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Decrement of postprandial insulin secretion determines the progressive nature of type-2 diabetes.

Authors
Shim, WS; Kim, SK; Kim, HJ; Kang, ES; Ahn, CW; Lim, SK; Lee, HC; Cha, BS
Citation
European journal of endocrinology, 155(4):615-622, 2006
Journal Title
European journal of endocrinology
ISSN
0804-46431479-683X
Abstract
OBJECTIVE: Type-2 diabetes is a progressive disease. However, little is known about whether decreased fasting or postprandial pancreatic beta-cell responsiveness is more prominent with increased duration of diabetes. The aim of this study was to evaluate the relationship between insulin secretion both during fasting and 2 h postprandial, and the duration of diabetes in type-2 diabetic patients.



DESIGN: Cross-sectional clinical investigation.



METHODS: We conducted a meal tolerance test in 1466 type-2 diabetic patients and calculated fasting (M0) and postprandial (M1) beta-cell responsiveness.



RESULTS: The fasting C-peptide, postprandial C-peptide, M0, and M1 values were lower, but HbA1c values were higher, in patients with diabetes duration > 10 years than those in other groups. There was no difference in the HbA1c levels according to the tertiles of their fasting C-peptide level. However, in a group of patients with highest postprandial C-peptide tertile, the HbA1c values were significantly lower than those in other groups. After adjustment of age, sex, and body mass index (BMI), the duration of diabetes was found to be negatively correlated with fasting C-peptide (gamma = -0.102), postprandial C-peptide (gamma = -0.356), M0 (gamma = -0.263), and M1 (gamma = -0.315; P < 0.01 respectively). After adjustment of age, sex, and BMI, HbA1c was found to be negatively correlated with postprandial C-peptide (gamma = -0.264), M(0) (gamma = -0.379), and M1 (gamma = -0.522), however, positively correlated with fasting C-peptide (gamma = 0.105; P < 0.01 respectively). In stepwise multiple regression analysis, M0, M1, and homeostasis model assessment for insulin resistance (HOMA-IR) emerged as predictors of HbAlc after adjustment for age, sex, and BMI (R2 = 0.272, 0.080, and 0.056 respectively).



CONCLUSIONS: With increasing duration of diabetes, the decrease of postprandial insulin secretion is becoming more prominent, and postprandial beta-cell responsiveness may be a more important determinant for glycemic control than fasting beta-cell responsiveness.
MeSH terms
AdultAgedBiological Markers/bloodC-Peptide/bloodCross-Sectional StudiesDiabetes Mellitus, Type 2/metabolism*Disease ProgressionFasting/bloodFemaleHemoglobin A, Glycosylated/analysisHumansInsulin/secretion*Insulin-Secreting Cells/secretionMaleMiddle AgedPostprandial PeriodRegression AnalysisStatistical Distributions
DOI
10.1530/eje.1.02249
PMID
16990662
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Endocrinology & Metabolism
AJOU Authors
김, 혜진
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