Evidence map›Paper›PMID 37484963›Full record

ReviewFrontiers in endocrinology2023

Metabolite-sensing GPCRs controlling interactions between adipose tissue and inflammation.

Elaine M Duncan, Luca Vita, Bethany Dibnah, Brian D Hudson

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  3. Article
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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

4 authors at 1 institution in 1 country.

Elaine M DuncanCentre for Translational Pharmacology, University of Glasgow, Glasgow, United Kingdom.
Luca VitaCentre for Translational Pharmacology, University of Glasgow, Glasgow, United Kingdom.
Bethany DibnahCentre for Translational Pharmacology, University of Glasgow, Glasgow, United Kingdom.
Brian D HudsonCentre for Translational Pharmacology, University of Glasgow, Glasgow, United Kingdom.
University of Glasgow · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic disorders including obesity, diabetes and non-alcoholic steatohepatitis are a group of conditions characterised by chronic low-grade inflammation of metabolic tissues. There is now a growing appreciation that various metabolites released from adipose tissue serve as key signalling mediators, influencing this interaction with inflammation. G protein-coupled receptors (GPCRs) are the largest family of signal transduction proteins and most historically successful drug targets. The signalling pathways for several key adipose metabolites are mediated through GPCRs expressed both on the adipocytes themselves and on infiltrating macrophages. These include three main groups of GPCRs: the FFA4 receptor, which is activated by long chain free fatty acids; the HCA

Indexed as

Metabolic DiseasesReceptors, G-Protein-CoupledAdipocytesAdipose TissueHumansInflammationObesityReceptors, G-Protein-Coupledadiposefree fatty acidG protein-coupled receptorhydroxy carboxylic acidsinflammationmetabolite signallingsuccinate

Identifiers

PMID37484963
PMCPMC10357040
OpenAlexW4383343642

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.