AI Article Synopsis

  • FTO gene variations have been linked to an increased risk of type 2 diabetes (T2D) in a Japanese population, but their connection to fat mass and BMI remains debated.
  • In a study of 760 T2D patients and 693 controls, FTO SNPs were generally not linked to BMI or T2D risk in a combined analysis, but did show significant associations in men when analyzed separately.
  • The findings imply that the impact of FTO polymorphisms on T2D risk in Japanese men is primarily due to their influence on peak BMI before diagnosis.

Article Abstract

Aim: Several studies have demonstrated that polymorphisms within the fat-mass and obesity-associated gene (FTO) are associated with type 2 diabetes (T2D). However, whether the effects of the FTO locus on T2D susceptibility are independent of fat-mass increases remains controversial. To investigate this issue, we examined the association of FTO variants with T2D and various aspects of BMI history during adult life in a Japanese population.

Methods: We genotyped SNPs within FTO (rs1121980 and rs1558902) in 760 Japanese patients with T2D who had reached a lifetime maximum BMI (BMImax) before or at the time of diagnosis and 693 control individuals with information regarding their BMImax.

Results: The BMImax showed the strongest association with T2D risk among the BMIs evaluated in this study. In the sex-combined analysis, FTO SNPs were not associated with any of the BMI variables or with T2D, but in sex-stratified analyses, both SNPs were significantly associated with the BMImax and rs1558902 was associated with T2D in men. The association of the SNPs with T2D remained significant after adjustments for the current BMI and age, whereas the T2D association of the SNP was no longer significant after adjustments for BMImax and age.

Conclusions: These results suggest that the effects of FTO polymorphisms on T2D susceptibility in Japanese men are mediated through their effect on increasing the BMImax before or at the time of diagnosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098825PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0165523PLOS

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