Postoperative oral glucose tolerance and stimulated insulin secretion: A predictor of endocrine graft function more than 10 years after pancreas-kidney transplantation

被引:16
作者
Pfeffer, F
Nauck, MA
Drognitz, O
Benz, S
von Dobschuetz, E
Hopt, UT
机构
[1] Univ Freiburg, Dept Gen Surg, D-79106 Freiburg, Germany
[2] Diabeteszentrum Bad Lauterberg, Bad Lauterberg im Harz, Germany
关键词
D O I
10.1097/01.TP.0000098821.26466.DE
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. After pancreas transplantation, endocrine function is determined by the insulin secretory capacity of the transplanted pancreas. The authors evaluated the predictive value of postoperative oral glucose tolerance test (OGTT) and stimulated insulin secretion on long-term endocrine function. Methods. Forty-one patients after pancreas-kidney transplantation with systemic venous drainage were studied. Patients were categorized to have normal glucose tolerance (NGT) or impaired glucose tolerance (IGT) (World Health Organization criteria: NGT, <7.8 mM; IGT, 7.8-11.1 mM 120 min after glucose intake) and high or low total insulin secretion. Mean follow-up of graft function and patient outcome was 10.2+/-0.5 years after OGTT. Results. Patients with IGT had grafts with a longer ischemia time and a significantly worst urine amylase excretion as compared with patients with NGT. Using Kaplan-Meier survival analysis, patients with NGT had better long-term pancreatic function as compared with IGT in the follow-up after performing the first OGTT (mean, 10.9+/-0.2 vs. 8.8+/-0.9 years of graft function; P=0.02), but there was no difference in patient survival and kidney graft function. Also, high insulin secretion predicted significantly longer pancreas graft function as compared with low insulin secretion (P=0.04). Conclusions. Although IGT does not lead to poorer long-term patient survival and kidney graft function, it does predict compromised long-term endocrine function of the transplanted pancreas. Therefore, postoperative OGTT are useful tools for identification of patients at risk of, long-term endocrine graft failure after pancreas transplantation.
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页码:1427 / 1431
页数:5
相关论文
共 28 条
[1]  
AHN KJ, 1992, TRANSPLANT P, V24, P1581
[2]  
BASRI N, 1992, TRANSPLANT P, V24, P1780
[3]   Prediction of the long-term metabolic success of the pancreatic graft function [J].
Battezzati, A ;
Benedini, S ;
Caldara, R ;
Calori, G ;
Secchi, A ;
Pozza, G ;
Luzi, L .
TRANSPLANTATION, 2001, 71 (11) :1560-1565
[4]   Impairment of microcirculation in the early reperfusion period predicts the degree of graft pancreatitis in clinical pancreas transplantation [J].
Benz, S ;
Bergt, S ;
Obermaier, R ;
Wiessner, R ;
Pfeffer, F ;
Schareck, W ;
Hopt, UT .
TRANSPLANTATION, 2001, 71 (06) :759-763
[5]  
Cecka J M, 1996, Clin Transpl, P1
[6]   PATHOGENESIS OF NIDDM - A BALANCED OVERVIEW [J].
DEFRONZO, RA ;
BONADONNA, RC ;
FERRANNINI, E .
DIABETES CARE, 1992, 15 (03) :318-368
[7]   SYSTEMIC VENOUS DRAINAGE OF PANCREAS ALLOGRAFTS AS INDEPENDENT CAUSE OF HYPERINSULINEMIA IN TYPE-I DIABETIC RECIPIENTS [J].
DIEM, P ;
ABID, M ;
REDMON, JB ;
SUTHERLAND, DER ;
ROBERTSON, RP .
DIABETES, 1990, 39 (05) :534-540
[8]   Glucose intolerance after renal transplantation depends upon prednisolone dose and recipient age [J].
Hjelmesaeth, J ;
Hartmann, A ;
Kofstad, J ;
Stenstrom, J ;
Leivestad, T ;
Egeland, T ;
Fauchald, P .
TRANSPLANTATION, 1997, 64 (07) :979-983
[9]   Determinants of insulin secretion after renal transplantation [J].
Hjelmesæth, J ;
Jenssen, T ;
Hagen, M ;
Egeland, T ;
Hartmann, A .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2003, 52 (05) :573-578
[10]   EFFECTS OF PANCREAS TRANSPLANTATION ON POSTPRANDIAL GLUCOSE-METABOLISM [J].
KATZ, H ;
HOMAN, M ;
VELOSA, J ;
ROBERTSON, P ;
RIZZA, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (18) :1278-1283