98%
921
2 minutes
20
Background: Limited information is available regarding endothelial glycocalyx degradation during sepsis in horses. Plasma syndecan-1 concentrations are increased in consequence of sepsis in other species and have been useful for prognostication.
Objectives: To determine whether plasma syndecan-1 levels are increased in adult horses affected with sepsis.
Study Design: Retrospective cohort study.
Methods: Adult horses were assigned to one of three groups based on results of physical and laboratory examinations, clinical diagnosis, and results of previously described SIRS classification: Group 1 horses included healthy, nonseptic horses; Group 2 included horses in which clinical illness was identified but that were not considered to be septic; Group 3 included horses with a clinical diagnosis of sepsis. Plasma syndecan-1 concentration was determined in blood obtained at admission into the hospital for each horse, using an equine specific ELISA. Data were analysed using ANOVA and linear regression (p ≤ 0.05).
Results: One hundred and ninety-one horses were included and divided into three groups. Scores for SIRS were highest for Group 3 horses and lowest in Groups 1 and 2. Plasma syndecan-1 concentrations in Group 3 horses (50.73 ± 84.24 μg/ml; n = 42) were greater than those for Group 1 (15.69 ± 11.28 μg/ml; n = 66) and Group 2 (16.88 ± 15.30 μg/ml; n = 83). There was no difference regarding syndecan concentrations between Groups 1 and 2.
Main Limitations: Retrospective study design, solitary time point of measurement for each patient, and lack of a widely accepted consensus regarding definitive diagnosis of sepsis in adult horses.
Conclusions: Circulating plasma levels of syndecan-1, a biochemical marker of endothelial glycocalyx damage, are increased in septic adult horses.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1111/evj.13862 | DOI Listing |
Pediatr Blood Cancer
October 2025
Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark.
Endothelial damage may play a key role in several non-infectious toxicities following hematopoietic stem cell transplantation (HSCT). We explored damage to the endothelial glycocalyx in 113 children undergoing HSCT by measuring syndecan-1 plasma levels. Syndecan-1 levels were elevated in patients with severe sinusoidal obstruction syndrome (SOS) and steroid-refractory/dependent acute graft-versus-host disease, but remained low in milder cases.
View Article and Find Full Text PDFBurns
July 2025
Firefighters' Burn and Surgical Research Laboratory, MedStar Health Research Institute, Washington, DC, United States; Departments of Surgery and Biochemistry, Georgetown University School of Medicine, Washington, DC, United States; The Burn Center, MedStar Washington Hospital Center, Washington, DC
Introduction: Burn shock is mediated by a complex inflammatory response leading to endothelial cell dysfunction (EnD) and increased vascular permeability in large total body surface area (TBSA) injuries. Smaller TBSA burns do not induce systemic EnD. Previous studies in animal models have examined systemic markers of endothelial cell dysfunction following thermal injury and have aimed to characterize this dysfunction in various end organs.
View Article and Find Full Text PDFProteomics
August 2025
Department of Biotechnology, Biomedical Research Foundation, Academy of Athens, Athens, Greece.
Multiple myeloma (MM) remains incurable; gaps in our understanding of MM molecular pathogenesis and drugs' resistance mechanisms are involved in the failure of therapies. This study aims to identify proteins significantly impacting MM patients' response to commonly used therapeutic regimens. Bone marrow CD138+ selected plasma cells were isolated from patients who had achieved Response (Responders, R) and those who were Non-Responders (NR) to their primary MM therapy.
View Article and Find Full Text PDFCell Rep
August 2025
Department of Pathology, Albert Einstein College of Medicine, Bronx, NY, USA. Electronic address:
Durable serological protection is maintained through the persistence of antigen-specific plasma cells (PCs), but key factors regulating the survival of nascent PCs remain unclear. Previously, we reported that bone marrow (BM) PCs partially organize into clusters that are enriched for long-lived PCs, suggesting that clusters are survival niches. Here, we report that acute blockade of a proliferation-inducing ligand (APRIL) and B cell activating factor (BAFF) using transmembrane activator and CAML interactor (TACI)-Fc rapidly disrupts clusters and mobilizes BM PCs.
View Article and Find Full Text PDFFront Immunol
August 2025
Department of Respiratory and Critical Care Medicine, Tianjin Medical University General Hospital, Tianjin, China.
Introduction: Neutrophil extracellular traps (NETs) play a critical role in inflammation and coagulation imbalance. Recent studies have demonstrated that activation of gasdermin D (GSDMD) protein and its pore-forming activity are essential drivers of NET generation. This study investigated the association between GSDMD-NETs axis activation and sepsis-induced coagulopathy (SIC), as well as the potential association with glycocalyx damage.
View Article and Find Full Text PDF