4.6 Article

Genetic architecture of human thinness compared to severe obesity

期刊

PLOS GENETICS
卷 15, 期 1, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pgen.1007603

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资金

  1. European Research Council
  2. Wellcome Trust [098497/Z/12/Z, WT098051, WT206194]
  3. Medical Research Council [MRC_MC_UU_12012/5]
  4. NIHR Cambridge Biomedical Research Centre
  5. Bernard Wolfe Health Neuroscience Endowment
  6. European Community [279153]
  7. Economic and Social Research Council
  8. Wellcome Trust
  9. MRC [076467/Z/05/Z]
  10. Common Fund of the Office of the Director of the National Institutes of Health
  11. NCI
  12. NHGRI
  13. NHLBI
  14. NIDA
  15. NIMH
  16. NINDS
  17. 23andMe
  18. Economic and Social Research Council [ES/M008592/1] Funding Source: researchfish
  19. ESRC [ES/S008349/1, ES/M008592/1] Funding Source: UKRI
  20. MRC [MR/N01104X/1, G0900554, MC_UU_12012/5, MR/N01104X/2, G1001799, MC_UU_12012/1, MC_UU_00014/1] Funding Source: UKRI

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The variation in weight within a shared environment is largely attributable to genetic factors. Whilst many genes/loci confer susceptibility to obesity, little is known about the genetic architecture of healthy thinness. Here, we characterise the heritability of thinness which we found was comparable to that of severe obesity (h(2) = 28.07 vs 32.33% respectively), although with incomplete genetic overlap (r = -0.49, 95% CI [-0.17, -0.82], p = 0.003). In a genome-wide association analysis of thinness (n = 1,471) vs severe obesity (n = 1,456), we identified 10 loci previously associated with obesity, and demonstrate enrichment for established BMI-associated loci (p(binomial) = 3.05x10(-5)). Simulation analyses showed that different association results between the extremes were likely in agreement with additive effects across the BMI distribution, suggesting different effects on thinness and obesity could be due to their different degrees of extremeness. In further analyses, we detected a novel obesity and BMI-associated locus at PKHD1 (rs2784243, obese vs. thin p = 5.99x10(-6), obese vs. controls p = 2.13x10(-6) p(BMI) = 2.3x10(-13)), associations at loci recently discovered with much larger sample sizes (e.g. FAM150B and PRDM6-CEP120), and novel variants driving associations at previously established signals (e.g. rs205262 at the SNRPC/C6orf106 locus and rs112446794 at the PRDM6-CEP120 locus). Our ability to replicate loci found with much larger sample sizes demonstrates the value of clinical extremes and suggest that characterisation of the genetics of thinness may provide a more nuanced understanding of the genetic architecture of body weight regulation and may inform the identification of potential anti-obesity targets. Author summary Obesity-associated disorders are amongst the leading causes of morbidity and mortality worldwide. Most genome-wide association studies (GWAS) have focused on body mass index (BMI = weight in Kg divided by height squared (m(2))) and obesity, but to date no genetic association study testing thin and healthy individuals has been performed. In this study, we recruited a first of its kind cohort of 1,471 clinically ascertained thin and healthy individuals and contrasted the genetic architecture of the trait with that of severe early onset obesity. We show that thinness, like obesity, is a heritable trait with a polygenic component. In a GWAS of persistent healthy thinness vs. severe obesity with a total sample size of 2,927, we are able to find evidence of association in loci that have only been recently discovered using large cohorts with >40,000 individuals. We also find a novel BMI-associated locus at PKHD1 in UK Biobank highlighted by our association study. This work illustrates the value and increased power brought upon by using clinically ascertained extremes to study complex traits and provides a valuable resource on which to study resistance to obesity in an increasingly obesogenic environment.

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