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Published on: June 28, 2019
Omacor (prescription omega-3-acid ethyl esters 90): From severe rhythm disorders to hypertriglyceridemia
1Experimental Cardiology Laboratory, Heart Center, Department of Internal Medicine and Cardiology, Philipps University of Marburg, 35043 Marburg, Germany. Rupp@staff.uni-marburg.de
Insights
Omega-3 ethyl esters, like Omacor, help prevent cardiac remodeling and arrhythmias post-myocardial infarction. Clinical trials show reduced mortality and arrhythmic events with this specific medication.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Biochemistry
Background:
- Adverse cardiac remodeling post-myocardial infarction (MI) and severe rhythm disorders remain critical therapeutic targets.
- Omega-3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), can modulate ion channels and exchangers to counteract cardiac remodeling.
- Existing therapies have limitations in preventing adverse cardiac remodeling and rhythm disorders.
Purpose of the Study:
- To evaluate the efficacy of omega-3 fatty acid ethyl esters (Omacor) in preventing adverse cardiac remodeling and rhythm disorders.
- To differentiate Omacor from fish oil and generic n-3 polyunsaturated fatty acid supplementation.
- To highlight the specific benefits of Omacor in post-MI patients and those with heart failure.
Main Methods:
- Analysis of data from the GISSI-Prevenzione and GISSI-HF trials.
- Comparison of omega-3 fatty acid ethyl esters (Omacor) with fish oil and placebo.
- Review of clinical trial data regarding anti-arrhythmogenic actions and cardiovascular benefits.
Main Results:
- Omacor, administered as ethyl esters, demonstrated sustained intestinal absorption and reduced environmental toxin content.
- DHA component of Omacor showed potential in inhibiting ischemia-induced arrhythmias in animal models.
- GISSI-HF and GISSI-Prevenzione trials showed Omacor reduced severe arrhythmic events, mortality, and arrhythmic death.
- Higher dosages (3-4 g/day) of Omacor showed enhanced cardiovascular benefits and improved hypertriglyceridemia.
Conclusions:
- Omega-3 acid ethyl esters (Omacor) are effective in secondary prevention post-MI, reducing mortality and arrhythmic events.
- Omacor should be precisely referred to as a medication, distinct from fish oil or general supplementation.
- The anti-arrhythmogenic and cardiovascular benefits of Omacor are supported by clinical trial evidence, particularly at higher doses.
Abstract:
Despite progress made in post-myocardial infarction (MI) revascularization and background therapy for the failing heart, the prevention of adverse cardiac remodeling associated with severe rhythm disorders remains an important drug target. Part of the remodeling can be counteracted by modulating the activity of ion channels and exchangers by omega-3 acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). In the GISSI-Prevenzione and GISSI-HF trials, omega-3 fatty acids were administered as ethyl esters (Omacor Solvay Pharmaceuticals) and not as triglycerides present in fish oil. Ethyl esters result in a sustained intestinal absorption of EPA and DHA and require various purification steps during production, thereby minimizing the content of environmental toxins. Also the rather high (38%) DHA content of Omacor should not be ignored since in rats with low dose intake of omega-3 acids, DHA but not EPA inhibited ischemia-induced arrhythmias. In patients on multiple tablets, 840 mg EPA+DHA in one capsule is preferred to increase compliance. It is not justified to refer to Omacor as "n-3 polyunsaturated fatty acid supplementation" or even "fish oil" and, based on controlled clinical trials, there is no evidence that fish oil could be a substitute of Omacor. To avoid further confusion, guidelines should be precise and refer to the medication, eg, as in NICE guideline CG48: "Omega-3-acid ethyl esters treatment licensed for secondary prevention post-MI." The anti-arrhythmogenic action of Omacor should be seen in the context of implantable cardioverter-defibrillator trials (DINAMIT, IRIS) where non-sudden death was increased and total mortality unaltered. However, Omacor administered in the GISSI-HF trial reduced the incidence of severe arrhythmic events and mortality. Also in the GISSI-Prevenzione trial, arrhythmic death and mortality were reduced. At higher dosages (daily, 3-4 g) Omacor exhibits more pronounced cardiovascular benefits and, as a licensed indication, improves hypertriglyceridemia and related lipid parameters.
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