Type 2 & other diabetes

Time-dependent effect of GLP-1 receptor agonists on cardiovascular benefits: a real-world study

Cardiovasc DiabetolPublished Retrospective cohort study

Authors' conclusion

In this real-world type 2 diabetes population, discontinuation of GLP-1 RA treatment was associated to a higher risk of major cardiovascular events, in both subjects with and without a history of CV events.

Study context

Population
Persons with T2D followed at a single center after first GLP-1 RA prescription, 2009–2019, with and without a history of cardiovascular (CV) events
Participants
550 persons
Exposure
GLP-1 RA cessation vs continuation
  • Primary preventionn = 395
  • Secondary preventionn = 155
Outcome
MACE risk with GLP-1 RA cessation by time
Methodological detailssingle-centre, multivariable Cox regression with GLP-1 RA treatment as time-dependent covariate
  • Single-centre
  • Multivariable Cox regression with GLP-1 RA treatment as time-dependent covariate

Main finding

As reported in the abstract

Multivariable Cox model, time-dependent covariate
Hazard ratio (95% CI)P value
GLP-1 RA cessation (primary prevention)
3.40(1.82–6.32)
P < 0.001
GLP-1 RA cessation (secondary prevention)
2.71(1.46–5.01)
P = 0.002

Observational data: associations, not effects.

Further findings

MACE risk by age at GLP-1 initiation (primary prevention)

HR (95% CI)P value
Age at GLP-1 initiation1.08 (1.03–1.14)P = 0.001

Follow-up and treatment duration

Median treatment duration Primary prevention 3.2 years (0-10.8) · Secondary prevention 2.5 years (0-10.3)

MACE risk by age at GLP-1 initiation (primary prevention)

Changes in BMI and HbA1c did not have an impact on MACE risk (primary prevention)

Weight and HbA1c during follow-up

Continuers had significantly greater weight loss and lower HbA1c than those who withdrew treatment

Original publication

Time-dependent effect of GLP-1 receptor agonists on cardiovascular benefits: a real-world study. Cardiovasc Diabetol. Published 25 March 2023. doi:10.1186/s12933-023-01800-z

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