Mardones Lorena, Petermann-Rocha Fanny, Martínez-Sanguinetti María Adela, Leiva Ana María, Troncoso Pantoja Claudia Andrea, Martorell Miquel, Ulloa Natalia, Lasserre Laso Nicole Francisca, Pérez-Bravo Francisco, Celis-Morales Carlos, Villagrán Marcelo
Universidad Católica de la Santísima Concepción.
Institute of Cardiovascular and Medical Sciences. University of Glasgow.
Nutr Hosp. 2019 Jul 1;36(3):589-598. doi: 10.20960/nh.2275.
Background: genetic variants of the FTO gene confer the highest risk of obesity identified so far. Associations between the FTO gene and alterations in metabolic markers have been reported in different populations but not in Chileans. The aim of this study was therefore to investigate the association of rs3751812 gene polymorphism with adiposity and metabolic markers in the Chilean adult population. Methods: genotype of the FTO gene was determined in 409 participants from the GENADIO study. Adiposity markers (body weight, BMI, % fat mass and waist circumference), metabolic markers (glycemia, insulin, HOMAIR, total cholesterol, LDL cholesterol, HDL cholesterol, triglycerides, leptin, ALT, GGT, PCRhs) and blood pressure were measured. The association between the FTO genotype and the different markers was determined using linear regression analyses. Results: there was an association between the polymorphism and all adiposity markers as well as insulin, HOMAIR, leptin and HDL cholesterol (p < 0.05) in the fully adjusted model. For total cholesterol, triglycerides, LDL cholesterol, ALT, GGT and PCRhs, the association disappeared after adjustment by body mass index. Conclusion: our findings verify the association between the FTO rs3751812 polymorphism with obesity, hyperinsulinemia, hyperleptinemia and lower levels of HDL cholesterol in the Chilean population. These alterations could increase the risk of diabetes mellitus type II and metabolic syndrome.
FTO基因的遗传变异赋予了迄今为止所发现的最高肥胖风险。FTO基因与代谢标志物改变之间的关联已在不同人群中报道,但智利人群中尚未见报道。因此,本研究的目的是调查rs3751812基因多态性与智利成年人群肥胖及代谢标志物之间的关联。方法:在来自GENADIO研究的409名参与者中确定FTO基因的基因型。测量肥胖标志物(体重、BMI、体脂百分比和腰围)、代谢标志物(血糖、胰岛素、HOMAIR、总胆固醇、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇、甘油三酯、瘦素、谷丙转氨酶、γ-谷氨酰转肽酶、PCRhs)和血压。使用线性回归分析确定FTO基因型与不同标志物之间的关联。结果:在完全调整模型中,该多态性与所有肥胖标志物以及胰岛素、HOMAIR、瘦素和高密度脂蛋白胆固醇之间存在关联(p<0.05)。对于总胆固醇、甘油三酯、低密度脂蛋白胆固醇、谷丙转氨酶、γ-谷氨酰转肽酶和PCRhs,在通过体重指数调整后,这种关联消失。结论:我们的研究结果证实了智利人群中FTO rs3751812多态性与肥胖、高胰岛素血症、高瘦素血症及较低水平的高密度脂蛋白胆固醇之间的关联。这些改变可能会增加2型糖尿病和代谢综合征的风险。