Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Turki, Abrar, Stockler, Sylvia, Sirrs, Sandra, Salvarinova, Ramona, Ho, Gloria, Branov, Jennifer, Rosen-Heath, Annie, Bosdet, Taryn, Elango, Rajavel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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
_version_ 1784708852772503552
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
work_keys_str_mv AT turkiabrar developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT stocklersylvia developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT sirrssandra developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT salvarinovaramona developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT hogloria developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT branovjennifer developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT rosenheathannie developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT bosdettaryn developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia
AT elangorajavel developmentofminimallyinvasive13cglucosebreathtesttoexaminedifferentexogenouscarbohydratesourcesinpatientswithglycogenstoragediseasetypeia