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Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease

BACKGROUND AND AIMS: Cardiovascular outcomes trials have demonstrated that lowering low-density lipoprotein cholesterol (LDL-C) reduces the risk for future cardiovascular events. We assessed the potential cardiovascular benefits of bempedoic acid through a simulation study in patients with atheroscl...

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Autores principales: Gunn, Laura H., McKay, Ailsa J., Feng, Amy, Louie, Michael J., Ballantyne, Christie M., Ray, Kausik K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9833227/
https://www.ncbi.nlm.nih.gov/pubmed/36644205
http://dx.doi.org/10.1016/j.athplu.2022.05.003
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author Gunn, Laura H.
McKay, Ailsa J.
Feng, Amy
Louie, Michael J.
Ballantyne, Christie M.
Ray, Kausik K.
author_facet Gunn, Laura H.
McKay, Ailsa J.
Feng, Amy
Louie, Michael J.
Ballantyne, Christie M.
Ray, Kausik K.
author_sort Gunn, Laura H.
collection PubMed
description BACKGROUND AND AIMS: Cardiovascular outcomes trials have demonstrated that lowering low-density lipoprotein cholesterol (LDL-C) reduces the risk for future cardiovascular events. We assessed the potential cardiovascular benefits of bempedoic acid through a simulation study in patients with atherosclerotic cardiovascular disease (ASCVD) and elevated LDL-C. METHODS: The validated SMART prediction model was used to estimate the baseline 10-year risk of three-point major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, and non-fatal stroke) in patients with ASCVD who were enrolled in four Phase 3, randomized, placebo-controlled bempedoic acid studies. The predicted change in 10-year cardiovascular risk associated with bempedoic acid was estimated for each patient based on the Cholesterol Treatment Trialists’ model. Data were analyzed in two cohorts: Cohort 1 included mostly patients treated with moderate-high intensity statins, and Cohort 2 included patients who were intolerant of more than low-intensity statin. RESULTS: A total of 2884 patients were included in Cohort 1 and 226 in Cohort 2. Weighted average baseline 10-year cardiovascular event risk was 26.1% and 31.6% for Cohorts 1 and 2, respectively. The least squares mean percent difference (95% confidence interval (CI) of the predicted absolute change in 10-year cardiovascular event risk with bempedoic acid was −3.3% (−3.7% to −2.9%) for patients in Cohort 1 and -6.0% (−7.7% to −4.3%) for patients in Cohort 2 compared with placebo (p < 0.0001 for both). CONCLUSIONS: Among patients with ASCVD who could potentially benefit from additional LDL-C lowering, our simulation predicted a lower absolute cardiovascular event risk after initiating bempedoic acid as compared with placebo.
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spelling pubmed-98332272023-01-12 Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease Gunn, Laura H. McKay, Ailsa J. Feng, Amy Louie, Michael J. Ballantyne, Christie M. Ray, Kausik K. Atheroscler Plus Full Length Article BACKGROUND AND AIMS: Cardiovascular outcomes trials have demonstrated that lowering low-density lipoprotein cholesterol (LDL-C) reduces the risk for future cardiovascular events. We assessed the potential cardiovascular benefits of bempedoic acid through a simulation study in patients with atherosclerotic cardiovascular disease (ASCVD) and elevated LDL-C. METHODS: The validated SMART prediction model was used to estimate the baseline 10-year risk of three-point major adverse cardiovascular events (cardiovascular death, non-fatal myocardial infarction, and non-fatal stroke) in patients with ASCVD who were enrolled in four Phase 3, randomized, placebo-controlled bempedoic acid studies. The predicted change in 10-year cardiovascular risk associated with bempedoic acid was estimated for each patient based on the Cholesterol Treatment Trialists’ model. Data were analyzed in two cohorts: Cohort 1 included mostly patients treated with moderate-high intensity statins, and Cohort 2 included patients who were intolerant of more than low-intensity statin. RESULTS: A total of 2884 patients were included in Cohort 1 and 226 in Cohort 2. Weighted average baseline 10-year cardiovascular event risk was 26.1% and 31.6% for Cohorts 1 and 2, respectively. The least squares mean percent difference (95% confidence interval (CI) of the predicted absolute change in 10-year cardiovascular event risk with bempedoic acid was −3.3% (−3.7% to −2.9%) for patients in Cohort 1 and -6.0% (−7.7% to −4.3%) for patients in Cohort 2 compared with placebo (p < 0.0001 for both). CONCLUSIONS: Among patients with ASCVD who could potentially benefit from additional LDL-C lowering, our simulation predicted a lower absolute cardiovascular event risk after initiating bempedoic acid as compared with placebo. Elsevier 2022-05-28 /pmc/articles/PMC9833227/ /pubmed/36644205 http://dx.doi.org/10.1016/j.athplu.2022.05.003 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
Gunn, Laura H.
McKay, Ailsa J.
Feng, Amy
Louie, Michael J.
Ballantyne, Christie M.
Ray, Kausik K.
Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease
title Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease
title_full Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease
title_fullStr Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease
title_full_unstemmed Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease
title_short Estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease
title_sort estimated cardiovascular benefits of bempedoic acid in patients with established cardiovascular disease
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9833227/
https://www.ncbi.nlm.nih.gov/pubmed/36644205
http://dx.doi.org/10.1016/j.athplu.2022.05.003
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