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

被引:22
作者
Piccini, Sara [1 ,2 ]
Favacchio, Giuseppe [2 ]
Panico, Cristina [1 ,3 ]
Morenghi, Emanuela [4 ]
Folli, Franco [5 ]
Mazziotti, Gherardo [1 ,2 ]
Lania, Andrea Gerardo [1 ,2 ]
Mirani, Marco [2 ]
机构
[1] Humanitas Univ, Dept Biomed Sci, Via Rita Levi Montalcini 4, I-20072 Milan, Italy
[2] IRCCS Humanitas Res Hosp, Endocrinol Diabetol & Androl Unit, Via Manzoni 56, I-20089 Milan, Italy
[3] IRCCS Humanitas Res Hosp, Dept Cardiol, Milan, Italy
[4] IRCCS Humanitas Res Hosp, Biostat Unit, Via Manzoni 56, I-20089 Milan, Italy
[5] Univ Milan, Dept Hlth Sci, Endocrinol & Metab, Milan, Italy
关键词
Diabetes; GLP-1 receptor agonists; Cardiovascular events; Real-world; GLUCAGON-LIKE PEPTIDE-1; TYPE-2; DIABETES-MELLITUS; 7-36; AMIDE; OUTCOMES; LIRAGLUTIDE; SEMAGLUTIDE; MICE;
D O I
10.1186/s12933-023-01800-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundGlucagon-like peptide-1 receptor agonists (GLP-1 RAs) have shown cardiovascular benefits in cardiovascular outcome trials in type 2 diabetes mellitus. However, the most convincing evidence was obtained in subjects with established cardiovascular (CV) disease. We analyzed the determinants of GLP-1 RA-mediated CV protection in a real-world population of persons with type 2 diabetes with and without a history of CV events with long-term follow-up.MethodsRetrospective cohort study of 550 individuals with type 2 diabetes (395 in primary CV prevention, 155 in secondary CV prevention), followed at a single center after the first prescription of a GLP-1 RA between 2009 and 2019. CV and metabolic outcomes were assessed.ResultsMedian duration of follow-up was 5.0 years (0.25-10.8) in primary prevention and 3.6 years (0-10.3) in secondary prevention, with a median duration of treatment of 3.2 years (0-10.8) and 2.5 years (0-10.3) respectively. In the multivariable Cox regression model considering GLP-1 RA treatment as a time-dependent covariate, in the primary prevention group, changes in BMI and glycated hemoglobin did not have an impact on MACE risk, while age at the time of GLP-1 initiation (HR 1.08, 95% CI 1.03-1.14, p = 0.001) and GLP-1 RA cessation by time (HR 3.40, 95% CI 1.82-6.32, p < 0.001) increased the risk of MACE. Regarding the secondary prevention group, only GLP-1 RA cessation by time (HR 2.71, 95% CI 1.46-5.01, p = 0.002) increased the risk of MACE. With respect to those who withdrew treatment, subjects who continued the GLP-1 RA had significantly greater weight loss and lower glycated hemoglobin levels during follow-up.ConclusionsIn 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.
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页数:14
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