sábado, 16 de diciembre de 2017

Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution. - PubMed - NCBI

Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution. - PubMed - NCBI



 2017 Dec 7;101(6):925-938. doi: 10.1016/j.ajhg.2017.10.007.

Penetrance of Polygenic Obesity Susceptibility Loci across the Body Mass Index Distribution.

Abstract

A growing number of single-nucleotide polymorphisms (SNPs) have been associated with body mass index (BMI) and obesity, but whether the effects of these obesity-susceptibility loci are uniform across the BMI distribution remains unclear. We studied the effects of 37 BMI-associated SNPs in 75,230 adults of European ancestry across BMI percentiles by using conditional quantile regression (CQR) and meta-regression (MR) models. The effects of nine SNPs (24%)-rs1421085 (FTO; p = 8.69 × 10-15), rs6235 (PCSK1; p = 7.11 × 10-6), rs7903146 (TCF7L2; p = 9.60 × 10-6), rs11873305 (MC4R; p = 5.08 × 10-5), rs12617233 (FANCL; p = 5.30 × 10-5), rs11672660 (GIPR; p = 1.64 × 10-4), rs997295 (MAP2K5; p = 3.25 × 10-4), rs6499653 (FTO; p = 6.23 × 10-4), and rs3824755 (NT5C2; p = 7.90 × 10-4)-increased significantly across the sample BMI distribution. We showed that such increases stemmed from unadjusted gene interactions that enhanced the effects of SNPs in persons with a high BMI. When 125 height-associated SNPs were analyzed for comparison, only one (<1%), rs6219 (IGF1, p = 1.80 × 10-4), showed effects that varied significantly across height percentiles. Cumulative gene scores of these SNPs (GS-BMI and GS-height) showed that only GS-BMI had effects that increased significantly across the sample distribution (BMI: p = 7.03 × 10-37; height: p = 0.499). Overall, these findings underscore the importance of gene-gene and gene-environment interactions in shaping the genetic architecture of BMI and advance a method for detecting such interactions by using only the sample outcome distribution.

KEYWORDS:

body mass index; conditional quantile regression; epistasis; gene score; gene-environment interactions; height; missing heritability; polygenic inheritance; quantitative trait distribution; variable allele penetrance

PMID:
 
29220676
 
DOI:
 
10.1016/j.ajhg.2017.10.007

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