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Genetic Risk Score in Diabetes Associated With Chronic Pancreatitis Versus Type 2 Diabetes Mellitus.
Goodarzi, Mark O; Nagpal, Tanvi; Greer, Phil; Cui, Jinrui; Chen, Yii-Der I; Guo, Xiuqing; Pankow, James S; Rotter, Jerome I; Alkaade, Samer; Amann, Stephen T; Baillie, John; Banks, Peter A; Brand, Randall E; Conwell, Darwin L; Cote, Gregory A; Forsmark, Christopher E; Gardner, Timothy B; Gelrud, Andres; Guda, Nalini; LaRusch, Jessica; Lewis, Michele D; Money, Mary E; Muniraj, Thiruvengadam; Papachristou, Georgios I; Romagnuolo, Joseph; Sandhu, Bimaljit S; Sherman, Stuart; Singh, Vikesh K; Wilcox, C Mel; Pandol, Stephen J; Park, Walter G; Andersen, Dana K; Bellin, Melena D; Hart, Phil A; Yadav, Dhiraj; Whitcomb, David C.
Afiliação
  • Goodarzi MO; Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Nagpal T; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, University of Pittsburgh and UPMC Medical Center, Pittsburgh, Pennsylvania, USA.
  • Greer P; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, University of Pittsburgh and UPMC Medical Center, Pittsburgh, Pennsylvania, USA.
  • Cui J; Division of Endocrinology, Diabetes, and Metabolism, Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Chen YI; Institute for Translational Genomics and Population Sciences and Department of Pediatrics, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, USA.
  • Guo X; Institute for Translational Genomics and Population Sciences and Department of Pediatrics, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, USA.
  • Pankow JS; Division of Epidemiology and Community Health, School of Public Health, University of Minnesota, Minneapolis, Minnesota, USA.
  • Rotter JI; Institute for Translational Genomics and Population Sciences and Department of Pediatrics, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California, USA.
  • Alkaade S; Department of Medicine, Saint Louis University, St. Louis, Missouri, USA.
  • Amann ST; Digestive Health Specialists, Tupelo, Mississippi, USA.
  • Baillie J; Gastroenterology, Virginia Commonwealth University, Richmond, Virginia, USA.
  • Banks PA; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
  • Brand RE; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, University of Pittsburgh and UPMC Medical Center, Pittsburgh, Pennsylvania, USA.
  • Conwell DL; Division of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Cote GA; Department of Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Forsmark CE; Department of Medicine, University of Florida, Gainesville, Florida, USA.
  • Gardner TB; Department of Medicine, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Gelrud A; GastroHealth and Miami Cancer Institute, Baptist Hospital, Miami, Florida, USA.
  • Guda N; GI Associates LLC, Aurora St. Luke's Medical Center, Milwaukee, Wisconsin, USA.
  • LaRusch J; Ariel Precision Medicine, Pittsburgh Pennsylvania, USA.
  • Lewis MD; Department of Medicine, Mayo Clinic, Jacksonville, Florida, USA.
  • Money ME; Meritus Medical Center, Hagerstown, Maryland, USA.
  • Muniraj T; Department of Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Papachristou GI; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, University of Pittsburgh and UPMC Medical Center, Pittsburgh, Pennsylvania, USA.
  • Romagnuolo J; Palmetto Primary and Specialty Care, Gastroenterology, Goose Creek, South Carolina, USA.
  • Sandhu BS; Richmond Gastroenterology Associates, St. Mary's Hospital, Richmond, Virginia, USA.
  • Sherman S; Department of Medicine, Indiana University, Indianapolis, Indiana, USA.
  • Singh VK; Department of Medicine, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
  • Wilcox CM; Department of Medicine, University of Alabama Birmingham, Birmingham, Alabama, USA.
  • Pandol SJ; Division of Gastroenterology, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Park WG; Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California, USA.
  • Andersen DK; Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Bellin MD; Department of Endocrinology, University of Minnesota, Minneapolis, Minnesota, USA.
  • Hart PA; Division of Gastroenterology, Hepatology, and Nutrition, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
  • Yadav D; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, University of Pittsburgh and UPMC Medical Center, Pittsburgh, Pennsylvania, USA.
  • Whitcomb DC; Division of Gastroenterology, Hepatology, and Nutrition, Department of Medicine, University of Pittsburgh and UPMC Medical Center, Pittsburgh, Pennsylvania, USA.
Clin Transl Gastroenterol ; 10(7): e00057, 2019 07.
Article em En | MEDLINE | ID: mdl-31232720
INTRODUCTION: Diabetes mellitus (DM) is a complication of chronic pancreatitis (CP). Whether pancreatogenic diabetes associated with CP-DM represents a discrete pathophysiologic entity from type 2 DM (T2DM) remains uncertain. Addressing this question is needed for development of specific measures to manage CP-DM. We approached this question from a unique standpoint, hypothesizing that if CP-DM and T2DM are separate disorders, they should be genetically distinct. To test this hypothesis, we sought to determine whether a genetic risk score (GRS) based on validated single nucleotide polymorphisms for T2DM could distinguish between groups with CP-DM and T2DM. METHODS: We used 60 T2DM single nucleotide polymorphisms to construct a weighted GRS in 1,613 subjects from the North American Pancreatitis Study 2 and 2,685 subjects from the Multi-Ethnic Study of Atherosclerosis, all of European origin. RESULTS: The mean GRS was identical between 321 subjects with CP-DM and 423 subjects with T2DM (66.53 vs 66.42, P = 0.95), and the GRS of both diabetic groups was significantly higher than that of nondiabetic controls (n = 3,554, P < 0.0001). Exploratory analyses attempting to enrich the CP-DM group for pancreatogenic diabetes, such as eliminating diabetes diagnosed before CP, requiring pancreas-specific comorbidities, or removing those with a family history of diabetes, did not improve the ability of the GRS to distinguish between CP-DM and T2DM. DISCUSSION: Recognizing that we lacked a gold standard to define CP-DM, our study suggests that CP-DM may be a subtype of T2DM, a notion that should be tested in future, large prospective studies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Diabetes Mellitus Tipo 2 / Pancreatite Crônica Tipo de estudo: Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Transl Gastroenterol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Diabetes Mellitus Tipo 2 / Pancreatite Crônica Tipo de estudo: Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Transl Gastroenterol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos