Content area

Abstract

Introduction

Despite the widespread use of glucagon-like peptide-1 (GLP-1) receptor agonists (GLP-1ras) to improve glycemic regulation, with a low risk of hypoglycemia and weight reduction, their effectiveness varies among individuals. This study aimed to identify predictors of the efficacy of GLP-1ra on Hemoglobin A1c (HbA1c) in patients with insulin-independent diabetes.

Methods

In total, 58 patients with insulin-independent diabetes were included. Patients were included if their β-cell function was evaluated via a glucagon stimulation test (GST) before the introduction of GLP-1ra therapy. β-Cell function-related indices, such as the C-peptide index (CPI), increments in C-peptide immunoreactivity (CPR) after glucagon stimulation (ΔCPR), and the area under the CPR curve (CPR-AUC) during the GST, were evaluated. HbA1c and body weight (BW) were measured at 6 and 12 months after the initiation of GLP-1ra.

Results

A univariate regression analysis revealed a significant correlation between CPR-AUC and changes in HbA1c at 6 months and with changes in BW at 6 and 12 months. A multivariate regression analysis revealed that CPR-AUC was significantly correlated with changes in HbA1c at 6 months. A receiver-operating characteristic analysis revealed that 21.9 ng/ml·min CPR-AUC was the optimal cut-off value to predict an HbA1c level < 7%, i.e., 53 mmol/mol.

Conclusion

Residual β-cell function, as assessed via CPR-AUC in the GST, is an effective predictor of the efficacy of GLP-1ras.

Details

Title
C-Peptide Area Under the Curve at Glucagon Stimulation Test Predicts Glucose Improvements by GLP-1 Receptor Analogue: A Retrospective Observational Study
Author
Ohbatake, Azusa 1 ; Yagi, Kunimasa 2 ; Karashima, Shigehiro 1 ; Shima, Yuki 1 ; Miyamoto, Yukiko 1 ; Asaka, Hiroyuki 1 ; Okazaki, Satoko 1 ; Kometani, Mitsuhiro 1 ; Kawashiri, Masa-aki 1 ; Takeda, Yoshiyu 1 ; Yoneda, Takashi 3 ; Chujo, Daisuke 4   VIAFID ORCID Logo 

 Kanazawa University Graduate School of Medical Science, Department of Internal Medicine, Kanazawa, Japan (GRID:grid.9707.9) (ISNI:0000 0001 2308 3329) 
 University of Toyama, First Department of Internal Medicine, Toyama, Japan (GRID:grid.267346.2) (ISNI:0000 0001 2171 836X) 
 Kanazawa University Graduate School of Medical Science, Department of Internal Medicine, Kanazawa, Japan (GRID:grid.9707.9) (ISNI:0000 0001 2308 3329); Kanazawa University Graduate School of Medical Science, Department of Health Promotion and Medicine of the Future, Kanazawa, Japan (GRID:grid.9707.9) (ISNI:0000 0001 2308 3329); Kanazawa University, Institute of Liberal Arts and Science, Kanazawa, Japan (GRID:grid.9707.9) (ISNI:0000 0001 2308 3329) 
 Kanazawa University Graduate School of Medical Science, Department of Internal Medicine, Kanazawa, Japan (GRID:grid.9707.9) (ISNI:0000 0001 2308 3329); National Center for Global Health and Medicine, Department of Diabetes, Endocrinology, and Metabolism, Tokyo, Japan (GRID:grid.45203.30) (ISNI:0000 0004 0489 0290) 
Pages
673-681
Publication year
2019
Publication date
Apr 2019
Publisher
Springer Nature B.V.
ISSN
18696953
e-ISSN
18696961
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2512384482
Copyright
Copyright Springer Nature B.V. Apr 2019