Atherothrombotic risk stratification and ezetimibe for secondary prevention
Open accessAbstract
Background Ezetimibe improves cardiovascular (CV) outcomes in patients stabilized after acute coronary syndrome (ACS) when added to statin therapy. After ACS, patients vary considerably in their risk for recurrent CV events.Objectives This study tested the hypothesis that atherothrombotic risk stratification may be useful to identify post-ACS patients who have the greatest potential for benefit from the addition of ezetimibe to statin therapy.Methods The TIMI (Thrombolysis In Myocardial Infarction) Risk Score for Secondary Prevention (TRS 2°P) is a simple 9-point risk stratification tool, previously developed in a large population with atherothrombosis to predict CV death, myocardial infarction (MI), and ischemic stroke (CV death/MI/ischemic cerebrovascular accident [iCVA]). The current study applied this tool prospectively to 17,717 post-ACS patients randomized either to ezetimibe and simvastatin or to placebo and simvastatin in IMPROVE-IT (Improved Reduction of Outcomes: Vytorin Efficacy International Trial). Treatment efficacy was assessed by baseline risk for CV death/MI/iCVA, the IMPROVE-IT composite endpoints (CE), and individual component endpoints at 7 years.Results All 9 clinical variables in the TRS 2°P were independent risk indicators for CV death/MI/iCVA (p < 0.001). The integer-based scheme showed a strong graded relationship with the rate of CV death/MI/iCVA, the trial CE, and the individual components (p trend <0.0001 for each). High-risk patients (n = 4,393; 25%), defined by ≥3 risk indicators, had a 6.3% (95% confidence interval: 2.9% to 9.7%) absolute risk reduction in CV death/MI/iCVA at 7 years with ezetimibe/simvastatin, thus translating to a number-needed-to-treat of 16. Intermediate-risk patients (2 risk indicators; n = 5,292; 30%) had a 2.2% (95% confidence interval: -0.3% to 4.6%) absolute risk reduction. Low-risk patients (0 to 1 risk indicators; n = 8,032; 45%) did not appear to derive benefit from the addition of ezetimibe (p interaction = 0.010). Similar findings were observed for the IMPROVE-IT primary CE.Conclusions Atherothrombotic risk stratification using the TRS 2°P identifies high-risk patients who derive greatest benefit from the addition of ezetimibe to statin therapy for secondary prevention after ACS. (Improved Reduction of Outcomes: Vytorin Efficacy International Trial [IMPROVE-IT]; NCT00202878).
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Type 1 diabetes mellitus is associated with high cardiovascular disease risk, particularly in patients with microalbuminuria and renal disease.
“T1DM is associated with high CVD risk, in particular in patients with microalbuminuria and renal disease [427].”
From 2019 ESC/EAS guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk (2019) · cites this paper as [427]
Risk scores and other cardiovascular biomarkers have been developed for risk stratification of secondary prevention patients but are not yet in widespread use.
“Recently, risk scores and other cardiovascular biomarkers have been developed for risk strati fi cation of secondary prevention patients (i.e., those who are already high risk because they have ASCVD) but are not yet in widespread use (17,18).”
From 10. Cardiovascular Disease and Risk Management: <i>Standards of Care in Diabetes—2023</i> (2023) · cites this paper as [17]
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References 30 · Cited by 204
Research works printed but not linked: 1
- Balakrishnan N, Rao CR, editors. Handbook of Statistics, Survival Methods, Vol. 23. Amsterdam, the Netherlands: Elsevier, 2004:1-25.
- Authors
- Bohula, E. A., Morrow, D. A., Giugliano, R. P., Blazing, M. A., He, P., Park, J.-G., Murphy, S. A., White, J. A., Kesaniemi, Y. A., Pedersen, T. R., Brady, A. J., Mitchel, Y., Cannon, C. P., & Braunwald, E.
- Affiliations
- Brigham and Women's Hospital (US)
- Duke University (US)
- Oslo University Hospital (NO)
- Glasgow Royal Infirmary (GB)
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- Corresponding author
- Bohula, Erin A.
- ORCID
- Venue
- Journal of the American College of Cardiology
- Publisher
- Elsevier BV
- Published
- 2017-02
- Volume
- 69
- Issue
- 8
- Pages
- 911-921
- ISSN
- 0735-1097 (ISSN-L)
- OpenAlex
- W2589921037
- Cited by
- 204
- References
- 30
- Citations by year
- 2026: 11 · 2025: 20 · 2024: 6 · 2023: 17 · 2022: 20 · 2021: 25 · 2020: 32 · 2019: 36 · 2018: 23 · 2017: 14
- FWCI
- 29.42
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Journal of the American College of Cardiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Eli Lilly and Company
- AstraZeneca
- GlaxoSmithKline
- Gilead Sciences
- Daiichi-Sankyo
- Eisai
- Topics
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Acute Myocardial Infarction Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Antiplatelet Therapy and Cardiovascular Diseases
- Keywords
- ezetimibe, acute coronary syndrome, secondary prevention, simvastatin, IMPROVE-IT trial, cardiovascular mortality, myocardial infarction, ischemic stroke, lipid-lowering therapy, risk prediction, number needed to treat, statin therapy, cardiovascular risk reduction
- MeSH terms
- Ezetimibe, Aged, Female, Humans, Male, Middle Aged, Myocardial Infarction, Prospective Studies, Treatment Outcome, Risk Assessment, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Simvastatin, Acute Coronary Syndrome, Secondary Prevention
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