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Biological constraints on GWAS SNPs at suggestive significance thresholds reveal additional BMI loci.
Hammond, Reza K; Pahl, Matthew C; Su, Chun; Cousminer, Diana L; Leonard, Michelle E; Lu, Sumei; Doege, Claudia A; Wagley, Yadav; Hodge, Kenyaita M; Lasconi, Chiara; Johnson, Matthew E; Pippin, James A; Hankenson, Kurt D; Leibel, Rudolph L; Chesi, Alessandra; Wells, Andrew D; Grant, Struan Fa.
Afiliação
  • Hammond RK; Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia, Philadelphia, United States.
  • Pahl MC; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, United States.
  • Su C; Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia, Philadelphia, United States.
  • Cousminer DL; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, United States.
  • Leonard ME; Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia, Philadelphia, United States.
  • Lu S; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, United States.
  • Doege CA; Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia, Philadelphia, United States.
  • Wagley Y; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, United States.
  • Hodge KM; Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia, Philadelphia, United States.
  • Lasconi C; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, United States.
  • Johnson ME; Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia, Philadelphia, United States.
  • Pippin JA; Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, United States.
  • Hankenson KD; Naomi Berrie Diabetes Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, United States.
  • Leibel RL; Department of Pathology and Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University, New York, United States.
  • Chesi A; Columbia Stem Cell Initiative, Vagelos College of Physicians and Surgeons, Columbia University, New York, United States.
  • Wells AD; Department of Orthopaedic Surgery, University of Michigan Medical School, Ann Arbor, United States.
  • Grant SF; Center for Spatial and Functional Genomics, Children's Hospital of Philadelphia, Philadelphia, United States.
Elife ; 102021 01 18.
Article em En | MEDLINE | ID: mdl-33459256
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Massa Corporal / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Índice de Massa Corporal / Polimorfismo de Nucleotídeo Único / Estudo de Associação Genômica Ampla Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article