Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci

Author:

Hammond Reza K12,Pahl Matthew C12,Su Chun12,Cousminer Diana L12,Leonard Michelle E12,Lu Sumei12,Doege Claudia A345,Wagley Yadav6,Hodge Kenyaita M12,Lasconi Chiara12ORCID,Johnson Matthew E12,Pippin James A12,Hankenson Kurt D6,Leibel Rudolph L7,Chesi Alessandra12,Wells Andrew D189,Grant Struan FA12101112ORCID

Affiliation:

1. Center for Spatial and Functional Genomics, Children’s Hospital of Philadelphia, Philadelphia, United States

2. Division of Human Genetics, The Children’s Hospital of Philadelphia, Philadelphia, United States

3. Naomi Berrie Diabetes Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, United States

4. Department of Pathology and Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University, New York, United States

5. Columbia Stem Cell Initiative, Vagelos College of Physicians and Surgeons, Columbia University, New York, United States

6. Department of Orthopaedic Surgery, University of Michigan Medical School, Ann Arbor, United States

7. Division of Molecular Genetics (Pediatrics) and the Naomi Berrie Diabetes Center, Columbia University Vagelos College of Physicians and Surgeons, New York, United States

8. Department of Pathology, The Children’s Hospital of Philadelphia, Philadelphia, United States

9. Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States

10. Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States

11. Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, United States

12. Division of Diabetes and Endocrinology, The Children’s Hospital of Philadelphia, Philadelphia, United States

Abstract

To uncover novel significant association signals (p<5×10−8), 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 × 10−8≤p<5×10−4) 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<5×10−5 in the 2010 GWAS, of which 13 achieved genome-wide significance by 2018, including at NAV1, MTIF3, and ADCY3. 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.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Human Genome Research Institute

Children's Hospital of Philadelphia

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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