AI Article Synopsis

  • Obesity is a significant global health issue influenced by genetics and environment, with the FTO gene identified as a key genetic factor.
  • This study analyzed FTO gene variations (specifically rs9939609 and rs17817449) in 169 normal-weight and 123 extremely obese subjects to assess their impact on obesity and related health metrics.
  • Results indicated a strong link between FTO variants and extreme obesity, with specific haplotypes increasing obesity risk, and certain polymorphisms affecting BMI and triglyceride levels, though no effect on the onset age of obesity was observed.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7197983PMC
http://dx.doi.org/10.1590/1678-4685-GMB-2018-0264DOI Listing

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