Glucose, insulin secretion, and insulin secretory pulses were measured by deconvolution of peripheral C-peptide concentrations in 10 IDDM recipients of a combined kidney-pancreas allograft 6 mo post-transplantation and were compared with 10 matched nondiabetic control subjects. Seven of the 10 recipients were restudied 2 yr post-transplantation. To control for immunosuppressive therapy, 6 patients with a kidney allograft also were studied. Pancreatic insulin secretion rates were evaluated over a 24-h period with three mixed meals. Six months post-transplantation, fasting (5.3 ± 0.1 vs. 5.3 ± 0.1 mM), average 24-h (6.0 ± 0.1 vs. 5.7 ± 0.1 mM), and meal-related (6.1 ± 0.3 vs. 5.8 ± 0.2 mM) plasma glucose levels were not different in control subjects and recipients, respectively. Total 24-h insulin secretion rates were similar between the two groups (150 ± 15 vs. 182 ± 24 nmol · m−2 · 24 h−1). However, post-transplantation, the relationship between basal and meal-stimulated insulin secretion was altered with increased basal insulin secretion (52.2 ± 6.4 vs. 97.4 ± 12.5 pmol · m−2 · min−1 P < 0.004) and reduced meal-related secretion. The proportion of total 24-h insulin secretion comprised by basal secretion was 44 ± 4% in the control subjects vs. 73 ± 5% in recipients. The number of ultradian oscillations of insulin secretion identified in each 24-h period by pulse analysis was similar in control subjects and recipients (11.9 ± 0.9 vs. 10.4 ± 0.5 oscillations/24 h). Two years post-transplantation, the glucose profiles and oscillatory insulin secretory patterns remained intact. Basal insulin secretion was 76 ± 11 pmol · m−2 · min−1 and 24-h insulin secretion was 167 ± nmol m−2 24 h−1. Six kidney-transplant recipients studied showed that 47 ± 3% of 24-h insulin secretion was basal secretion. This finding supported the idea that altered meal secretory patterns observed in the kidney-pancreas recipients were not the result of immunosuppressive therapy. After combined kidney-pancreas transplantation 1) plasma glucose profiles remain normal 2 yr post-transplantation, 2) clearance of C-peptide is reduced, 3) basal insulin secretion is increased but meal responses are reduced, and 4) the normal oscillatory pattern of insulin secretion persists.
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Original Articles|
October 01 1992
Insulin Secretory Profiles and C-Peptide Clearance Kinetics at 6 Months and 2 Years After Kidney-Pancreas Transplantation
John D Blackman;
John D Blackman
Departments of Medicine and Surgery, University of Chicago, Pritzker School of Medicine
Chicago, Illinois
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Kenneth S Polonsky;
Kenneth S Polonsky
Departments of Medicine and Surgery, University of Chicago, Pritzker School of Medicine
Chicago, Illinois
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Jonathan B Jaspan;
Jonathan B Jaspan
Departments of Medicine and Surgery, University of Chicago, Pritzker School of Medicine
Chicago, Illinois
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Jeppe Sturis;
Jeppe Sturis
Departments of Medicine and Surgery, University of Chicago, Pritzker School of Medicine
Chicago, Illinois
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Eve Van Cauter;
Eve Van Cauter
Departments of Medicine and Surgery, University of Chicago, Pritzker School of Medicine
Chicago, Illinois
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J Richard Thistlethwaite
J Richard Thistlethwaite
Departments of Medicine and Surgery, University of Chicago, Pritzker School of Medicine
Chicago, Illinois
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Address correspondence and reprint requests to Kenneth S. Polonsky, MD, University of Chicago, Department of Medicine, Box 435, 5841 S. Maryland Avenue, Chicago, IL 60637.
Diabetes 1992;41(10):1346–1354
Article history
Received:
August 16 1991
Revision Received:
May 26 1992
Accepted:
May 26 1992
PubMed:
1397710
Citation
John D Blackman, Kenneth S Polonsky, Jonathan B Jaspan, Jeppe Sturis, Eve Van Cauter, J Richard Thistlethwaite; Insulin Secretory Profiles and C-Peptide Clearance Kinetics at 6 Months and 2 Years After Kidney-Pancreas Transplantation. Diabetes 1 October 1992; 41 (10): 1346–1354. https://doi.org/10.2337/diab.41.10.1346
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