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The Second-Meal Phenomenon in Type 2 Diabetes

OBJECTIVE: In health, the rise in glucose after lunch is less if breakfast is eaten. We evaluated the second-meal effect in type 2 diabetes. RESEARCH DESIGN AND METHODS: Metabolic changes after lunch in eight obese type 2 diabetic subjects were compared on 3 days: breakfast eaten, no breakfast, and...

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Detalles Bibliográficos
Autores principales: Jovanovic, Ana, Gerrard, Jean, Taylor, Roy
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699724/
https://www.ncbi.nlm.nih.gov/pubmed/19366973
http://dx.doi.org/10.2337/dc08-2196
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author Jovanovic, Ana
Gerrard, Jean
Taylor, Roy
author_facet Jovanovic, Ana
Gerrard, Jean
Taylor, Roy
author_sort Jovanovic, Ana
collection PubMed
description OBJECTIVE: In health, the rise in glucose after lunch is less if breakfast is eaten. We evaluated the second-meal effect in type 2 diabetes. RESEARCH DESIGN AND METHODS: Metabolic changes after lunch in eight obese type 2 diabetic subjects were compared on 3 days: breakfast eaten, no breakfast, and no breakfast but intravenous arginine 1 h before lunch. RESULTS: Despite comparable insulin levels, the rise in plasma glucose after lunch was considerably less if breakfast had been eaten (0.68 ± 1.49 vs. 12.32 ± 1.73 vs. 7.88 ± 1.03 mmol · h(−1) · l(−1); P < 0.0001). Arginine administration almost halved the lunch rise in plasma glucose (12.32 ± 1.73 vs. 7.88 ± 1.03 mmol · h(−1) · l(−1)). The plasma free fatty acid concentration at lunchtime directly related to plasma glucose rise after lunch (r = 0.67, P = 0.0005). CONCLUSIONS: The second-meal effect is preserved in type 2 diabetes. Premeal administration of a nonglucose insulin secretagogue results in halving the postprandial glucose rise and has therapeutic potential.
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spelling pubmed-26997242010-07-01 The Second-Meal Phenomenon in Type 2 Diabetes Jovanovic, Ana Gerrard, Jean Taylor, Roy Diabetes Care Original Research OBJECTIVE: In health, the rise in glucose after lunch is less if breakfast is eaten. We evaluated the second-meal effect in type 2 diabetes. RESEARCH DESIGN AND METHODS: Metabolic changes after lunch in eight obese type 2 diabetic subjects were compared on 3 days: breakfast eaten, no breakfast, and no breakfast but intravenous arginine 1 h before lunch. RESULTS: Despite comparable insulin levels, the rise in plasma glucose after lunch was considerably less if breakfast had been eaten (0.68 ± 1.49 vs. 12.32 ± 1.73 vs. 7.88 ± 1.03 mmol · h(−1) · l(−1); P < 0.0001). Arginine administration almost halved the lunch rise in plasma glucose (12.32 ± 1.73 vs. 7.88 ± 1.03 mmol · h(−1) · l(−1)). The plasma free fatty acid concentration at lunchtime directly related to plasma glucose rise after lunch (r = 0.67, P = 0.0005). CONCLUSIONS: The second-meal effect is preserved in type 2 diabetes. Premeal administration of a nonglucose insulin secretagogue results in halving the postprandial glucose rise and has therapeutic potential. American Diabetes Association 2009-07 2009-04-14 /pmc/articles/PMC2699724/ /pubmed/19366973 http://dx.doi.org/10.2337/dc08-2196 Text en © 2009 by the American Diabetes Association. https://creativecommons.org/licenses/by-nc-nd/3.0/Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ (https://creativecommons.org/licenses/by-nc-nd/3.0/) for details.
spellingShingle Original Research
Jovanovic, Ana
Gerrard, Jean
Taylor, Roy
The Second-Meal Phenomenon in Type 2 Diabetes
title The Second-Meal Phenomenon in Type 2 Diabetes
title_full The Second-Meal Phenomenon in Type 2 Diabetes
title_fullStr The Second-Meal Phenomenon in Type 2 Diabetes
title_full_unstemmed The Second-Meal Phenomenon in Type 2 Diabetes
title_short The Second-Meal Phenomenon in Type 2 Diabetes
title_sort second-meal phenomenon in type 2 diabetes
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699724/
https://www.ncbi.nlm.nih.gov/pubmed/19366973
http://dx.doi.org/10.2337/dc08-2196
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