Cargando…

Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial

INTRODUCTION: Increasing the frequency of blood glucose monitoring aids the evaluation of glycemic variability and blood glucose control by antidiabetic drugs. It remains unclear, however, whether GLP-1 receptor agonists or basal insulin has a better effect on glycemic variability in type 2 diabetes...

Descripción completa

Detalles Bibliográficos
Autores principales: Yin, Ting-Ting, Bi, Yan, Li, Ping, Shen, Shan-Mei, Xiong, Xiao-Lu, Gao, Li-Jun, Jiang, Can, Wang, Yan, Feng, Wen-Huan, Zhu, Da-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984915/
https://www.ncbi.nlm.nih.gov/pubmed/29744819
http://dx.doi.org/10.1007/s13300-018-0412-6
_version_ 1783328678393937920
author Yin, Ting-Ting
Bi, Yan
Li, Ping
Shen, Shan-Mei
Xiong, Xiao-Lu
Gao, Li-Jun
Jiang, Can
Wang, Yan
Feng, Wen-Huan
Zhu, Da-Long
author_facet Yin, Ting-Ting
Bi, Yan
Li, Ping
Shen, Shan-Mei
Xiong, Xiao-Lu
Gao, Li-Jun
Jiang, Can
Wang, Yan
Feng, Wen-Huan
Zhu, Da-Long
author_sort Yin, Ting-Ting
collection PubMed
description INTRODUCTION: Increasing the frequency of blood glucose monitoring aids the evaluation of glycemic variability and blood glucose control by antidiabetic drugs. It remains unclear, however, whether GLP-1 receptor agonists or basal insulin has a better effect on glycemic variability in type 2 diabetes mellitus (T2DM) patients who are inadequately controlled by metformin. We used a continuous glucose monitoring system (CGMS) to compare patients on a GLP-1 receptor agonist with patients on basal insulin in terms of glycemic variability. METHODS: This prospective randomized study assigned T2DM patients treated with metformin (N = 39) to either exenatide treatment or insulin glargine treatment for 16 weeks. Glycemic variability was assessed using a CGMS; hemoglobin A1c (HbA1c), β-cell function, weight, body mass index (BMI), and waist circumference were also evaluated. RESULTS: Mean blood glucose level, continuous overlapping net glycemic action, mean amplitude of glycemic excursions, percentage of the time that the blood glucose value was > 10.0 mmol/L, and highest blood glucose level (P  < 0.01–0.05) significantly decreased in both groups. Standard deviation of the mean glucose value, largest amplitude of glycemic excursions, and waist circumference significantly decreased for those treated with exenatide (P  < 0.05), while no changes were observed with insulin glargine treatment. Percentage of the time that the blood glucose value was > 7.8 mmol/L decreased after insulin glargine use (P  < 0.05) but not with the exenatide intervention. Similar decreases in fasting blood glucose and HbA1c and increases in the 1/homeostasis model assessment of insulin resistance, disposition index 30, and disposition index 120 were observed in both groups (P  < 0.01–0.05). Reductions in weight and BMI were greater with exenatide than with insulin glargine treatment (P  < 0.05). CONCLUSIONS: In overweight and obese patients with T2DM inadequately controlled by metformin, exenatide and insulin glargine have similar efficacies in terms of glycemic variability, HbA1c alleviation, and β-cell function, but exenatide has a greater effect on body weight and BMI.
format Online
Article
Text
id pubmed-5984915
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Springer Healthcare
record_format MEDLINE/PubMed
spelling pubmed-59849152018-06-13 Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial Yin, Ting-Ting Bi, Yan Li, Ping Shen, Shan-Mei Xiong, Xiao-Lu Gao, Li-Jun Jiang, Can Wang, Yan Feng, Wen-Huan Zhu, Da-Long Diabetes Ther Original Research INTRODUCTION: Increasing the frequency of blood glucose monitoring aids the evaluation of glycemic variability and blood glucose control by antidiabetic drugs. It remains unclear, however, whether GLP-1 receptor agonists or basal insulin has a better effect on glycemic variability in type 2 diabetes mellitus (T2DM) patients who are inadequately controlled by metformin. We used a continuous glucose monitoring system (CGMS) to compare patients on a GLP-1 receptor agonist with patients on basal insulin in terms of glycemic variability. METHODS: This prospective randomized study assigned T2DM patients treated with metformin (N = 39) to either exenatide treatment or insulin glargine treatment for 16 weeks. Glycemic variability was assessed using a CGMS; hemoglobin A1c (HbA1c), β-cell function, weight, body mass index (BMI), and waist circumference were also evaluated. RESULTS: Mean blood glucose level, continuous overlapping net glycemic action, mean amplitude of glycemic excursions, percentage of the time that the blood glucose value was > 10.0 mmol/L, and highest blood glucose level (P  < 0.01–0.05) significantly decreased in both groups. Standard deviation of the mean glucose value, largest amplitude of glycemic excursions, and waist circumference significantly decreased for those treated with exenatide (P  < 0.05), while no changes were observed with insulin glargine treatment. Percentage of the time that the blood glucose value was > 7.8 mmol/L decreased after insulin glargine use (P  < 0.05) but not with the exenatide intervention. Similar decreases in fasting blood glucose and HbA1c and increases in the 1/homeostasis model assessment of insulin resistance, disposition index 30, and disposition index 120 were observed in both groups (P  < 0.01–0.05). Reductions in weight and BMI were greater with exenatide than with insulin glargine treatment (P  < 0.05). CONCLUSIONS: In overweight and obese patients with T2DM inadequately controlled by metformin, exenatide and insulin glargine have similar efficacies in terms of glycemic variability, HbA1c alleviation, and β-cell function, but exenatide has a greater effect on body weight and BMI. Springer Healthcare 2018-05-09 2018-06 /pmc/articles/PMC5984915/ /pubmed/29744819 http://dx.doi.org/10.1007/s13300-018-0412-6 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research
Yin, Ting-Ting
Bi, Yan
Li, Ping
Shen, Shan-Mei
Xiong, Xiao-Lu
Gao, Li-Jun
Jiang, Can
Wang, Yan
Feng, Wen-Huan
Zhu, Da-Long
Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial
title Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial
title_full Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial
title_fullStr Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial
title_full_unstemmed Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial
title_short Comparison of Glycemic Variability in Chinese T2DM Patients Treated with Exenatide or Insulin Glargine: A Randomized Controlled Trial
title_sort comparison of glycemic variability in chinese t2dm patients treated with exenatide or insulin glargine: a randomized controlled trial
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5984915/
https://www.ncbi.nlm.nih.gov/pubmed/29744819
http://dx.doi.org/10.1007/s13300-018-0412-6
work_keys_str_mv AT yintingting comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT biyan comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT liping comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT shenshanmei comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT xiongxiaolu comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT gaolijun comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT jiangcan comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT wangyan comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT fengwenhuan comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial
AT zhudalong comparisonofglycemicvariabilityinchineset2dmpatientstreatedwithexenatideorinsulinglarginearandomizedcontrolledtrial