Carrasco-Luna Joaquín, Navarro-Solera María, Gombert Marie, Martín-Carbonell Vanessa, Carrasco-García Álvaro, Del Castillo-Villaescusa Cristina, García-Pérez Miguel Ángel, Codoñer-Franch Pilar
Department of Pediatrics, Obstetrics and Gynecology, University of Valencia, 46010 Valencia, Spain.
Department for Biotechnology, Faculty of Experimental Science, Catholic University of Valencia, 46001 Valencia, Spain.
Children (Basel). 2023 Jul 14;10(7):1221. doi: 10.3390/children10071221.
Obesity is a multifactorial disease whose onset and development are shaped by the individual genetic background. The melanocortin 4 receptor gene () is involved in the regulation of food intake and energy expenditure. Some of the single nucleotide polymorphisms (SNPs) of this gene are related to obesity and metabolic risk factors. The present study was undertaken to assess the relationship between three polymorphism SNPs, namely, rs17782313, rs17773430 and rs34114122, and obesity and metabolic risk factors. One hundred seventy-eight children with obesity aged between 7 and 16 years were studied to determine anthropometric variables and biochemical and inflammatory parameters. Our results highlight that metabolic risk factors, especially alterations in carbohydrate metabolism, were related to rs17782313. The presence of the minor C allele in the three variants (C-C-C) was significantly associated with anthropometric measures indicative of obesity, such as the body mass and fat mass indexes, and increased the values of insulinemia to 21.91 µIU/mL with respect to the wild type values. Our study suggests that the C-C-C haplotype of the SNPs rs17782313, rs17773430 and rs34114122 of the gene potentiates metabolic risk factors at early ages in children with obesity.
肥胖是一种多因素疾病,其发病和发展受个体遗传背景影响。黑皮质素4受体基因()参与食物摄入和能量消耗的调节。该基因的一些单核苷酸多态性(SNP)与肥胖和代谢风险因素有关。本研究旨在评估rs17782313、rs17773430和rs34114122这三种多态性SNP与肥胖及代谢风险因素之间的关系。对178名7至16岁的肥胖儿童进行了研究,以确定人体测量学变量以及生化和炎症参数。我们的研究结果表明,代谢风险因素,尤其是碳水化合物代谢的改变,与rs17782313有关。三种变体(C-C-C)中次要C等位基因的存在与表明肥胖的人体测量指标显著相关,如体重和脂肪量指数,并且相对于野生型值,胰岛素血症值增加到21.91 µIU/mL。我们的研究表明,基因的SNP rs17782313、rs17773430和rs34114122的C-C-C单倍型在肥胖儿童的早期会增强代谢风险因素。