Metabolism - Clinical and Experimental
Volume 56, Issue 12 , Pages 1729-1734, December 2007

Impact of reduced meal frequency without caloric restriction on glucose regulation in healthy, normal-weight middle-aged men and women

  • Olga Carlson

      Affiliations

    • Diabetes Section, Laboratory of Clinical Investigation, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Bronwen Martin

      Affiliations

    • Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Kim S. Stote

      Affiliations

    • Beltsville Human Nutrition Research Center, US Department of Agriculture, Agriculture Research Service, Beltsville, MD, USA
  • ,
  • Erin Golden

      Affiliations

    • Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Stuart Maudsley

      Affiliations

    • Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Samer S. Najjar

      Affiliations

    • Laboratory of Cardiovascular Science, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Luigi Ferrucci

      Affiliations

    • Clinical Research Branch, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Donald K. Ingram

      Affiliations

    • Laboratory of Experimental Gerontology, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Dan L. Longo

      Affiliations

    • Laboratory of Immunology, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • William V. Rumpler

      Affiliations

    • Beltsville Human Nutrition Research Center, US Department of Agriculture, Agriculture Research Service, Beltsville, MD, USA
  • ,
  • David J. Baer

      Affiliations

    • Beltsville Human Nutrition Research Center, US Department of Agriculture, Agriculture Research Service, Beltsville, MD, USA
  • ,
  • Josephine Egan

      Affiliations

    • Diabetes Section, Laboratory of Clinical Investigation, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
  • ,
  • Mark P. Mattson

      Affiliations

    • Laboratory of Neurosciences, National Institute on Aging Intramural Research Program, Baltimore, MD, USA
    • Corresponding Author InformationCorresponding author.

Received 16 May 2007; accepted 3 July 2007.

Abstract 

An unresolved issue in the field of diet and health is if and how changes in meal frequency affect energy metabolism in humans. We therefore evaluated the influence of reduced meal frequency without a reduction in energy intake on glucose metabolism in normal-weight, healthy male and female subjects. The study was a randomized crossover design, with two 8-week treatment periods (with an intervening 11-week off-diet period) in which subjects consumed all of their calories for weight maintenance distributed in either 3 meals or 1 meal per day (consumed between 4:00 pm and 8:00 pm). Energy metabolism was evaluated at designated time points throughout the study by performing morning oral glucose tolerance tests and measuring levels of glucose, insulin, glucagon, leptin, ghrelin, adiponectin, resistin, and brain-derived neurotrophic factor (BDNF). Subjects consuming 1 meal per day exhibited higher morning fasting plasma glucose levels, greater and more sustained elevations of plasma glucose concentrations, and a delayed insulin response in the oral glucose tolerance test compared with subjects consuming 3 meals per day. Levels of ghrelin were elevated in response to the 1-meal-per-day regimen. Fasting levels of insulin, leptin, ghrelin, adiponectin, resistin, and BDNF were not significantly affected by meal frequency. Subjects consuming a single large daily meal exhibit elevated fasting glucose levels and impaired morning glucose tolerance associated with a delayed insulin response during a 2-month diet period compared with those consuming 3 meals per day. The impaired glucose tolerance was reversible and was not associated with alterations in the levels of adipokines or BDNF.

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PII: S0026-0495(07)00280-6

doi:10.1016/j.metabol.2007.07.018

Metabolism - Clinical and Experimental
Volume 56, Issue 12 , Pages 1729-1734, December 2007