SERUM SOLUBLE ENDOGLIN IN PEDIATRIC SEPTIC SHOCK–ASSOCIATED MULTIPLE ORGAN DYSFUNCTION SYNDROME

Author:

Atreya Mihir R.,Cvijanovich Natalie Z.1,Fitzgerald Julie C.2,Weiss Scott L.2,Bigham Michael T.3,Jain Parag N.4,Schwarz Adam J.5,Lutfi Riad6,Nowak Jeffrey7,Thomas Neal J.8,Quasney Michael9,Haileselassie Bereketeab10,Baines Torrey D.11,Zingarelli Basilia,

Affiliation:

1. UCSF Benioff Children's Hospital Oakland, Oakland, California

2. Children's Hospital of Philadelphia, Philadelphia, Pennsylvania

3. Akron Children's Hospital, Akron, Ohio

4. Texas Children's Hospital and Baylor College of Medicine, Houston, Texas

5. Children's Hospital of Orange County, Orange, California

6. Riley Hospital for Children, Indianapolis, Indiana

7. Children's Hospital and Clinics of Minnesota, Minneapolis, Minnesota

8. Penn State Hershey Children's Hospital, Hershey, Pennsylvania

9. CS Mott Children's Hospital at the University of Michigan, Ann Arbor, Michigan

10. Lucile Packard Children's Hospital Stanford, Palo Alto, California

11. University of Florida Health Shands Children's Hospital, Gainesville, Florida

Abstract

ABSTRACT Background: Endothelial activation is a key driver of multiple organ dysfunction syndrome (MODS). Soluble endoglin (sENG) is expressed by mature and progenitor endothelial cells and thought to have angiogenic properties. We sought to determine the association between sENG and pediatric sepsis-associated MODS. Methods: Prospective observational study of pediatric septic shock. Primary outcome of interest was complicated course—a composite of death by (or) MODS on day 7 of illness. Secondary outcomes included individual organ dysfunctions. Endothelial biomarkers including sENG were measured using multiplex Luminex assays among patients with existing data on the Pediatric Sepsis Biomarker Risk Model (PERSEVERE-II) data. Multivariable regression was used to test the independent association between sENG and clinical outcomes. Serum sENG concentrations across PERSEVERE-II mortality risk strata and correlations with established markers of endothelial dysfunction were determined. Results: Three hundred six critically ill children with septic shock were included. Serum sENG concentrations were higher among those with primary and secondary outcomes of interest, with the exception of acute neurological dysfunction. Soluble endoglin was independently associated with increased odds of complicated course (adjusted odds ratio, 1.53; 95% confidence interval, 1.02–2.27; P = 0.038) and acute renal dysfunction (adjusted odds ratio, 1.84; 95% confidence interval, 1.18–2.876; P = 0.006). Soluble endoglin demonstrated graded responses across PERSEVERE-II risk strata and was positively correlated with endothelial biomarkers, except angiopoietin-1. Conclusions: Serum sENG is independently associated with complicated course and acute renal dysfunction in pediatric septic shock. Future studies are required to validate our observational data, and mechanistic studies are necessary to elucidate whether endoglin plays an organ-specific role in the development or resolution of acute renal dysfunction in sepsis.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Critical Care and Intensive Care Medicine,Emergency Medicine

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