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Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance
BACKGROUND: Rebaudioside A and erythritol are nonnutritive sweeteners. There have been several studies of their glycemic effects, but the outcomes remain controversial. The purpose of this study was to evaluate the glycemic effects of rebaudioside A and erythritol as a sweetener in people with gluco...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Diabetes Association
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995183/ https://www.ncbi.nlm.nih.gov/pubmed/27352150 http://dx.doi.org/10.4093/dmj.2016.40.4.283 |
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author | Shin, Dong Hee Lee, Ji Hye Kang, Myung Shin Kim, Tae Hoon Jeong, Su Jin Kim, Chong Hwa Kim, Sang Soo Kim, In Joo |
author_facet | Shin, Dong Hee Lee, Ji Hye Kang, Myung Shin Kim, Tae Hoon Jeong, Su Jin Kim, Chong Hwa Kim, Sang Soo Kim, In Joo |
author_sort | Shin, Dong Hee |
collection | PubMed |
description | BACKGROUND: Rebaudioside A and erythritol are nonnutritive sweeteners. There have been several studies of their glycemic effects, but the outcomes remain controversial. The purpose of this study was to evaluate the glycemic effects of rebaudioside A and erythritol as a sweetener in people with glucose intolerance. METHODS: This trial evaluated the glycemic effect after 2 weeks of consumption of rebaudioside A and erythritol as sweeteners in a pre-diabetic population. The patients were evaluated for fructosamine, fasting plasma glucose, C-peptide, insulin, and 2-hour plasma glucose before and after consumption of sweetener. The primary outcome was a change in fructosamine levels from the baseline to the end of treatment. Secondary outcomes were the changes in levels of fasting plasma glucose and 2-hour plasma glucose. RESULTS: From the baseline to the end of experiment, the changes in fructosamine levels after consumption of rebaudioside A and erythritol, did not differ significantly (244.00±19.57 vs. 241.68±23.39 µmol/L, P=0.366). The change in levels from the baseline to end of the study for rebaudioside A and erythritol were fasting plasma glucose (102.56±10.72 vs. 101.32±9.20 mg/dL), 2-hour plasma glucose (154.92±54.53 vs. 141.92±42.22 mg/dL), insulin (7.56±4.29 vs. 7.20±5.12 IU/mL), and C-peptide (2.92±1.61 vs. 2.73±1.31 ng/mL), respectively, and also did not differ significantly (P>0.05 for all). CONCLUSION: Our study suggests that consumption of rebaudioside A and erythritol does not alter the glucose homeostasis in people with glucose intolerance. |
format | Online Article Text |
id | pubmed-4995183 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-49951832016-08-24 Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance Shin, Dong Hee Lee, Ji Hye Kang, Myung Shin Kim, Tae Hoon Jeong, Su Jin Kim, Chong Hwa Kim, Sang Soo Kim, In Joo Diabetes Metab J Original Article BACKGROUND: Rebaudioside A and erythritol are nonnutritive sweeteners. There have been several studies of their glycemic effects, but the outcomes remain controversial. The purpose of this study was to evaluate the glycemic effects of rebaudioside A and erythritol as a sweetener in people with glucose intolerance. METHODS: This trial evaluated the glycemic effect after 2 weeks of consumption of rebaudioside A and erythritol as sweeteners in a pre-diabetic population. The patients were evaluated for fructosamine, fasting plasma glucose, C-peptide, insulin, and 2-hour plasma glucose before and after consumption of sweetener. The primary outcome was a change in fructosamine levels from the baseline to the end of treatment. Secondary outcomes were the changes in levels of fasting plasma glucose and 2-hour plasma glucose. RESULTS: From the baseline to the end of experiment, the changes in fructosamine levels after consumption of rebaudioside A and erythritol, did not differ significantly (244.00±19.57 vs. 241.68±23.39 µmol/L, P=0.366). The change in levels from the baseline to end of the study for rebaudioside A and erythritol were fasting plasma glucose (102.56±10.72 vs. 101.32±9.20 mg/dL), 2-hour plasma glucose (154.92±54.53 vs. 141.92±42.22 mg/dL), insulin (7.56±4.29 vs. 7.20±5.12 IU/mL), and C-peptide (2.92±1.61 vs. 2.73±1.31 ng/mL), respectively, and also did not differ significantly (P>0.05 for all). CONCLUSION: Our study suggests that consumption of rebaudioside A and erythritol does not alter the glucose homeostasis in people with glucose intolerance. Korean Diabetes Association 2016-08 2016-06-15 /pmc/articles/PMC4995183/ /pubmed/27352150 http://dx.doi.org/10.4093/dmj.2016.40.4.283 Text en Copyright © 2016 Korean Diabetes Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Shin, Dong Hee Lee, Ji Hye Kang, Myung Shin Kim, Tae Hoon Jeong, Su Jin Kim, Chong Hwa Kim, Sang Soo Kim, In Joo Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance |
title | Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance |
title_full | Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance |
title_fullStr | Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance |
title_full_unstemmed | Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance |
title_short | Glycemic Effects of Rebaudioside A and Erythritol in People with Glucose Intolerance |
title_sort | glycemic effects of rebaudioside a and erythritol in people with glucose intolerance |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995183/ https://www.ncbi.nlm.nih.gov/pubmed/27352150 http://dx.doi.org/10.4093/dmj.2016.40.4.283 |
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