Evidence map›Paper›PMID 27861524›Full record

ArticlePloS one2016

Factors Associated with Worse Lung Function in Cystic Fibrosis Patients with Persistent Staphylococcus aureus.

Sibylle Junge, Dennis Görlich, Martijn den Reijer, Bärbel Wiedemann, Burkhard Tümmler, Helmut Ellemunter, Angelika Dübbers, Peter Küster, Manfred Ballmann, Cordula Koerner-Rettberg and 19 more

Registry-linked trialOpen access · goldAbstract readMulticenter Study
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 NCT00669760 (Dissection of Staphylococcus Aureus Infection From Colonization in Cystic Fibrosis Patients, a Non-interventional, Prospective, Longitudinal Multicenter Study.), which is not on this map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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.

NCT00669760 completednot on this map

Dissection of Staphylococcus Aureus Infection From Colonization in Cystic Fibrosis Patients, a Non-interventional, Prospective, Longitudinal Multicenter Study.

TypeobservationalSponsorUniversity Hospital MuensterRan2008 to 2015Enrolled195ConditionsCystic FibrosisArmsnon-interventional study
3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. State-of-the-Art Review: Transformative Changes in the Care of People With Cystic Fibrosis: Implications for Infectious Diseases Specialists.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Thymidine-dependent Staphylococcus aureus and lung function in patients with cystic fibrosis: a 10-year retrospective case-control study.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2024
    Article
  7. Antibiotics (Basel, Switzerland) · 2023
    Article
  8. Article
  9. Nuclease activity and protein A release ofFrontiers in immunology · 2023
    Article
  10. Article
  11. Clinical Features and Treatment Outcomes of PulmonaryOpen forum infectious diseases · 2022
    Article
  12. Article
  13. Article
  14. Pathogens (Basel, Switzerland) · 2021
    Review
  15. Article
  16. Observational
  17. Article
  18. Dual-purpose isocyanides produced byProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  19. Observational
  20. Article
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

29 authors at 16 institutions in 3 countries.

Sibylle JungeClinic for Paediatric Pulmonology, Allergology and Neonatology, Hannover, Hannover, Germany.
Dennis GörlichInstitute of Biostatistics and Clinical Research, University Hospital Münster, Münster, Germany.
Martijn den ReijerDepartment of Medical Microbiology and Infectious Diseases, Erasmus Medical Center Rotterdam, Rotterdam, The Netherlands.
Bärbel WiedemannInstitute of Medical Informatics and Biometrics, Technical University Dresden, Dresden, Germany.
Burkhard TümmlerClinical Research Group, Clinic for Paediatric Pulmonology, Allergology and Neonatology, Medizinische Hochschule Hannover, Hannover, Germany.
Helmut EllemunterCF-Center Innsbruck, Department of Child and Adolescent Health, Medical University of Innsbruck, Innsbruck, Austria.
Angelika DübbersDepartment of Paediatrics, University Hospital Münster, Münster, Germany.
Peter KüsterDepartment of Paediatrics, Clemenshospital Münster, Münster, Germany.
Manfred BallmannRuhr University, Paediatric Clinic at St Josef Hospital, Bochum, Germany.
Cordula Koerner-RettbergRuhr University, Paediatric Clinic at St Josef Hospital, Bochum, Germany.
Jörg Große-OnnebrinkDepartment of Paediatrics, University Hospital Essen, Essen, Germany.
Eberhardt HeuerPaediatricians "Kinderärztliche Ambulanz", Hamburg, Germany.
Wolfgang SextroPaediatricians "Kinderärztliche Ambulanz", Hamburg, Germany.
Jochen G MainzCF Center, Department of Paediatrics, Jena University Hospital, Jena, Germany.
Jutta HammermannDepartment of Paediatrics, University Clinics Dresden, Dresden, Germany.
Joachim RiethmüllerDepartment of Pediatrics, University Clinics Tübingen, Tübingen, Germany.
Ute Graepler-MainkaDepartment of Pediatrics, University Clinics Tübingen, Tübingen, Germany.
Doris StaabDepartment of Paediatric Pulmonology and Immunology, Charité Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany.
Bettina WollschlägerUniversity Hospital Halle, Halle, Germany.
Rüdiger SzczepanskiChildren's Hospital Osnabrück, Osnabrück, Germany.
Antje SchusterDepartment of Paediatrics, University of Düsseldorf, Düsseldorf, Germany.
Friedrich-Karl TegtmeyerPark Schönefeld Clinics, Kassel, Germany.
Sivagurunathan SutharsanRuhrlandklinik, Essen, Germany.
Alexandra WaldUniversity Clinics Leipzig, Leipzig, Germany.
Jerzy-Roch NoferCenter for Laboratory Medicine, University Hospital Münster, Münster, Germany.
Willem van WamelDepartment of Medical Microbiology and Infectious Diseases, Erasmus Medical Center Rotterdam, Rotterdam, The Netherlands.
Karsten BeckerInstitute of Medical Microbiology, University Hospital Münster, Münster, Germany.
Georg PetersInstitute of Medical Microbiology, University Hospital Münster, Münster, Germany.
Barbara C KahlInstitute of Medical Microbiology, University Hospital Münster, Münster, Germany.ORCID http://orcid.org/0000-0001-5155-3383
University Hospital Münster · DEErasmus MC · NLSt. Josef-Hospital · DETechnische Universität Dresden · DECharité - Universitätsmedizin Berlin · DEClemenshospital Münster · DEEssen University Hospital · DEHeinrich Heine University Düsseldorf · DEInnsbruck Medical University · ATJena University Hospital · DEMarienhospital Osnabrück · DEMedizinische Hochschule Hannover · DERuhrlandklinik · DEUniversity Hospital in Halle · DEUniversity Hospital Leipzig · DEVitos Orthopedic Clinic Kassel · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStaphylococcus aureus is an important pathogen in cystic fibrosis (CF). However, it is not clear which factors are associated with worse lung function in patients with persistent S. aureus airway cultures. Our main hypothesis was that patients with high S. aureus density in their respiratory specimens would more likely experience worsening of their lung disease than patients with low bacterial loads.

methodsTherefore, we conducted an observational prospective longitudinal multi-center study and assessed the association between lung function and S. aureus bacterial density in respiratory samples, co-infection with other CF-pathogens, nasal S. aureus carriage, clinical status, antibiotic therapy, IL-6- and IgG-levels against S. aureus virulence factors.

results195 patients from 17 centers were followed; each patient had an average of 7 visits. Data were analyzed using descriptive statistics and generalized linear mixed models. Our main hypothesis was only supported for patients providing throat specimens indicating that patients with higher density experienced a steeper lung function decline (p<0.001). Patients with exacerbations (n = 60), S. aureus small-colony variants (SCVs, n = 84) and co-infection with Stenotrophomonas maltophilia (n = 44) had worse lung function (p = 0.0068; p = 0.0011; p = 0.0103). Patients with SCVs were older (p = 0.0066) and more often treated with trimethoprim/sulfamethoxazole (p = 0.0078). IL-6 levels positively correlated with decreased lung function (p<0.001), S. aureus density in sputa (p = 0.0016), SCVs (p = 0.0209), exacerbations (p = 0.0041) and co-infections with S. maltophilia (p = 0.0195) or A. fumigatus (p = 0.0496).

conclusionsIn CF-patients with chronic S. aureus cultures, independent risk factors for worse lung function are high bacterial density in throat cultures, exacerbations, elevated IL-6 levels, presence of S. aureus SCVs and co-infection with S. maltophilia.

trial registrationClinicalTrials.gov NCT00669760.

Indexed as

Staphylococcus aureusAdolescentAdultAntibodies, BacterialBacterial LoadChildCoinfectionCystic FibrosisDisease ProgressionFemaleForced Expiratory VolumeHumansImmunoglobulin GInterleukin-6MaleNasal MucosaAntibodies, BacterialImmunoglobulin GInterleukin-6

Identifiers

PMID27861524
PMCPMC5115705
OpenAlexW2557099177

What OpenQuestion holds

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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.