Evidence map›Paper›PMID 23284998›Full record

ArticlePloS one2012

Statistical and biological gene-lifestyle interactions of MC4R and FTO with diet and physical activity on obesity: new effects on alcohol consumption.

Dolores Corella, Carolina Ortega-Azorín, Jose V Sorlí, M Isabel Covas, Paula Carrasco, Jordi Salas-Salvadó, Miguel Ángel Martínez-González, Fernando Arós, José Lapetra, Lluís Serra-Majem and 9 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 3 pooled it
5.0field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 3 syntheses or guidelines pooled it, 80 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 13 institutions in 2 countries.

Dolores CorellaDepartment of Preventive Medicine and Public Health, School of Medicine, University of Valencia, Valencia, Spain. dolores.corella@uv.es
Carolina Ortega-Azorín
Jose V Sorlí
M Isabel Covas
Paula Carrasco
Jordi Salas-Salvadó
Miguel Ángel Martínez-González
Fernando Arós
José Lapetra
Lluís Serra-Majem
Rosa Lamuela-Raventos
Enrique Gómez-Gracia
Miquel Fiol
Xavier Pintó
Emilio Ros
Amelia Martí
Oscar Coltell
Jose M Ordovás
Ramon Estruch
Instituto de Salud Carlos III · ESUniversitat de València · ESUniversidad de Navarra · ESBellvitge University Hospital · ESHospital Clínic de Barcelona · ESHospital Txagorritxu · ESHospital Universitario Son Dureta · ESSpanish National Centre for Cardiovascular Research · ESUniversidad de Las Palmas de Gran Canaria · ESUniversidad de Málaga · ESUniversidad Rovira i Virgili · ESUniversitat de Barcelona · ESUniversitat Jaume I · ES

Funding

HSRD VA CDA 11-263
6 · The paper itself

Abstract

backgroundFat mass and obesity (FTO) and melanocortin-4 receptor (MC4R) and are relevant genes associated with obesity. This could be through food intake, but results are contradictory. Modulation by diet or other lifestyle factors is also not well understood.

objectiveTo investigate whether MC4R and FTO associations with body-weight are modulated by diet and physical activity (PA), and to study their association with alcohol and food intake.

methodsAdherence to Mediterranean diet (AdMedDiet) and physical activity (PA) were assessed by validated questionnaires in 7,052 high cardiovascular risk subjects. MC4R rs17782313 and FTO rs9939609 were determined. Independent and joint associations (aggregate genetic score) as well as statistical and biological gene-lifestyle interactions were analyzed.

resultsFTO rs9939609 was associated with higher body mass index (BMI), waist circumference (WC) and obesity (P<0.05 for all). A similar, but not significant trend was found for MC4R rs17782313. Their additive effects (aggregate score) were significant and we observed a 7% per-allele increase of being obese (OR=1.07; 95%CI 1.01-1.13). We found relevant statistical interactions (P<0.05) with PA. So, in active individuals, the associations with higher BMI, WC or obesity were not detected. A biological (non-statistical) interaction between AdMedDiet and rs9939609 and the aggregate score was found. Greater AdMedDiet in individuals carrying 4 or 3-risk alleles counterbalanced their genetic predisposition, exhibiting similar BMI (P=0.502) than individuals with no risk alleles and lower AdMedDiet. They also had lower BMI (P=0.021) than their counterparts with low AdMedDiet. We did not find any consistent association with energy or macronutrients, but found a novel association between these polymorphisms and lower alcohol consumption in variant-allele carriers (B+/-SE: -0.57+/-0.16 g/d per-score-allele; P=0.001).

conclusionStatistical and biological interactions with PA and diet modulate the effects of FTO and MC4R polymorphisms on obesity. The novel association with alcohol consumption seems independent of their effects on BMI.

Indexed as

Life StyleAgedAged, 80 and overAlcohol DrinkingAlpha-Ketoglutarate-Dependent Dioxygenase FTOBody Mass IndexFemaleHumansMaleMiddle AgedObesityProteinsReceptor, Melanocortin, Type 4Alpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanProteinsReceptor, Melanocortin, Type 4

Identifiers

PMID23284998
PMCPMC3528751
OpenAlexW2095856537

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.