Evidence map›Paper›PMID 42656713›Full record

ArticleFrontiers in medicine2026

Age-related differences in circulating heparanase-1 activity in sepsis and correlation with systemic vascular endotheliopathy.

Colin J Sallee, Aaron S Noa, Mouli Bhowmik, Amber C Nobles, Zhangjie Wang, Jian Liu, Jillian R Richter, J Edwin Blalock, Rakesh P Patel, Amit Gaggar and 1 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Colin J SalleeDivision of Pediatric Critical Care Medicine, Department of Pediatrics, David Geffen School of Medicine, University of California, Los Angeles, CA, United States.
Aaron S NoaHeersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Mouli BhowmikDivision of Pediatric Critical Care Medicine, Department of Pediatrics, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Amber C NoblesDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Zhangjie WangGlycan Therapeutics, Raleigh, NC, United States.
Jian LiuDivision of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Jillian R RichterDivision of Trauma and Acute Care Surgery, Department of Surgery, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
J Edwin BlalockDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Rakesh P PatelDepartment of Pathology, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Amit GaggarDivision of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
Robert P RichterDivision of Pediatric Critical Care Medicine, Department of Pediatrics, Heersink School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.

Funding

Role of heme and PGP matrikines in lung inflammationR01HL153113 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GAGGAR, AMIT, PATEL, RAKESH P. · 2020 to 2023
$2.2M
Mechanisms driving endothelial angiopoietin-2 expression and vascular dysfunction during pediatric sepsisK08GM144788 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI RICHTER, ROBERT P · 2021 to 2025
$930k
NHLBI NIH HHS R01 HL153113NIGMS NIH HHS K08 GM144788
6 · The paper itself

Abstract

Background: Heparanase-1 (HPSE)-mediated degradation of endothelial glycocalyx heparan sulfate (HS) contributes to vascular endotheliopathy in sepsis, yet age-dependent differences in HPSE biology remain undefined. Thus, we sought to determine age-related differences in circulating HPSE activity during sepsis and its association with markers of endotheliopathy and organ dysfunction. Methods: Heparanase-1 enzymatic activity and HS disaccharide levels were measured in plasma from children (10 sepsis, 10 controls) and adults (16 sepsis, 15 controls) from prospective observational cohorts using liquid chromatography-tandem mass spectrometry. Associations with plasma angiopoietin-2 levels and change in serum albumin (markers of endotheliopathy) in addition to organ failure scores were assessed using Spearman correlations. Results: Heparanase-1 activity and circulating HS were elevated in both sepsis cohorts compared to controls, with moderate-to-strong correlations between HPSE activity and HS levels. However, adults with sepsis demonstrated approximately 10-fold higher plasma HPSE activity than children (median 1,256 vs. 116, Conclusion: Heparanase-1-mediated glycocalyx degradation is a conserved feature of sepsis across the age spectrum, but the magnitude, cellular source, and clinical implications of circulating HPSE activity differ markedly by age, underscoring the need for age-stratified therapeutic approaches.

Indexed as

adultschildrenendothelial glycocalyxheparanase activityheparan sulfatesepsisvascular endotheliopathy

Identifiers

PMID42656713
PMCPMC13506940

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.