Diabetes Clinical Trial
Official title:
Measurement of ß-cell Function and Insulin Sensitivity in Non-diabetic Patients With En-bloc Liver, Pancreas and Small Bowel Transplant Using a Hyperglycemic Clamp
Under chronic immunosuppressive and corticosteroid therapy, transplant patients have a tendency to develop in the long-term diabetes. Patients who have received extra pancreatic tissue with their liver and small bowel transplantation have not yet developed insulin resistance or diabetes mellitus. We would like to investigate to which level insulin secretory capacity the extra pancreas together with the native pancreas has in these transplant patients using the hyperglycemic clamp. These data will be compared with the data obtained from healthy controls.
The glycemic control in type 1 diabetic recipients of islet cell grafts is correlated with
the ß-cell mass. In the standard technique for liver/small bowel transplant procedure
previously described by Grant et al, the pancreas was removed. This surgical method was
modified by Sudan et al and the donor pancreas was transplanted intact in these non-diabetic
patients. Under chronic immunosuppressive and corticosteroid therapy, these patients with
extra ß-cell mass have not developed insulin resistance or diabetes mellitus. To which level
insulin secretory capacity the extra pancreas allograft together with the native pancreas
has in these transplant patients are not yet known.
Among the measures of pancreatic ß-cell-secretory capacity, the first-phase and steady state
insulin secretion from the hyperglycemic clamp studies are believed to give the most robust
estimates. Moreover, the hyperglycemic clamp and the euglycemic clamp yield comparable
estimates of insulin sensitivity and, so that under appropriate conditions, the
hyperglycemic clamp technique may be used to assess both insulin sensitivity and insulin
secretion in the same individual in a single experiment.
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Observational Model: Case Control, Time Perspective: Prospective
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