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A Controlled Mouse Model for Neonatal Polymicrobial Sepsis
Published on: January 27, 2019
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Increased plasma nucleosomes are associated with severe sepsis in foals
E M Birckhead1, S L Raidal1, S Das1
1Gulbali Institute, School of Agricultural, Environmental and Veterinary Sciences, Faculty of Science and Health, Charles Sturt University, Locked Bag 588, Booroma St, Wagga Wagga, NSW 2678, Australia.
Veterinary Journal (London, England : 1997)
|January 10, 2025
Summary
Nucleosome levels were significantly increased in foals with severe sepsis, indicating a potential biomarker for this life-threatening condition in neonatal horses. Further research is needed to confirm diagnostic utility.
Area of Science:
- Veterinary Medicine
- Equine Neonatal Health
- Immunology
Background:
- Sepsis is a leading cause of mortality in neonatal foals.
- Diagnosis is challenging due to non-specific clinical signs and limited diagnostic tools.
- Increased nucleosome levels are associated with sepsis in humans and other animals.
Purpose of the Study:
- To investigate whether circulating nucleosome levels are elevated in foals with sepsis.
- To determine if nucleosome levels correlate with disease severity, specifically severe sepsis in foals.
Main Methods:
- Plasma samples were collected from clinically healthy, sick non-septic, and septic foals.
- An enzyme-linked immunosorbent assay (ELISA) was used to quantify nucleosome levels.
- Septic foals were further classified as severe sepsis based on hypoperfusion and/or organ dysfunction.
Main Results:
- Nucleosome levels were significantly higher in foals with severe sepsis compared to all other groups.
- No significant difference in nucleosome levels was observed between sick non-septic and clinically healthy foals.
- The study acknowledges potential confounding factors like non-age-matched groups.
Conclusions:
- Elevated nucleosome levels show promise as a biomarker for severe sepsis in neonatal foals.
- Nucleosome analysis may aid in assessing and understanding equine neonatal sepsis.
- Larger, age-matched studies are recommended to validate these findings and explore related biomarkers.
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