Evidence map›Paper›PMID 24767768›Full record

ArticleThe Lancet. Respiratory medicine2014

Respiratory microbiome in IPF: cause, effect, or biomarker?

Philip L Molyneaux, Toby M Maher

Abstract readComment
PubMed Publisher
In one paragraph

Article in The Lancet. Respiratory medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Schisandrin B attenuates bleomycin-induced pulmonary fibrosis in mice through AKT-mTOR pathway.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2024
    Article
  4. Persistent microbial infections and idiopathic pulmonary fibrosis - an insight intoFrontiers in cellular and infection microbiology · 2024
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Microbiota and IPF: hidden and detected relationships.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2021
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Idiopathic Pulmonary Fibrosis: Novel Concepts of Proton Pump Inhibitors as Antifibrotic Drugs.American journal of respiratory and critical care medicine · 2016
    Review
  18. The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis.American journal of respiratory and critical care medicine · 2014
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Philip L MolyneauxNational Heart and Lung Institute, Imperial College, Guy Scadding Building, Royal Brompton Campus, London SW3 6LY, UK; Interstitial Lung Disease Unit, Royal Brompton Hospital, London, UK. Electronic address: p.molyneaux@imperial.ac.uk.
Toby M MaherNational Heart and Lung Institute, Imperial College, Guy Scadding Building, Royal Brompton Campus, London SW3 6LY, UK; Interstitial Lung Disease Unit, Royal Brompton Hospital, London, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

DNA, BacterialMicrobiotaFemaleHumansIdiopathic Pulmonary FibrosisLungMaleStaphylococcusStreptococcusDNA, Bacterial

Identifiers

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.