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

Wan Sub Shim, Soo Kyung Kim, Hae Jin Kim, Eun Seok Kang, Chul Woo Ahn, Sung Kil Lim, Hyun Chul Lee, Bong Soo Cha

Research output: Contribution to journalArticle

23 Citations (Scopus)

Abstract

Objective: Type-2 diabetes is a progressive disease. However, little is known about whether decreased fasting or postprandial pancreatic β-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 (Mo) and postprandial (Ml) β-cell responsiveness. Results: The fasting C-peptide, postprandial C-peptide, Mo, and M1 values were lower, but HbAlc values were higher, in patients with diabetes duration > 10 years than those in other groups. There was no difference in the HbAlc 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 (γ=-0.102), postprandial C-peptide (γ=-0.356), Mo (γ=-0.263), and M1 (γ=-0.315; P<0.01 respectively). After adjustment of age, sex, and BMI, HbA1c was found to be negatively correlated with postprandial C-peptide (γ=-0.264), Mo (γ=-0.379), and M1 (γ=-0.522), however, positively correlated with fasting C-peptide (γ=0.105; P < 0.01 respectively). In stepwise multiple regression analysis, MO, M1, and homeostasis model assessment for insulin resistance (HOMA-IR) emerged as predictors of HbA1c 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 β-cell responsiveness may be a more important determinant for glycemic control than fasting β-cell responsiveness.

Original languageEnglish
Pages (from-to)615-622
Number of pages8
JournalEuropean Journal of Endocrinology
Volume155
Issue number4
DOIs
Publication statusPublished - 2006 Oct 1

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C-Peptide
Type 2 Diabetes Mellitus
Fasting
Insulin
Social Adjustment
Body Mass Index
Meals
Insulin Resistance
Homeostasis
Regression Analysis

All Science Journal Classification (ASJC) codes

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Cite this

Shim, Wan Sub ; Kim, Soo Kyung ; Kim, Hae Jin ; Kang, Eun Seok ; Ahn, Chul Woo ; Lim, Sung Kil ; Lee, Hyun Chul ; Cha, Bong Soo. / Decrement of postprandial insulin secretion determines the progressive nature of type-2 diabetes. In: European Journal of Endocrinology. 2006 ; Vol. 155, No. 4. pp. 615-622.
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abstract = "Objective: Type-2 diabetes is a progressive disease. However, little is known about whether decreased fasting or postprandial pancreatic β-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 (Mo) and postprandial (Ml) β-cell responsiveness. Results: The fasting C-peptide, postprandial C-peptide, Mo, and M1 values were lower, but HbAlc values were higher, in patients with diabetes duration > 10 years than those in other groups. There was no difference in the HbAlc 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 (γ=-0.102), postprandial C-peptide (γ=-0.356), Mo (γ=-0.263), and M1 (γ=-0.315; P<0.01 respectively). After adjustment of age, sex, and BMI, HbA1c was found to be negatively correlated with postprandial C-peptide (γ=-0.264), Mo (γ=-0.379), and M1 (γ=-0.522), however, positively correlated with fasting C-peptide (γ=0.105; P < 0.01 respectively). In stepwise multiple regression analysis, MO, M1, and homeostasis model assessment for insulin resistance (HOMA-IR) emerged as predictors of HbA1c 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 β-cell responsiveness may be a more important determinant for glycemic control than fasting β-cell responsiveness.",
author = "Shim, {Wan Sub} and Kim, {Soo Kyung} and Kim, {Hae Jin} and Kang, {Eun Seok} and Ahn, {Chul Woo} and Lim, {Sung Kil} and Lee, {Hyun Chul} and Cha, {Bong Soo}",
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Decrement of postprandial insulin secretion determines the progressive nature of type-2 diabetes. / Shim, Wan Sub; Kim, Soo Kyung; Kim, Hae Jin; Kang, Eun Seok; Ahn, Chul Woo; Lim, Sung Kil; Lee, Hyun Chul; Cha, Bong Soo.

In: European Journal of Endocrinology, Vol. 155, No. 4, 01.10.2006, p. 615-622.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Decrement of postprandial insulin secretion determines the progressive nature of type-2 diabetes

AU - Shim, Wan Sub

AU - Kim, Soo Kyung

AU - Kim, Hae Jin

AU - Kang, Eun Seok

AU - Ahn, Chul Woo

AU - Lim, Sung Kil

AU - Lee, Hyun Chul

AU - Cha, Bong Soo

PY - 2006/10/1

Y1 - 2006/10/1

N2 - Objective: Type-2 diabetes is a progressive disease. However, little is known about whether decreased fasting or postprandial pancreatic β-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 (Mo) and postprandial (Ml) β-cell responsiveness. Results: The fasting C-peptide, postprandial C-peptide, Mo, and M1 values were lower, but HbAlc values were higher, in patients with diabetes duration > 10 years than those in other groups. There was no difference in the HbAlc 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 (γ=-0.102), postprandial C-peptide (γ=-0.356), Mo (γ=-0.263), and M1 (γ=-0.315; P<0.01 respectively). After adjustment of age, sex, and BMI, HbA1c was found to be negatively correlated with postprandial C-peptide (γ=-0.264), Mo (γ=-0.379), and M1 (γ=-0.522), however, positively correlated with fasting C-peptide (γ=0.105; P < 0.01 respectively). In stepwise multiple regression analysis, MO, M1, and homeostasis model assessment for insulin resistance (HOMA-IR) emerged as predictors of HbA1c 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 β-cell responsiveness may be a more important determinant for glycemic control than fasting β-cell responsiveness.

AB - Objective: Type-2 diabetes is a progressive disease. However, little is known about whether decreased fasting or postprandial pancreatic β-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 (Mo) and postprandial (Ml) β-cell responsiveness. Results: The fasting C-peptide, postprandial C-peptide, Mo, and M1 values were lower, but HbAlc values were higher, in patients with diabetes duration > 10 years than those in other groups. There was no difference in the HbAlc 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 (γ=-0.102), postprandial C-peptide (γ=-0.356), Mo (γ=-0.263), and M1 (γ=-0.315; P<0.01 respectively). After adjustment of age, sex, and BMI, HbA1c was found to be negatively correlated with postprandial C-peptide (γ=-0.264), Mo (γ=-0.379), and M1 (γ=-0.522), however, positively correlated with fasting C-peptide (γ=0.105; P < 0.01 respectively). In stepwise multiple regression analysis, MO, M1, and homeostasis model assessment for insulin resistance (HOMA-IR) emerged as predictors of HbA1c 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 β-cell responsiveness may be a more important determinant for glycemic control than fasting β-cell responsiveness.

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