Evidence map›Paper›PMID 35078737›Full record

ArticleJournal of cystic fibrosis : official journal of the European Cystic Fibrosis Society2022

The lung microbiota in children with cystic fibrosis captured by induced sputum sampling.

Rebecca Weiser, Juliette Oakley, Katherine Ronchetti, Jo-Dee Tame, Sven Hoehn, Tomasz P Jurkowski, Eshwar Mahenthiralingam, Julian T Forton

Open access · hybridAbstract read
PubMed Publisher
In one paragraph

Article in Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Genome-wide association study of susceptibility toThe European respiratory journal · 2024
    Article
  5. The ageing of people living with cystic fibrosis: what to expect now?European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  6. Changing profile of bacterial infection and microbiome in cystic fibrosis: when to use antibiotics in the era of CFTR-modulator therapy.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  7. Considerations for the use of inhaled antibiotics forBMJ open respiratory research · 2024
    Article
  8. The presence of cystic fibrosis-related diabetes modifies the sputum microbiome in cystic fibrosis disease.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Rebecca WeiserMicrobiomes Microbes and Informatics Group, Organisms and Environment Division, School of Biosciences, Cardiff University, Sir Martin Evans Building, Park Place, Cardiff, UK. Electronic address: WeiserR@Cardiff.ac.uk.
Juliette OakleyDepartment of Paediatric Respiratory Medicine, Noah's Ark Children's Hospital for Wales, Cardiff, UK; School of Medicine, Cardiff University, UK.
Katherine RonchettiDepartment of Paediatric Respiratory Medicine, Noah's Ark Children's Hospital for Wales, Cardiff, UK; Department of Paediatric Physiotherapy, Noah's Ark Children's Hospital for Wales, Cardiff, UK.
Jo-Dee TameDepartment of Paediatric Respiratory Medicine, Noah's Ark Children's Hospital for Wales, Cardiff, UK; Department of Paediatric Physiotherapy, Noah's Ark Children's Hospital for Wales, Cardiff, UK.
Sven HoehnMolecular Biosciences Division, School of Biosciences, Cardiff University, Sir Martin Evans Building, Park Place, Cardiff, UK.
Tomasz P JurkowskiMolecular Biosciences Division, School of Biosciences, Cardiff University, Sir Martin Evans Building, Park Place, Cardiff, UK.
Eshwar MahenthiralingamMicrobiomes Microbes and Informatics Group, Organisms and Environment Division, School of Biosciences, Cardiff University, Sir Martin Evans Building, Park Place, Cardiff, UK.
Julian T FortonDepartment of Paediatric Respiratory Medicine, Noah's Ark Children's Hospital for Wales, Cardiff, UK; School of Medicine, Cardiff University, UK.
Cardiff University · GBNoah's Ark Children's Hospital for Wales · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

backgroundSpatial topography of the cystic fibrosis (CF) lung microbiota is poorly understood in childhood. How best to sample the respiratory tract in children for microbiota analysis, and the utility of microbiota profiling in clinical management of early infection remains unclear. By comparison with bronchoalveolar lavage (BAL), we assessed the ability of induced sputum (IS) sampling to characterise the lower airway microbiota.

methodsSample sets from IS and two or three matched BAL compartments were obtained for microbiota analysis as part of the CF-Sputum Induction Trial (UKCRN_14615, ISRCTNR_12473810). Microbiota profiles and pathogen detection were compared between matched samples.

resultsTwenty-eight patients, aged 1.1-17.7 years, provided 30 sample sets. Within-patient BAL comparisons revealed spatial heterogeneity in 8/30 (27%) sample sets indicating that the lower airway microbiota from BAL is frequently compartmentalised in children with CF. IS samples closely resembled one or more matched BAL compartments in 15/30 (50%) sets, and were related in composition in a further 9/30 (30%). IS detected 86.2% of the Top 5 genera found across matched BAL samples. The sensitivity of IS to detect specific CF-pathogens identified in matched BAL samples at relative abundance ≥5% varied between 43 and 100%, with negative predictive values between 73 and 100%.

conclusionsSpatial heterogeneity of the lower airway microbiota was observed in BAL samples and presents difficulties for consistent lung sampling. IS captured a microbiota signature representative of the lower airway in 80% of cases, and is a straightforward, non-invasive intervention that can be performed frequently to aid pathogen diagnosis and understand microbiota evolution in children with CF.

Indexed as

Cystic FibrosisMicrobiotaBronchoalveolar Lavage FluidChildHumansLungSputumCystic fibrosisInduced sputumMicrobiomeMicrobiotaSputum induction

Identifiers

PMID35078737
OpenAlexW4206966368

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.