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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...

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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
Descripción
Sumario: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.