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Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia
BACKGROUND: Glycogen storage disease type Ia (GSD Ia) is an autosomal recessive disorder caused by deficiency of glucose-6-phosphatase (G6Pase), resulting in fasting hypoglycemia. Dietary treatment with provision of uncooked cornstarch (UCCS) or a novel modified cornstarch (Glycosade®) is available...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109185/ https://www.ncbi.nlm.nih.gov/pubmed/35585965 http://dx.doi.org/10.1016/j.ymgmr.2022.100880 |
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author | Turki, Abrar Stockler, Sylvia Sirrs, Sandra Salvarinova, Ramona Ho, Gloria Branov, Jennifer Rosen-Heath, Annie Bosdet, Taryn Elango, Rajavel |
author_facet | Turki, Abrar Stockler, Sylvia Sirrs, Sandra Salvarinova, Ramona Ho, Gloria Branov, Jennifer Rosen-Heath, Annie Bosdet, Taryn Elango, Rajavel |
author_sort | Turki, Abrar |
collection | PubMed |
description | BACKGROUND: Glycogen storage disease type Ia (GSD Ia) is an autosomal recessive disorder caused by deficiency of glucose-6-phosphatase (G6Pase), resulting in fasting hypoglycemia. Dietary treatment with provision of uncooked cornstarch (UCCS) or a novel modified cornstarch (Glycosade®) is available to treat hypoglycemia, yet choice of carbohydrate to achieve a desirable glycemic control is debated.(13)C-glucose breath test ((13)C-GBT) can be used to examine glucose metabolism from different carbohydrate sources via (13)CO(2) in breath. OBJECTIVES: Our objectives were: 1) establishing the use of a minimally invasive (13)C-GBT to examine in vivo glucose metabolism in healthy adults, and 2) using (13)C-GBT to measure utilization of the standard UCCS vs. Glycosade® in GSD Ia and healthy controls. DESIGN: Experiment 1- Ten healthy adults (6F: 4 M, 22-33y) underwent (13)C-GBT protocol twice as a proof-of-principle, once with oral isotope dose (glucose 75 g + [U-(13)C(6)] d-glucose 75 mg) and once without isotope (only glucose 75 g) to test sensitivity of natural (13)C-enrichment. Breath samples were collected at baseline and every 20 min for 240 min. Rate of CO(2) production was measured at 120 min using indirect calorimetry. Finger-prick blood glucose was measured using a glucometer hourly to test hypoglycemia (glucose <4 mmol/L). Experiment 2- Three GSD Ia (12y, 13y, and 28y) and six healthy controls (2F: 4 M, 10-32y) underwent (13)C-GBT protocol twice: with UCCS or Glycosade® (based on their current prescribed dose 42-100 g) after ~4 h fast based on our GSD Ia patients with fasting tolerance. RESULTS: Findings 1- Maximum (13)C-enrichments occurred at 200 min without and with [U-(13)C(6)] d-glucose in all healthy adults, suggesting natural enrichment is sensitive for the (13)C-GBT. Findings 2-Glycosade® utilization was lower than UCCS utilization in 12y and 13y GSD Ia, but was similar in the 28y GSD Ia. CONCLUSIONS: (13)C-GBT is a novel minimally invasive functional test to examine glucose metabolism in GSD Ia, and test new products like Glycosade®, which has the potential to improve nutritional management and individualized carbohydrate supply in GSD. |
format | Online Article Text |
id | pubmed-9109185 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-91091852022-05-17 Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia Turki, Abrar Stockler, Sylvia Sirrs, Sandra Salvarinova, Ramona Ho, Gloria Branov, Jennifer Rosen-Heath, Annie Bosdet, Taryn Elango, Rajavel Mol Genet Metab Rep Research Paper BACKGROUND: Glycogen storage disease type Ia (GSD Ia) is an autosomal recessive disorder caused by deficiency of glucose-6-phosphatase (G6Pase), resulting in fasting hypoglycemia. Dietary treatment with provision of uncooked cornstarch (UCCS) or a novel modified cornstarch (Glycosade®) is available to treat hypoglycemia, yet choice of carbohydrate to achieve a desirable glycemic control is debated.(13)C-glucose breath test ((13)C-GBT) can be used to examine glucose metabolism from different carbohydrate sources via (13)CO(2) in breath. OBJECTIVES: Our objectives were: 1) establishing the use of a minimally invasive (13)C-GBT to examine in vivo glucose metabolism in healthy adults, and 2) using (13)C-GBT to measure utilization of the standard UCCS vs. Glycosade® in GSD Ia and healthy controls. DESIGN: Experiment 1- Ten healthy adults (6F: 4 M, 22-33y) underwent (13)C-GBT protocol twice as a proof-of-principle, once with oral isotope dose (glucose 75 g + [U-(13)C(6)] d-glucose 75 mg) and once without isotope (only glucose 75 g) to test sensitivity of natural (13)C-enrichment. Breath samples were collected at baseline and every 20 min for 240 min. Rate of CO(2) production was measured at 120 min using indirect calorimetry. Finger-prick blood glucose was measured using a glucometer hourly to test hypoglycemia (glucose <4 mmol/L). Experiment 2- Three GSD Ia (12y, 13y, and 28y) and six healthy controls (2F: 4 M, 10-32y) underwent (13)C-GBT protocol twice: with UCCS or Glycosade® (based on their current prescribed dose 42-100 g) after ~4 h fast based on our GSD Ia patients with fasting tolerance. RESULTS: Findings 1- Maximum (13)C-enrichments occurred at 200 min without and with [U-(13)C(6)] d-glucose in all healthy adults, suggesting natural enrichment is sensitive for the (13)C-GBT. Findings 2-Glycosade® utilization was lower than UCCS utilization in 12y and 13y GSD Ia, but was similar in the 28y GSD Ia. CONCLUSIONS: (13)C-GBT is a novel minimally invasive functional test to examine glucose metabolism in GSD Ia, and test new products like Glycosade®, which has the potential to improve nutritional management and individualized carbohydrate supply in GSD. Elsevier 2022-05-11 /pmc/articles/PMC9109185/ /pubmed/35585965 http://dx.doi.org/10.1016/j.ymgmr.2022.100880 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Turki, Abrar Stockler, Sylvia Sirrs, Sandra Salvarinova, Ramona Ho, Gloria Branov, Jennifer Rosen-Heath, Annie Bosdet, Taryn Elango, Rajavel Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia |
title | Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia |
title_full | Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia |
title_fullStr | Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia |
title_full_unstemmed | Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia |
title_short | Development of minimally invasive (13)C-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type Ia |
title_sort | development of minimally invasive (13)c-glucose breath test to examine different exogenous carbohydrate sources in patients with glycogen storage disease type ia |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109185/ https://www.ncbi.nlm.nih.gov/pubmed/35585965 http://dx.doi.org/10.1016/j.ymgmr.2022.100880 |
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