Evidence map›Paper›PMID 24937177›Full record

ArticleAmerican journal of respiratory and critical care medicine2014

Pseudomonas aeruginosa in vitro phenotypes distinguish cystic fibrosis infection stages and outcomes.

Nicole Mayer-Hamblett, Margaret Rosenfeld, Ronald L Gibson, Bonnie W Ramsey, Hemantha D Kulasekara, George Z Retsch-Bogart, Wayne Morgan, Daniel J Wolter, Christopher E Pope, Laura S Houston and 5 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
8.0field-weighted citation impact, top 2% 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

69 citing papers in PubMed, 115 citations in OpenAlex.

  1. Amikacin liposome inhalation suspension for chronic Pseudomonas aeruginosa infection in cystic fibrosis.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2020
    Trial
  2. Impact of Sustained Eradication of New Pseudomonas aeruginosa Infection on Long-term Outcomes in Cystic Fibrosis.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2015
    Trial
  3. Article
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  7. mBio · 2024
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  8. Insights onMicroorganisms · 2024
    Article
  9. bioRxiv : the preprint server for biology · 2024
    Article
  10. Article
  11. Microbiology spectrum · 2024
    Article
  12. Oral Cavity Microbiome Impact on Respiratory Infections Among Children.Pediatric health, medicine and therapeutics · 2024
    Review
  13. Review
  14. bioRxiv : the preprint server for biology · 2023
    Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Mutational background influencesProceedings of the National Academy of Sciences of the United States of America · 2022
    Article

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 5 institutions in 1 country.

Nicole Mayer-Hamblett1 Department of Pediatrics.
Margaret Rosenfeld
Ronald L Gibson
Bonnie W Ramsey
Hemantha D Kulasekara
George Z Retsch-Bogart
Wayne Morgan
Daniel J Wolter
Christopher E Pope
Laura S Houston
Bridget R Kulasekara
Umer Khan
Jane L Burns
Samuel I Miller
Lucas R Hoffman
Seattle Children's Hospital · USUniversity of Washington · USHuman Genome Sciences (United States) · USUniversity of Arizona · USUniversity of North Carolina at Chapel Hill · US

Funding

Institute of Translational Health SciencesUL1TR000423 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$49.4M
Translational Research Center to Expedite Novel Therapies in Cystic FibrosisP30DK089507 · NIDDK · SEATTLE CHILDREN'S HOSPITAL · PI Christopher Hooper Goss · 2010 to 2026
$21.4M
Pseudomonas aeruginosa Adaptation During Early CF Airway Infection and TreatmentR01HL098084 · NHLBI · UNIVERSITY OF WASHINGTON · PI HOFFMAN, LUCAS R · 2009 to 2012
$1.6M
Pseudomonas Aeruginosa Early CF Adaptive Changes: A Translational StudyK02HL105543 · NHLBI · UNIVERSITY OF WASHINGTON · PI HOFFMAN, LUCAS R · 2011 to 2014
$400k
NCATS NIH HHS UL1 TR000423NCATS NIH HHS UL1TR000423NHLBI NIH HHS K02 HL105543NHLBI NIH HHS K02HL105543NHLBI NIH HHS R01 HL098084NHLBI NIH HHS R01HL098084NIDDK NIH HHS P30 DK089507NIDDK NIH HHS P30DK089507
6 · The paper itself

Abstract

rationalePseudomonas aeruginosa undergoes phenotypic changes during cystic fibrosis (CF) lung infection. Although mucoidy is traditionally associated with transition to chronic infection, we hypothesized that additional in vitro phenotypes correlate with this transition and contribute to disease.

objectivesTo characterize the relationships between in vitro P. aeruginosa phenotypes, infection stage, and clinical outcomes.

methodsA total of 649 children with CF and newly identified P. aeruginosa were followed for a median 5.4 years during which a total of 2,594 P. aeruginosa isolates were collected. Twenty-six in vitro bacterial phenotypes were assessed among the isolates, including measures of motility, exoproduct production, colony morphology, growth, and metabolism. MEASUREMENTS AND MAIN

resultsP. aeruginosa phenotypes present at the time of culture were associated with both stage of infection (new onset, intermittent, or chronic) and the primary clinical outcome, occurrence of a pulmonary exacerbation (PE) in the subsequent 2 years. Two in vitro P. aeruginosa phenotypes best distinguished infection stages: pyoverdine production (31% of new-onset cultures, 48% of intermittent, 69% of chronic) and reduced protease production (31%, 39%, and 65%, respectively). The best P. aeruginosa phenotypic predictors of subsequent occurrence of a PE were mucoidy (odds ratio, 1.75; 95% confidence interval, 1.19-2.57) and reduced twitching motility (odds ratio, 1.43; 95% confidence interval, 1.11-1.84).

conclusionsIn this large epidemiologic study of CF P. aeruginosa adaptation, P. aeruginosa isolates exhibited two in vitro phenotypes that best distinguished early and later infection stages. Among the many phenotypes tested, mucoidy and reduced twitching best predicted subsequent PE. These phenotypes indicate potentially useful prognostic markers of transition to chronic infection and advancing lung disease.

Indexed as

AdolescentChildChild, PreschoolCystic FibrosisDisease ProgressionFemaleHumansInfantIn Vitro TechniquesLogistic ModelsMaleMulticenter Studies as TopicOutcome Assessment, Health CarePhenotypeProspective StudiesPseudomonas aeruginosaepidemiologyexacerbationmucoid Pseudomonas aeruginosapulmonary functionrisk factors

Identifiers

PMID24937177
PMCPMC4226041
OpenAlexW2143954504

What OpenQuestion holds

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Read underepoch 390

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.