Analyze Diet
Journal of veterinary internal medicine2023; 37(2); 697-702; doi: 10.1111/jvim.16647

Effect of plasma transfusion on serum amyloid A concentration in healthy neonatal foals and foals with failure of transfer of passive immunity.

Abstract: Anecdotal evidence suggests plasma transfusions increase serum amyloid A (SAA) concentrations in healthy neonatal foals making this marker of inflammation inappropriate for therapeutic decision making in such animals. Objective: Administration of hyperimmune fresh frozen plasma (FFP) increases SAA concentration in healthy foals and in foals with failure of transfer of passive immunity (FTPI). Methods: Eighty-six healthy foals. Methods: Prospective cohort study. Foals <24 hours of age receiving plasma transfusion for treatment of FTPI (serum immunoglobulin G [IgG] concentrations 8 g/L; n = 33) were enrolled. A healthy nontransfused group of foals (IgG >8 g/L; n = 21) also was included. Serum amyloid A concentration was determined before (t0h) and after (t24h) administration of FFP. Changes in blood SAA concentration were assessed using linear regression models. Results: No statistical differences were found in SAA concentration at t0h or t24h among the 3 groups (P > .05, for all comparisons). The variation in SAA concentration before (t0h) and after (t24h) plasma transfusion showed that administration of FFP was not associated with the changes in SAA concentration (P > .05). An association between SAA concentration at t0h and at 24 hours (P < .05) was identified, where foals with higher SAA concentration at t0h also had higher SAA concentration at t24h. Conclusions: Administration of FFP to newborn foals was not associated with changes in SAA concentration.
Publication Date: 2023-02-24 PubMed ID: 36825688PubMed Central: PMC10061169DOI: 10.1111/jvim.16647Google 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

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 explores the influence of plasma transfusion on the concentration of serum amyloid A (SAA) in healthy newborn foals and those with a failure of transfer of passive immunity (FTPI). The researchers show that despite anecdotal claims, there’s no significant effect of plasma transfusion on SAA levels, so it can continue to be used as an inflammation marker in therapeutic decision-making for neonatal foals.

Objective and Methods

  • The objective of the study was to find out if the administration of hyperimmune fresh frozen plasma (FFP) affects SAA concentration in healthy foals and in foals with FTPI.
  • The study followed a prospective cohort design, where the researchers monitored 86 healthy foals that were less than 24 hours old. Foals receiving plasma transfusion as part of FTPI treatment (serum Immunoglobulin G [IgG] concentrations less than 8 g/L; n = 17), or as a preventative measure against Rhodococcus equi infection (IgG more than 8 g/L; n = 33), were enrolled. A third, healthy, non-transfused group of foals (IgG more than 8 g/L; n = 21) was also included for comparison.
  • Serum amyloid A concentration was determined before and after the administration of FFP (t0h and t24h). Changes in SAA concentration in the blood were analyzed using linear regression models.

Results

  • The researchers found no statistical differences between SAA concentrations at t0h or t24h among the three groups of foals (P > .05, showing no statistically significant difference). This indicates that receiving transfusion didn’t result in measurable differences in SAA levels across the groups.
  • The comparison of SAA concentration before and after plasma transfusion revealed that administration of FFP wasn’t associated with changes in SAA concentration (P > .05, indicating a lack of statistical significance).
  • An association between SAA concentration at t0h and t24h (P < .05, indicating statistical significance) was identified, where foals with higher SAA concentration at t0h also demonstrated higher SAA concentration at t24h, suggesting a consistent level in individual subjects over time.

Conclusions

  • The study concluded that the administration of FFP to newborn foals was not associated with changes in SAA concentration, refuting the anecdotal evidence that plasma transfusion increases SAA concentration in neonatal foals.
  • This means that SAA can remain a useful biomarker for inflammation in neonatal foals that have received FFP transfusion, either for FTPI treatment or as a preventative measure against Rhodococcus equi infection.

Cite This Article

APA
Palmisano M, Javsicas L, McNaughten J, Gamsjäger L, Renaud DL, Gomez DE. (2023). Effect of plasma transfusion on serum amyloid A concentration in healthy neonatal foals and foals with failure of transfer of passive immunity. J Vet Intern Med, 37(2), 697-702. https://doi.org/10.1111/jvim.16647

Publication

ISSN: 1939-1676
NlmUniqueID: 8708660
Country: United States
Language: English
Volume: 37
Issue: 2
Pages: 697-702

Researcher Affiliations

Palmisano, Megan
  • Department of Clinical Studies, University of Pennsylvania, Kennett Square, Pennsylvania, USA.
Javsicas, Laura
  • Rhinebeck Equine LLP, Rhinebeck, New York, USA.
McNaughten, Justin
  • Palm Beach Equine Clinic, Wellington, Florida, USA.
Gamsjäger, Lisa
  • Department of Population Health and Pathobiology, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.
Renaud, David L
  • Department of Population Medicine, Ontario Veterinary College, University of Guelph, Guelph, Canada.
Gomez, Diego E
  • Department of Clinical Studies, Ontario Veterinary College, University of Guelph, Guelph, Canada.

MeSH Terms

  • Animals
  • Horses
  • Animals, Newborn
  • Serum Amyloid A Protein / analysis
  • Prospective Studies
  • Blood Component Transfusion / veterinary
  • Plasma / chemistry
  • Immunoglobulin G
  • Horse Diseases

Conflict of Interest Statement

Authors declare no conflict of interest.

References

This article includes 44 references
  1. Giguère S, Gaskin JM, Miller C, Bowman JL. Evaluation of a commercially available hyperimmune plasma product for prevention of naturally acquired pneumonia caused by Rhodococcus equi in foals.. J Am Vet Med Assoc 2002 Jan 1;220(1):59-63.
    pubmed: 12680449doi: 10.2460/javma.2002.220.59google scholar: lookup
  2. Giguère S, Cohen ND, Chaffin MK, Slovis NM, Hondalus MK, Hines SA, Prescott JF. Diagnosis, treatment, control, and prevention of infections caused by Rhodococcus equi in foals.. J Vet Intern Med 2011 Nov-Dec;25(6):1209-20.
  3. Caston SS, McClure SR, Martens RJ, Chaffin MK, Miles KG, Griffith RW, Cohen ND. Effect of hyperimmune plasma on the severity of pneumonia caused by Rhodococcus equi in experimentally infected foals.. Vet Ther 2006 Winter;7(4):361-75.
    pubmed: 17216591
  4. Madigan JE, Hietala S, Muller N. Protection against naturally acquired Rhodococcus equi pneumonia in foals by administration of hyperimmune plasma.. J Reprod Fertil Suppl 1991;44:571-8.
    pubmed: 1795301
  5. Crump LM, Foreman JH, Riddle WT. Evaluation of hyperimmune equine plasma for the treatment of failure of passive transfer in foals. AAEP Lexington, KY: American Association of Equine Practitioner; 1992.
  6. LeBlanc MM. Responses to plasma transfusion in clinically healthy and clinically ill foals. AAEP Lexington, KY: American Association of Equine Practitioners; 1987.
  7. McClure JT, DeLuca JL, Lunn DP, Miller J. Evaluation of IgG concentration and IgG subisotypes in foals with complete or partial failure of passive transfer after administration of intravenous serum or plasma.. Equine Vet J 2001 Nov;33(7):681-6.
    pubmed: 11770990doi: 10.2746/042516401776249273google scholar: lookup
  8. McClure JT, DeLuca JL, Lunn DP, Miller J. Evaluation of IgG concentration and IgG subisotypes in foals with complete or partial failure of passive transfer after administration of intravenous serum or plasma.. Equine Vet J 2001 Nov;33(7):681-6.
    pubmed: 11770990doi: 10.2746/042516401776249273google scholar: lookup
  9. Wilkins PA, Dewan-Mix S. Efficacy of intravenous plasma to transfer passive immunity in clinically healthy and clinically ill equine neonates with failure of passive transfer.. Cornell Vet 1994 Jan;84(1):7-14.
    pubmed: 8313712
  10. Becht JL, Semrad SD. Hematology, blood typing, and immunology of the neonatal foal.. Vet Clin North Am Equine Pract 1985 Apr;1(1):91-116.
    pubmed: 3907769doi: 10.1016/s0749-0739(17)30771-xgoogle scholar: lookup
  11. Jeffcott LB. Some practical aspects of the transfer of passive immunity to newborn foals.. Equine Vet J 1974 Jul;6(3):109-15.
  12. Petersen HH, Nielsen JP, Heegaard PM. Application of acute phase protein measurements in veterinary clinical chemistry.. Vet Res 2004 Mar-Apr;35(2):163-87.
    pubmed: 15099494doi: 10.1051/vetres:2004002google scholar: lookup
  13. Husebekk A, Husby G, Sletten K, Marhaug G, Nordstoga K. Characterization of amyloid protein AA and its serum precursor SAA in the horse.. Scand J Immunol 1986 Jun;23(6):703-9.
  14. 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.
    pubmed: 15950503doi: 10.1016/j.tvjl.2005.04.021google scholar: lookup
  15. Coutinho da Silva MA, Canisso IF, MacPherson ML, Johnson AE, Divers TJ. Serum amyloid A concentration in healthy periparturient mares and mares with ascending placentitis.. Equine Vet J 2013 Sep;45(5):619-24.
    pubmed: 23432049doi: 10.1111/evj.12034google scholar: lookup
  16. Paltrinieri S, Giordano A, Villani M, Manfrin M, Panzani S, Veronesi MC. Influence of age and foaling on plasma protein electrophoresis and serum amyloid A and their possible role as markers of equine neonatal septicaemia.. Vet J 2008 Jun;176(3):393-6.
    pubmed: 17644376doi: 10.1016/j.tvjl.2007.05.018google scholar: lookup
  17. Stoneham SJ, Palmer L, Cash R, Rossdale PD. Measurement of serum amyloid A in the neonatal foal using a latex agglutination immunoturbidimetric assay: determination of the normal range, variation with age and response to disease.. Equine Vet J 2001 Nov;33(6):599-603.
    pubmed: 11720032doi: 10.2746/042516401776563472google scholar: lookup
  18. Po E. The effects of equine plasma transfusion on markers of inflammation in healthy neonatal foals. Veterinary Clinical Medicine Urbana, IL: University of Illinois at Urbana‐Champaign; 2016:116.
  19. Sprayberry KA. Neonatal transfusion medicine: the use of blood, plasma, oxygen carrying solutions and adjunctive therapies in foals. Clin Tech Equine Pract 2003;2(1):31‐41.
  20. Barr B, Nieman NM. Serum amyloid A as an aid in diagnosing sepsis in equine neonates.. Equine Vet J 2022 Sep;54(5):922-926.
    pubmed: 34773677doi: 10.1111/evj.13540google scholar: lookup
  21. Viner M, Mazan M, Bedenice D, Mapes S, Pusterla N. Comparison of serum amyloid A in horses with infectious and noninfectious respiratory diseases. J Equine Vet 2017;49:11‐13.
  22. Dohoo IR, Martin SW, Stryhn H. Veterinary Epidemiologic Research. Charlottetown, Prince Edward Island, Canada: VER Inc; 2009.
  23. Alsemgeest SP, Taverne MA, Boosman R, van der Weyden BC, Gruys E. Peripartum acute-phase protein serum amyloid-A concentration in plasma of cows and fetuses.. Am J Vet Res 1993 Jan;54(1):164-7.
    pubmed: 7678954
  24. Alsemgeest SP, Jonker FH, Taverne MA, Kalsbeek HC, Wensing T, Gruys E. Serum amyloid-A (SAA) and haptoglobin (Hp) plasma concentrations in newborn calves.. Theriogenology 1995 Jan 15;43(2):381-7.
    pubmed: 16727630doi: 10.1016/0093-691x(94)00031-ogoogle scholar: lookup
  25. Peetsalu K, Tummeleht L, Kuks A, Orro T. Serum amyloid A and haptoglobin concentrations in relation to growth and colostrum intake in neonatal lambs. Livest Sci 2019;220:217‐220.
  26. Allen BV, Blackmore DJ. Relationship between paired plasma and serum viscosity and plasma proteins in the horse.. Res Vet Sci 1984 May;36(3):360-3.
    pubmed: 6463380
  27. 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.
    pubmed: 21783263doi: 10.1016/j.vetimm.2011.06.037google scholar: lookup
  28. McDonald TL, Larson MA, Mack DR, Weber A. Elevated extrahepatic expression and secretion of mammary-associated serum amyloid A 3 (M-SAA3) into colostrum.. Vet Immunol Immunopathol 2001 Dec;83(3-4):203-11.
    pubmed: 11730930doi: 10.1016/s0165-2427(01)00380-4google scholar: lookup
  29. Nolen‐Walston R. How to interpret serum amyloid a concentrations. AAEP Lexington, KY: American Association of Equine Practitioners; 2015.
  30. Orro T, Jacobsen S, LePage JP, Niewold T, Alasuutari S, Soveri T. Temporal changes in serum concentrations of acute phase proteins in newborn dairy calves.. Vet J 2008 May;176(2):182-7.
    pubmed: 17412622doi: 10.1016/j.tvjl.2007.02.010google scholar: lookup
  31. Secor EJ, Matychak MB, Felippe MJ. Transfer of tumour necrosis factor-α via colostrum to foals.. Vet Rec 2012 Jan;170(2):51.
    pubmed: 22027187doi: 10.1136/vr.100220google scholar: lookup
  32. 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.
    pmc: PMC7163734pubmed: 30565319doi: 10.1111/evj.13062google scholar: lookup
  33. Akiko C, Aoki T, Itoh M. Hematological and blood biochemical characteristics of newborn heavy draft foals after dystocia. J Equine Vet 2017;50:69‐75.
  34. Pearson JM, Homerosky ER, Caulkett NA, Campbell JR, Levy M, Pajor EA, Windeyer MC. Quantifying subclinical trauma associated with calving difficulty, vigour, and passive immunity in newborn beef calves.. Vet Rec Open 2019;6(1):e000325.
    pmc: PMC6347876pubmed: 30740228doi: 10.1136/vetreco-2018-000325google scholar: lookup
  35. Uhlar CM, Whitehead AS. Serum amyloid A, the major vertebrate acute-phase reactant.. Eur J Biochem 1999 Oct;265(2):501-23.
  36. Ousey JC. Peripartal endocrinology in the mare and foetus.. Reprod Domest Anim 2004 Aug;39(4):222-31.
  37. Nagel C, Aurich C. Induction of parturition in horses - from physiological pathways to clinical applications.. Domest Anim Endocrinol 2022 Jan;78:106670.
  38. Duggan V. Serum amyloid A in the neonatal foal: the significance of peri-parturient events.. Vet J 2008 Jun;176(3):267-9.
    pubmed: 17928246doi: 10.1016/j.tvjl.2007.08.029google scholar: lookup
  39. Harvey JW, Asquith RL, McNulty PK, Kivipelto J, Bauer JE. Haematology of foals up to one year old.. Equine Vet J 1984 Jul;16(4):347-53.
  40. Axon JE, Palmer JE. Clinical pathology of the foal.. Vet Clin North Am Equine Pract 2008 Aug;24(2):357-85, vii.
    pubmed: 18652960doi: 10.1016/j.cveq.2008.03.005google scholar: lookup
  41. Faramarzi B, Rich L. Haematological profile in foals during the first year of life.. Vet Rec 2019 Apr 20;184(16):503.
    pubmed: 30995997doi: 10.1136/vr.104461google scholar: lookup
  42. Tóthová C, Nagy O, Seidel H. Serum concentrations of selected acute phase proteins and enzyme activities after injection of a combined mineral preparation in calves. Acta Vet Brno 2009;59(5–6):467‐480.
  43. Schwartz D, Pusterla N, Jacobsen S, Christopher MM. Analytical validation of a new point-of-care assay for serum amyloid A in horses.. Equine Vet J 2018 Sep;50(5):678-683.
    pubmed: 29344980doi: 10.1111/evj.12807google scholar: lookup
  44. McDonald TL, Weber A, Smith JW. A monoclonal antibody sandwich immunoassay for serum amyloid A (SAA) protein.. J Immunol Methods 1991 Nov 22;144(2):149-55.
    pubmed: 1720442doi: 10.1016/0022-1759(91)90081-pgoogle scholar: lookup

Citations

This article has been cited 0 times.