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Residual Atherosclerotic Cardiovascular Disease Risk in Statin Users: A Systematic Review and Meta-Analysis
Alexandre H Watanabe1, Lori D Bash1, Tracy Westley2
1Merck & Co, Inc Rahway NJ.
Insights
Even with statin therapy, individuals face significant residual atherosclerotic cardiovascular disease (ASCVD) risk. This highlights ongoing gaps in treatment and the need for optimized risk management strategies.
Area of Science:
- Cardiology
- Public Health
- Pharmacology
Background:
- Statins are primary lipid-lowering agents for adults.
- Residual atherosclerotic cardiovascular disease (ASCVD) risk in statin users requires further investigation.
- This study quantifies real-world residual ASCVD risk in patients on statin therapy.
Purpose of the Study:
- To estimate the residual ASCVD risk in adult statin users in a real-world setting.
- To synthesize current evidence on ASCVD events and mortality among statin users.
- To identify potential gaps in cardiovascular risk management for patients on statins.
Main Methods:
- Systematic literature review and meta-analysis adhering to PRISMA guidelines.
- Inclusion of observational studies published between January 2013 and August 2023.
- Assessment of five key outcomes: composite ASCVD events/all-cause death, myocardial infarction, ischemic stroke, cardiovascular death, and coronary revascularization.
Main Results:
- Pooled residual composite risk was 12.3 per 1000 person-years (PPY), higher in those with prior ASCVD (15.8 PPY) than those at risk (6.4 PPY).
- Specific event rates included myocardial infarction (8.23 PPY), ischemic stroke (6.0 PPY), cardiovascular death (4.3 PPY), and coronary revascularization (7.4 PPY).
- Significant variability was observed across studies for all assessed outcomes.
Conclusions:
- A meaningful residual ASCVD risk exists among statin users in real-world practice.
- Findings underscore persistent gaps in achieving optimal cardiovascular risk reduction.
- Comprehensive and optimized risk management strategies are crucial for statin-treated patients.
Background:
Statins are the cornerstone of lipid-lowering therapy, reducing low-density lipoprotein cholesterol in adults. However, residual atherosclerotic cardiovascular disease (ASCVD) risk among statin users remains unclear. This study estimated residual ASCVD risk in statin users in practice.
Methods:
We conducted a systematic literature review and meta-analyses following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, including observational studies published January 1, 2013, to August 1, 2023, that reported ASCVD risk in adult statin users. Five outcomes were assessed: composite risk (major adverse cardiovascular events or all-cause death), myocardial infarction, ischemic stroke, cardiovascular-related death, and coronary revascularization. Meta-analysis methods were used to synthesize individual study estimates. For each outcome, forest plots present study-level estimates and the pooled incidence rate per 1000 person-years (PPY).
Results:
The meta-analysis of residual composite risk (major adverse cardiovascular events or all-cause death) in the overall population was 12.3 PPY (range, 0.2-72.0). Rates were lower in adults at risk of ASCVD (6.4 PPY [range, 3.7-9.8 PPY]) and higher in adults with prior ASCVD (15.8 PPY [range, 0.2-72.0 PPY]). Meta-analysis for myocardial infarction showed 8.23 PPY (range, 1.1-88.82 PPY) in the overall patient population, and a lower rate of ischemic stroke with a rate of 6.0 PPY (range, 1.4-18.8 PPY). A rate of 4.3 PPY (range, 0.4-22.9 PPY) was estimated for cardiovascular-related death, and 7.4 PPY for coronary revascularization (range, 3.1-27.6 PPY).
Conclusions:
Despite substantial between-study variability, this real-world meta-analysis indicates meaningful residual ASCVD risk among statin users, underscoring persistent treatment gaps and need for comprehensive, optimized risk management.
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