Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci.
Where this comes from
- Record sourced from PubMed, PMID 33459256.
- Also identified by DOI 10.7554/eLife.62206 and PMC identifier 7815306.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
To uncover novel significant association signals (p<5×10<sup>-8</sup>), genome-wide association studies (GWAS) requires increasingly larger sample sizes to overcome statistical correction for multiple testing. As an alternative, we aimed to identify associations among suggestive signals (5 × 10<sup>-8</sup>≤p<5×10<sup>-4</sup>) in increasingly powered GWAS efforts using chromatin accessibility and direct contact with gene promoters as biological constraints. We conducted retrospective analyses of three GIANT BMI GWAS efforts using ATAC-seq and promoter-focused Capture C data from human adipocytes and embryonic stem cell (ESC)-derived hypothalamic-like neurons. This approach, with its extremely low false-positive rate, identified 15 loci at p<5×10<sup>-5</sup> in the 2010 GWAS, of which 13 achieved genome-wide significance by 2018, including at <i>NAV1</i>, <i>MTIF3</i>, and <i>ADCY3</i>. Eighty percent of constrained 2015 loci achieved genome-wide significance in 2018. We observed similar results in waist-to-hip ratio analyses. In conclusion, biological constraints on sub-significant GWAS signals can reveal potentially true-positive loci for further investigation in existing data sets without increasing sample size.
Medical subject headings
- Body Mass Index
- Genome-Wide Association Study
- Polymorphism, Single Nucleotide