Evidence map›Paper›PMID 33299985›Full record

ArticleCritical care explorations2020

Endothelial Biomarkers Are Associated With Indirect Lung Injury in Sepsis-Associated Pediatric Acute Respiratory Distress Syndrome.

Jane E Whitney, Rui Feng, Natalka Koterba, Fang Chen, Jenny Bush, Kathryn Graham, Simon F Lacey, Jan Joseph Melenhorst, Samir M Parikh, Scott L Weiss and 1 more

Open access · goldAbstract read
In one paragraph

Article in Critical care explorations, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
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

21 citing papers in PubMed, 28 citations in OpenAlex.

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  11. Translational medicine for acute lung injury.Journal of translational medicine · 2024
    Review
  12. Pathobiology, Severity, and Risk Stratification of Pediatric Acute Respiratory Distress Syndrome: From the Second Pediatric Acute Lung Injury Consensus Conference.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2023
    Review
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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 at 4 institutions in 1 country.

Jane E WhitneyDivision of Medical Critical Care, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Rui FengDepartment of Biostatistics, Epidemiology & Informatics, Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
Natalka KoterbaCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA.
Fang ChenCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA.
Jenny BushPediatric Sepsis Program, Children's Hospital of Philadelphia, Philadelphia, PA.
Kathryn GrahamPediatric Sepsis Program, Children's Hospital of Philadelphia, Philadelphia, PA.
Simon F LaceyCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA.
Jan Joseph MelenhorstCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA.
Samir M ParikhDivision of Nephrology, Harvard Medical School, Boston, MA.
Scott L WeissPediatric Sepsis Program, Children's Hospital of Philadelphia, Philadelphia, PA.
Nadir YehyaPediatric Sepsis Program, Children's Hospital of Philadelphia, Philadelphia, PA.
Children's Hospital of Philadelphia · USUniversity of Pennsylvania · USBeth Israel Deaconess Medical Center · USBoston Children's Hospital · US

Funding

Pediatric Critical Care Scientist Development ProgramK12HD047349 · NICHD · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HEATHER T. KEENAN, Kevin M Watt · 2004 to 2026
$17.0M
Mitochondrial Dysfunction in Pediatric SepsisK23GM110496 · NIGMS · CHILDREN'S HOSP OF PHILADELPHIA · PI WEISS, SCOTT L · 2015 to 2018
$723k
Clinical and Proteomic Characterization of Nucleosomes in Pediatric Acute Respiratory Distress SyndromeK23HL136688 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI YEHYA, NADIR · 2017 to 2020
$694k
NHLBI NIH HHS K23 HL136688NHLBI NIH HHS L30 HL149099NICHD NIH HHS K12 HD047349NIGMS NIH HHS K23 GM110496
6 · The paper itself

Abstract

objectivesAcute respiratory distress syndrome occurring in the setting of direct versus indirect lung injury may reflect different pathobiologies amenable to different treatment strategies. We sought to test whether a panel of plasma biomarkers differed between children with sepsis-associated direct versus indirect acute respiratory distress syndrome. We hypothesized that a biomarker profile indicative of endothelial activation would be associated with indirect acute respiratory distress syndrome.

designObservational cohort.

settingAcademic PICU. SUBJECTS: Patients less than 18 years old with sepsis-associated direct (pneumonia,

interventionsNone. MEASUREMENTS AND MAIN

resultsOf 58 biomarkers examined, 33 differed by acute respiratory distress syndrome subtype. We used classification and regression tree methodology to examine associations between clinical and biochemical markers and acute respiratory distress syndrome subtype. The classification and regression tree model using only clinical variables (age, sex, race, oncologic comorbidity, and Pediatric Risk of Mortality-III score) performed worse than the classification and regression tree model using five clinical variables and 58 biomarkers. The best classification and regression tree model used only four endothelial biomarkers, including elevated angiopoietin-2/angiopoietin-1 ratio, vascular cell-adhesion molecule, and von Willebrand factor, to identify indirect acute respiratory distress syndrome. Test characteristics were 89% (80-97%) sensitivity, 80% (69-92%) specificity, positive predictive value 84% (74-93%), and negative predictive value 86% (76-96%).

conclusionsIndirect lung injury in children with acute respiratory distress syndrome is characterized by a biomarker profile indicative of endothelial activation, excess inflammation, and worse outcomes. A model using four biomarkers has the potential to be useful for more precisely identifying patients with acute respiratory distress syndrome whose pathobiology may respond to endothelial-targeted therapies in future trials.

Indexed as

acute respiratory distress syndromechildrenendotheliumlung injurypediatricsepsis

Identifiers

PMID33299985
PMCPMC7721219
OpenAlexW3111211519

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.