Evidence map›Paper›PMID 27810876›Full record

ArticleFEMS microbiology ecology2017

Impact of cystic fibrosis disease on archaea and bacteria composition of gut microbiota.

Francesco Miragoli, Sara Federici, Susanna Ferrari, Andrea Minuti, Annalisa Rebecchi, Eugenia Bruzzese, Vittoria Buccigrossi, Alfredo Guarino, Maria Luisa Callegari

Open access · hybridAbstract read
In one paragraph

Article in FEMS microbiology ecology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Observational
  7. Article
  8. Effect ofNutrients · 2023
    Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. The Gut-Lung Axis in Cystic Fibrosis.Journal of bacteriology · 2021
    Review
  15. Review
  16. Intestinal Dysbiosis in Young Cystic Fibrosis Rabbits.Journal of personalized medicine · 2021
    Article
  17. Article
  18. Review
  19. Article
  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

9 authors at 2 institutions in 1 country.

Francesco MiragoliCentro Ricerche Biotecnologiche, Università Cattolica del Sacro Cuore, Cremona 26100, Italy.
Sara FedericiCentro Ricerche Biotecnologiche, Università Cattolica del Sacro Cuore, Cremona 26100, Italy.
Susanna FerrariCentro Ricerche Biotecnologiche, Università Cattolica del Sacro Cuore, Cremona 26100, Italy.
Andrea MinutiIstituto di Zootecnica, Università Cattolica del Sacro Cuore, Piacenza 29122, Italy.
Annalisa RebecchiCentro Ricerche Biotecnologiche, Università Cattolica del Sacro Cuore, Cremona 26100, Italy.
Eugenia BruzzeseDepartment of Translational Medical Sciences, Section of Pediatrics, University Federico II, Naples 80131, Italy.
Vittoria BuccigrossiDepartment of Translational Medical Sciences, Section of Pediatrics, University Federico II, Naples 80131, Italy.
Alfredo GuarinoDepartment of Translational Medical Sciences, Section of Pediatrics, University Federico II, Naples 80131, Italy.
Maria Luisa CallegariCentro Ricerche Biotecnologiche, Università Cattolica del Sacro Cuore, Cremona 26100, Italy marialuisa.callegari@unicatt.it.
Università Cattolica del Sacro Cuore · ITFederico II University Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis is often associated with intestinal inflammation due to several factors, including altered gut microbiota composition. In this study, we analyzed the fecal microbiota among patients with cystic fibrosis of 10-22 years of age, and compared the findings with age-matched healthy subjects. The participating patients included 14 homozygotes and 14 heterozygotes with the delF508 mutation, and 2 heterozygotes presenting non-delF508 mutations. We used PCR-DGGE and qPCR to analyze the presence of bacteria, archaea and sulfate-reducing bacteria. Overall, our findings confirmed disruption of the cystic fibrosis gut microbiota. Principal component analysis of the qPCR data revealed no differences between homozygotes and heterozygotes, while both groups were distinct from healthy subjects who showed higher biodiversity. Archaea were under the detection limit in all homozygotes subjects, whereas methanogens were detected in 62% of both cystic fibrosis heterozygotes and healthy subjects. Our qPCR results revealed a low frequency of sulfate-reducing bacteria in the homozygote (13%) and heterozygote (13%) patients with cystic fibrosis compared with healthy subjects (87.5%). This is a pioneer study showing that patients with cystic fibrosis exhibit significant reduction of H

Indexed as

BiodiversityGastrointestinal MicrobiomeAdolescentAdultArchaeaBacteriaChildColonCystic FibrosisEuryarchaeotaFecesFemaleHumansIntestinesMaleMicrobiotacystic fibrosisgut microbiotamethanogen archaeaqPCRsulfate-reducing bacteria, DGGE-PCR

Identifiers

PMID27810876
PMCPMC5155554
OpenAlexW2547397706

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.