Evidence map›Paper›PMID 30755592›Full record

ArticleTranslational psychiatry2019

Immunoglobulin G modulation of the melanocortin 4 receptor signaling in obesity and eating disorders.

Nicolas Lucas, Romain Legrand, Christine Bôle-Feysot, Jonathan Breton, Moïse Coëffier, Kirsti Akkermann, Anu Järv, Jaanus Harro, Pierre Déchelotte, Sergueï O Fetissov

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
2.5field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 40 citations in OpenAlex.

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  3. A systematic review on the role of microbiota in the pathogenesis and treatment of eating disorders.European psychiatry : the journal of the Association of European Psychiatrists · 2020
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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

10 authors at 3 institutions in 2 countries.

Nicolas LucasInserm UMR1073, Nutrition, Gut and Brain Laboratory, 76183, Rouen, France.
Romain LegrandInserm UMR1073, Nutrition, Gut and Brain Laboratory, 76183, Rouen, France.
Christine Bôle-FeysotInserm UMR1073, Nutrition, Gut and Brain Laboratory, 76183, Rouen, France.
Jonathan BretonInserm UMR1073, Nutrition, Gut and Brain Laboratory, 76183, Rouen, France.
Moïse CoëffierInserm UMR1073, Nutrition, Gut and Brain Laboratory, 76183, Rouen, France.
Kirsti AkkermannDivision of Clinical Psychology, Department of Psychology, University of Tartu, Näituse 2, 50409, Tartu, Estonia.
Anu JärvTartu University Clinics, Psychiatric Hospital, University of Tartu, Ludvig Puusepa 1a, 50406, Tartu, Estonia.
Jaanus HarroDivision of Neuropsychopharmacology, Department of Psychology, University of Tartu, Ravila 14A, 50411, Tartu, Estonia.ORCID http://orcid.org/0000-0002-4484-2096
Pierre DéchelotteInserm UMR1073, Nutrition, Gut and Brain Laboratory, 76183, Rouen, France.ORCID http://orcid.org/0000-0001-5224-6166
Sergueï O FetissovInserm UMR1073, Nutrition, Gut and Brain Laboratory, 76183, Rouen, France. Serguei.Fetissov@univ-rouen.fr.
Inserm · FRUniversity of Tartu · EETartu University Hospital · EE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanocortin 4 receptor (MC4R) plays a key role in regulation of appetite activated by its main ligand α-melanocyte-stimulating hormone (α-MSH) in both central and peripheral targets. α-MSH also binds to circulating immunoglobulins (Igs) but the functional significance of such immune complexes (ICs) in MC4R signaling in normal and pathological conditions of altered appetite has remained unknown. To address this question, we analyzed plasma levels, affinity kinetics, and binding epitopes of α-MSH-reactive IgG extracted from plasma samples of female patients with hyperphagic obesity, anorexia nervosa, bulimia nervosa, binge-eating disorder, and healthy controls. Ability of α-MSH/IgG IC to bind and activate human MC4R were studied in vitro and to influence feeding behavior in vivo in rodents. We found that α-MSH-reactive IgG were low in obese but increased in anorectic and bulimic patients and displayed different epitope and kinetics of IC formation. Importantly, while α-MSH/IgG IC from all subjects were binding and activating MC4R, the receptor binding affinity was decreased in obesity. Additionally, α-MSH/IgG IC had lower MC4R-mediated cAMP activation threshold as compared with α-MSH alone in all but not obese subjects. Furthermore, the cellular internalization rate of α-MSH/IgG IC by MC4R-expressing cells was decreased in obese but increased in patients with anorexia nervosa. Moreover, IgG from obese patients prevented central anorexigenic effect of α-MSH. These findings reveal that MC4R is physiologically activated by IC formed by α-MSH/IgG and that different levels and molecular properties of α-MSH-reactive IgG underlie biological activity of such IC relevant to altered appetite in obesity and eating disorders.

Indexed as

AdolescentAdultalpha-MSHAnimalsCyclic AMPFeeding and Eating DisordersFemaleHEK293 CellsHumansImmunoglobulin GMaleMice, Inbred C57BLMiddle AgedObesityRats, Sprague-DawleyReceptor, Melanocortin, Type 4alpha-MSHCyclic AMPImmunoglobulin GMC4R protein, humanReceptor, Melanocortin, Type 4

Identifiers

PMID30755592
PMCPMC6372612
OpenAlexW2911671507

What OpenQuestion holds

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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.