Type 2 & other diabetes

One‐year usage patterns of SGLT ‐2 inhibitors and GLP ‐1 receptor agonists in individuals with type 2 diabetes in a real‐world population

Diabetes Obes MetabPublished Observational cohort study

Authors' conclusion

Distinct clinical and biochemical characteristics are associated with poor adherence versus discontinuation. Understanding these patterns is crucial for developing targeted strategies to improve sustained use, ultimately enhancing treatment outcomes for people with type 2 diabetes.

Study context

Population
Individuals with T2D initiating an SGLT2i or GLP-1 RA, Scottish Care Information Diabetes Collaboration database
Exposure
Usage patterns of SGLT2i and GLP-1 RA subclasses; characteristics associated with each usage category
Outcome
Usage category: adherent, poor adherence or three discontinuation categories including a proxy for intolerance
Follow-up
1 year
Methodological detailselectronic health records, real-world
  • Electronic health records
  • Real-world

Main finding

As reported in the abstract

  • SGLT2i: poor adherence more common in younger individuals, with greater socioeconomic deprivation and higher HbA1c
  • SGLT2i: intolerance more frequent in older, leaner females and in those with prior genital thrush
  • GLP-1RA: newer agents associated with more favourable usage patterns
  • GLP-1RA: poor adherence more frequent with liraglutide, lixisenatide and exenatide vs semaglutide; intolerance more common with lixisenatide
  • GLP-1RA: poor adherence associated with younger age and prior GLP-1RA use; intolerance with lower BMI, female sex and more advanced CKD

Observational data: associations, not effects.

Original publication

One‐year usage patterns of SGLT ‐2 inhibitors and GLP ‐1 receptor agonists in individuals with type 2 diabetes in a real‐world population. Diabetes Obes Metab. Published 4 November 2025. doi:10.1111/dom.70269

Composed by AI from the published abstract and checked against it. How Briefs are made →

Get them every week

New studies on this topic in My Week and in your Monday e-mail.

We e-mail you a sign-in link and a code. No password, no spam.