Central Laboratory, Clinical Medical College & Affiliated Hospital of Chengdu University, Chengdu 610106, China.
Institute for Global Food Security, School of Biological Sciences, Queen's University Belfast, Belfast BT9 5DL, UK.
Nutrients. 2023 Jun 6;15(12):2643. doi: 10.3390/nu15122643.
Childhood metabolic syndrome (MetS) is prevalent around the world and is associated with a high likelihood of suffering from severe diseases such as cardiovascular disease later in adulthood. MetS is associated with genetic susceptibility that involves gene polymorphisms. The fat mass and obesity-associated gene () encodes an RNA N6-methyladenosine demethylase that regulates RNA stability and molecular functions. Human contains genetic variants that significantly contribute to the early onset of MetS in children and adolescents. Emerging evidence has also uncovered that polymorphisms in intron 1, such as rs9939609 and rs9930506 polymorphisms, are significantly associated with the development of MetS in children and adolescents. Mechanistic studies reported that polymorphisms lead to aberrant expressions of and the adjacent genes that promote adipogenesis and appetite and reduce steatolysis, satiety, and energy expenditure in the carriers. The present review highlights the recent observations on the key polymorphisms that are associated with child and adolescent MetS with an exploration of the molecular mechanisms underlying the development of increased waist circumference, hypertension, and hyperlipidemia in child and adolescent MetS.
儿童代谢综合征(MetS)在全球范围内普遍存在,并且与成年后患严重疾病(如心血管疾病)的可能性较高相关。MetS 与涉及基因突变的遗传易感性有关。脂肪量和肥胖相关基因()编码一种 RNA N6-甲基腺苷去甲基酶,可调节 RNA 稳定性和分子功能。人类包含可显著导致儿童和青少年 MetS 早期发病的遗传变异体。新出现的证据还揭示了内含子 1 中的 突变,如 rs9939609 和 rs9930506 突变,与儿童和青少年 MetS 的发展显著相关。机制研究报告称,突变导致和相邻基因的异常表达,从而促进脂肪生成和食欲,并减少携带者的脂肪分解、饱腹感和能量消耗。本综述强调了与儿童和青少年 MetS 相关的关键 突变的最新观察结果,并探讨了导致儿童和青少年 MetS 腰围增加、高血压和血脂异常的分子机制。