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Multi-ancestry polygenic mechanisms of type 2 diabetes.
Smith, Kirk; Deutsch, Aaron J; McGrail, Carolyn; Kim, Hyunkyung; Hsu, Sarah; Huerta-Chagoya, Alicia; Mandla, Ravi; Schroeder, Philip H; Westerman, Kenneth E; Szczerbinski, Lukasz; Majarian, Timothy D; Kaur, Varinderpal; Williamson, Alice; Zaitlen, Noah; Claussnitzer, Melina; Florez, Jose C; Manning, Alisa K; Mercader, Josep M; Gaulton, Kyle J; Udler, Miriam S.
Afiliação
  • Smith K; Diabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Deutsch AJ; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • McGrail C; Programs in Metabolism and Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Kim H; Diabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Hsu S; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Huerta-Chagoya A; Programs in Metabolism and Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Mandla R; Department of Medicine, Harvard Medical School, Boston, MA, USA.
  • Schroeder PH; Biomedical Sciences Graduate Program, University of California, San Diego, La Jolla, CA, USA.
  • Westerman KE; Diabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Szczerbinski L; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Majarian TD; Programs in Metabolism and Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Kaur V; Committee on Genetics, Genomics and Systems Biology, University of Chicago, Chicago, IL, USA.
  • Williamson A; Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, IL, USA.
  • Zaitlen N; Programs in Metabolism and Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Claussnitzer M; Clinical and Translational Epidemiology Unit, Massachusetts General Hospital, Boston, MA, USA.
  • Florez JC; Diabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Manning AK; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Mercader JM; Programs in Metabolism and Medical & Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Gaulton KJ; Diabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
  • Udler MS; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Nat Med ; 30(4): 1065-1074, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38443691
ABSTRACT
Type 2 diabetes (T2D) is a multifactorial disease with substantial genetic risk, for which the underlying biological mechanisms are not fully understood. In this study, we identified multi-ancestry T2D genetic clusters by analyzing genetic data from diverse populations in 37 published T2D genome-wide association studies representing more than 1.4 million individuals. We implemented soft clustering with 650 T2D-associated genetic variants and 110 T2D-related traits, capturing known and novel T2D clusters with distinct cardiometabolic trait associations across two independent biobanks representing diverse genetic ancestral populations (African, n = 21,906; Admixed American, n = 14,410; East Asian, n =2,422; European, n = 90,093; and South Asian, n = 1,262). The 12 genetic clusters were enriched for specific single-cell regulatory regions. Several of the polygenic scores derived from the clusters differed in distribution among ancestry groups, including a significantly higher proportion of lipodystrophy-related polygenic risk in East Asian ancestry. T2D risk was equivalent at a body mass index (BMI) of 30 kg m-2 in the European subpopulation and 24.2 (22.9-25.5) kg m-2 in the East Asian subpopulation; after adjusting for cluster-specific genetic risk, the equivalent BMI threshold increased to 28.5 (27.1-30.0) kg m-2 in the East Asian group. Thus, these multi-ancestry T2D genetic clusters encompass a broader range of biological mechanisms and provide preliminary insights to explain ancestry-associated differences in T2D risk profiles.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 Limite: Humans Idioma: En Revista: Nat Med Assunto da revista: BIOLOGIA MOLECULAR / MEDICINA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 Limite: Humans Idioma: En Revista: Nat Med Assunto da revista: BIOLOGIA MOLECULAR / MEDICINA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos