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Diurnal pattern of insulin action in type 1 diabetes implications for a closed-Loop system

  • Ling Hinshaw
  • , Chiara Dalla Man
  • , Debashis K. Nandy
  • , Ahmed Saad
  • , Adil E. Bharucha
  • , James A. Levine
  • , Robert A. Rizza
  • , Rita Basu
  • , Rickey E. Carter
  • , Claudio Cobelli
  • , Yogish C. Kudva
  • , Ananda Basu

    Research output: Contribution to journalArticlepeer-review

    Abstract

    We recently demonstrated a diurnal pattern to insulin action (i.e., insulin sensitivity [SI]) in healthy individuals with higher SI at breakfast than at dinner. To determine whether such a pattern exists in type 1 diabetes, we studied 19 subjects with C-peptide- negative diabetes (HbA1c 7.1±0.6%) on insulin pump therapy with normal gastric emptying. Identical mixed meals were ingested during breakfast, lunch, and dinner at 0700, 1300, and 1900 h in randomized Latin square of order on 3 consecutive days when measured daily physical activity was equal. The triple tracer technique enabled measurement of glucose fluxes. Insulin was administered according to the customary insulin:carbohydrate ratio for each participant. Although postprandial glucose excursions did not differ among meals, insulin concentration was higher (P < 0.01) and endogenous glucose production less suppressed (P <0.049) at breakfast than at lunch. There were no differences in meal glucose appearance or in glucose disappearance between meals. Although there was no statistical difference (P = 0.34) in SI between meals in type 1 diabetic subjects, the diurnal pattern of SI taken across the three meals in its entirety differed (P = 0.016) from that of healthy subjects. Although the pattern in healthy subjects showed decreasing SI between breakfast and lunch, the reverse SI pattern was observed in type 1 diabetic subjects. The results suggest that in contrast to healthy subjects, SI diurnal pattern in type 1 diabetes is specific to the individual and cannot be extrapolated to the type 1 diabetic population as a whole, implying that artificial pancreas algorithms may need to be personalized.

    Original languageEnglish (US)
    Pages (from-to)2223-2229
    Number of pages7
    JournalDiabetes
    Volume62
    Issue number7
    DOIs
    StatePublished - Jul 2013

    ASJC Scopus subject areas

    • Internal Medicine
    • Endocrinology, Diabetes and Metabolism

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