Cardiovascular Outcomes in a SELECT-Like Obesity Cohort: Real-World Insights From the Swedish AROS Database
Viveca Ritsinger1,2, Josefine Fagerström3, Håkan Nero3
1Division of Cardiology, Department of Medicine Solna, Karolinska Institute, Stockholm, Sweden.
Background:
In the SELECT trial, semaglutide reduced major adverse cardiovascular outcomes (MACE) in individuals with overweight or obesity and established cardiovascular disease (CVD) but without diabetes. However, real-world cardiovascular event rates in comparable populations remain uncharacterised. We therefore aimed to (1) assess real-world cardiovascular outcomes in a SELECT-like cohort with obesity, (2) compare them to the general population and a broader population of individuals with obesity and (3) evaluate the cardiovascular preventive potential of semaglutide in this SELECT-like cohort with obesity.
Methods:
We used healthcare registries and electronic health records from three Swedish regions (2013-2023), covering ~40% of the national population, to identify individuals aged ≥ 45 years with obesity (body mass index [BMI] ≥ 30 kg/m2) and established CVD but without diabetes, in alignment with the SELECT trial criteria. Cardiovascular outcomes in this SELECT-like obesity cohort were compared with matched individuals from the general population as well as with a broader population of individuals with obesity, irrespective of CVD status or other comorbid conditions. To estimate the number needed to treat (NNT), the relative treatment effect of semaglutide observed in the SELECT trial was applied to the absolute risks identified in the SELECT-like obesity cohort.
Results:
The SELECT-like obesity cohort (n = 9652) had a mean (SD) age of 68.4 (11.3) years, a mean BMI of 33.1 kg/m2 (SD 3.5) and 57.9% were men. Most had a history of myocardial infarction (48.1%) or stroke (41.7%). Over a mean (SD) follow-up of 5.4 (3.2) years, MACE occurred in 21.7%. Compared with the SELECT trial, this real-world population had a higher mean age, had a higher proportion of females, and more often had a prior stroke. Applying the estimated effect of semaglutide from the SELECT trial, the NNT to prevent one MACE was 35 (95% CI, 24-66). Compared with the General population cohort (n = 48 260), the SELECT-like obesity cohort had a higher burden of cardiovascular and obesity-related comorbidities and an increased risk of adverse cardiovascular outcomes, including MACE (HR 2.3 [2.2-2.4]) and heart failure (HR 2.7 [2.5-2.9]).
Conclusion:
In a real-world setting, despite the use of extensive preventive medications, individuals with obesity and CVD had a higher risk of adverse cardiovascular outcomes and mortality compared with the SELECT trial as well as the general population. These findings highlight the substantial disease burden and the need for improved secondary CVD prevention strategies.
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