Effect of delay in treatment intensification in people with type 2 diabetes and suboptimal glycaemia after basal insulin initiation: A real-world observational study.

basal insulin delay in intensification micro- and macrovascular complications suboptimal glycaemia therapeutic inertia type 2 diabetes mellitus

Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
19 Oct 2023
Historique:
revised: 25 09 2023
received: 16 08 2023
accepted: 03 10 2023
medline: 20 10 2023
pubmed: 20 10 2023
entrez: 19 10 2023
Statut: aheadofprint

Résumé

Despite global recommendations for type 2 diabetes mellitus treatment to maintain optimal glycaemic targets, a significant proportion of people remain in suboptimal glycaemic control. Our objective was to investigate the impact of intensification delay after basal insulin (BI) initiation on long-term complications in people with suboptimal glycaemia. We conducted a retrospective cohort study in individuals with type 2 diabetes mellitus initiated on BI. Those with suboptimal glycaemia (glycated haemoglobin ≥7% or ≥53 mmol/mol) within 12 months of BI initiation were divided into early (treatment intensified within 5 years), or late (≥5 years) intensification groups. We estimated the age-stratified risks of micro- and macrovascular complications among these groups compared with those with optimal glycaemia (glycated haemoglobin <7%). Of the 13 916 people with suboptimal glycaemia, 52.5% (n = 7304) did not receive any treatment intensification. In those aged <65 years, compared with the optimal glycaemia group late intensification was associated with a 56% higher risk of macrovascular complications (adjusted hazard ratio 1.56; 95% confidence intervals 1.08, 2.26). In elderly people (≥65 years), late intensification was associated with a higher risk of cardiovascular-related death (1.62; 1.03, 2.54) and a lower risk of microvascular complications (0.26; 0.08, 0.83). Those who had late intensification were at an increased risk of cardiovascular death if they were ≥65 years and an increased risk of macrovascular complications if they were <65 years. These findings highlight the critical need for earlier intensification of treatment and adopting personalized treatment strategies to improve patient outcomes.

Identifiants

pubmed: 37857573
doi: 10.1111/dom.15337
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Sanofi

Informations de copyright

© 2023 The Authors. Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Sharmin Shabnam (S)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Leicester General Hospital, Leicester, UK.

Sophia Abner (S)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
IQVIA, London, UK.

Clare L Gillies (CL)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Leicester General Hospital, Leicester, UK.

Melanie J Davies (MJ)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Leicester General Hospital, Leicester, UK.

Terry Dex (T)

Department of Medical Affairs, Sanofi, Bridgewater, New Jersey, USA.

Kamlesh Khunti (K)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Leicester General Hospital, Leicester, UK.

David R Webb (DR)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Leicester General Hospital, Leicester, UK.

Francesco Zaccardi (F)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Leicester General Hospital, Leicester, UK.

Samuel Seidu (S)

Leicester Real World Evidence Unit, Diabetes Research Centre, University of Leicester, Leicester, UK.
Diabetes Research Centre, University of Leicester, Leicester General Hospital, Leicester, UK.
NIHR Leicester Biomedical Research Centre, Leicester General Hospital, Leicester, UK.

Classifications MeSH