Abstract: In hospitalized foals, limited data are available on the utility of sequential measurement of SAA concentrations and the value of these data in a clinical setting. Objective: To determine serum amyloid A (SAA) concentrations in ill neonatal foals at multiple timepoints during hospitalization, and to evaluate a potential association with systemic inflammatory response syndrome (SIRS) status, blood culture (BC) result, and survival. Methods: Hospitalized ill foals (n = 90, ≤ 14 days). Methods: In this retrospective study, foals were classified based on SIRS criteria: "SIRS" or "NonSIRS," BC results, and survival. Serum amyloid A concentrations on admission (ADM), day 1 (D1) and day 2 (D2) were compared within and between groups, using nonparametric tests. Results are presented as median (IQR) (effect size; 95% CI). Results: Serum amyloid A concentrations were higher in SIRS than in NonSIRS foals both on ADM (401 mg/L (99; 855) vs 67 mg/L (23; 685), [ES 129, 95% CI, 15-385]), and on D1 (836 mg/L (616; 1240) vs 212 mg/L (69; 890), [ES 501, 95% CI, 121-724]). On D2, but not on ADM, foals with a positive BC had higher SAA (1244 mg/L (757; 2004)) than BC negative foals (153 mg/L (57; 695), [ES 1002; 95% CI, 282-1418]). On D1, but not on ADM, SAA was higher in non-survivors (729 mg/L (469; 1347) than in survivors (323 mg/L (75; 889), [ES 373; 95% CI, 28-651]). Conclusions: Serum amyloid A measurements on D1 and D2 of hospitalization likely reflect both the severity of disease and response to initial treatment. Repeated SAA measurements during hospitalization can aid clinicians in determining severity of disease and can be useful as a prognosticator in ill neonatal foals.
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Overview
This study examined the changes in serum amyloid A (SAA) levels over time in sick newborn foals in the hospital, seeking to understand how these changes relate to inflammation, infection status, and survival outcomes.
Introduction and Objective
SAA is an acute phase protein that increases in response to inflammation and infection.
In neonatal foals, it’s important to know if sequential SAA measurements can help evaluate illness severity, guide treatment decisions, and predict outcomes.
The main objectives were to measure SAA concentrations at multiple timepoints—on admission (ADM), day 1 (D1), and day 2 (D2)—in hospitalized ill foals and assess associations with:
Systemic inflammatory response syndrome (SIRS) status
Survival versus non-survival during hospitalization
Methods
This was a retrospective study including 90 hospitalized foals aged 14 days or younger.
Foals were categorized based on three criteria:
SIRS or NonSIRS based on clinical and laboratory parameters.
Positive or negative blood cultures (presence or absence of bloodstream infection).
Outcome: survivor or non-survivor during hospitalization.
SAA concentrations were measured at three timepoints: admission (ADM), day 1 (D1), and day 2 (D2).
Statistical analysis involved nonparametric tests comparing SAA levels within and between groups, reporting medians, interquartile ranges (IQR), effect sizes (ES), and 95% confidence intervals (CI).
Key Results
SAA and SIRS status:
On admission (ADM), foals with SIRS had significantly higher SAA (median 401 mg/L) compared to NonSIRS foals (67 mg/L).
On Day 1 (D1), this difference remained with even higher SAA in SIRS foals (836 mg/L vs. 212 mg/L).
SAA and blood culture results:
At admission, SAA levels were not significantly different between foals with positive and negative blood cultures.
On Day 2 (D2), foals with positive blood cultures had markedly higher SAA (1244 mg/L) compared to those with negative cultures (153 mg/L), suggesting delayed or ongoing infection response.
SAA and survival:
On Day 1 (D1), non-survivors showed significantly higher SAA concentrations (729 mg/L) than survivors (323 mg/L), indicating higher systemic inflammation in fatal cases.
No significant differences in SAA at admission were observed based on survival.
Conclusions and Clinical Implications
Sequential SAA measurements provide valuable information on the severity and progression of illness in hospitalized neonatal foals.
Elevated SAA on Day 1 and Day 2 correlates with SIRS, bloodstream infection, and poorer outcomes.
Because SAA changes may lag behind clinical signs and blood culture positivity, multiple measurements over time are useful for tracking response to treatment.
Clinicians can use repeated SAA testing as a prognostic tool to stratify risk, monitor disease severity, and potentially guide therapeutic decisions in ill neonatal foals.
This approach enhances the clinical utility of SAA beyond a single measurement at admission, emphasizing the importance of dynamic monitoring during hospitalization.
Cite This Article
APA
van den Brom-Spierenburg AJ, Siegers EW, Westermann CM, Vernooij JCM, Sloet van Oldruitenborgh-Oosterbaan MM, Theelen MJP.
(2026).
Sequential measurement of serum amyloid A concentrations in ill hospitalized neonatal foals.
J Vet Intern Med, 40(2), aalag035.
https://doi.org/10.1093/jvimsj/aalag035
The authors declare no conflicts of interest. Serum amyloid A test kits were partly funded by Vrienden Diergeneeskunde. The funding organization was not involved in the design, execution, or reporting of this study.
References
This article includes 24 references
Hultén C, Tulamo RM, Suominen MM, Burvall K, Marhaug G, Forsberg M. A non-competitive chemiluminescence enzyme immunoassay for the equine acute phase protein serum amyloid A (SAA)—a clinically useful inflammatory marker in the horse.. Vet Immunol Immunopathol 1999;68:267-281.
Nieman NM, Chan DS. Comparison of the diagnostic predictability of serum amyloid A, white blood cell count and immunoglobulin G tests as indicators of early-onset, acute-phase morbidities in newborn foals.. Equine Vet Educ 2022;34:e533-e539.
Theelen MJP, Wilson WD, Byrne BA. Differences in isolation rate and antimicrobial susceptibility of bacteria isolated from foals with sepsis at admission and after ≥ 48 hours of hospitalization.. J Vet Intern Med 2020;34:955-963.
Singer M, Deutschman CS, Warren Seymour C. The third international consensus definitions for sepsis and septic shock (sepsis-3).. JAMA 2016;315:801-810.
Lankenfeld A, Weber C, Rohn K, Venner M. Kinetics of serum amyloid A during the treatment period of foals with pneumonia (Kinetik Von serum amyloid A Während Der Behandlungszeit Von Fohlen Mit Pneumonie).. Pferdeheilkunde 2021;37:128-137.
Palmisano M, Javsicas L, McNaughten J, Gamsjäger L, Renaud DL, Gomez DE. Effect of plasma transfusion on serum amyloid A concentration in healthy neonatal foals and foals with failure of passive immunity.. J Vet Intern Med 2023;37:697-702.