Exenatide Twice Daily Plus Glargine Versus Aspart 70/30 Twice Daily in Patients With Type 2 Diabetes With Inadequate Glycemic Control on Premixed Human Insulin and Metformin

Copyright © 2021 AACE. Published by Elsevier Inc. All rights reserved..

OBJECTIVE: Many patients with type 2 diabetes treated with premixed insulin gradually have inadequate glycemic control and switch to a basal-bolus regimen, which raises some concerns for weight gain and increased hypoglycemic risk. Switching to combination use of glp-1 agonist and basal insulin may be an alternative option.

METHODS: After a 12-week premixed human insulin 70/30 dosage optimization period, 200 patients with HbA1c of 7.0% to 10.0% were randomized into 24-week treatment groups with exenatide twice a day plus glargine or with aspart 70/30 twice a day.

RESULTS: After 24 weeks, the patients receiving exenatide plus glargine (n = 90) had improved HbA1c control compared with those receiving aspart 70/30 (n = 90) (least squares mean change: ‒0.59 vs ‒0.13%; difference [95% CI]: ‒0.45 [‒0.74 to ‒0.17]) in the full analysis set population. Weight decreased 3.5 kg with exenatide and decreased 0.4 kg with aspart 70/30 (P < .001). The insulin dose was reduced 10.7 units/day (95% CI, ‒12.2 to ‒9.2 units; P < .001) with exenatide, and increased 9.7 units/day (95% CI, 8.2 to 11.2 units; P < .001) with aspart 70/30. The most common adverse events were gastrointestinal adverse effects in the exenatide group (nausea [21%], vomiting [16%], diarrhea [13%]). The incidence of hypoglycemia was similar in 2 groups (27% for exenatide and 38% for aspart 70/30; P = .1).

CONCLUSION: In premixed human insulin‒treated patients with type 2 diabetes with inadequate glycemic control, switching to exenatide twice a day plus glargine was superior to aspart 70/30 twice a day for glycemic and weight control.

Medienart:

E-Artikel

Erscheinungsjahr:

2021

Erschienen:

2021

Enthalten in:

Zur Gesamtaufnahme - volume:27

Enthalten in:

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists - 27(2021), 8 vom: 15. Aug., Seite 790-797

Sprache:

Englisch

Beteiligte Personen:

Chen, Xi [VerfasserIn]
Xu, Yongping [VerfasserIn]
Zhang, Jianhua [VerfasserIn]
Shao, Shiyin [VerfasserIn]
Duan, Yanran [VerfasserIn]
Liu, Peiwen [VerfasserIn]
Shen, Liya [VerfasserIn]
Zhang, Jing [VerfasserIn]
Zeng, Jiaoe [VerfasserIn]
Lin, Mei [VerfasserIn]
Zhao, Shi [VerfasserIn]
Ma, Jianhua [VerfasserIn]
Zhao, Tao [VerfasserIn]
Hu, Juping [VerfasserIn]
Liao, Yong [VerfasserIn]
Chen, Xiaowen [VerfasserIn]
Hu, Shufang [VerfasserIn]
Xue, Yaoming [VerfasserIn]
Zeng, Zhaoyang [VerfasserIn]
He, Wentao [VerfasserIn]
Liu, Zhelong [VerfasserIn]
Li, Wenjun [VerfasserIn]
Liu, Liegang [VerfasserIn]
Yin, Ping [VerfasserIn]
Yu, Xuefeng [VerfasserIn]

Links:

Volltext

Themen:

2ZM8CX04RZ
9100L32L2N
9P1872D4OL
Aspart 70/30
Blood Glucose
D933668QVX
Exenatide
Glargine
Glp-1 agonist
Glycated Hemoglobin A
Hypoglycemic Agents
Insulin
Insulin Aspart
Insulin Glargine
Journal Article
Metformin
Randomized Controlled Trial
Randomized controlled trial

Anmerkungen:

Date Completed 10.08.2021

Date Revised 07.12.2022

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.eprac.2021.03.015

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM323867170