The future of pharmacological therapy for risk factor reduction. Hyperlipidaemia
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Updated: Oct 17, 2026

Differential Effects of Lipid-lowering Drugs in Modulating Morphology of Cholesterol Particles
Published on: November 10, 2017
1Department of Internal Medicine, University Hospital, Linköping, Sweden.
Insights
Drug treatment for high lipid levels (hyperlipidemia) requires lifelong therapy. Guidelines prioritize safety, efficacy, and patient compliance, classifying drugs as first- or second-line based on these factors.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Hyperlipidemia management requires lifelong drug treatment.
- Guidelines for drug treatment of hyperlipidemia have been established by the European Atherosclerosis Society.
- Drug therapy should only be initiated after excluding secondary causes, failure of dietary interventions, and careful individual assessment.
Purpose of the Study:
- To outline the criteria for selecting plasma lipid-lowering drugs.
- To classify current hyperlipidemia drugs into first- and second-line treatments.
- To discuss the potential for newer lipid-lowering drugs to become first-line therapies.
Main Methods:
- Review of European Atherosclerosis Society guidelines for hyperlipidemia drug treatment.
- Evaluation of drugs based on long-term efficacy, compliance, clinical endpoint effect, and safety.
- Classification of drugs into first- and second-line categories.
Main Results:
- First-line drugs currently include cholestyramine, nicotinic acid, and gemfibrozil.
- Second-line drugs include lovastatin, simvastatin, probucol, and "third generation" fibrates.
- Newer drugs like lovastatin, simvastatin, and probucol show promise for future first-line use due to better patient compliance.
Conclusions:
- Long-term efficacy, safety, and patient compliance are crucial for selecting hyperlipidemia drugs.
- Current guidelines categorize drugs, with a trend towards incorporating newer, more compliant options as first-line treatments.
- Continued research and experience may lead to a shift in first-line hyperlipidemia drug recommendations.
Abstract:
The European Atherosclerosis Society has produced guidelines for the drug treatment of hyperlipidaemia. This, of necessity, is lifelong and therefore should be prescribed only after exclusion of secondary causes for the disorder, after dietary advice has failed to produce desirable plasma lipid levels and after careful consideration of the individual case. A plasma lipid-lowering drug should be efficacious on a long term basis on plasma lipid levels, should fulfil conditions for long term compliance regarding simplicity of administration and lack of subjective side effects, have a documented effect on the clinical endpoint (e.g. myocardial infarction) and be safe on a long term basis. Based on these conditions, plasma lipid-lowering drugs can be classed as first- or second-line treatments. At present, examples of first-line drugs are cholestyramine, nicotinic acid and gemfibrozil, while second-line drugs are lovastatin, simvastatin, probucol and 'third generation' fibrates. With increasing experience with the newer drugs regarding clinical efficacy and long term safety, one hopes that lovastatin, simvastatin and probucol will fulfil all criteria and become first-line drugs. These have advantages over cholestyramine and nicotinic acid in terms of better patient compliance.
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