Evidence map›Paper›PMID 30241412›Full record

ReviewInternational journal of molecular sciences2018

Specialized Pro-Resolving Lipid Mediators in Cystic Fibrosis.

Réginald Philippe, Valerie Urbach

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. MicroRNAs in shaping the resolution phase of inflammation.Seminars in cell & developmental biology · 2022
    Review
  8. Review
  9. Mucosal Immunity in Cystic Fibrosis.Journal of immunology (Baltimore, Md. : 1950) · 2021
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Lipidomics Conquers a Niche, Consolidates Growth.International journal of molecular sciences · 2019
    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

2 authors at 1 institution in 1 country.

Réginald PhilippeINSERM, U1151, Institut Necker Enfants Malades, 75993 Paris, France. reginald.philippe@inserm.fr.
Valerie UrbachINSERM, U1151, Institut Necker Enfants Malades, 75993 Paris, France. valerie.urbach@inserm.fr.ORCID 0000-0001-7437-9365
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In cystic fibrosis (CF), impaired airway surface hydration (ASL) and mucociliary clearance that promote chronic bacterial colonization, persistent inflammation, and progressive structural damage to the airway wall architecture are typically explained by ion transport abnormalities related to the mutation of the gene coding for the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) channel. However, the progressive and unrelenting inflammation of the CF airway begins early in life, becomes persistent, and is excessive relative to the bacterial burden. Intrinsic abnormalities of the inflammatory response in cystic fibrosis have been suggested but the mechanisms involved remain poorly understood. This review aims to give an overview of the recent advances in the understanding of the defective resolution of inflammation in CF including the abnormal production of specialized pro-resolving lipid mediators (lipoxin and resolvin) and their impact on the pathogenesis of the CF airway disease.

Indexed as

Cystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDocosahexaenoic AcidsHumansInflammationLipoxinsMutationCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorDocosahexaenoic AcidsLipoxinscystic fibrosislipoxinresolvin

Identifiers

PMID30241412
PMCPMC6213393
OpenAlexW2892306013

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.