Abstract

Diminished postprandial secretion of incretins and insulin represents one of the key pathophysiological mechanisms behind type 2 diabetes (T2D). We tested the effects of two energy- and macronutrient-matched meals: A standard meat (M-meal) and a vegan (V-meal) on postprandial incretin and insulin secretion in participants with T2D. A randomized crossover design was used in 20 participants with T2D. Plasma concentrations of glucose, insulin, C-peptide, glucagon-like peptide-1 (GLP-1), amylin, and gastric inhibitory peptide (GIP) were determined at 0, 30, 60, 120, and 180 min. Beta-cell function was assessed with a mathematical model, using C-peptide deconvolution. Repeated-measures ANOVA was used for statistical analysis. Postprandial plasma glucose responses were similar after both test meals (p = 0.64). An increase in the stimulated secretion of insulin (by 30.5%; 95% CI 21.2 to 40.7%; p < 0.001), C-peptide (by 7.1%; 95% CI 4.1 to 9.9%; p < 0.001), and amylin (by 15.7%; 95% CI 11.8 to 19.7%; p < 0.001) was observed following consumption of the V-meal. An increase in stimulated secretion of GLP-1 (by 19.2%; 95% CI 12.4 to 26.7%; p < 0.001) and a decrease in GIP (by −9.4%; 95% CI −17.3 to −0.7%; p = 0.02) were observed after the V-meal. Several parameters of beta-cell function increased after the V-meal, particularly insulin secretion at a fixed glucose value 5 mmol/L, rate sensitivity, and the potentiation factor. Our results showed an increase in postprandial incretin and insulin secretion, after consumption of a V-meal, suggesting a therapeutic potential of plant-based meals for improving beta-cell function in T2D.

Highlights

  • The role of diet in the development of glucose intolerance and progression to type 2 diabetes (T2D) has been studied intensively [1,2,3]

  • We have investigated postprandial incretin and insulin secretion after ingestion of two meals matched for energy and macronutrient content: a standard meat burger and a plant-based burger, in men with T2D

  • Overall postprandial plasma glucose responses did not differ between meals, and we detected significantly higher stimulated insulin and C-peptide responses, higher concentrations of glucagon-like peptide -1 (GLP-1), and lower levels of gastric inhibitory peptide (GIP), after the plant-based meal compared with the standard M-meal

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Summary

Introduction

The role of diet in the development of glucose intolerance and progression to type 2 diabetes (T2D) has been studied intensively [1,2,3]. Namely glucagon-like peptide -1 (GLP-1) and gastric inhibitory peptide (GIP), which are released from the small intestine in response to nutrient ingestion to enhance glucose-dependent insulin secretion, aid in the overall maintenance of glucose homeostasis [5]. GLP-1 [6], and amylin [7] play a role in energy intake through appetite regulation The release of these satiety hormones depends on meal. Prospective observational studies indicate a positive relationship between a high consumption of red meat and T2D incidence [9,10]. People who eat any processed meats are one third more likely to develop diabetes compared with those who do not consume any [11]. We have investigated postprandial incretin and insulin secretion after ingestion of two meals matched for energy and macronutrient content: a standard meat burger and a plant-based burger, in men with T2D. Our results provide insight into the pathophysiology of T2D and potentially help build the evidence base for dietary recommendations for people with T2D

Trial Design
Participants and Eligibility Criteria
Randomization and Masking
Interventions
Anthropometric Measures and Blood Pressure
Metabolic Parameters
Gastrointestinal and Appetite Hormones
Beta-cell Function and Insulin Resistance
Statistical Analysis
Results
Postprandial Glucose and Insulin Response
Incretins
Correlations of Changes in Gastrointestinal Hormones with Glucose Metabolism
Discussion
Insulin Secretion and Beta-cell Function
Amylin
Strengths and Limitations
Full Text
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