Evidence map›Paper›PMID 40114142›Full record

ArticleBMC pediatrics2025

FTO and NOS3 genes associated with pediatric obesity: Corações de Ouro Preto study.

Aline Priscila Batista, Thomás Viana de Souza, Luiz Antônio Alves de Menezes-Júnior, Anna Carolina Motta Costa, Camila Blanco Cangussu, Luciano Garcia Lourenção, Wandeir Wagner de Oliveira, Gabriel Trindade Avelar, Daniela Fonseca Abdo Rocha, Iriane Marques de Carvalho Rodrigues and 3 more

Abstract read
In one paragraph

Article in BMC pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

13 authors.

Aline Priscila BatistaBiological Sciences Research Center, Postgraduate Program in Biological Sciences, Institute of Exact and Biological Sciences, Federal University of Ouro Preto, Ouro Preto, MG, Brazil. alinepriop@gmail.com.ORCID http://orcid.org/0000-0001-8305-1011
Thomás Viana de SouzaLaboratory of Epidemiology, School of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0002-9815-5021
Luiz Antônio Alves de Menezes-JúniorPostgraduate Program in Health and Nutrition, School of Nutrition, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0002-4497-5358
Anna Carolina Motta CostaSchool of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0002-9746-9379
Camila Blanco CangussuSchool of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0009-0001-2248-1955
Luciano Garcia LourençãoSchool of Nursing, Federal University of Rio Grande, Rio Grande, RS, Brazil.ORCID http://orcid.org/0000-0002-1240-4702
Wandeir Wagner de OliveiraLaboratory of Cardiometabolism, School of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0003-4784-0966
Gabriel Trindade AvelarSchool of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0003-4560-0299
Daniela Fonseca Abdo RochaSchool of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0003-4881-9827
Iriane Marques de Carvalho RodriguesSchool of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0009-0005-0589-7878
André Versiani Caldeira RochaSchool of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0009-0006-9419-8477
Joana Paula Mendes de MouraSchool of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0001-6737-2915
George Luiz Lins Machado-CoelhoLaboratory of Epidemiology, School of Medicine, Federal University of Ouro Preto, Ouro Preto, MG, Brazil.ORCID http://orcid.org/0000-0002-9806-9721

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 306467/2018-6Fundação de Amparo à Pesquisa do Estado de Minas Gerais APQ-01933-21
6 · The paper itself

Abstract

backgroundObesity is the largest global public health epidemic, increasingly affecting children and adolescents. Studies suggest that genetic markers such as single nucleotide polymorphisms (SNPs) may be associated with the development of obesity. Obesity susceptibility genes identified include alpha-ketoglutarate-dependent dioxygenase (FTO), endothelial nitric oxide (NOS3) and apolipoprotein B (APOB). Furthermore genetic predisposition can interact with other environmental factors, such as clinical risk factors for obesity. In this context, the potential interaction between these SNPs and clinical risk factors such as non-exclusive breastfeeding, high birth weight, and a family history of chronic diseases warrants investigation. There is a clear need for more research on the FTO, NOS3 and APOB genes in Brazilian children. The purpose of this study was to evaluate the associations between SNPs in the FTO (rs1121980), NOS3 (rs1799983) and APOB (rs693) genes and obesity as well as to investigate the combined influence of significant SNPs in children and adolescents in Ouro Preto, Minas Gerais, Brazil.

methodsA cross-sectional population-based study was conducted with elementary school students aged 6-17 years in Ouro Preto, Minas Gerais, between April and December 2021. The study evaluated sociodemographic, clinical, and biochemical variables and the SNPs rs1121980, rs1799983 and rs693 in the FTO, NOS3 and APOB genes, respectively, for associations with obesity.

resultsThe study revealed that the prevalence of obesity was notably high, reaching 8.5% in the study population. Homozygotes for the risk alleles of the FTO and NOS3 genes (genotypes AA and TT, respectively) remained significant, with both showing a more than twofold increased likelihood of being obese [OR: 2.07 (CI: 1.02-4.20) and 2.49 (CI: 1.08-5.73), respectively]. The same combination of alleles associated with clinical risk factors (nonexclusive breastfeeding, high birth weight, family history of diabetes, obesity and dyslipidemia) was associated with a significantly greater chance of being obese at a young age.

conclusionsOur results support the idea that the SNP rs1121980 in the FTO gene and rs1799983 in the NOS3 gene can affect the occurrence of obesity in Brazilian children and adolescents living in urban areas.

Indexed as

Alpha-Ketoglutarate-Dependent Dioxygenase FTONitric Oxide Synthase Type IIIPediatric ObesityPolymorphism, Single NucleotideAdolescentBrazilChildCross-Sectional StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansMaleRisk FactorsAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanNitric Oxide Synthase Type IIINOS3 protein, humanAdolescent healthEpidemiologyGeneticsNative American child healthObesity

Identifiers

PMID40114142
PMCPMC11924821

What Socratic holds

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Registered trials

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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 Socratic graph.