Genetic variants in the fat mass and obesity-associated (FTO) gene confer risk for extreme obesity and modulate adiposity in a Brazilian population.
Ana Carolina Proença da FonsecaBruna MarchesiniVerônica Marques ZembrzuskiDanielle Dutra VoigtVivianne Galante RamosJoão Regis Ivar CarneiroJosé Firmino Nogueira NetoGiselda Maria Kalil de CabelloPedro Hernán CabelloPublished in: Genetics and molecular biology (2020)
Obesity is a major public health problem worldwide. It has a complex etiology, influenced by environmental and genetic factors. FTO has been recognized as an important genetic factor for obesity development. This study evaluated the contribution of FTO polymorphisms (rs9939609 and rs17817449) for extreme obesity in terms of the period of obesity onset, anthropometric, and biochemical parameters. The haplotype and the combined effects of FTO risk alleles on obesity susceptibility were evaluated. We investigated 169 normal-weight subjects (body mass index, BMI: 22.8 [21.0; 24.0] kg/m2) and 123 extremely obese individuals (BMI: 47.6 [44.1; 53.1] kg/m2). Genotyping was performed by real time PCR. Our results showed a strong association between FTO variants and extreme obesity. Carriers of the AT haplotype had an increased risk for extreme obesity. Gene scores suggested that the risk of developing extreme obesity was increased 1.37-fold per risk allele added. Both polymorphisms also influenced BMI and body weight. Additionally, rs17817449 influenced triglyceride levels. No effect of FTO variants on the period of obesity onset was found. In conclusion, the FTO polymorphisms showed a strong association with development of extreme phenotype of obesity and adiposity modulation in a Brazilian population.
Keyphrases
- weight gain
- insulin resistance
- weight loss
- metabolic syndrome
- body mass index
- high fat diet induced
- type diabetes
- public health
- adipose tissue
- genome wide
- climate change
- body weight
- physical activity
- skeletal muscle
- gene expression
- risk assessment
- body composition
- high resolution
- dna methylation
- real time pcr
- transcription factor