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Variant level heritability estimates of type 2 diabetes in African Americans.
Armstrong, Nicole D; Patki, Amit; Srinivasasainagendra, Vinodh; Ge, Tian; Lange, Leslie A; Kottyan, Leah; Namjou, Bahram; Shah, Amy S; Rasmussen-Torvik, Laura J; Jarvik, Gail P; Meigs, James B; Karlson, Elizabeth W; Limdi, Nita A; Irvin, Marguerite R; Tiwari, Hemant K.
Affiliation
  • Armstrong ND; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA. nmda@uab.edu.
  • Patki A; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Srinivasasainagendra V; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.
  • Ge T; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Lange LA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
  • Kottyan L; Division of Biomedical Informatics and Personalized Medicine, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Namjou B; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Shah AS; Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Rasmussen-Torvik LJ; Department of Pediatrics, Cincinnati Children's Hospital Medical Center &, The University of Cincinnati, Cincinnati, OH, USA.
  • Jarvik GP; Department of Preventive Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
  • Meigs JB; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA.
  • Karlson EW; Division of General Internal Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Limdi NA; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Irvin MR; Program in Medical and Population Genetics, Broad Institute, Cambridge, MA, USA.
  • Tiwari HK; Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Sci Rep ; 14(1): 14009, 2024 06 18.
Article in En | MEDLINE | ID: mdl-38890458
ABSTRACT
Type 2 diabetes (T2D) is caused by both genetic and environmental factors and is associated with an increased risk of cardiorenal complications and mortality. Though disproportionately affected by the condition, African Americans (AA) are largely underrepresented in genetic studies of T2D, and few estimates of heritability have been calculated in this race group. Using genome-wide association study (GWAS) data paired with phenotypic data from ~ 19,300 AA participants of the Reasons for Geographic and Racial Differences in Stroke (REGARDS) study, Genetics of Hypertension Associated Treatments (GenHAT) study, and the Electronic Medical Records and Genomics (eMERGE) network, we estimated narrow-sense heritability using two

methods:

Linkage-Disequilibrium Adjusted Kinships (LDAK) and Genome-Wide Complex Trait Analysis (GCTA). Study-level heritability estimates adjusting for age, sex, and genetic ancestry ranged from 18% to 34% across both methods. Overall, the current study narrows the expected range for T2D heritability in this race group compared to prior estimates, while providing new insight into the genetic basis of T2D in AAs for ongoing genetic discovery efforts.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Black or African American / Genetic Predisposition to Disease / Diabetes Mellitus, Type 2 / Genome-Wide Association Study Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Black or African American / Genetic Predisposition to Disease / Diabetes Mellitus, Type 2 / Genome-Wide Association Study Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Sci Rep Year: 2024 Document type: Article Affiliation country: United States