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Published on: November 10, 2017
Prognostic Implication of LDL-C Variability and Its Association with Lipid-Lowering Strategies: Insights from the
Jaeoh Lee1, Sripal Bangalore2, Kyeong Ho Yun3
1Division of Cardiology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Visit-to-visit variability in low-density lipoprotein cholesterol (LDL-C) was similar with statin-ezetimibe but higher with treat-to-target strategies. Increased LDL-C variability predicts adverse cardiovascular events, regardless of lipid-lowering approach.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Lipid-lowering strategies aim to reduce cardiovascular risk.
- Understanding LDL-C variability is crucial for optimizing treatment.
- Previous trials provide data for comparative analysis.
Purpose of the Study:
- To compare visit-to-visit LDL-C variability across different lipid-lowering strategies.
- To assess the prognostic implications of LDL-C variability on cardiovascular outcomes.
Main Methods:
- Analysis of two randomized clinical trials (RACING and LODESTAR).
- Evaluation of LDL-C variability using standard deviation (SD), coefficient of variation, and variation independent of mean.
- Primary endpoint: composite of death, myocardial infarction, stroke, or coronary revascularization.
Main Results:
- LDL-C variability was similar with moderate-intensity statin plus ezetimibe compared to high-intensity statins.
- Higher LDL-C variability was observed with a treat-to-target strategy.
- Increased LDL-C variability (by SD) independently predicted the primary endpoint (HR 1.024, p<0.001).
- Each 1-SD increase in LDL-C variability was associated with increased risk of MI (2.1%), stroke (3.5%), and revascularization (2.7%).
Conclusions:
- Moderate-intensity statin plus ezetimibe did not increase LDL-C variability compared to high-intensity statins.
- Treat-to-target strategies were associated with increased LDL-C variability.
- Elevated LDL-C variability is linked to higher risks of adverse cardiovascular outcomes, even with guideline-directed statin therapy.
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