Fat mass obesity-associated (FTO) (rs9939609) and melanocortin 4 receptor (MC4R) (rs17782313) SNP are positively associated with obesity and blood pressure in Mexican school-aged children

被引:22
|
作者
Garcia-Solis, Pablo [1 ]
Reyes-Bastidas, Marissa [1 ]
Flores, Karla [2 ]
Garcia, Olga P. [2 ]
Rosado, Jorge L. [2 ]
Mendez-Villa, Lorena [1 ]
Garcia-G, Carlota [1 ]
Garcia-Gutierrez, David [1 ]
Kuri-Garcia, Aaron [2 ]
Hernandez-Montiel, Hebert L. [1 ]
Soriano-Leon, Ofelia [1 ]
Elena Villagran-Herrera, Maria [1 ]
Solis-Sainz, Juan C. [1 ]
机构
[1] Univ Autonoma Queretaro, Fac Med, Dept Invest Biomed, Clavel 200, Queretaro 76170, Qro, Mexico
[2] Univ Autonoma Queretaro, Fac Ciencias Nat, Av Ciencias S-N, Juriquilla 76230, Qro, Mexico
关键词
Fat mass obesity-associated; Melanocortin; 4; receptor; SNP; Obesity; Blood pressure; INSULIN-RESISTANCE; GENE; RISK; DYSLIPIDEMIA; HYPERTENSION; PREVALENCE; VARIANTS; LOCI;
D O I
10.1017/S0007114516003779
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Childhood overweight and obesity are worldwide public health problems and risk factors for chronic diseases. The presence of SNP in several genes has been associated with the presence of obesity. A total of 580 children (8-13 years old) from Queretaro, Mexico, participated in this cross-sectional study, which evaluated the associations of rs9939609 (fat mass obesity-associated (FTO)), rs17782313 (melanocortin 4 receptor (MC4R)) and rs6548238 (transmembrane protein 18 (TMEM18)) SNP with obesity and metabolic risk factors. Overweight and obesity prevalence was 19.8 and 19.1%, respectively. FTO, MC4R and TMEM18 risk allele frequency was 17, 9.8 and 89.5%, respectively. A significant association between FTO homozygous and MC4R heterozygous risk alleles and obesity was found (OR 3.9; 95% CI 1.46, 10.22, and OR 2.1; 95% CI 1.22, 3.71; respectively). The FTO heterozygous subjects showed higher systolic and diastolic blood pressures, compared with the homozygous for the ancestral allele subjects. These results remain significant after considering adiposity as a covariate. The FTO and MC4R genotypes were not significantly associated with total cholesterol, HDL-cholesterol and insulin concentration. No association was found between TMEM18 risk allele and obesity and/or metabolic alterations. Our results show that, in addition to a higher BMI, there is also an association of the risk genotype with blood pressure in the presence of the FTO risk genotype. The possible presence of a risk genotype in obese children must be considered to offer a more comprehensive therapeutic approach in order to delay and/or prevent the development of chronic diseases.
引用
收藏
页码:1834 / 1840
页数:7
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