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Transethnic Evaluation Identifies Low-Frequency Loci Associated With 25-Hydroxyvitamin D Concentrations.
Hong, Jaeyoung; Hatchell, Kathryn E; Bradfield, Jonathan P; Bjonnes, Andrew; Chesi, Alessandra; Lai, Chao-Qiang; Langefeld, Carl D; Lu, Lingyi; Lu, Yingchang; Lutsey, Pamela L; Musani, Solomon K; Nalls, Mike A; Robinson-Cohen, Cassianne; Roizen, Jeffery D; Saxena, Richa; Tucker, Katherine L; Ziegler, Julie T; Arking, Dan E; Bis, Joshua C; Boerwinkle, Eric; Bottinger, Erwin P; Bowden, Donald W; Gilsanz, Vicente; Houston, Denise K; Kalkwarf, Heidi J; Kelly, Andrea; Lappe, Joan M; Liu, Yongmei; Michos, Erin D; Oberfield, Sharon E; Palmer, Nicholette D; Rotter, Jerome I; Sapkota, Bishwa; Shepherd, John A; Wilson, James G; Basu, Saonli; de Boer, Ian H; Divers, Jasmin; Freedman, Barry I; Grant, Struan F A; Hakanarson, Hakon; Harris, Tamara B; Kestenbaum, Bryan R; Kritchevsky, Stephen B; Loos, Ruth J F; Norris, Jill M; Norwood, Arnita F; Ordovas, Jose M; Pankow, James S; Psaty, Bruce M.
Afiliação
  • Hong J; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
  • Hatchell KE; Department of Population Health Sciences, University of Wisconsin-Madison School of Medicine and Public Health, Madison, Wisconsin.
  • Bradfield JP; Center for Applied Genomics, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Bjonnes A; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts.
  • Chesi A; The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Lai CQ; USDA-ARS Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts.
  • Langefeld CD; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Lu L; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Lu Y; The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Lutsey PL; Division of Epidemiology and Community Health, University of Minnesota, Minneapolis, Minnesota.
  • Musani SK; Department of Medicine, University of Mississippi Medical Center, Jackson, Mississippi.
  • Nalls MA; Data Tecnica International, Glen Echo, Maryland.
  • Robinson-Cohen C; Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland.
  • Roizen JD; Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington, Seattle, Washington.
  • Saxena R; Center for Applied Genomics, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Tucker KL; Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Ziegler JT; Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts.
  • Arking DE; Department of Biomedical and Nutritional Sciences, University of Massachusetts Lowell, Lowell, Massachusetts.
  • Bis JC; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Boerwinkle E; McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Bottinger EP; Cardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, Washington.
  • Bowden DW; University of Texas Health Science Center at Houston, Houston, Texas.
  • Gilsanz V; The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.
  • Houston DK; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Kalkwarf HJ; Department of Radiology, Children's Hospital of Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles, California.
  • Kelly A; Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Lappe JM; Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Liu Y; The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Michos ED; Perelman School of Medicine at University of Pennsylvania, Philadelphia, Pennsylvania.
  • Oberfield SE; Creighton University, Omaha, Nebraska.
  • Palmer ND; Department of Epidemiology and Prevention, Division of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Rotter JI; Ciccarone Center for the Prevention of Heart Disease, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Sapkota B; Division of Pediatric Endocrinology, Diabetes and Metabolism, Columbia University Medical Center, New York, New York.
  • Shepherd JA; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Wilson JG; Institute for Translational Genomics and Population Sciences, Department of Pediatrics and Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California.
  • Basu S; Department of Pediatrics, College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
  • de Boer IH; University of California San Francisco School of Medicine, San Francisco, California.
  • Divers J; Department of Physiology and Biophysics, University of Mississippi Medical Center, Jackson, Mississippi.
  • Freedman BI; Division of Biostatistics, University of Minnesota, Minneapolis, Minnesota.
  • Grant SFA; Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington, Seattle, Washington.
  • Hakanarson H; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Harris TB; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Kestenbaum BR; Center for Applied Genomics, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Kritchevsky SB; Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Loos RJF; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Norris JM; Center for Applied Genomics, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Norwood AF; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Ordovas JM; Laboratory of Epidemiology and Population Sciences, National Institute on Aging, Bethesda, Maryland.
  • Pankow JS; Kidney Research Institute, Division of Nephrology, Department of Medicine, University of Washington, Seattle, Washington.
  • Psaty BM; Department of Internal Medicine, Section on Gerontology and Geriatric Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
J Clin Endocrinol Metab ; 103(4): 1380-1392, 2018 04 01.
Article em En | MEDLINE | ID: mdl-29325163
Context: Vitamin D inadequacy is common in the adult population of the United States. Although the genetic determinants underlying vitamin D inadequacy have been studied in people of European ancestry, less is known about populations with Hispanic or African ancestry. Objective: The Trans-Ethnic Evaluation of Vitamin D (TRANSCEN-D) genomewide association study (GWAS) consortium was assembled to replicate genetic associations with 25-hydroxyvitamin D [25(OH)D] concentrations from the Study of Underlying Genetic Determinants of Vitamin D and Highly Related Traits (SUNLIGHT) meta-analyses of European ancestry and to identify genetic variants related to vitamin D concentrations in African and Hispanic ancestries. Design: Ancestry-specific (Hispanic and African) and transethnic (Hispanic, African, and European) meta-analyses were performed with Meta-Analysis Helper software (METAL). Patients or Other Participants: In total, 8541 African American and 3485 Hispanic American (from North America) participants from 12 cohorts and 16,124 European participants from SUNLIGHT were included in the study. Main Outcome Measures: Blood concentrations of 25(OH)D were measured for all participants. Results: Ancestry-specific analyses in African and Hispanic Americans replicated single nucleotide polymorphisms (SNPs) in GC (2 and 4 SNPs, respectively). An SNP (rs79666294) near the KIF4B gene was identified in the African American cohort. Transethnic evaluation replicated GC and DHCR7 region SNPs. Additionally, the transethnic analyses revealed SNPs rs719700 and rs1410656 near the ANO6/ARID2 and HTR2A genes, respectively. Conclusions: Ancestry-specific and transethnic GWASs of 25(OH)D confirmed findings in GC and DHCR7 for African and Hispanic American samples and revealed findings near KIF4B, ANO6/ARID2, and HTR2A. The biological mechanisms that link these regions with 25(OH)D metabolism warrant further investigation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina D / Deficiência de Vitamina D Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vitamina D / Deficiência de Vitamina D Idioma: En Ano de publicação: 2018 Tipo de documento: Article