Abstract

Introduction

Patients aged ≥ 65 years continue to be underrepresented in clinical studies related to type 2 diabetes mellitus (T2DM). Accordingly, the REALI pooled analysis was performed to evaluate the effectiveness and safety of insulin glargine 300 U/mL (Gla-300) across different age subgroups, using data from 14 interventional and non-interventional studies.

Methods

Pooled efficacy and safety data were collected from 8106 European patients with uncontrolled T2DM who were initiated on or switched to Gla-300 injected once daily for 24 weeks. Patients were categorised into five age subgroups: < 50 (N = 727), 50–59 (N = 2030), 60–69 (N = 3054), 70–79 (N = 1847) and ≥ 80 years (N = 448).

Results

Mean baseline haemoglobin A1c (HbA1c) decreased linearly from the youngest (9.10%) to the oldest (8.46%) age subgroup. Following Gla-300 initiation, there were similar HbA1c reductions across age groups, with a least squares mean (95% confidence interval) change in HbA1c from baseline to week 24 of − 1.09% (− 1.18 to − 1.00), − 1.08% (− 1.14 to − 1.03), − 1.12% (− 1.17 to − 1.07), − 1.18% (− 1.24 to − 1.12) and − 1.11% (− 1.23 to − 0.99) in the < 50, 50–59, 60–69, 70–79 and ≥ 80 years subgroups, respectively. The incidences and event rates of reported hypoglycaemia were overall low. Compared to younger age subgroups, lower incidences of symptomatic hypoglycaemia occurring at any time of the day (5.9 vs. 7.6–9.4% for the younger subgroups) or during the night (0.5 vs. 1.6–2.5%) were recorded in patients aged ≥ 80 years. By contrast, the highest incidence of severe hypoglycaemia occurring any time of the day was reported in the subgroup aged ≥ 80 years (1.1 vs. 0.1–0.6% for the younger age subgroups).

Conclusion

Gla-300 initiated in patients with uncontrolled T2DM provides glycaemic improvement with a favourable safety profile across a wide range of ages.

Details

Title
Impact of Age on the Effectiveness and Safety of Insulin Glargine 300 U/mL: Results from the REALI European Pooled Data Analysis
Author
Bonadonna, Riccardo C 1 ; Didac, Mauricio 2 ; Müller-Wieland, Dirk 3 ; Freemantle Nick 4 ; Bigot, Gregory 5 ; Mauquoi Celine 6 ; Ciocca, Alice 7 ; Bonnemaire Mireille 7 ; Gourdy Pierre 8 

 Azienda Ospedaliero–Universitaria di Parma, Parma, Italy (GRID:grid.411482.a); University of Parma, Department of Medicine and Surgery, Parma, Italy (GRID:grid.10383.39) (ISNI:0000 0004 1758 0937) 
 CIBERDEM, Institut de Recerca Hospital de la Santa Creu i Sant Pau, Department of Endocrinology and Nutrition, Barcelona, Spain (GRID:grid.413396.a) (ISNI:0000 0004 1768 8905) 
 University Hospital Aachen, Department of Medicine I, Aachen, Germany (GRID:grid.412301.5) (ISNI:0000 0000 8653 1507) 
 University College London, Institute of Clinical Trials and Methodology, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201) 
 IVIDATA Group, Paris, France (GRID:grid.83440.3b) 
 International Drug Development Institute (IDDI), Louvain-la-Neuve, Belgium (GRID:grid.482598.a) 
 General Medicines, Sanofi, Paris, France (GRID:grid.417924.d) 
 Toulouse University Hospital, Endocrinology, Diabetology and Nutrition Department, Toulouse, France (GRID:grid.411175.7) (ISNI:0000 0001 1457 2980); Toulouse University, Institute of Metabolic and Cardiovascular Diseases, UMR1048 INSERM/UPS, Toulouse, France (GRID:grid.508721.9) 
Pages
1073-1097
Publication year
2021
Publication date
Apr 2021
Publisher
Springer Nature B.V.
ISSN
18696953
e-ISSN
18696961
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2512387715
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.