Prevalence of residual B-cell function related to age at onset and genetic profile in newly diagnosed type I diabetics

Acta Diabetol Lat. 1987 Oct-Dec;24(4):317-23. doi: 10.1007/BF02742964.

Abstract

Patients with type I (insulin-dependent) diabetes mellitus maintain B-cell function for a varying period of time after onset. This is commonly held to account for post-initial remission. To estimate residual B-cell function we measured plasma and 24-h urinary C-peptide in 68 type I diabetic patients (age range 4-35 years, within 10-180 days of the onset of symptoms, typed for HLA-A, -B, -C and DR loci. A positive correlation (r = 0.26; p less than 0.05) was found between urinary C-peptide levels and the age of the patient. The analysis of variance of urinary C-peptide values on the basis of the presence or absence of DR3 and DR4 antigens revealed that the DR3-positive patients had reduced excretion (15.2 +/- 9.2 SD micrograms/24h) with respect to the others (22.7 +/- 15.5 SD micrograms/24h) (F = 6.35; p less than 0.05). No interaction effect was found in DR3/4 positive patients. Hence, late onset patients appear to have higher residual C-peptide secretion. In the light of these findings, the assessment of B-cell function and genetic profile may be useful in predicting which patients are likely to have remission periods and identifying the metabolic consequences of even minimal endogenous insulin secretion.

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • C-Peptide / blood
  • C-Peptide / urine
  • Child
  • Child, Preschool
  • Diabetes Mellitus, Type 1 / physiopathology*
  • Female
  • HLA-DR Antigens / analysis
  • Humans
  • Islets of Langerhans / physiopathology*
  • Male

Substances

  • C-Peptide
  • HLA-DR Antigens