Evidence map›Paper›PMID 30455959›Full record

ArticlePharmacology research & perspectives2018

Oral administration of the selective GPR120/FFA4 agonist compound A is not effective in alleviating tissue inflammation in mouse models of prototypical autoimmune diseases.

Melanie Wannick, Siegfried Bezdek, Nathalie Guillen, Markus Thieme, Fibi Meshrkey, Sadegh Mousavi, Michaela Seeling, Falk Nimmerjahn, Attila Mócsai, Detlef Zillikens and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2018. 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
1.2field-weighted citation impact, top 21% 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, 17 citations in OpenAlex.

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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 3 institutions in 2 countries.

Melanie WannickDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.
Siegfried BezdekDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.
Nathalie GuillenDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.
Markus ThiemeDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.
Fibi MeshrkeyDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.
Sadegh MousaviDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.
Michaela SeelingChair of Genetics Department of Biology University of Erlangen-Nuremberg Erlangen Germany.
Falk NimmerjahnChair of Genetics Department of Biology University of Erlangen-Nuremberg Erlangen Germany.
Attila MócsaiDepartment of Physiology Semmelweis University School of Medicine MTA-SE "Lendület" Inflammation Physiology Research Group of the Hungarian Academy of Sciences Semmelweis University Budapest Hungary.
Detlef ZillikensCenter for Research on Inflammation of the Skin (CRIS) University of Lübeck Lübeck Germany.
Tanya SezinDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.
Christian D SadikDepartment of Dermatology, Allergy, and Venereology University of Lübeck Lübeck Germany.ORCID 0000-0001-6701-048X
University of Lübeck · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DESemmelweis University · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ω3-polyunsaturated free fatty acids (ω3-PUFAs), particularly docosahexaenoic (DHA) and eicosapentaenoic acid (EPA), are thought to exert health promoting effects in metabolic and in inflammatory diseases. The molecular mechanisms of these beneficial effects are only partially understood. DHA and EPA activate

Indexed as

Acetic AcidAdministration, OralAnimalsAnti-Inflammatory Agents, Non-SteroidalArthritis, RheumatoidAza CompoundsDisease Models, AnimalFatty Acids, Omega-3HumansImiquimodMiceMice, Inbred C57BLPemphigoid, BullousPsoriasisReceptors, G-Protein-CoupledTreatment Outcome3-(2-chloro-5-(trifluoromethoxy)phenyl)-3-azaspiro(5.5)undecane-9-acetic acidAcetic AcidAnti-Inflammatory Agents, Non-SteroidalAza CompoundsFatty Acids, Omega-3FFAR4 protein, humanImiquimodReceptors, G-Protein-Coupledautoimmune diseasecompound AGPR120/FFAR4pemphigoid diseasepsoriasisrheumatoid arthritis

Identifiers

PMID30455959
PMCPMC6223243
OpenAlexW2899724956

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.