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Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals

BTI320 is a proprietary fractionated mannan polysaccharide being studied for attenuation of postprandial glucose excursion. The apparent blood glucose‐lowering effect of this compound is effective in lowering postprandial hyperinsulinemia, participating in the metabolic regulation of other lipid mol...

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Autores principales: Luke, David R., Lee, Karen Ka Yan, Rausch, Carl W., Cheng, Camille
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585810/
https://www.ncbi.nlm.nih.gov/pubmed/29870598
http://dx.doi.org/10.1002/cpdd.583
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author Luke, David R.
Lee, Karen Ka Yan
Rausch, Carl W.
Cheng, Camille
author_facet Luke, David R.
Lee, Karen Ka Yan
Rausch, Carl W.
Cheng, Camille
author_sort Luke, David R.
collection PubMed
description BTI320 is a proprietary fractionated mannan polysaccharide being studied for attenuation of postprandial glucose excursion. The apparent blood glucose‐lowering effect of this compound is effective in lowering postprandial hyperinsulinemia, participating in the metabolic regulation of other lipid molecules; the consequence of this activity is yet to be validated with BTI320 with respect to the risk of cardiovascular disease. The primary objective of the study was to determine the postprandial glucose and insulin responses to 3 test meals containing rice alone or consumed with BTI320 (study A) or 3 test meals (Sprite(TM)) alone or consumed with BTI320 (study B). Twenty overweight but otherwise healthy volunteers, 4 female and 6 male (mean age 29 years, BMI 27–28 kg/m(2)) in study A and 6 female and 4 male (mean age 32 years, BMI 25‐32 kg/m(2)) in study B participated in the BTI320 evaluations. Standardized postprandial response methodology was utilized. In study A the addition of 6‐ and 12‐g BTI320 tablets reduced postprandial glucose responses to white rice by 19% and 32% and reduced postprandial insulin responses by 16% and 24%, respectively (P ≤ .05). In study B 2.6 and 5.2 g BTI320 reduced the glycemic index by 10% and 14%, respectively, and led to 14% and 18% decreases in the insulinemic index of the soft drink (P ≤ .05). These 2 studies demonstrated that the consumption of BTI320 before carbohydrate food or sugary beverage significantly reduced postprandial glucose levels and insulin responses to that meal or beverage in a dose‐dependent manner.
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spelling pubmed-65858102019-06-27 Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals Luke, David R. Lee, Karen Ka Yan Rausch, Carl W. Cheng, Camille Clin Pharmacol Drug Dev Articles BTI320 is a proprietary fractionated mannan polysaccharide being studied for attenuation of postprandial glucose excursion. The apparent blood glucose‐lowering effect of this compound is effective in lowering postprandial hyperinsulinemia, participating in the metabolic regulation of other lipid molecules; the consequence of this activity is yet to be validated with BTI320 with respect to the risk of cardiovascular disease. The primary objective of the study was to determine the postprandial glucose and insulin responses to 3 test meals containing rice alone or consumed with BTI320 (study A) or 3 test meals (Sprite(TM)) alone or consumed with BTI320 (study B). Twenty overweight but otherwise healthy volunteers, 4 female and 6 male (mean age 29 years, BMI 27–28 kg/m(2)) in study A and 6 female and 4 male (mean age 32 years, BMI 25‐32 kg/m(2)) in study B participated in the BTI320 evaluations. Standardized postprandial response methodology was utilized. In study A the addition of 6‐ and 12‐g BTI320 tablets reduced postprandial glucose responses to white rice by 19% and 32% and reduced postprandial insulin responses by 16% and 24%, respectively (P ≤ .05). In study B 2.6 and 5.2 g BTI320 reduced the glycemic index by 10% and 14%, respectively, and led to 14% and 18% decreases in the insulinemic index of the soft drink (P ≤ .05). These 2 studies demonstrated that the consumption of BTI320 before carbohydrate food or sugary beverage significantly reduced postprandial glucose levels and insulin responses to that meal or beverage in a dose‐dependent manner. John Wiley and Sons Inc. 2018-06-05 2019-04 /pmc/articles/PMC6585810/ /pubmed/29870598 http://dx.doi.org/10.1002/cpdd.583 Text en © 2018 The Authors. Clinical Pharmacology in Drug Development Published by Wiley Periodicals, Inc. on behalf of The American College of Clinical Pharmacology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Articles
Luke, David R.
Lee, Karen Ka Yan
Rausch, Carl W.
Cheng, Camille
Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals
title Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals
title_full Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals
title_fullStr Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals
title_full_unstemmed Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals
title_short Phase 1 Study of the Pharmacology of BTI320 Before High‐Glycemic Meals
title_sort phase 1 study of the pharmacology of bti320 before high‐glycemic meals
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6585810/
https://www.ncbi.nlm.nih.gov/pubmed/29870598
http://dx.doi.org/10.1002/cpdd.583
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