Your browser doesn't support javascript.
loading
Metabolite Profiles of Incident Diabetes and Heterogeneity of Treatment Effect in the Diabetes Prevention Program.
Chen, Zsu-Zsu; Liu, Jinxi; Morningstar, Jordan; Heckman-Stoddard, Brandy M; Lee, Christine G; Dagogo-Jack, Samuel; Ferguson, Jane F; Hamman, Richard F; Knowler, William C; Mather, Kieren J; Perreault, Leigh; Florez, Jose C; Wang, Thomas J; Clish, Clary; Temprosa, Marinella; Gerszten, Robert E.
Afiliação
  • Chen ZZ; Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center, Boston, MA.
  • Liu J; Department of Epidemiology and Biostatistics, Biostatistics Center and Milken Institute School of Public Health, George Washington University, Rockville, MD.
  • Morningstar J; Medical University of South Carolina, Charleston, SC.
  • Heckman-Stoddard BM; Division of Cancer Prevention, National Cancer Institute, Bethesda, MD.
  • Lee CG; Division of Diabetes, Endocrinology, and Metabolic Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD.
  • Dagogo-Jack S; Division of Endocrinology, Diabetes, and Metabolism, University of Tennessee Health Science Center, Memphis, TN.
  • Ferguson JF; Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Hamman RF; Department of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Aurora, CO.
  • Knowler WC; Diabetes Epidemiology and Clinical Research Section, Phoenix Epidemiology and Clinical Research Branch, National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, AZ.
  • Mather KJ; Department of Medicine, Indiana University School of Medicine, Indianapolis, IN.
  • Perreault L; Division of Endocrinology, Metabolism, and Diabetes, University of Colorado Anschutz Medical Campus, Aurora, CO.
  • Florez JC; Diabetes Unit and Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA.
  • Wang TJ; Harvard Medical School, Boston, MA.
  • Clish C; Broad Institute of MIT and Harvard, Cambridge, MA.
  • Temprosa M; Division of Cardiovascular Medicine, Vanderbilt University Medical Center, Nashville, TN.
  • Gerszten RE; Broad Institute of MIT and Harvard, Cambridge, MA.
Diabetes ; 68(12): 2337-2349, 2019 12.
Article em En | MEDLINE | ID: mdl-31582408
Novel biomarkers of type 2 diabetes (T2D) and response to preventative treatment in individuals with similar clinical risk may highlight metabolic pathways that are important in disease development. We profiled 331 metabolites in 2,015 baseline plasma samples from the Diabetes Prevention Program (DPP). Cox models were used to determine associations between metabolites and incident T2D, as well as whether associations differed by treatment group (i.e., lifestyle [ILS], metformin [MET], or placebo [PLA]), over an average of 3.2 years of follow-up. We found 69 metabolites associated with incident T2D regardless of treatment randomization. In particular, cytosine was novel and associated with the lowest risk. In an exploratory analysis, 35 baseline metabolite associations with incident T2D differed across the treatment groups. Stratification by baseline levels of several of these metabolites, including specific phospholipids and AMP, modified the effect that ILS or MET had on diabetes development. Our findings highlight novel markers of diabetes risk and preventative treatment effect in individuals who are clinically at high risk and motivate further studies to validate these interactions.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Citosina / Diabetes Mellitus Tipo 2 Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Citosina / Diabetes Mellitus Tipo 2 Idioma: En Ano de publicação: 2019 Tipo de documento: Article