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Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration.
Lanktree, Matthew B; Elbers, Clara C; Li, Yun; Zhang, Guosheng; Duan, Qing; Karczewski, Konrad J; Guo, Yiran; Tragante, Vinicius; North, Kari E; Cushman, Mary; Asselbergs, Folkert W; Wilson, James G; Lange, Leslie A; Drenos, Fotios; Reiner, Alex P; Barnes, Michael R; Keating, Brendan J.
Afiliação
  • Lanktree MB; Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
  • Elbers CC; Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, PA Complex Genetics Section, Department of Medical Genetics (DBG), University Medical Center Utrecht, Utrecht, The Netherlands.
  • Li Y; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Zhang G; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Duan Q; Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Karczewski KJ; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA.
  • Guo Y; Center for Applied Genomics, Abramson Research Center, Children's Hospital of Philadelphia, Philadelphia, PA.
  • Tragante V; Department of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands Department of Medical Genetics, Biomedical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • North KE; Department of Epidemiology, School of Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC.
  • Cushman M; Departments of Medicine and Pathology,University of Vermont, Colchester, VT.
  • Asselbergs FW; Department of Cardiology, Division Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Wilson JG; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, MS.
  • Lange LA; Department of Genetics, University of North Carolina School of Medicine at Chapel Hill, Chapel Hill, NC.
  • Drenos F; Centre for Cardiovascular Genetics, Institute of Cardiovascular Science, Faculty of Population Health Sciences, University College London, London, United Kindom.
  • Reiner AP; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Barnes MR; William Harvey Research Institute, Barts and the London School of Medicine, Queen Mary University of London, London, United Kindom.
  • Keating BJ; Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, PA Division of Transplantation, Department of Surgery, University of Pennsylvania, Philadelphia, PA.
J Lipid Res ; 56(9): 1781-6, 2015 Sep.
Article em En | MEDLINE | ID: mdl-26199122
Meta-analyses of European populations has successfully identified genetic variants in over 150 loci associated with lipid levels, but results from additional ethnicities remain limited. Previously, we reported two novel lipid loci identified in a sample of 7,657 African Americans using a gene-centric array including 50,000 SNPs in 2,100 candidate genes. Initial discovery and follow-up of signals with P < 10(-5) in additional African American samples confirmed CD36 and ICAM1. Using an additional 8,244 African American female samples from the Women's Health Initiative SNP Health Association Resource genome-wide association study dataset, we further examined the previous meta-analyses results by attempting to replicate 20 additional putative lipid signals with P < 10(-4). Replication confirmed rs868213, located in a splice donor region of exocyst complex component 3-like 1 (EXOC3L1) as a novel signal for HDL (additive allelic effect ß = 0.02; P = 1.4 × 10(-8); meta-analyses of discovery and replication). EXOC3L1 is strongly expressed in vascular endothelium and forms part of the exocyst complex, a key facilitator of the trafficking of lipid receptors. Increasing sample sizes for genetic studies in nonEuropean populations will continue to improve our understanding of lipid metabolism.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte Vesicular / Estudo de Associação Genômica Ampla / Lipoproteínas HDL Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte Vesicular / Estudo de Associação Genômica Ampla / Lipoproteínas HDL Tipo de estudo: Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article