Evidence map›Paper›PMID 31507425›Full record

ArticleFrontiers in pharmacology2019

Arachidonic Acid and Docosahexaenoic Acid Metabolites in the Airways of Adults With Cystic Fibrosis: Effect of Docosahexaenoic Acid Supplementation.

Elisabetta Teopompi, Patrizia Risé, Roberta Pisi, Carola Buccellati, Marina Aiello, Giovanna Pisi, Candida Tripodi, Valentina Fainardi, Enrico Clini, Alfredo Chetta and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  4. Murine Alox8 versus the human ALOX15B ortholog: differences and similarities.Pflugers Archiv : European journal of physiology · 2024
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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

12 authors at 4 institutions in 1 country.

Elisabetta TeopompiRespiratory Disease Unit, Department of Medicine and Surgery, University Hospital, Parma, Parma, Italy.
Patrizia RiséDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milano, Italy.
Roberta PisiRespiratory Disease Unit, Department of Medicine and Surgery, University Hospital, Parma, Parma, Italy.
Carola BuccellatiDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milano, Italy.
Marina AielloRespiratory Disease Unit, Department of Medicine and Surgery, University Hospital, Parma, Parma, Italy.
Giovanna PisiDepartment of Pediatrics, CF Unit Children Hospital, University Hospital of Parma, Parma, Italy.
Candida TripodiDepartment of Pediatrics, CF Unit Children Hospital, University Hospital of Parma, Parma, Italy.
Valentina FainardiDepartment of Pediatrics, CF Unit Children Hospital, University Hospital of Parma, Parma, Italy.
Enrico CliniDepartment of Medical and Surgical Sciences, University of Modena Reggio Emilia, Modena, Italy.
Alfredo ChettaRespiratory Disease Unit, Department of Medicine and Surgery, University Hospital, Parma, Parma, Italy.
G Enrico RovatiDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milano, Italy.
Angelo SalaDepartment of Pharmacological and Biomolecular Sciences, University of Milan, Milano, Italy.
University of Parma · ITUniversity of Milan · ITIstituto di Biomedicina e di Immunologia Molecolare Alberto Monroy · ITUniversity of Modena and Reggio Emilia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cystic fibrosis (CF) is an autosomal recessive disorder, caused by genetic mutations in CF transmembrane conductance regulator protein. Several reports have indicated the presence of specific fatty acid alterations in CF patients, most notably decreased levels of plasmatic and tissue docosahexaenoic acid (DHA), the precursor of specialized pro-resolving mediators. We hypothesized that DHA supplementation could restore the production of DHA-derived products and possibly contribute to a better control of the chronic pulmonary inflammation observed in CF subjects. Sputum samples from 15 CF and 10 chronic obstructive pulmonary disease (COPD) subjects were collected and analyzed by LC/MS/MS, and blood fatty acid were profiled by gas chromatography upon lipid extraction and transmethylation. Interestingly, CF subjects showed increased concentrations of leukotriene B

Indexed as

15-lipoxygenasearachidonic acid (AA or eicosatetraenoic acid)docosahexaenoic acid-DHAinflammatory mediatorssputum

Identifiers

PMID31507425
PMCPMC6716427
OpenAlexW2963746551

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.