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Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study

AIM: To investigate possible changes of blood glucose levels after oral intake of lactulose in healthy subjects. METHODS: The study was performed as prospective, randomized, two-part study with 4-way cross-over design with n = 12 in each study arm. Capillary blood glucose levels were determined over...

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Autores principales: Steudle, Jasmin, Schön, Christiane, Wargenau, Manfred, Pauly, Lioba, Schwejda-Güttes, Susann, Gaigg, Barbara, Kuchinka-Koch, Angelika, Stover, John F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081387/
https://www.ncbi.nlm.nih.gov/pubmed/30090645
http://dx.doi.org/10.4292/wjgpt.v9.i3.22
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author Steudle, Jasmin
Schön, Christiane
Wargenau, Manfred
Pauly, Lioba
Schwejda-Güttes, Susann
Gaigg, Barbara
Kuchinka-Koch, Angelika
Stover, John F
author_facet Steudle, Jasmin
Schön, Christiane
Wargenau, Manfred
Pauly, Lioba
Schwejda-Güttes, Susann
Gaigg, Barbara
Kuchinka-Koch, Angelika
Stover, John F
author_sort Steudle, Jasmin
collection PubMed
description AIM: To investigate possible changes of blood glucose levels after oral intake of lactulose in healthy subjects. METHODS: The study was performed as prospective, randomized, two-part study with 4-way cross-over design with n = 12 in each study arm. Capillary blood glucose levels were determined over a time period of 180 min after intake of a single dose of 10 g or 20 g lactulose provided as crystal or liquid formulation. During the manufacturing process of lactulose, impurities with sugars (e.g., lactose, fructose, galactose) occur. Water and 20 g glucose were used as control and reference. Because lactulose is used as a functional food ingredient, it may also be consumed by people with impaired glucose tolerance, including diabetics. Therefore, it is of interest to determine whether the described carbohydrate impurities may increase blood glucose levels after ingestion. RESULTS: The blood glucose concentration-time curves after intake of 10 g lactulose, 20 g lactulose, and water were almost identical. None of the three applications showed any changes in blood glucose levels. After intake of 20 g glucose, blood glucose concentration increased by approximately 3 mmol/L (mean C(max) = 8.3 mmol/L), reaching maximum levels after approximately 30 min and returning to baseline within approximately 90 min, which was significantly different to the corresponding 20 g lactulose formulations (P < 0.0001). Comparing the two lactulose formulations, crystals and liquid, in the dosage of 10 g and 20 g, there was no difference in the blood glucose profile and calculated pharmacokinetic parameters despite the different amounts of carbohydrate impurities (1.5% for crystals and 26.45% for liquid). Anyhow, the absolute amount of single sugars was low with 0.3 g in crystals and 5.29 g in liquid formulation in the 20 g dosages. Lactulose was well tolerated by most volunteers, and only some reported mild to moderate mainly gastrointestinal side effects. CONCLUSION: The unchanged blood glucose levels after lactulose intake in healthy subjects suggest its safe use in subjects with impaired glucose tolerance.
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spelling pubmed-60813872018-08-08 Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study Steudle, Jasmin Schön, Christiane Wargenau, Manfred Pauly, Lioba Schwejda-Güttes, Susann Gaigg, Barbara Kuchinka-Koch, Angelika Stover, John F World J Gastrointest Pharmacol Ther Randomized Controlled Trial AIM: To investigate possible changes of blood glucose levels after oral intake of lactulose in healthy subjects. METHODS: The study was performed as prospective, randomized, two-part study with 4-way cross-over design with n = 12 in each study arm. Capillary blood glucose levels were determined over a time period of 180 min after intake of a single dose of 10 g or 20 g lactulose provided as crystal or liquid formulation. During the manufacturing process of lactulose, impurities with sugars (e.g., lactose, fructose, galactose) occur. Water and 20 g glucose were used as control and reference. Because lactulose is used as a functional food ingredient, it may also be consumed by people with impaired glucose tolerance, including diabetics. Therefore, it is of interest to determine whether the described carbohydrate impurities may increase blood glucose levels after ingestion. RESULTS: The blood glucose concentration-time curves after intake of 10 g lactulose, 20 g lactulose, and water were almost identical. None of the three applications showed any changes in blood glucose levels. After intake of 20 g glucose, blood glucose concentration increased by approximately 3 mmol/L (mean C(max) = 8.3 mmol/L), reaching maximum levels after approximately 30 min and returning to baseline within approximately 90 min, which was significantly different to the corresponding 20 g lactulose formulations (P < 0.0001). Comparing the two lactulose formulations, crystals and liquid, in the dosage of 10 g and 20 g, there was no difference in the blood glucose profile and calculated pharmacokinetic parameters despite the different amounts of carbohydrate impurities (1.5% for crystals and 26.45% for liquid). Anyhow, the absolute amount of single sugars was low with 0.3 g in crystals and 5.29 g in liquid formulation in the 20 g dosages. Lactulose was well tolerated by most volunteers, and only some reported mild to moderate mainly gastrointestinal side effects. CONCLUSION: The unchanged blood glucose levels after lactulose intake in healthy subjects suggest its safe use in subjects with impaired glucose tolerance. Baishideng Publishing Group Inc 2018-08-07 2018-08-07 /pmc/articles/PMC6081387/ /pubmed/30090645 http://dx.doi.org/10.4292/wjgpt.v9.i3.22 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Randomized Controlled Trial
Steudle, Jasmin
Schön, Christiane
Wargenau, Manfred
Pauly, Lioba
Schwejda-Güttes, Susann
Gaigg, Barbara
Kuchinka-Koch, Angelika
Stover, John F
Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study
title Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study
title_full Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study
title_fullStr Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study
title_full_unstemmed Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study
title_short Blood glucose response after oral intake of lactulose in healthy volunteers: A randomized, controlled, cross-over study
title_sort blood glucose response after oral intake of lactulose in healthy volunteers: a randomized, controlled, cross-over study
topic Randomized Controlled Trial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081387/
https://www.ncbi.nlm.nih.gov/pubmed/30090645
http://dx.doi.org/10.4292/wjgpt.v9.i3.22
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