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Residual β-Cell Function in Children With IDDM: Reproducibility of Testing and Factors Influencing Insulin Secretory Reserve

  1. Cheril Clarson, BM, BS, FRCP(C),
  2. Denis Daneman, MD, BCh, FRCP(C),
  3. Allan L Drash, MD,
  4. Dorothy J Becker, MD, BCh, FCP(SA) and
  5. Robert M Ehrlich, MD, FRCP(C)
  1. Divisions of Endocrinology, Departments of Pediatrics Hospital for Sick Children, University of Toronto Toronto, Canada
  2. Children's Hospital of Pittsburgh, University of Pittsburgh Pittsburgh, Pennsylvania
  1. Address correspondence and reprint requests to Dr. Denis Daneman, The Hospital for Sick Children, 555 University Avenue, Toronto, Canada M5G 1X8.

Abstract

Reproducibility of C-peptide secretion was assessed in 20 children (group 1) by their responses to two Sustacal- (a mixed liquid meal) stimulation tests performed 7–14 days apart. For the 12 C-peptide-positive children (basal C-peptide ≥0.03 pmol/ml) there were no differences in the basal or stimulated values between tests 1 and 2. The effect of exogenous insulin on C-peptide secretion was assessed in 20 other children (group 2) by their responses to two Sustacal tests, one test without and one with soluble insulin (0.25 U/kg) injected subcutaneously before testing. Eleven children were C-peptide positive and had no differences in C-peptide response between tests 1 and 2. The results from test 1 in groups 1 and 2 were combined with those from 44 others undergoing a single Sustacal test (group 3, N = 84). There was a close correlation between basal and peak C-peptide concentrations in the 44 C-peptide-positive children (r = .88, P < .001). Peak C-peptide concentrations correlated inversely with HbA1 (r = −.29, P < .01), insulin dose in units per kilogram (r = −.40, P < .001), and duration of diabetes (r = .33, P < .001) and positively with age at onset of diabetes (r = .34, P < .001). The C-peptide-positive children had reduced glucose response to Sustacal, lower HbA1 concentration, lower insulin requirement, later age of onset, and shorter duration of diabetes than children who were C-peptide negative.

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