A Randomized Controlled, Double-Masked, Crossover Study of a GPR119 Agonist on Glucagon Counterregulation During Hypoglycemia in Type 1 Diabetes

Hypoglycemia is the limiting factor for optimal glycemic control in people with type 1 diabetes (T1D). Activation of α-cell GPR119 receptors increases glucagon counterregulatory responses to hypoglycemia in preclinical studies. We assessed the effect of MBX-2982, a GPR119 agonist, on glucagon counterregulatory responses to experimental hypoglycemia in participants with T1D. Activation of GPR119 with MBX-2982 did not improve glucagon counterregulatory responses to hypoglycemia in participants with T1D, though increases in fasting glucagon-like peptide 1 and responses during a mixed-meal test demonstrated appropriate target engagement. GPR119 agonists are unlikely to be effective agents to mitigate hypoglycemia risk in people with T1D.

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Publication Details

Journal
Diabetes
Published
2025-04-02
DOI
https://doi.org/10.2337/db25-0096
Citations
6
Primary Topic
Diabetes Treatment and Management
Type
article
Field-Weighted Citation Impact
7.77
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article

A Randomized Controlled, Double-Masked, Crossover Study of a GPR119 Agonist on Glucagon Counterregulation During Hypoglycemia in Type 1 Diabetes

Martin Chase Marak, David Kelley, Anna Casu, Marcus Hompesch et al.
6 citations
Diabetes
Diabetes Treatment and Management
7.77
article

A Randomized Controlled, Double-Masked, Crossover Study of a GPR119 Agonist on Glucagon Counterregulation During Hypoglycemia in Type 1 Diabetes

Martin Chase Marak, David Kelley, Anna Casu, Marcus Hompesch, Richard E. Pratley, Justine M. Mucinski, Tumpa Dutta, Gina Mercouffer, Fanchao Yi, Anika Bilal
article en
6 citations

Abstract

Hypoglycemia is the limiting factor for optimal glycemic control in people with type 1 diabetes (T1D). Activation of α-cell GPR119 receptors increases glucagon counterregulatory responses to hypoglycemia in preclinical studies. We assessed the effect of MBX-2982, a GPR119 agonist, on glucagon counterregulatory responses to experimental hypoglycemia in participants with T1D. Activation of GPR119 with MBX-2982 did not improve glucagon counterregulatory responses to hypoglycemia in participants with T1D, though increases in fasting glucagon-like peptide 1 and responses during a mixed-meal test demonstrated appropriate target engagement. GPR119 agonists are unlikely to be effective agents to mitigate hypoglycemia risk in people with T1D.

DiabetesVol. 74(7)
Merck & Co., Inc., Rahway, NJ, USA (United States) (US), Building Engineering and Science Talent (US), Translational Research Institute for Metabolism and Diabetes (US), Jaeb Center for Health Research (US)
Good health and well-being
Openalex Percentile: Top 3%
Diabetes Treatment and Management
7.77
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