Song Yongyan, Li Shujin, Liu Hao, Liu Xinyu, Li Jing, Wang Yunhan, Yang Jin
Central Laboratory, Clinical Medical College & Affiliated Hospital of Chengdu University, Chengdu, Sichuan, PR China.
Clinical Medical College of Chengdu University, Chengdu, Sichuan, PR China.
Pediatr Res. 2025 Apr 1. doi: 10.1038/s41390-025-04020-1.
The relationship between polymorphisms in fat mass and obesity-associated gene (FTO) and the components of metabolic syndrome (MetS) has been explored among children and adolescents, but the results are inconsistent and inconclusive.
Electronic databases including Medline, Scopus, Embase, Web of Science, CNKI, and Google Scholar were searched for eligible studies, and data were extracted from each study. Standardized mean differences were calculated to examine the differences in the components of MetS between FTO genotypes.
Forty-six studies (45,100 subjects), seven studies (4216 subjects), and six studies (2699 subjects) were included in the meta-analyses for FTOrs9939609, FTOrs1421085, and FTOrs17817449 polymorphisms, respectively. A-allele carriers of FTOrs9939609 polymorphism had higher levels of waist circumference (WC), systolic blood pressure, and fasting blood glucose, but lower levels of high-density lipoprotein cholesterol (HDL-C) than TT homozygotes (p < 0.05 for all). C-allele carriers of FTOrs1421085 polymorphism had higher levels of WC and lower levels of HDL-C than TT homozygotes (p < 0.05 for both). No significant associations between FTOrs17817449 polymorphism and the components of MetS were detected.
The meta-analysis demonstrates that A allele of FTOrs9939609 and C allele of FTOrs1421085 polymorphisms confer a higher risk of MetS among children and adolescents.
Genetic polymorphisms are closely related to metabolic syndrome in children and adolescents. The rs9939609 polymorphism in fat mass and obesity-associated gene is apparently associated with a higher risk of metabolic syndrome among children and adolescents. The findings of this study can provide reference for gene diagnosis and gene therapy of metabolic syndrome in children and adolescents.
已在儿童和青少年中探索了脂肪量与肥胖相关基因(FTO)多态性与代谢综合征(MetS)各组分之间的关系,但结果不一致且尚无定论。
检索包括Medline、Scopus、Embase、Web of Science、中国知网和谷歌学术在内的电子数据库以查找符合条件的研究,并从每项研究中提取数据。计算标准化均值差以检验FTO基因不同基因型之间MetS各组分的差异。
分别有46项研究(45100名受试者)、7项研究(4216名受试者)和6项研究(2699名受试者)纳入了针对FTO rs9939609、FTO rs1421085和FTO rs17817449多态性的荟萃分析。与TT纯合子相比,FTO rs9939609多态性的A等位基因携带者腰围(WC)、收缩压和空腹血糖水平较高,但高密度脂蛋白胆固醇(HDL-C)水平较低(所有p<0.05)。与TT纯合子相比,FTO rs1421085多态性的C等位基因携带者WC水平较高,HDL-C水平较低(两者p<0.05)。未检测到FTO rs17817449多态性与MetS各组分之间存在显著关联。
荟萃分析表明,FTO rs9939609的A等位基因和FTO rs1421085多态性的C等位基因使儿童和青少年患MetS的风险更高。
基因多态性与儿童和青少年的代谢综合征密切相关。脂肪量与肥胖相关基因中的rs9939609多态性显然与儿童和青少年患代谢综合征的较高风险相关。本研究结果可为儿童和青少年代谢综合征的基因诊断和基因治疗提供参考。