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Patterns of Plasma Glucagon Dynamics Do Not Match Metabolic Phenotypes in Young Women.
Gar, Christina; Rottenkolber, Marietta; Sacco, Vanessa; Moschko, Sarah; Banning, Friederike; Hesse, Nina; Popp, Daniel; Hübener, Christoph; Seissler, Jochen; Lechner, Andreas.
Afiliação
  • Gar C; Diabetes Research Group, Medizinische Klinik IV, Medical Center of the University of Munich (Klinikum der Universitaet Muenchen), Munich, Germany.
  • Rottenkolber M; Clinical Cooperation Group Type 2 Diabetes, Helmholtz Zentrum Muenchen, Neuherberg, Germany.
  • Sacco V; German Center for Diabetes Research, Neuherberg, Germany.
  • Moschko S; Diabetes Research Group, Medizinische Klinik IV, Medical Center of the University of Munich (Klinikum der Universitaet Muenchen), Munich, Germany.
  • Banning F; Clinical Cooperation Group Type 2 Diabetes, Helmholtz Zentrum Muenchen, Neuherberg, Germany.
  • Hesse N; German Center for Diabetes Research, Neuherberg, Germany.
  • Popp D; Diabetes Research Group, Medizinische Klinik IV, Medical Center of the University of Munich (Klinikum der Universitaet Muenchen), Munich, Germany.
  • Hübener C; Clinical Cooperation Group Type 2 Diabetes, Helmholtz Zentrum Muenchen, Neuherberg, Germany.
  • Seissler J; German Center for Diabetes Research, Neuherberg, Germany.
  • Lechner A; Diabetes Research Group, Medizinische Klinik IV, Medical Center of the University of Munich (Klinikum der Universitaet Muenchen), Munich, Germany.
J Clin Endocrinol Metab ; 103(3): 972-982, 2018 03 01.
Article em En | MEDLINE | ID: mdl-29244078
ABSTRACT
Context The role of hyperglucagonemia in type 2 diabetes is still debated.

Objective:

We analyzed glucagon dynamics during oral glucose tolerance tests (oGTTs) in young women with one out of three metabolic phenotypes healthy control (normoglycemic after a normoglycemic pregnancy), normoglycemic high-risk (normoglycemic after a pregnancy complicated by gestational diabetes), and prediabetes/screening-diagnosed type 2 diabetes. We asked if glucagon patterns were homogeneous within the metabolic phenotypes. Design and

Setting:

Five-point oGTT, sandwich enzyme-linked immunosorbent assay for glucagon, and functional data analysis with unsupervised clustering.

Participants:

Cross-sectional analysis of 285 women from the monocenter observational study Prediction, Prevention, and Subclassification of gestational and type 2 Diabetes, recruited between November 2011 and May 2016.

Results:

We found four patterns of glucagon dynamics that did not match the metabolic phenotypes. Elevated fasting glucagon and delayed glucagon suppression was overrepresented with prediabetes/diabetes, but this was only detected in 21% of this group. It also occurred in 8% of the control group.

Conclusions:

We conclude that hyperglucagonemia may contribute to type 2 diabetes in a subgroup of affected individuals but that it is not a sine qua non for the disease. This should be considered in future pathophysiological studies and when testing pharmacotherapies addressing glucagon signaling.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Estado Pré-Diabético / Glucagon / Diabetes Gestacional / Diabetes Mellitus Tipo 2 Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Estado Pré-Diabético / Glucagon / Diabetes Gestacional / Diabetes Mellitus Tipo 2 Tipo de estudo: Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Pregnancy Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha