Evidence map›Paper›PMID 33513903›Full record

ReviewLife (Basel, Switzerland)2021

Lung Microbiome in Cystic Fibrosis.

Filippo Scialo, Felice Amato, Gustavo Cernera, Monica Gelzo, Federica Zarrilli, Marika Comegna, Lucio Pastore, Andrea Bianco, Giuseppe Castaldo

Open access · goldAbstract readReview
In one paragraph

Review in Life (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. BioMed research international · 2026
    Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Insights intoMicroorganisms · 2024
    Article
  9. Beyond the organ: lung microbiome shapes transplant indications and outcomes.European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery · 2024
    Review
  10. Review
  11. Review
  12. Review
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

9 authors at 2 institutions in 1 country.

Filippo ScialoDipartimento di Scienze Mediche Traslazionali, University of Campania "L. Vanvitelli", 80131 Napoli, Italy.ORCID 0000-0002-1121-7315
Felice AmatoCEINGE, Biotecnologie Avanzate, 80145 Napoli, Italy.ORCID 0000-0002-0596-2933
Gustavo CerneraCEINGE, Biotecnologie Avanzate, 80145 Napoli, Italy.
Monica GelzoCEINGE, Biotecnologie Avanzate, 80145 Napoli, Italy.ORCID 0000-0002-1500-0746
Federica ZarrilliCEINGE, Biotecnologie Avanzate, 80145 Napoli, Italy.ORCID 0000-0003-1614-6816
Marika ComegnaCEINGE, Biotecnologie Avanzate, 80145 Napoli, Italy.
Lucio PastoreCEINGE, Biotecnologie Avanzate, 80145 Napoli, Italy.ORCID 0000-0001-6894-9317
Andrea BiancoDipartimento di Scienze Mediche Traslazionali, University of Campania "L. Vanvitelli", 80131 Napoli, Italy.ORCID 0000-0002-4692-5901
Giuseppe CastaldoCEINGE, Biotecnologie Avanzate, 80145 Napoli, Italy.
Ceinge Biotecnologie Avanzate (Italy) · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The defective mucociliary clearance due to CFTR malfunctioning causes predisposition to the colonization of pathogens responsible for the recurrent inflammation and rapid deterioration of lung function in patients with cystic fibrosis (CF). This has also a profound effect on the lung microbiome composition, causing a progressive reduction in its diversity, which has become a common characteristic of patients affected by CF. Although we know that the lung microbiome plays an essential role in maintaining lung physiology, our comprehension of how the microbial components interact with each other and the lung, as well as how these interactions change during the disease's course, is still at an early stage. Many challenges exist and many questions still to be answered, but there is no doubt that manipulation of the lung microbiome could help to develop better therapies for people affected by CF.

Indexed as

CFTRcystic fibrosislungmicrobiome

Identifiers

PMID33513903
PMCPMC7911450
OpenAlexW3122258336

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.