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Polygenic subtype identified in ACCORD trial displays a favorable type 2 diabetes phenotype in the UKBiobank population.
Hershberger, Courtney; Mariam, Arshiya; Pantalone, Kevin M; Buse, John B; Motsinger-Reif, Alison A; Rotroff, Daniel M.
Afiliación
  • Hershberger C; Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.
  • Mariam A; Center for Quantitative Metabolic Research, Cleveland Clinic, Cleveland, OH, 44195, USA.
  • Pantalone KM; Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.
  • Buse JB; Center for Quantitative Metabolic Research, Cleveland Clinic, Cleveland, OH, 44195, USA.
  • Motsinger-Reif AA; Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, 44195, USA.
  • Rotroff DM; Center for Quantitative Metabolic Research, Cleveland Clinic, Cleveland, OH, 44195, USA.
Hum Genomics ; 18(1): 70, 2024 Jun 22.
Article en En | MEDLINE | ID: mdl-38909264
ABSTRACT

INTRODUCTION:

We previously identified a genetic subtype (C4) of type 2 diabetes (T2D), benefitting from intensive glycemia treatment in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial. Here, we characterized the population of patients that met the C4 criteria in the UKBiobank cohort. RESEARCH DESIGN AND

METHODS:

Using our polygenic score (PS), we identified C4 individuals in the UKBiobank and tested C4 status with risk of developing T2D, cardiovascular disease (CVD) outcomes, and differences in T2D medications.

RESULTS:

C4 individuals were less likely to develop T2D, were slightly older at T2D diagnosis, had lower HbA1c values, and were less likely to be prescribed T2D medications (P < .05). Genetic variants in MAS1 and IGF2R, major components of the C4 PS, were associated with fewer overall T2D prescriptions.

CONCLUSION:

We have confirmed C4 individuals are a lower risk subpopulation of patients with T2D.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Herencia Multifactorial / Diabetes Mellitus Tipo 2 Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Herencia Multifactorial / Diabetes Mellitus Tipo 2 Límite: Aged / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Hum Genomics Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos