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A high-protein breakfast induces greater insulin and glucose-dependent insulinotropic peptide responses to a subsequent lunch meal in individuals with type 2 diabetes
Plain-language guide to PMID 25733459 (2015): single-blind and crossover controlled clinical trial study of Glucagon and GIP (Gastric Inhibitory Polypeptide) in 2 men.
Key Facts
- PMID
- 25733459
- Journal
- The Journal of nutrition
- Year
- 2015
- Study type
- Controlled Clinical Trial
- Authors
- Park YM et al. (7 authors)
- DOI
- 10.3945/jn.114.202549
What This Study Did, in Plain Language
What Was Tested
The paper reports a study of Glucagon and GIP (Gastric Inhibitory Polypeptide), published as a controlled clinical trial.
This study examined the effects of high-protein vs. high-carbohydrate breakfast meals on the metabolic and incretin responses after the breakfast and lunch meals.
Why It Was Studied
The previous meal modulates the postprandial glycemic responses to a subsequent meal; this is termed the second-meal phenomenon.
Who Took Part
The study group was 2 men.
By PubMed's age tags, the people studied were young adults, adults and middle-aged adults, both men and women.
On day 7, subjects completed an 8-h testing day.
After an overnight fast, the subjects consumed their respective breakfast followed by a standard 500-kcal high-carbohydrate lunch meal 4 h later.
How the Study Was Run
The researchers set it up as a single-blind and crossover study.
In this single-blind Glucagon study one party knew the assignments and the other did not.
Each person switched between Glucagon and the comparison at some point, usually with a gap in between.
Blood samples were taken throughout the day for assessment of 4-h postbreakfast and 4-h postlunch total area under the curve (AUC) for glucose, insulin, C-peptide, glucagon, glucose-dependent insulinotropic peptide (GIP), and glucagon-like peptide 1 (GLP-1).
What Was Measured
PubMed files the paper under topics including Blood Glucose, Body Mass Index, Breakfast, C-Peptide, Diabetes Mellitus, Type 2, Diet and Diet Records.
Author keywords: GIP, GLP-1, glucagon, high carbohydrate, postprandial glucose and second-meal phenomenon.
What This Means in Plain Language
The paper is a single-blind and crossover study of Glucagon and GIP (Gastric Inhibitory Polypeptide) in 2 men.
With fewer than 40 people, it is a small study, so it is better read as an early signal for further research than as a settled answer.
The abstract goes on to report its results in about 7 sentences; this page does not restate them, so read the paper for the findings and their limits.
The publication is from 2015 (The Journal of nutrition), a journal based in United States.
More context: the Glucagon compound page and the GIP (Gastric Inhibitory Polypeptide) compound page, all human trials.
Our Notes on the Compounds
Glucagon: A 29-amino-acid pancreatic hormone that raises blood glucose; used as a rescue medicine for severe low blood sugar and as a diagnostic aid.
GIP (Gastric Inhibitory Polypeptide): A 42-amino-acid gut hormone that boosts insulin release after meals; one of the two receptors tirzepatide acts on.
Related Pages
Source: PubMed record. This explanation is written by PeptideWhiz from the public record. For research and education only. Not medical advice; no dosing information is given.