Diabetes Research and Clinical Practice
Volume 83, Issue 2 , Pages 280-288, February 2009

Classical and model-based estimates of beta-cell function during a mixed meal vs. an OGTT in a population-based cohort

  • Josina M. Rijkelijkhuizen

      Affiliations

    • EMGO Institute, VU University Medical Center, Van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands
    • Corresponding Author InformationCorresponding author. Tel.: +31 20 4449831; fax: +31 20 4448181.
  • ,
  • Cynthia J. Girman

      Affiliations

    • Merck & Co., Inc., Department of Epidemiology, Clinical and Quantitative Sciences, North Wales, PA, USA
  • ,
  • Andrea Mari

      Affiliations

    • Institute of Biomedical Engineering, National Research Council, Padua, Italy
  • ,
  • Marjan Alssema

      Affiliations

    • EMGO Institute, VU University Medical Center, Van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands
  • ,
  • Thomas Rhodes

      Affiliations

    • Merck & Co., Inc., Department of Epidemiology, Clinical and Quantitative Sciences, North Wales, PA, USA
  • ,
  • Giel Nijpels

      Affiliations

    • EMGO Institute, VU University Medical Center, Van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands
    • Department of General Practice, VU University Medical Center, Amsterdam, The Netherlands
  • ,
  • Piet J. Kostense

      Affiliations

    • EMGO Institute, VU University Medical Center, Van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands
    • Department of Clinical Epidemiology and Biostatistics, VU University Medical Center, Amsterdam, The Netherlands
  • ,
  • Peter P. Stein

      Affiliations

    • Merck & Co., Clinical Research, Inc., Clinical and Quantitative Sciences, Rahway, NJ, USA
  • ,
  • Elisabeth M. Eekhoff

      Affiliations

    • Department of Endocrinology, VU University Medical Center, Amsterdam, The Netherlands
  • ,
  • Robert J. Heine

      Affiliations

    • EMGO Institute, VU University Medical Center, Van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands
    • Department of Endocrinology, VU University Medical Center, Amsterdam, The Netherlands
  • ,
  • Jacqueline M. Dekker

      Affiliations

    • EMGO Institute, VU University Medical Center, Van der Boechorststraat 7, 1081 BT Amsterdam, The Netherlands

Received 13 February 2008; received in revised form 7 November 2008; accepted 12 November 2008. published online 22 December 2008.

Abstract 

This study compared classical and model-based beta-cell responses during an oral glucose tolerance test (OGTT) and a meal tolerance test (MTT) in a population-based cohort. Individuals with normal glucose metabolism (NGM, n=161), impaired glucose metabolism (IGM, n=19) and type 2 diabetes mellitus (DM, n=20) underwent a 75g-OGTT and an MTT (75g carbohydrates, 50g fat, 24g proteins). Classical estimates of beta-cell function (insulinogenic index and the ratio of areas under insulin and glucose curves) were calculated. Mathematical modelling was used to determine beta-cell glucose sensitivity, rate sensitivity and potentiation. Insulin sensitivity was characterized by three surrogate estimates. Both classical and model-based estimates of beta-cell function were higher during MTT than during OGTT (P<0.05). Regarding the model-based parameters, especially beta-cell sensitivity was increased following MTT as compared with OGTT (P<0.05). Both during OGTT and MTT, across most parameters describing beta-cell function, the largest reduction in beta-cell response occurred between IGM and DM, while the largest reduction in insulin sensitivity occurred between NGM and IGM. We conclude that beta-cell response is stronger after a mixed meal than after an OGTT with equal carbohydrate quantity, both for classical and model-based parameters. The higher response was mostly explained by higher beta-cell sensitivity during the meal.

Keywords: Insulin secretion, Insulin sensitivity, Beta-cell glucose sensitivity, Mixed meal, OGTT, General population

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PII: S0168-8227(08)00575-5

doi:10.1016/j.diabres.2008.11.017

Diabetes Research and Clinical Practice
Volume 83, Issue 2 , Pages 280-288, February 2009