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Published on: November 10, 2017
Same evidence, varying viewpoints: Three questions illustrating important differences between United States and
David I Feldman1, Erin D Michos1, Neil J Stone2
1The Ciccarone Center for the Prevention of Cardiovascular Disease, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Insights
Comparing lipid management guidelines, the US approach prioritizes cost-effectiveness for atherosclerotic cardiovascular disease (ASCVD) prevention, while the European guideline broadens eligibility for intensive therapy. Both aim to reduce cardiovascular risk through statin and non-statin treatments.
Area of Science:
- Cardiology
- Preventive Medicine
- Pharmacoeconomics
Background:
- The 2018 AHA/ACC and 2019 ESC/EAS guidelines offer differing recommendations for managing atherosclerotic cardiovascular disease (ASCVD) risk via lipid management.
- Recent clinical trial data on non-statin therapies and ASCVD risk reduction informs comparisons between these guidelines.
Purpose of the Study:
- To analyze key differences between the US and European lipid management guidelines.
- To evaluate guideline recommendations regarding ASCVD event rates, the role of subclinical atherosclerosis, and LDL-C targets for primary and secondary prevention.
Main Methods:
- Comparative analysis of the 2018 AHA/ACC Multisociety Guideline and the 2019 ESC/EAS Dyslipidemia Guideline.
- Utilizing recent randomized clinical trial data on non-statin lipid-lowering therapy and ASCVD risk reduction to address specific clinical questions.
Main Results:
- The US guideline emphasizes cost-effectiveness, restricting intensive non-statin therapy to very high-risk individuals.
- The European guideline expands eligibility for aggressive lipid-lowering, including lower LDL-C targets (below 55 mg/dL) and broader application in primary and secondary prevention.
- Current healthcare constraints make the European approach more challenging to implement globally.
Conclusions:
- The US guideline offers more affordable and attainable ASCVD prevention strategies by limiting intensive therapy based on risk and cost.
- Future research should focus on trials assessing both cost-effectiveness and efficacy to reconcile differing guideline recommendations.
- Aligning guidelines requires a balance between therapeutic intensity, cost, and global healthcare accessibility.
Abstract:
In 2018, the AHA/ACC Multisociety Guideline on the Management of Blood Cholesterol was released. Less than one year later, the 2019 ESC/EAS Dyslipidemia Guideline was published. While both provide important recommendations for managing atherosclerotic cardiovascular disease (ASCVD) risk through lipid management, differences exist. Prior to the publication of both guidelines, important randomized clinical trial data emerged on non-statin lipid lowering therapy and ASCVD risk reduction. To illustrate important differences in guideline recommendations, we use this data to help answer three key questions: 1) Are ASCVD event rates similar in high-risk primary and stable secondary prevention? 2) Does imaging evidence of subclinical atherosclerosis justify aggressive use of statin and non-statin therapy (if needed) to reduce LDL-C levels below 55 mg/dL as recommended in the European Guideline? 3) Do LDL-C levels below 70 mg/dL achieve a large absolute risk reduction in secondary ASCVD prevention? The US guideline prioritizes both the added efficacy and cost implications of non-statin therapy, which limits intensive therapy to individuals with the highest risk of ASCVD. The European approach broadens the eligibility criteria by incorporating goals of therapy in both primary and secondary prevention. The current cost and access constraints of healthcare worldwide, especially amidst a COVID-19 pandemic, makes the European recommendations more challenging to implement. By restricting non-statin therapy to a subgroup of high- and, in particular, very high-risk individuals, the US guideline provides primary and secondary ASCVD prevention recommendations that are more affordable and attainable. Ultimately, finding a common ground for both guidelines rests on our ability to design trials that assess cost-effectiveness in addition to efficacy and safety.
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