Evidence map›Paper›PMID 27606687›Full record

ArticlePloS one2016

Extremes of Interferon-Stimulated Gene Expression Associate with Worse Outcomes in the Acute Respiratory Distress Syndrome.

Jerry A Nick, Silvia M Caceres, Jennifer E Kret, Katie R Poch, Matthew Strand, Anna V Faino, David P Nichols, Milene T Saavedra, Jennifer L Taylor-Cousar, Mark W Geraci and 6 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00548795 (A Prospective Assessment of Viral-induced Adaptation of Neutrophil Response in ARDS - Ancillary to ARDS Network Trials), which is not on this map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 17% 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.

NCT00548795 completednot on this map

A Prospective Assessment of Viral-induced Adaptation of Neutrophil Response in ARDS - Ancillary to ARDS Network Trials

TypeobservationalSponsorNational Jewish HealthRan2007 to 2012Enrolled132ConditionsRespiratory Distress Syndrome, Adult
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  3. Article
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  5. Article
  6. Distribution ofMicroorganisms · 2022
    Article
  7. Article
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  15. Article
  16. Review
  17. Article
  18. Fifty Years of Research in ARDS. Genomic Contributions and Opportunities.American journal of respiratory and critical care medicine · 2017
    Review
  19. Review
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

16 authors at 6 institutions in 1 country.

Jerry A NickDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America.
Silvia M CaceresDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America.
Jennifer E KretSt Louis County Department of Public Health, Berkeley, Missouri, United States of America.
Katie R PochDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America.
Matthew StrandDivision of Biostatistics and Bioinformatics, National Jewish Health, Denver, Colorado, United States of America.
Anna V FainoDivision of Biostatistics and Bioinformatics, National Jewish Health, Denver, Colorado, United States of America.
David P NicholsDepartment of Pediatrics, National Jewish Health, Denver, Colorado, United States of America.
Milene T SaavedraDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America.
Jennifer L Taylor-CousarDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America.
Mark W GeraciDivision of Pulmonary Science and Critical Care Medicine, Department of Medicine, University of Colorado Denver School of Medicine, Aurora, Colorado, United States of America.
Ellen L BurnhamDivision of Pulmonary Science and Critical Care Medicine, Department of Medicine, University of Colorado Denver School of Medicine, Aurora, Colorado, United States of America.
Michael B FesslerImmunity, Inflammation, and Disease Laboratory, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, North Carolina, United States of America.
Benjamin T SurattDepartment of Medicine, University of Vermont College of Medicine, Burlington, Vermont, United States of America.
Edward AbrahamOffice of the Dean, Wake Forest School of Medicine, Winston-Salem, North Carolina, United States of America.
Marc MossDivision of Pulmonary Science and Critical Care Medicine, Department of Medicine, University of Colorado Denver School of Medicine, Aurora, Colorado, United States of America.
Kenneth C MalcolmDepartment of Medicine, National Jewish Health, Denver, Colorado, United States of America.
National Jewish Health · USUniversity of Colorado Denver · USNational Institute of Environmental Health Sciences · USSt. Louis County Missouri · USUniversity of Vermont · USWake Forest University · US

Funding

Cell Signaling of Host DefenseZIAES102005 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI FESSLER, MICHAEL B · 2009 to 2025
$41.7M
Role of Interleukin-18 in Acute Lung InjuryP01HL068743 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI DINARELLO, CHARLES ANTHONY · 2002 to 2006
$7.4M
Cell Signaling of Host DefenseZ01ES102005 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI FESSLER, MICHAEL B · 2006 to 2008
$3.3M
Viral-induced Adaptation of Neutrophil Response in ARDSR01HL090991 · NHLBI · NATIONAL JEWISH HEALTH · PI NICK, JERRY A · 2007 to 2010
$1.7M
Intramural NIH HHS Z01 ES102005NHLBI NIH HHS P01 HL068743NHLBI NIH HHS R01 HL090991
6 · The paper itself

Abstract

Acute Respiratory Distress Syndrome (ARDS) severity may be influenced by heterogeneity of neutrophil activation. Interferon-stimulated genes (ISG) are a broad gene family induced by Type I interferons, often as a response to viral infections, which evokes extensive immunomodulation. We tested the hypothesis that over- or under-expression of immunomodulatory ISG by neutrophils is associated with worse clinical outcomes in patients with ARDS. Genome-wide transcriptional profiles of circulating neutrophils isolated from patients with sepsis-induced ARDS (n = 31) and healthy controls (n = 19) were used to characterize ISG expression. Hierarchical clustering of expression identified 3 distinct subject groups with Low, Mid and High ISG expression. ISG accounting for the greatest variability in expression were identified (MX1, IFIT1, and ISG15) and used to analyze a prospective cohort at the Colorado ARDS Network site. One hundred twenty ARDS patients from four urban hospitals were enrolled within 72 hours of initiation of mechanical ventilation. Circulating neutrophils were isolated from patients and expression of ISG determined by PCR. Samples were stratified by standard deviation from the mean into High (n = 21), Mid, (n = 82) or Low (n = 17) ISG expression. Clinical outcomes were compared between patients with High or Low ISG expression to those with Mid-range expression. At enrollment, there were no differences in age, gender, co-existing medical conditions, or type of physiologic injury between cohorts. After adjusting for age, race, gender and BMI, patients with either High or Low ISG expression had significantly worse clinical outcomes than those in the Mid for number of 28-day ventilator- and ICU-free days (P = 0.0006 and 0.0004), as well as 90-day mortality and 90-day home with unassisted breathing (P = 0.02 and 0.004). These findings suggest extremes of ISG expression by circulating neutrophils from ARDS patients recovered early in the syndrome are associated with poorer clinical outcomes.

Indexed as

Case-Control StudiesCell SeparationFemaleGene Expression ProfilingGene Expression RegulationHumansInterferon-alphaInterferonsKaplan-Meier EstimateMaleMiddle AgedMultivariate AnalysisNeutrophilsOdds RatioRespiratory Distress SyndromeRisk FactorsInterferon-alphaInterferons

Identifiers

PMID27606687
PMCPMC5015849
OpenAlexW2510558112

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.