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Residual beta-cell function in children with IDDM: reproducibility of testing and factors influencing insulin
Insights
C-peptide secretion is reproducible in children with diabetes. Higher C-peptide levels correlate with better diabetes control, including lower HbA1 and insulin needs.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Diabetes Research
Background:
- Assessing endogenous insulin production is crucial for managing type 1 diabetes.
- C-peptide is a reliable marker of insulin secretion.
- Understanding factors influencing C-peptide secretion aids in treatment strategies.
Purpose of the Study:
- To evaluate the reproducibility of C-peptide secretion in children with diabetes.
- To investigate the effect of exogenous insulin on C-peptide levels.
- To identify correlations between C-peptide secretion and glycemic control parameters.
Main Methods:
- Two Sustacal (mixed liquid meal) stimulation tests were performed 7-14 days apart to assess C-peptide secretion reproducibility.
- Exogenous soluble insulin was administered subcutaneously before testing in a separate group to evaluate its effect.
- Combined data from multiple groups (N=84) were analyzed for correlations.
Main Results:
- C-peptide secretion demonstrated good reproducibility between tests in C-peptide-positive children.
- Peak C-peptide concentrations correlated inversely with HbA1, insulin dose, and diabetes duration.
- Positive correlations were observed between peak C-peptide and age at diabetes onset.
- C-peptide-positive children exhibited better glycemic control and lower insulin requirements.
Conclusions:
- C-peptide secretion is a reproducible measure in pediatric diabetes patients.
- Higher C-peptide levels are associated with improved diabetes control indicators.
- These findings support C-peptide as a valuable biomarker for assessing beta-cell function in children with diabetes.
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 greater than or equal to 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 less than .001). Peak C-peptide concentrations correlated inversely with HbA1 (r = -.29, P less than .01), insulin dose in units per kilogram (r = -.40, P less than .001), and duration of diabetes (r = .33, P less than .001) and positively with age at onset of diabetes (r = .34, P less than .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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