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Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease
The gluten free diet (GFD) has a high glycemic index and low-fiber content, which potentially influences glycemic excursions in type 1 diabetes (T1D) and celiac disease (CD). Participants in this case-control study of youth with T1D+CD (n = 10) and T1D only (n = 7) wore blinded continuous glucose mo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364400/ https://www.ncbi.nlm.nih.gov/pubmed/28338063 http://dx.doi.org/10.1038/srep45286 |
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author | Pham-Short, Anna Donaghue, Kim C Ambler, Geoffrey Garnett, Sarah Craig, Maria E. |
author_facet | Pham-Short, Anna Donaghue, Kim C Ambler, Geoffrey Garnett, Sarah Craig, Maria E. |
author_sort | Pham-Short, Anna |
collection | PubMed |
description | The gluten free diet (GFD) has a high glycemic index and low-fiber content, which potentially influences glycemic excursions in type 1 diabetes (T1D) and celiac disease (CD). Participants in this case-control study of youth with T1D+CD (n = 10) and T1D only (n = 7) wore blinded continuous glucose monitoring systems for six days. Blood glucose levels (BGLs) were compared between groups for each meal, including pre-meal, peak, 2-hour postprandial and time-to-peak. Participants consumed a test-breakfast of GF cereal and milk for three days and kept weighed food diaries; nutrient intake was analyzed and compared to national recommendations. Youth with T1D+CD had shorter time-to-peak BGL (77 vs 89 mins, P = 0.03), higher peak (9.3 vs 7.3 mmol/L, P = 0.001) and higher postprandial BGLs than T1D (8.4 vs 7.0 mmol/L, P = 0.01), despite similar pre-meal BGLs (9.2 vs 8.6 mmol/L, P = 0.28). Regarding test breakfast, greater pre and post-meal BGL difference correlated with longer CD duration (R = 0.53, P = 0.01). Total energy and macronutrient intake didn’t differ between groups; however the majority of participants collectively had inadequate intake of calcium (76%), folate (71%) and fiber (53%), with excessive saturated fat (12%) and sodium (>2,000 mg/day). The GFD is associated with greater glycemic excursions and inadequate nutritional intake in youth with T1D+CD. Clinical management should address both glycemic variability and dietary quality. |
format | Online Article Text |
id | pubmed-5364400 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53644002017-03-24 Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease Pham-Short, Anna Donaghue, Kim C Ambler, Geoffrey Garnett, Sarah Craig, Maria E. Sci Rep Article The gluten free diet (GFD) has a high glycemic index and low-fiber content, which potentially influences glycemic excursions in type 1 diabetes (T1D) and celiac disease (CD). Participants in this case-control study of youth with T1D+CD (n = 10) and T1D only (n = 7) wore blinded continuous glucose monitoring systems for six days. Blood glucose levels (BGLs) were compared between groups for each meal, including pre-meal, peak, 2-hour postprandial and time-to-peak. Participants consumed a test-breakfast of GF cereal and milk for three days and kept weighed food diaries; nutrient intake was analyzed and compared to national recommendations. Youth with T1D+CD had shorter time-to-peak BGL (77 vs 89 mins, P = 0.03), higher peak (9.3 vs 7.3 mmol/L, P = 0.001) and higher postprandial BGLs than T1D (8.4 vs 7.0 mmol/L, P = 0.01), despite similar pre-meal BGLs (9.2 vs 8.6 mmol/L, P = 0.28). Regarding test breakfast, greater pre and post-meal BGL difference correlated with longer CD duration (R = 0.53, P = 0.01). Total energy and macronutrient intake didn’t differ between groups; however the majority of participants collectively had inadequate intake of calcium (76%), folate (71%) and fiber (53%), with excessive saturated fat (12%) and sodium (>2,000 mg/day). The GFD is associated with greater glycemic excursions and inadequate nutritional intake in youth with T1D+CD. Clinical management should address both glycemic variability and dietary quality. Nature Publishing Group 2017-03-24 /pmc/articles/PMC5364400/ /pubmed/28338063 http://dx.doi.org/10.1038/srep45286 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pham-Short, Anna Donaghue, Kim C Ambler, Geoffrey Garnett, Sarah Craig, Maria E. Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease |
title | Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease |
title_full | Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease |
title_fullStr | Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease |
title_full_unstemmed | Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease |
title_short | Greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease |
title_sort | greater postprandial glucose excursions and inadequate nutrient intake in youth with type 1 diabetes and celiac disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364400/ https://www.ncbi.nlm.nih.gov/pubmed/28338063 http://dx.doi.org/10.1038/srep45286 |
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