Non-severe hypoglycemia in type 1 diabetes: a randomized crossover trial comparing two quantities of oral carbohydrates at different insulin-induced hypoglycemia ranges.


Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2023
Historique:
received: 15 03 2023
accepted: 09 05 2023
medline: 20 6 2023
pubmed: 19 6 2023
entrez: 19 6 2023
Statut: epublish

Résumé

Non-severe hypoglycemia (NS-H) is challenging for people living with type 1 diabetes (PWT1D) and often results from relative iatrogenic hyper-insulinemia. Current guidelines recommend a one-size-fits-all approach of 15-20 g of simple carbohydrates (CHO) every 15 min regardless of the triggering conditions of the NS-H event. We aimed to test different amounts of CHO to treat insulin-induced NS-H at various glucose ranges. This is a randomized, four-way, crossover study involving PWT1D, testing NS-H treatment outcomes with 16 g vs. 32 g CHO at two plasma glucose (PG) ranges: A: 3.0-3.5 mmol/L and B: <3.0 mmol/L. Across all study arms, participants consumed an additional 16 g of CHO if PG was still <3.0 mmol/L at 15 min and <4.0 mmol/L at 45 min post-initial treatment. Subcutaneous insulin was used in a fasting state to induce NS-H. Participants had frequent venous sampling of PG, insulin, and glucagon levels. Participants ( NS-H, in the context of hyper-insulinemia, is difficult to treat in PWT1D. Initial consumption of 32 g of CHO revealed some advantages at the 3.0-3.5 mmol/L range. This was not reproduced at lower PG ranges since participants needed additional CHO regardless of the amount of initial consumption. ClinicalTrials.gov, identifier NCT03489967.

Identifiants

pubmed: 37334295
doi: 10.3389/fendo.2023.1186680
pmc: PMC10272543
doi:

Substances chimiques

Blood Glucose 0
Glucagon 9007-92-5
Hypoglycemic Agents 0
Insulin 0

Banques de données

ClinicalTrials.gov
['NCT03489967']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1186680

Subventions

Organisme : CIHR
ID : 148464
Pays : Canada
Organisme : CIHR
ID : JT1-157204
Pays : Canada

Informations de copyright

Copyright © 2023 Taleb, Gingras, Cheng, Parent, Messier, Bovan, Shohoudi, Brazeau and Rabasa-Lhoret.

Déclaration de conflit d'intérêts

RR-L has received research grants from Astra-Zeneca, Eli Lilly, Merck, Novo-Nordisk, and Sanofi-Aventis. He has been a consultant or member of advisory panels of Abbott, Amgen, Astra-Zeneca, Boehringer, Carlina Technology, Eli Lilly, Janssen, Medtronic, Merck, Neomed, Novo-Nordisk, Roche, Sanofi-Aventis, and Takeda. He has received honoraria for conferences by Abbott, Astra-Zeneca, Eli Lilly, Janssen, Medtronic, Merck, Novo-Nordisk, and Sanofi-Aventis. He has received in kind contributions related to closed-loop technology from Animas, Medtronic, and Roche. He also benefits from unrestricted grants for clinical and educational activities from Eli Lilly, Lifescan, Medtronic, Merck, Novo Nordisk, and Sanofi. He holds intellectual property in the field of type 2 diabetes risk biomarkers, catheter life, and the closed-loop system. RR-L and VM received purchase fees from Eli Lilly in relation with closed-loop technology. NT has received consultant fees from Dexcom, Eli Lilly, and Viatris. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Nadine Taleb (N)

Montreal Clinical Research Institute, Montreal, Canada.
Biomedical Sciences Department, Faculty of Medicine, Université de Montréal, Montreal, Canada.
Endocrinology Division, Centre hospitalier de l'Université de Montréal, Montreal, Canada.

Véronique Gingras (V)

Montreal Clinical Research Institute, Montreal, Canada.
Research Centre, CHU Sainte-Justine, Montreal, Canada.
Department of Nutrition, Faculty of Medicine, Université de Montréal, Montreal, Canada.

Ran Cheng (R)

Montreal Clinical Research Institute, Montreal, Canada.
Endocrinology Division, Centre hospitalier de l'Université de Montréal, Montreal, Canada.

Valérie Parent (V)

Montreal Clinical Research Institute, Montreal, Canada.

Virginie Messier (V)

Montreal Clinical Research Institute, Montreal, Canada.

Danijela Bovan (D)

Montreal Clinical Research Institute, Montreal, Canada.

Azadeh Shohoudi (A)

Montreal Clinical Research Institute, Montreal, Canada.

Anne-Sophie Brazeau (AS)

School of Human Nutrition, McGill University, Montreal, Canada.
Montreal Diabetes Research Center, Montreal, Canada.

Rémi Rabasa-Lhoret (R)

Montreal Clinical Research Institute, Montreal, Canada.
Endocrinology Division, Centre hospitalier de l'Université de Montréal, Montreal, Canada.
Department of Nutrition, Faculty of Medicine, Université de Montréal, Montreal, Canada.
Montreal Diabetes Research Center, Montreal, Canada.

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