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.
Insights
Individuals with obesity and cardiovascular disease (CVD) face higher risks, even with preventive care. Semaglutide shows potential for preventing major adverse cardiovascular events (MACE) in this high-risk group.
Area of Science:
- Cardiology
- Endocrinology
- Public Health
Background:
- Semaglutide demonstrated cardiovascular benefits in the SELECT trial for individuals with obesity and established cardiovascular disease (CVD) but without diabetes.
- Real-world cardiovascular event rates in similar populations are not well-characterized.
- This study aimed to assess real-world outcomes and semaglutide's preventive potential in a SELECT-like cohort.
Purpose of the Study:
- To evaluate real-world cardiovascular outcomes in a cohort mirroring the SELECT trial criteria (obesity, established CVD, no diabetes).
- To compare cardiovascular event rates in this cohort against the general population and a broader obesity cohort.
- To estimate the cardiovascular preventive potential of semaglutide in this specific high-risk population.
Main Methods:
- Utilized Swedish healthcare registries and electronic health records (2013-2023) for individuals aged ≥45 years with obesity (BMI ≥30 kg/m²) and established CVD, excluding diabetes.
- Compared outcomes of the SELECT-like obesity cohort (n=9652) with matched general population and broader obesity cohorts.
- Applied semaglutide's relative treatment effect from the SELECT trial to estimate the number needed to treat (NNT) for major adverse cardiovascular events (MACE).
Main Results:
- The SELECT-like cohort (mean age 68.4 years, BMI 33.1 kg/m², 57.9% male) experienced a 21.7% MACE rate over 5.4 years.
- This real-world cohort had higher mean age, more females, and more prior strokes compared to the SELECT trial.
- The estimated NNT to prevent one MACE with semaglutide was 35 (95% CI, 24-66). The cohort showed significantly higher MACE (HR 2.3) and heart failure (HR 2.7) risks versus the general population.
Conclusions:
- Despite preventive medications, individuals with obesity and CVD exhibit elevated cardiovascular risks and mortality compared to both the SELECT trial and general populations.
- These findings underscore the significant disease burden in this demographic.
- There is a critical need for enhanced secondary cardiovascular disease prevention strategies for individuals with obesity and established CVD.
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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