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Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting
The Aspergillus niger-derived prolyl endoprotease (AN-PEP) has previously been shown to degrade gluten in healthy subjects when added to an intragastrically infused meal. The current study investigated the efficacy of AN-PEP in a physiological meal setting. In this randomized placebo-controlled cros...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638938/ https://www.ncbi.nlm.nih.gov/pubmed/29026170 http://dx.doi.org/10.1038/s41598-017-13587-7 |
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author | König, Julia Holster, Savanne Bruins, Maaike J. Brummer, Robert J. |
author_facet | König, Julia Holster, Savanne Bruins, Maaike J. Brummer, Robert J. |
author_sort | König, Julia |
collection | PubMed |
description | The Aspergillus niger-derived prolyl endoprotease (AN-PEP) has previously been shown to degrade gluten in healthy subjects when added to an intragastrically infused meal. The current study investigated the efficacy of AN-PEP in a physiological meal setting. In this randomized placebo-controlled crossover study, 18 gluten-sensitive subjects consumed a porridge containing 0.5 g gluten together with two tablets either containing a high or low dose of AN-PEP, or placebo. Gastric and duodenal content was sampled over 180 minutes, and areas under the curve of gluten concentrations were calculated. The primary outcome, i.e. success rate of high dose AN-PEP defined as at least 50% gluten degradation compared to placebo in the duodenum, was achieved in 10 of 13 comparisons. In the stomach, gluten levels were reduced from 176.9 (median, interquartile range 73.5–357.8) to 22.0 (10.6–50.8, p = 0.001) in the high dose and to 25.4 μg × min/ml (16.4–43.7, p = 0.001) in the low dose. In the duodenum, gluten levels were reduced from 14.1 (8.3–124.7) in the placebo to 6.3 (3.5–19.8, p = 0.019) in the high dose and to 7.4 μg × min/ml in the low dose (3.8–12.0, p = 0.015). Thus even in a physiological meal setting, AN-PEP significantly degraded most gluten in the stomach before it entered the duodenum. |
format | Online Article Text |
id | pubmed-5638938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56389382017-10-18 Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting König, Julia Holster, Savanne Bruins, Maaike J. Brummer, Robert J. Sci Rep Article The Aspergillus niger-derived prolyl endoprotease (AN-PEP) has previously been shown to degrade gluten in healthy subjects when added to an intragastrically infused meal. The current study investigated the efficacy of AN-PEP in a physiological meal setting. In this randomized placebo-controlled crossover study, 18 gluten-sensitive subjects consumed a porridge containing 0.5 g gluten together with two tablets either containing a high or low dose of AN-PEP, or placebo. Gastric and duodenal content was sampled over 180 minutes, and areas under the curve of gluten concentrations were calculated. The primary outcome, i.e. success rate of high dose AN-PEP defined as at least 50% gluten degradation compared to placebo in the duodenum, was achieved in 10 of 13 comparisons. In the stomach, gluten levels were reduced from 176.9 (median, interquartile range 73.5–357.8) to 22.0 (10.6–50.8, p = 0.001) in the high dose and to 25.4 μg × min/ml (16.4–43.7, p = 0.001) in the low dose. In the duodenum, gluten levels were reduced from 14.1 (8.3–124.7) in the placebo to 6.3 (3.5–19.8, p = 0.019) in the high dose and to 7.4 μg × min/ml in the low dose (3.8–12.0, p = 0.015). Thus even in a physiological meal setting, AN-PEP significantly degraded most gluten in the stomach before it entered the duodenum. Nature Publishing Group UK 2017-10-12 /pmc/articles/PMC5638938/ /pubmed/29026170 http://dx.doi.org/10.1038/s41598-017-13587-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article König, Julia Holster, Savanne Bruins, Maaike J. Brummer, Robert J. Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting |
title | Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting |
title_full | Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting |
title_fullStr | Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting |
title_full_unstemmed | Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting |
title_short | Randomized clinical trial: Effective gluten degradation by Aspergillus niger-derived enzyme in a complex meal setting |
title_sort | randomized clinical trial: effective gluten degradation by aspergillus niger-derived enzyme in a complex meal setting |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5638938/ https://www.ncbi.nlm.nih.gov/pubmed/29026170 http://dx.doi.org/10.1038/s41598-017-13587-7 |
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