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  • 1
    ISSN: 1432-0428
    Keywords: C-peptide ; insulin antibodies ; glucose tolerance ; segmental pancreatic transplantation ; pancreatic transplant rejection ; brittle diabetes mellitus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Plasma C-peptide and serum insulin antibody levels were determined in 5 diabetic patients undergoing vascularized pancreatic transplantation. The grafts functioned well at first and exogenous insulin could be withdrawn, but one to 7 weeks later the grafts were rejected. After the transplantation there was an increase in the fasting plasma C-peptide level, and B-cell stimulation with glucose or glucagon evoked a C-peptide response. Healing of ischaemic damage was reflected in an increase in the C-peptide level. During graft rejection the C-peptide level fell. Measurement of plasma C-peptide levels provides a direct index of the B-cell function of the pancreatic graft. After transplantation the insulin antibody level fell exponentially, with an apparent half life of 10–11 days, whereas the level of total IgG was variable. The results indicate that formation of insulin antibodies ceases immediately on removal of the immunogenic stimulus, that is, on withdrawal of xenogeneic insulin.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Diabetologia 19 (1980), S. 427-432 
    ISSN: 1432-0428
    Keywords: Insulin ; C-peptide ; proinsulin ; diabetic ; mothers ; infants ; neonatal hypoglycaemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Serum concentrations of glucose, C-peptide, IRI (Immunoreactive insulin) and proinsulin were determined in 31 insulin-dependent diabetic mothers and their newborn infants and in 13 nondiabetic mothers and their babies at the time of delivery. Eleven mothers with long-term diabetes had insulin antibodies and low or undetectable C-peptide levels (mean ± SEM: 0.04±0.01 nmol/l). Diabetic mothers without insulin antibodies had a mean C peptide value of 1.18 nmol/1 (range 0.05–3.00) and the non-diabetics 0.95 nmol/l (0.28–2.4). Blood glucose values (2 to 4 hours after birth) of less than 1.7 mmol/l were observed in 7 of the 11 babies with antibodies and in 3 of the 20 babies without antibodies. C-peptide in the 31 babies of diabetic mothers correlated to maternal glucose (p 〈 0.05). In addition the mean glucose value (2–4 hours) was negatively correlated to IRI and proinsulin (p 〈 0.01) in the babies without antibodies, confirming that elevated maternal glucose leads to increased insulin secretion at the time of birth, which may lead to hypoglycaemia. In babies without antibodies birth weight correlated to their C-peptide (p 〈 0.01) and proinsulin (p 〈 0.01). The 31 babies of the diabetic mothers were born with higher C-peptide (1.01±0.16 nmol/ 1) than babies of non-diabetic mothers (0.39±0.04 nmol/1). The newborn infants secrete significantly more proinsulin than their mothers. Babies of mothers with insulin antibodies were born with the same concentrations of antibodies (Pearson correlation coefficient = 0.98) as in their mothers, but total IRI was higher in these babies, due in part to human proinsulin being bound to the antibodies. There were significant correlations between insulin antibodies on the one hand, and IRI, proinsulin and C-peptide on the other, in the 11 babies, p 〈 0.001, p 〈 0.001 and p 〈 0.01, respectively, the last indicating increasing B-cell activity with higher antibody levels.
    Type of Medium: Electronic Resource
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