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Association between 1,5-Anhydroglucitol and Acute C Peptide Response to Arginine among Patients with Type 2 Diabetes.

Authors :
Shen Y
Si Y
Lu J
Ma X
Zhang L
Mo Y
Lu W
Zhu W
Bao Y
Hu G
Zhou J
Source :
Journal of diabetes research [J Diabetes Res] 2020 Jul 21; Vol. 2020, pp. 4243053. Date of Electronic Publication: 2020 Jul 21 (Print Publication: 2020).
Publication Year :
2020

Abstract

Objective: The aim of this study was to explore the association of 1,5-anhydroglucitol with acute C peptide response (ACPR) to arginine among patients with type 2 diabetes.<br />Methods: Patients with type 2 diabetes were enrolled from the Department of Endocrinology and Metabolism, Shanghai Sixth People's Hospital. ACPR was assessed using arginine stimulation test. Decreased β -cell function was defined as ACPR < 2.1. Multivariable logistic regression models were used to demonstrate the association between 1,5-anhydroglucitol and decreased β -cell function.<br />Results: Finally, 623 patients with type 2 diabetes were enrolled into the analysis. Multivariable-adjusted odds ratios for decreased β -cell function across quartiles of 1,5-anhydroglucitol were 1.00, 0.47 (95% confidence interval (CI) 0.23-0.99), 0.41 (95% CI 0.20-0.84), and 0.27 (95% CI 0.13-0.57) ( P <subscript>trend</subscript> = 0.042), respectively. When 1,5-anhydroglucitol was considered as a continuous variable after logarithm, the corresponding odds ratio was 0.40 (95% CI 0.23-0.71).<br />Conclusions: We demonstrated a dose-response linear association between 1,5-anhydroglucitol and ACPR. 1,5-Anhydroglucitol was likely to be associated with β -cell function. Further analysis with large sample size and prospective study design is warranted to validate our findings.<br />Competing Interests: The authors declare that they have no conflicts of interest.<br /> (Copyright © 2020 Yun Shen et al.)

Details

Language :
English
ISSN :
2314-6753
Volume :
2020
Database :
MEDLINE
Journal :
Journal of diabetes research
Publication Type :
Academic Journal
Accession number :
32775460
Full Text :
https://doi.org/10.1155/2020/4243053