Evidence map›Paper›PMID 30114376›Full record

ArticleAmerican journal of respiratory and critical care medicine2019

Early Plasma Matrix Metalloproteinase Profiles. A Novel Pathway in Pediatric Acute Respiratory Distress Syndrome.

Matt S Zinter, Kevin L Delucchi, Michele Y Kong, Benjamin E Orwoll, Aaron S Spicer, Michelle J Lim, Mustafa F Alkhouli, Anna E Ratiu, Anne V McKenzie, Patrick S McQuillen and 4 more

Abstract readEditorial
In one paragraph

Article in American journal of respiratory and critical care medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

39 citing papers in PubMed, 55 citations in OpenAlex.

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  17. 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
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 1 country.

Matt S Zinter1 Division of Critical Care and.
Kevin L Delucchi2 Department of Psychiatry, and.
Michele Y Kong3 Division of Critical Care Medicine, Department of Pediatrics, University of Alabama School of Medicine, Birmingham, Alabama; and.
Benjamin E Orwoll1 Division of Critical Care and.
Aaron S Spicer1 Division of Critical Care and.
Michelle J Lim4 Division of Critical Care, Department of Pediatrics, Mattel Children's Hospital, University of California Los Angeles Geffen School of Medicine, Los Angeles, California.
Mustafa F Alkhouli1 Division of Critical Care and.
Anna E Ratiu4 Division of Critical Care, Department of Pediatrics, Mattel Children's Hospital, University of California Los Angeles Geffen School of Medicine, Los Angeles, California.
Anne V McKenzie1 Division of Critical Care and.
Patrick S McQuillen1 Division of Critical Care and.
Christopher C Dvorak5 Division of Allergy, Immunology, and Blood & Marrow Transplantation, Department of Pediatrics, Benioff Children's Hospital.
Carolyn S Calfee6 Department of Anesthesia and.
Michael A Matthay6 Department of Anesthesia and.
Anil Sapru1 Division of Critical Care and.
University of California, Los Angeles · USUniversity of California, San Francisco · USSociety of Critical Care Medicine · USUCSF Benioff Children's Hospital · US

Funding

Pediatric Scientist Development Program (PSDP) [K12]K12HD000850 · NICHD · YALE UNIVERSITY · PI Sallie R. Permar · 1987 to 2026
$44.1M
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
Precision Medicine in the Acute Respiratory Distress SyndromeR35HL140026 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CALFEE, CAROLYN · 2018 to 2024
$6.8M
Resolution of Clinical Lung InjuryR37HL051856 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MATTHAY, MICHAEL A. · 2006 to 2015
$3.9M
Coagulation and Fibrinolysis in Pediatric Insulin Titration TrialR01HL114484 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SAPRU, ANIL · 2012 to 2015
$1.6M
Targeted Genomic Analysis of Coagulation Pathways in Acute Lung InjuryK23HL085526 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SAPRU, ANIL · 2007 to 2011
$756k
Matrix Metalloproteinase Driven Lung Inflammation in RSV diseaseK08HL119359 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KONG, MICHELE · 2014 to 2018
$715k
NHLBI NIH HHS K08 HL119359NHLBI NIH HHS K23 HL085526NHLBI NIH HHS R01 HL114484NHLBI NIH HHS R35 HL140026NHLBI NIH HHS R37 HL051856NICHD NIH HHS K12 HD000850NICHD NIH HHS K12 HD047349
6 · The paper itself

Abstract

rationaleMMPs (Matrix metalloproteinases) and their endogenous tissue inhibitors may contribute to lung injury through extracellular matrix degradation and modulation of inflammation and fibrosis.

objectivesTo test for an association between MMP pathway proteins and inflammation, endothelial dysfunction, and clinical outcomes.

methodsWe measured MMPs in plasma collected on acute respiratory distress syndrome (ARDS) Day 1 from 235 children at five hospitals between 2008 and 2017. We used latent class analysis to identify patients with distinct MMP profiles and then associated those profiles with markers of inflammation (IL-1RA, -6, -8, -10, and -18; macrophage inflammatory protein-1α and -1β; tumor necrosis factor-α and -R2), endothelial injury (angiopoietin-2, von Willebrand factor, soluble thrombomodulin), impaired oxygenation (Pa MEASUREMENTS AND MAIN

resultsIn geographically distinct derivation and validation cohorts, approximately one-third of patients demonstrated an MMP profile characterized by elevated MMP-1, -2, -3, -7, and -8 and tissue inhibitor of metalloproteinase-1 and -2; and depressed active and total MMP-9. This MMP profile was associated with multiple markers of inflammation, endothelial injury, and impaired oxygenation on Day 1 of ARDS, and conferred fourfold increased odds of mortality or severe morbidity independent of the P/F ratio and other confounders (95% confidence interval, 2.1-7.6; P < 0.001). Logistic regression using both the P/F ratio and MMP profiles was superior to the P/F ratio alone in prognosticating mortality or severe morbidity (area under the receiver operating characteristic curve, 0.75; 95% confidence interval, 0.68-0.82 vs. area under the receiver operating characteristic curve, 0.66; 95% confidence interval, 0.58-0.73; P = 0.009).

conclusionsPediatric patients with ARDS have specific plasma MMP profiles associated with inflammation, endothelial injury, morbidity, and mortality. MMPs may play a role in the pathobiology of children with ARDS.

Indexed as

BiomarkersChildHumansMatrix MetalloproteinasesRespiratory Distress SyndromeBiomarkersMatrix Metalloproteinasesmatrix metalloproteinasespediatric acute lung injurypediatric acute respiratory distress syndromepediatric intensive care unittissue inhibitor of metalloproteinases

Identifiers

PMID30114376
PMCPMC6353006
OpenAlexW2886082206

What OpenQuestion holds

Textmetadata
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.