ID | 115897 |
Author |
Danne, Thomas
Hannover Medical School
Matsuhisa, Munehide
Tokushima University
Tokushima University Educator and Researcher Directory
KAKEN Search Researchers
Sussebach, Christian
Sanofi
Goyeau, Harmonie
Sanofi
Lauand, Felipe
Sanofi
Niemoeller, Elisabeth
Sanofi
Bolli, Geremia B.
Perugia University
|
Keywords | basal insulin
glycaemic control
hypoglycaemia
insulin analogues
meta-analysis
type 1 diabetes
|
Content Type |
Journal Article
|
Description | Severe hypoglycaemia (SH) remains a challenge to people with type 1 diabetes (T1DM), and new‐generation basal insulins may improve patient outcomes. This post hoc meta‐analysis explored the risk of SH with insulin glargine 300 U/mL (Gla‐300) versus glargine 100 U/mL (Gla‐100) in a pooled population with T1DM from three randomized, multicentre, 6‐month similarly designed phase 3 trials: EDITION 4, EDITION JP 1 and EDITION JUNIOR. Endpoints included incidence and time to first occurrence of SH. Among 629 and 626 participants randomized to Gla‐300 and Gla‐100, respectively, glycated haemoglobin reductions were similar. Fewer participants experienced ≥1 SH event with Gla‐300 (6.2%) than with Gla‐100 (9.3%). From baseline to month 6, the risk of a first SH event was lower with Gla‐300: hazard ratio 0.65 [95% confidence interval (CI) 0.44–0.98; stratified log‐rank test P = 0.038]. SH event rates were numerically lower with Gla‐300 versus Gla‐100 from baseline to month 6 [relative risk (RR) 0.80 (95% CI 0.49–1.29); P = 0.356] and baseline to week 8 [RR 0.73 (95% CI 0.37–1.44); P = 0.369]. Thus, Gla‐300 demonstrated similar glycaemic control with lower risk of SH versus Gla‐100, particularly during the titration period.
|
Journal Title |
Diabetes, Obesity and Metabolism: A Journal of Pharmacology and Therapeutics
|
ISSN | 14631326
|
NCID | AA11435496
|
Publisher | John Wiley & Sons
|
Volume | 22
|
Issue | 10
|
Start Page | 1880
|
End Page | 1885
|
Published Date | 2020-06-09
|
Rights | This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License(https://creativecommons.org/licenses/by-nc/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
|
EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
|
TextVersion |
Publisher
|
departments |
Institute of Advanced Medical Sciences
|