Type 2 Diabetes Mellitus Clinical Trial
Official title:
Acute and Second Meal Effects of Peanuts on Glycemic Response and Appetite in Obese Women With High Type 2 Diabetes Risk: a Randomized Crossover Trial
Nut consumption is associated with reduced risk of Type 2 diabetes. The aim of this study was to assess the effects of peanut (whole or peanut butter) to breakfast meals on glycemic, insulinemic and selected gut hormone responses, appetite, and food intake over two consecutive meals in obese women with high Type 2 diabetes risk. Fifteen women participated in a randomized crossover trial where 42.5g of whole peanuts (P), peanut butter (PB), or no peanuts (control-C) were added to a 75g available carbohydrate-matched breakfast meal. Postprandial concentrations of blood glucose, insulin, non-esterified free fatty acids (NEFA), glucagon-like peptide-1 (GLP-1), peptide YY (PYY), cholecystokinin (CCK), appetitive sensations and food intake were assessed after breakfast treatments and a standard lunch (75g available carbohydrate).
| Status | Completed |
| Enrollment | 15 |
| Est. completion date | February 2011 |
| Est. primary completion date | September 2010 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 18 Years to 50 Years |
| Eligibility |
Inclusion Criteria: - Body mass index between 30 - 35 kg/M2 - Not taking medications known to affect glycemia, fat metabolism, or appetite - Regular breakfast consumer (=100 kilocalories ingested within 2 hours of waking on =4d/wk) - No body weight fluctuation (<5kg in the past 3 months) - Willingness to eat all test foods - No self-reported allergy to the foods provided in the study - No self-reported sleep disorders - At least one of the following conditions: waist circumference = 88 cm; reported family history of Type 2 diabetes in first degree relatives; capillary glycemia between 5.5 - 7.0 mmol/L; and/or a 2-hour blood glucose of 7.8 - 11.1 mmol/L (impaired glucose tolerance) Exclusion Criteria: - Type 2 diabetes mellitus - Dyslipidemia - High blood pressure |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Brazil | Federal University of Viçosa | Viçosa | Minas Gerais |
| Lead Sponsor | Collaborator |
|---|---|
| Federal University of Vicosa | Coordenação de Aperfeiçoamento de Pessoal de Nível Superior., Fundação de Amparo à Pesquisa do estado de Minas Gerais, United States Agency for International Development (USAID) |
Brazil,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Change from baseline in glucose homeostasis at eight hours | Postprandial concentrations and incremental area under the curve of blood glucose, insulin and glucagon-like peptide-1, and incremental area above the curve of non-esterified free fatty acids were assessed after breakfast treatments and a standard lunch | Baseline (-10), 15, 45, 60, 90, 120, 180, 240, 265, 295, 310, 340, 370, 430 and 490 minutes | No |
| Secondary | Change from baseline in incretin hormones at four hours | Postprandial concentrations and the incremental area under the curve of peptide YY and cholecystokinin were assessed after breakfast treatments | Baseline (-10), 15, 45, 60, 90, 120, 180 and 240 minutes | No |
| Secondary | Change in food intake over 24 hours | All food consumed in laboratory and after leaving the laboratory in the experiment day were recorded | 24 hours | No |
| Secondary | Change from baseline in appetitive sensations at twelve hours | Appetite ratings were scored at baseline and in a pre-determined times on a 100 mm visual analogue scale anchored with descriptors of "not at all" and "extremely" | Baseline (-10), 15, 45, 60, 90, 120, 180, 240, 265, 295, 310, 340, 370, 430, 490, 550, 610, 670 and 730 minutes | No |
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