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Timing modulates the effect of sleep loss on glucose homeostasis

Abstract

Chronobiological factors may modulate the impact of sleep loss on glucose homeostasis. However, these interactions have not been systematically assessed in humans. Objective: To assess the effect of sleep loss during the late vs early night on glucose homeostasis. Design: Fifteen normal-weight men participated in three conditions of a randomized, balanced crossover study comprising two conditions with shortened sleep (i.e., 4 hours of sleep during the first or the second half of the night) and a control condition with 8 hours of sleep. Glucose, insulin, cortisol, and glucagon were measured. Insulin sensitivity and secretion were assessed with a Botnia clamp. Results: Compared with regular sleep duration, sleep loss reduced insulin sensitivity (M-value; P 5 0.031) irrespective of early- or late-night timing (P 5 0.691). The disposition index (i.e., the b-cell response adjusted for insulin sensitivity) also tended to be impaired by short sleep (P 5 0.056) but not by sleep timing (P 5 0.543). In contrast, sleep loss in the second half but not the first half of the night induced reductions in morning glucagon and cortisol levels (P,0.031) followed by a transient increase in cortisol (P , 0.044).

Original languageEnglish
Article numberjcem_201802636
JournalJournal of Clinical Endocrinology and Metabolism
Volume104
Issue number7
Pages (from-to)2801-2808
Number of pages8
ISSN0021-972X
DOIs
Publication statusPublished - 21.03.2019

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Research Areas and Centers

  • Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)

DFG Research Classification Scheme

  • 2.22-17 Endocrinology, Diabetology, Metabolism

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  • CRC/Transregio TRR 134: Ingestive Behaviour: Homeostasis and Reward

    Lehnert, H. (Speaker), Brüning, J. C. (Principal Investigator (PI)), Scholz, H. (Principal Investigator (PI)), Kloppenburg, P. (Principal Investigator (PI)), Hausen, A. C. (Principal Investigator (PI)), Jöhren, O. (Principal Investigator (PI)), Schulz, C. (Principal Investigator (PI)), Schwaninger, M. (Principal Investigator (PI)), Wunderlich, F. T. (Principal Investigator (PI)), Schmid, S. (Principal Investigator (PI)), Oster, H. (Principal Investigator (PI)), Klement, J. (Principal Investigator (PI)), Ott, V. (Principal Investigator (PI)), Stephan, K. E. (Principal Investigator (PI)), Tittgemeyer, M. (Principal Investigator (PI)), Oltmanns, K. (Principal Investigator (PI)), Münte, T. (Principal Investigator (PI)), Tronnier, V. M. (Principal Investigator (PI)), Schweiger, U. (Principal Investigator (PI)), Brassen, S. (Principal Investigator (PI)), Büchel, C. (Principal Investigator (PI)), Peters, J. (Principal Investigator (PI)), Schilbach, L. (Principal Investigator (PI)), Anders, S. (Principal Investigator (PI)), Martinetz, T. (Principal Investigator (PI)), Park, S. Q. (Principal Investigator (PI)), Brabant, E. G. (Principal Investigator (PI)), Kasten, M. (Principal Investigator (PI)), Klein, C. (Principal Investigator (PI)) & Krämer, U. (Principal Investigator (PI))

    01.01.14 → 31.12.18

    Project: DFG Joint Research › DFG Collaborative Research Centers (CRC)

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