Evidence map›Paper›PMID 36922513›Full record

ArticleNature communications2023

A rare human variant that disrupts GPR10 signalling causes weight gain in mice.

Fleur Talbot, Claire H Feetham, Jacek Mokrosiński, Katherine Lawler, Julia M Keogh, Elana Henning, Edson Mendes de Oliveira, Vikram Ayinampudi, Sadia Saeed, Amélie Bonnefond and 9 more

Open access · goldFull text read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 14 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

19 authors at 5 institutions in 3 countries.

Fleur Talbot *University of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.ORCID 0000-0002-8897-4103
Claire H Feetham *Division of Diabetes, Endocrinology and Gastroenterology, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Jacek Mokrosiński *University of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.ORCID 0000-0001-5008-0457
Katherine LawlerUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.ORCID 0000-0003-4188-1804
Julia M KeoghUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.
Elana HenningUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.
Edson Mendes de OliveiraUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.ORCID 0000-0002-7330-7826
Vikram AyinampudiUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.
Sadia SaeedDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID 0000-0003-3144-7772
Amélie BonnefondDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Mohammed ArslanSchool of Life Sciences, Forman Christian College, Lahore, Pakistan.
Giles S H YeoUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.ORCID 0000-0001-8823-3615
Philippe FroguelDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.ORCID 0000-0003-2972-0784
David A BechtoldDivision of Diabetes, Endocrinology and Gastroenterology, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0001-8676-8704
Antony AdamsonGenome Editing Unit, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0002-5408-0013
Neil HumphreysGenome Editing Unit, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.
Inês BarrosoUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.ORCID 0000-0001-5800-4520
Simon M LuckmanDivision of Diabetes, Endocrinology and Gastroenterology, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK. simon.luckman@manchester.ac.uk.
I Sadaf FarooqiUniversity of Cambridge Metabolic Research Laboratories and NIHR Cambridge Biomedical Research Centre, Wellcome-MRC Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK. isf20@cam.ac.uk.ORCID 0000-0001-7609-3504
University of Cambridge · GBUniversity of Manchester · GBCentre National de la Recherche Scientifique · FRForman Christian College · PKUniversity of Exeter · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H007172/1Biotechnology and Biological Sciences Research Council BB/M001067/1Biotechnology and Biological Sciences Research Council BB/P01867X/1Medical Research Council MR/P00279X/1Medical Research Council MR/S026193/1Wellcome TrustWellcome Trust 203513/Z/16/ZWellcome Trust 207462/Z/17/ZWellcome Trust 208363/Z/17/ZWellcome Trust WT098051
6 · The paper itself

Abstract

Disruption of brain-expressed G protein-coupled receptor-10 (GPR10) causes obesity in animals. Here, we identify multiple rare variants in GPR10 in people with severe obesity and in normal weight controls. These variants impair ligand binding and G protein-dependent signalling in cells. Transgenic mice harbouring a loss of function GPR10 variant found in an individual with obesity, gain excessive weight due to decreased energy expenditure rather than increased food intake. This evidence supports a role for GPR10 in human energy homeostasis. Therapeutic targeting of GPR10 may represent an effective weight-loss strategy.

Indexed as

ObesityReceptors, G-Protein-CoupledAnimalsEnergy MetabolismHumansMiceMice, TransgenicSignal TransductionWeight GainPRLHR protein, humanReceptors, G-Protein-Coupled

Identifiers

PMID36922513
PMCPMC10017677
OpenAlexW4324351637

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read62
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.