Evidence map›Paper›PMID 24105491›Full record

ArticleInternational journal of obesity (2005)2014

Association between melanocortin-4 receptor mutations and eating behaviors in obese patients: a case--control study.

M Valette, C Poitou, E Kesse-Guyot, F Bellisle, C Carette, J Le Beyec, S Hercberg, K Clément, S Czernichow

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In one paragraph

Article in International journal of obesity (2005), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 34% 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

4 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Genetics of Severe Obesity.Current diabetes reports · 2018
    Review
  3. Article
  4. Article
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

9 authors at 4 institutions in 1 country.

M ValetteSorbonne Paris Cité, Nutritional Epidemiology Research Unit-UMR U557 INSERM, U1125 INRA, CNAM, Paris 13 University, CRNH-IdF, Bobigny, France.
C Poitou1] Institute of cardiometabolism and nutrition (ICAN), Pitié Salpêtriére hospital, Paris, France [2] Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Nutrition and Endocrinology Department, Heart and Metabolism Division, Paris, France [3] CRNH-Ile de France, Paris, France [4] INSERM U872, Team Nutriomique, Paris, France [5] Pierre and Marie Curie University - Paris 6, Paris, France.
E Kesse-GuyotSorbonne Paris Cité, Nutritional Epidemiology Research Unit-UMR U557 INSERM, U1125 INRA, CNAM, Paris 13 University, CRNH-IdF, Bobigny, France.
F BellisleSorbonne Paris Cité, Nutritional Epidemiology Research Unit-UMR U557 INSERM, U1125 INRA, CNAM, Paris 13 University, CRNH-IdF, Bobigny, France.
C Carette1] INSERM U1016, CNRS UMR 8104, University of Paris-Descartes, Cochin Institute, Paris, France [2] AP-HP, Nutrition Department, Ambroise Paré Hospital, Boulogne-Billancourt, France.
J Le Beyec1] AP-HP, Nutrigenic unit, Endocrinology and Oncology Biochemistry Department, Pitié-Salpêtrière Hospital, Pierre and Marie Curie university - Paris 6, Paris, France [2] INSERM U773, Digestive Physiology and Neuroendocrinology team, CRB3, Paris, France.
S Hercberg1] Sorbonne Paris Cité, Nutritional Epidemiology Research Unit-UMR U557 INSERM, U1125 INRA, CNAM, Paris 13 University, CRNH-IdF, Bobigny, France [2] Department of Public Health, Avicenne Hospital (AP-HP), Bobigny, France.
K Clément1] Institute of cardiometabolism and nutrition (ICAN), Pitié Salpêtriére hospital, Paris, France [2] Assistance Publique-Hôpitaux de Paris, Pitié-Salpêtrière Hospital, Nutrition and Endocrinology Department, Heart and Metabolism Division, Paris, France [3] INSERM U872, Team Nutriomique, Paris, France [4] Pierre and Marie Curie University - Paris 6, Paris, France.
S Czernichow1] AP-HP, Nutrition Department, Ambroise Paré Hospital, Boulogne-Billancourt, France [2] INSERM U1018, Centre for Research in Epidemiology and Population Health, Villejuif, France [3] University of Versailles Saint Quentin en Yvelines, Boulogne-Billancourt, France.
Assistance Publique – Hôpitaux de Paris · FRCentre de Recherche Épidémiologie et StatistiqueInserm · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanocortin-4 receptor (MC4R) gene mutations are involved in the leptin-melanocortin pathways that control food intake. The effect of these mutations on eating behavior phenotypes is still debated. To determine the association between functional MC4R mutations and eating behaviors, dietary intake and physical activity, we sequenced the MC4R gene in 4653 obese adults. Among them, 19 adults carriers of functional MC4R mutation were matched on age, sex and body mass index with two randomly-paired controls without MC4R mutation (n=57). We found that eating behaviors and physical activity did not differ between groups. In particular, cases were not at increased risk of binge eating disorders. Subjects carriers of MC4R mutation reported a higher proportion of dietary carbohydrates intakes (43.2±7.1 and 39.2±8.1% of total energy intake, respectively, P=0.048) and a lower proportion of dietary lipids (34.3±6.7 and 38.5±6.7% of total energy intake, respectively, P=0.018). In conclusion, mutation carriers differ from controls by a higher consumption of carbohydrates counterbalanced by a lower consumption of lipids expressed as percentage of total energy intake. However, functional MC4R mutations do not have a higher risk of compulsive eating contrary to what was previously suggested.

Indexed as

AdultBody Mass IndexCase-Control StudiesEatingEnergy IntakeFeeding BehaviorFemaleHumansLeptinMaleMiddle AgedMutationObesityReceptor, Melanocortin, Type 4Receptors, Cell SurfaceSurveys and QuestionnairesLeptinMC4R protein, humanReceptor, Melanocortin, Type 4Receptors, Cell Surface

Identifiers

PMID24105491
OpenAlexW2100629594

What OpenQuestion holds

Textmetadata
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.