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Adipose Tissue Gene Expression Associations Reveal Hundreds of Candidate Genes for Cardiometabolic Traits.
Raulerson, Chelsea K; Ko, Arthur; Kidd, John C; Currin, Kevin W; Brotman, Sarah M; Cannon, Maren E; Wu, Ying; Spracklen, Cassandra N; Jackson, Anne U; Stringham, Heather M; Welch, Ryan P; Fuchsberger, Christian; Locke, Adam E; Narisu, Narisu; Lusis, Aldons J; Civelek, Mete; Furey, Terrence S; Kuusisto, Johanna; Collins, Francis S; Boehnke, Michael; Scott, Laura J; Lin, Dan-Yu; Love, Michael I; Laakso, Markku; Pajukanta, Päivi; Mohlke, Karen L.
Afiliação
  • Raulerson CK; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Ko A; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA; Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
  • Kidd JC; Department of Biostatistics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Currin KW; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Brotman SM; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Cannon ME; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Wu Y; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Spracklen CN; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Jackson AU; Department of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Stringham HM; Department of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Welch RP; Department of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Fuchsberger C; Center for Biomedicine, European Academy of Bolzano/Bozen, University of Lübeck, Bolzano/Bozen 39100, Italy.
  • Locke AE; McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO 63110, USA.
  • Narisu N; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Lusis AJ; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
  • Civelek M; Department of Biomedical Engineering, University of Virginia, Charlottesville, VA 22908, USA.
  • Furey TS; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA; Department of Biology, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Kuusisto J; Institute of Clinical Medicine, Kuopio University Hospital, University of Eastern Finland, Kuopio 70210, Finland.
  • Collins FS; National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
  • Boehnke M; Department of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Scott LJ; Department of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI 48109, USA.
  • Lin DY; Department of Biostatistics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Love MI; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA; Department of Biostatistics, University of North Carolina, Chapel Hill, NC 27599, USA.
  • Laakso M; Institute of Clinical Medicine, Kuopio University Hospital, University of Eastern Finland, Kuopio 70210, Finland.
  • Pajukanta P; Department of Human Genetics, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA; Institute for Precision Health, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA.
  • Mohlke KL; Department of Genetics, University of North Carolina, Chapel Hill, NC 27599, USA. Electronic address: mohlke@med.unc.edu.
Am J Hum Genet ; 105(4): 773-787, 2019 10 03.
Article em En | MEDLINE | ID: mdl-31564431
Genome-wide association studies (GWASs) have identified thousands of genetic loci associated with cardiometabolic traits including type 2 diabetes (T2D), lipid levels, body fat distribution, and adiposity, although most causal genes remain unknown. We used subcutaneous adipose tissue RNA-seq data from 434 Finnish men from the METSIM study to identify 9,687 primary and 2,785 secondary cis-expression quantitative trait loci (eQTL; <1 Mb from TSS, FDR < 1%). Compared to primary eQTL signals, secondary eQTL signals were located further from transcription start sites, had smaller effect sizes, and were less enriched in adipose tissue regulatory elements compared to primary signals. Among 2,843 cardiometabolic GWAS signals, 262 colocalized by LD and conditional analysis with 318 transcripts as primary and conditionally distinct secondary cis-eQTLs, including some across ancestries. Of cardiometabolic traits examined for adipose tissue eQTL colocalizations, waist-hip ratio (WHR) and circulating lipid traits had the highest percentage of colocalized eQTLs (15% and 14%, respectively). Among alleles associated with increased cardiometabolic GWAS risk, approximately half (53%) were associated with decreased gene expression level. Mediation analyses of colocalized genes and cardiometabolic traits within the 434 individuals provided further evidence that gene expression influences variant-trait associations. These results identify hundreds of candidate genes that may act in adipose tissue to influence cardiometabolic traits.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Expressão Gênica / Tecido Adiposo / Diabetes Mellitus Tipo 2 / Obesidade Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Expressão Gênica / Tecido Adiposo / Diabetes Mellitus Tipo 2 / Obesidade Idioma: En Ano de publicação: 2019 Tipo de documento: Article