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

IF 2 3区 医学 Q2 PEDIATRICS
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, André Versiani Caldeira Rocha, Joana Paula Mendes de Moura, George Luiz Lins Machado-Coelho
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引用次数: 0

Abstract

Background: Obesity 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.

Methods: A 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.

Results: The 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.

Conclusions: Our 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.

背景:肥胖症是全球最大的公共卫生流行病,对儿童和青少年的影响越来越大。研究表明,单核苷酸多态性(SNPs)等遗传标记可能与肥胖的发生有关。已发现的肥胖易感基因包括α-酮戊二酸依赖性二氧合酶(FTO)、内皮一氧化氮(NOS3)和脂蛋白 B(APOB)。此外,遗传易感性还可能与其他环境因素相互作用,如肥胖的临床风险因素。在这种情况下,这些 SNPs 与临床风险因素(如非纯母乳喂养、高出生体重和慢性病家族史)之间的潜在相互作用值得研究。显然,需要对巴西儿童的 FTO、NOS3 和 APOB 基因进行更多的研究。本研究旨在评估 FTO(rs1121980)、NOS3(rs1799983)和 APOB(rs693)基因中的 SNPs 与肥胖之间的关联,并调查巴西米纳斯吉拉斯州奥罗普雷图市儿童和青少年中重要 SNPs 的综合影响:2021 年 4 月至 12 月期间,对米纳斯吉拉斯州奥罗普雷图市 6-17 岁的小学生进行了一项基于人群的横断面研究。研究评估了社会人口学、临床和生化变量,以及 FTO、NOS3 和 APOB 基因中的 SNPs rs1121980、rs1799983 和 rs693 与肥胖的关系:研究显示,肥胖症的发病率很高,在研究人群中达到 8.5%。FTO 和 NOS3 基因风险等位基因的等位基因(基因型分别为 AA 和 TT)仍然具有显著性,这两种基因导致肥胖的可能性增加了两倍多[OR:分别为 2.07(CI:1.02-4.20)和 2.49(CI:1.08-5.73)]。与临床风险因素(非纯母乳喂养、高出生体重、糖尿病家族史、肥胖症和血脂异常)相关的等位基因组合与年轻时肥胖的几率显著增加有关:我们的研究结果表明,FTO 基因中的 SNP rs1121980 和 NOS3 基因中的 SNP rs1799983 可影响生活在城市地区的巴西儿童和青少年的肥胖发生率。
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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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