417437google scholar: lookup
  18. Wright IM, Smith MR, Humphrey DJ, Eaton-Evans TC, Hillyer MH. Endoscopic surgery in the treatment of contaminated and infected synovial cavities.. Equine Vet J 2003 Sep;35(6):613-9.
    doi: 10.2746/042516403775467225pubmed: 14515964google scholar: lookup
  19. Malark JA, Nixon AJ, Skinner KL, Mohammed H. Characteristics of digital flexor tendon sheath fluid from clinically normal horses.. Am J Vet Res 1991 Aug;52(8):1292-4.
    pubmed: 1928911
  20. Steel CM. Equine synovial fluid analysis.. Vet Clin North Am Equine Pract 2008 Aug;24(2):437-54, viii.
    doi: 10.1016/j.cveq.2008.05.004pubmed: 18652964google scholar: lookup
  21. Satoh M, Fujinaga T, Okumura M, Hagio M. Sandwich enzyme-linked immunosorbent assay for quantitative measurement of serum amyloid A protein in horses.. Am J Vet Res 1995 Oct;56(10):1286-91.
    pubmed: 8928944
  22. Jacobsen S, Niewold TA, Halling-Thomsen M, Nanni S, Olsen E, Lindegaard C, Andersen PH. Serum amyloid A isoforms in serum and synovial fluid in horses with lipopolysaccharide-induced arthritis.. Vet Immunol Immunopathol 2006 Apr 15;110(3-4):325-30.
    doi: 10.1016/j.vetimm.2005.10.012pubmed: 16337010google scholar: lookup
  23. Martí R, Varela E, Segura RM, Alegre J, Suriñach JM, Pascual C. Determination of D-lactate by enzymatic methods in biological fluids: study of interferences.. Clin Chem 1997 Jun;43(6 Pt 1):1010-5.
    pubmed: 9191554
  24. Kortekangas P, Peltola O, Toivanen A, Aro HT. Synovial-fluid D-lactic acid in bacterial and other acute joint effusions.. Scand J Rheumatol 1994;23(4):203-5.
    doi: 10.3109/03009749409103061pubmed: 8091146google scholar: lookup
  25. de Seny D, Cobraiville G, Charlier E, Neuville S, Esser N, Malaise D, Malaise O, Calvo FQ, Relic B, Malaise MG. Acute-phase serum amyloid a in osteoarthritis: regulatory mechanism and proinflammatory properties.. PLoS One 2013;8(6):e66769.
  26. Jacobsen S, Jensen JC, Frei S, Jensen AL, Thoefner MB. Use of serum amyloid A and other acute phase reactants to monitor the inflammatory response after castration in horses: a field study.. Equine Vet J 2005 Nov;37(6):552-6.
    doi: 10.2746/042516405775314853pubmed: 16295934google scholar: lookup
  27. Kjelgaard-Hansen M, Jacobsen S. Assay validation and diagnostic applications of major acute-phase protein testing in companion animals.. Clin Lab Med 2011 Mar;31(1):51-70.
    doi: 10.1016/j.cll.2010.10.002pubmed: 21295722google scholar: lookup
  28. nTodar K.nOnline textbook of bacteriology. WI: Maison, 2012. nhttp://www.textbookofbacteriology.net.
  29. Riordan T, Doyle D, Tabaqchali S. Synovial fluid lactic acid measurement in the diagnosis and management of septic arthritis.. J Clin Pathol 1982 Apr;35(4):390-4.
    doi: 10.1136/jcp.35.4.390pmc: PMC497667pubmed: 7076866google scholar: lookup
  30. Robinson CS, Timofte D, Singer ER, Rimmington L, Rubio-Martínez LM. Prevalence and antimicrobial susceptibility of bacterial isolates from horses with synovial sepsis: A cross-sectional study of 95 cases.. Vet J 2016 Oct;216:117-21.
    doi: 10.1016/j.tvjl.2016.07.004pubmed: 27687937google scholar: lookup
  31. Jacobsen S, Kjelgaard-Hansen M, Hagbard Petersen H, Jensen AL. Evaluation of a commercially available human serum amyloid A (SAA) turbidometric immunoassay for determination of equine SAA concentrations.. Vet J 2006 Sep;172(2):315-9.
    doi: 10.1016/j.tvjl.2005.04.021pubmed: 15950503google scholar: lookup

Citations

This article has been cited 16 times.
  1. Laus F, Gialletti R, Bazzano M, Laghi L, Dini F, Marchegiani A. Synovial Fluid Metabolome Can Differentiate between Healthy Joints and Joints Affected by Osteoarthritis in Horses. Metabolites 2023 Aug 4;13(8).
    doi: 10.3390/metabo13080913pubmed: 37623857google scholar: lookup
  2. Braconi D, Geminiani M, Psarelli EE, Giustarini D, Marzocchi B, Rossi R, Bernardini G, Spiga O, Gallagher JA, Le Quan Sang KH, Arnoux JB, Imrich R, Al-Sbou MS, Gornall M, Jackson R, Ranganath LR, Santucci A. Effects of Nitisinone on Oxidative and Inflammatory Markers in Alkaptonuria: Results from SONIA1 and SONIA2 Studies. Cells 2022 Nov 18;11(22).
    doi: 10.3390/cells11223668pubmed: 36429096google scholar: lookup
  3. Thurston CC, Stefanovski D, MacKinnon MC, Chapman HS, Richardson DW, Levine DG. Serum amyloid A and fibrinogen as markers for early detection of surgical site infection associated with internal fixation in the horse. Front Vet Sci 2022;9:960865.
    doi: 10.3389/fvets.2022.960865pubmed: 36299628google scholar: lookup
  4. Dey M, Al-Attar M, Peruffo L, Coope A, Zhao SS, Duffield S, Goodson N. Assessment and diagnosis of the acute hot joint: a systematic review and meta-analysis. Rheumatology (Oxford) 2023 May 2;62(5):1740-1756.
    doi: 10.1093/rheumatology/keac606pubmed: 36264140google scholar: lookup
  5. Vajs T, Nekouei O, Biermann NM. A Descriptive Study of the Clinical Presentation, Management, and Outcome of Horses with Acute Soft Tissue Trauma of the Tarsus and the Association with Synovial Involvement. Animals (Basel) 2022 Feb 21;12(4).
    doi: 10.3390/ani12040524pubmed: 35203232google scholar: lookup
  6. Haralambus R, Florczyk A, Sigl E, Gültekin S, Vogl C, Brandt S, Schnierer M, Gamerith C, Jenner F. Detection of synovial sepsis in horses using enzymes as biomarkers. Equine Vet J 2022 May;54(3):513-522.
    doi: 10.1111/evj.13459pubmed: 33977535google scholar: lookup
  7. Yoshimura S, Koziy RV, Dickinson R, Moshynskyy I, McKenzie JA, Simko E, Bracamonte JL. Use of serum amyloid A in serum and synovial fluid to detect eradication of infection in experimental septic arthritis in horses. Can J Vet Res 2020 Jul;84(3):198-204.
    pubmed: 32801454
  8. Sinovich M, Villarino NF, Singer E, Robinson CS, Rubio-Martínez LM. Can blood serum amyloid A concentrations in horses differentiate synovial sepsis from extrasynovial inflammation and determine response to treatment?. Vet Rec 2020 Sep 19;187(6):235.
    doi: 10.1136/vr.105153pubmed: 32098906google 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. Stack JD, Cousty M, Steele E, Handel I, Lechartier A, Vinardell T, David F. Comparison of Serum Amyloid A Measurements in Equine Synovial Fluid With Routine Diagnostic Methods to Detect Synovial Infection in a Clinical Environment. Front Vet Sci 2019;6:325.
    doi: 10.3389/fvets.2019.00325pubmed: 31632987google scholar: lookup
  11. Anderson JR, Smagul A, Simpson D, Clegg PD, Rubio-Martinez LM, Peffers MJ. The synovial fluid proteome differentiates between septic and nonseptic articular pathologies. J Proteomics 2019 Jun 30;202:103370.
    doi: 10.1016/j.jprot.2019.04.020pubmed: 31028944google scholar: lookup
  12. 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
  13. Anderson JR, Phelan MM, Clegg PD, Peffers MJ, Rubio-Martinez LM. Synovial Fluid Metabolites Differentiate between Septic and Nonseptic Joint Pathologies. J Proteome Res 2018 Aug 3;17(8):2735-2743.
    doi: 10.1021/acs.jproteome.8b00190pubmed: 29969035google scholar: lookup
  14. Souto PC, Santos MR, Orozco AMO, Bento LD, Ramirez-Lopez CJ, Girardi FM, Machado JCA, de Oliveira LL, da Fonseca LA. Enzyme-Linked Immunosorbent Assay (ELISA) Development for Equine Serum Amyloid A (SAA) Determination Using Recombinant Proteins. Methods Protoc 2025 Apr 7;8(2).
    doi: 10.3390/mps8020037pubmed: 40278511google scholar: lookup
  15. Koziy RV, Katselis GS, Yoshimura S, Simko E, Bracamonte JL. Temporal kinetics of serum amyloid A (SAA) concentration and identification of SAA isoforms in blood and synovial fluid of horses with experimentally induced septic arthritis, non-septic synovitis, and systemic inflammation. J Vet Diagn Invest 2025 Jan;37(1):42-54.
    doi: 10.1177/10406387241299873pubmed: 39688235google scholar: lookup
  16. Bundgaard L, Årman F, Åhrman E, Walters M, Auf dem Keller U, Malmström J, Jacobsen S. An Equine Protein Atlas Highlights Synovial Fluid Proteome Dynamics during Experimentally LPS-Induced Arthritis. J Proteome Res 2024 Nov 1;23(11):4849-4863.
    doi: 10.1021/acs.jproteome.4c00125pubmed: 39395021google scholar: lookup