University of Leicester
Browse

The Diabetes Unmet Need with Basal Insulin Evaluation (DUNE) study in type 2 diabetes: Achieving HbA1c targets with basal insulin in a real-world setting.

Download (588.44 kB)
journal contribution
posted on 2019-06-24, 11:00 authored by LF Meneghini, D Mauricio, E Orsi, NM Lalic, AMG Cali, J Westerbacka, P Stella, C Candelas Dea, V Pilorget, R Perfetti, K Khunti, DUNE investigators
AIMS: To describe in a real-world setting the achievement of physician-selected individualized HbA1c targets in individuals with type 2 diabetes, newly or recently initiated with basal insulin, and the association of hypoglycaemia with target achievement. MATERIALS AND METHODS: A 12-week, prospective, single-arm, observational study of adults with type 2 diabetes, either newly initiated with any basal insulin or start on basal insulin within the preceding 12 months. At enrollment, eligible participants from 28 countries were treated with or without oral antihyperglycaemic drugs and/or GLP-1 receptor agonists. RESULTS: Individualized targets for almost all of the 3139 evaluable participants (99.7%) had been set by their physicians, with 57% of participants having HbA1c targets between 7.0% and <7.5% (53 and <58 mmol/mol). By week 12, 28% and 27% of newly and previously initiated participants, respectively, achieved individualized HbA1c targets with modest average increases in daily insulin dose of 9 and 5 U (0.10 and 0.06 U/kg), respectively, from baseline (14 and 23 U [0.17 and 0.29 U/kg], respectively). Overall, 16% of participants experienced at least one episode of hypoglycaemia. Both the incidence and frequency of hypoglycaemia, but not the severity, were positively associated with a higher likelihood of achieving individualized HbA1c targets (P < 0.05). CONCLUSIONS: In this prospective real-world study, most participants using basal insulin did not achieve the individualized HbA1c targets set by their physicians. Participants who experienced symptomatic hypoglycaemia were more likely to achieve HbA1c targets than those who did not.

Funding

This study was sponsored by Sanofi. Sanofi designed and coordinated the clinical trial presented in this manuscript; Sanofi; Health Research K. K. acknowledges support from The National Institute for Health Research (NIHR) Collaboration for Leadership in Applied Health Research and Care—East Midlands (CLAHRC‐EM) and the NIHR Leicester Biomedical Research Centre. Editorial and writing assistance was provided by Arthur Holland, PhD, of Fishawack Communications Ltd and was funded by Sanofi.

History

Citation

Diabetes, Obesity and Metabolism, 2019, 21(6), pp. 1429-1436

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Diabetes Research Centre

Version

  • VoR (Version of Record)

Published in

Diabetes

Publisher

Wiley

eissn

1463-1326

Acceptance date

2019-01-02

Copyright date

2019

Available date

2019-06-24

Publisher version

https://onlinelibrary.wiley.com/doi/full/10.1111/dom.13673

Language

en

Usage metrics

    University of Leicester Publications

    Categories

    No categories selected

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC