Try our free symptom checker
Get a thorough self-assessment before your visit to the doctor.
Triglycerides may not get as much attention as cholesterol, but they matter just as much. When levels rise, fat quietly builds up in your bloodstream and in your arteries. Over time, this buildup increases the risk of cardiovascular problems. Even people who take statins and maintain good LDL cholesterol can still have high triglycerides. That leftover risk keeps doctors and patients worried.
If you eat better, exercise regularly, and follow your doctor’s advice yet your triglycerides stay high, you might wonder what else you can do. Vascepa, with its purified EPA formula, works differently from typical fish oil products. Let’s explore more below.
What exactly is Vascepa, and how does it work in the body?
Vascepa, known by its generic name icosapent ethyl (IPE), is a special type of omega-3 medicine that contains only EPA. Most regular fish oils contain both EPA and DHA, but Vascepa’s unique design leaves DHA out on purpose.
Why? Because DHA can sometimes raise LDL cholesterol, which is the “bad” kind. Vascepa focuses on EPA alone, giving the benefits of omega-3s without increasing LDL levels.
It became the first FDA-approved fish-oil-based prescription drug proven to lower cardiovascular risk in adults. The approval came after years of trials, beginning with MARINE and ANCHOR, which showed impressive drops in triglycerides for patients with very high or moderately high levels.
In 2019, after the REDUCE-IT study, the FDA expanded Vascepa’s use. Now, people who have triglycerides of 150 mg/dL or higher, and who already take statins for heart disease or diabetes, can use it to lower their cardiovascular risk even more.
So, what makes Vascepa stand out among heart medicines?
It protects your heart in ways that statins alone can’t. While statins focus on cutting cholesterol made in the liver, Vascepa reduces leftover risks linked to inflammation, unstable plaques, and fatty blood particles that slip past other treatments.
In short, Vascepa serves as a valuable add-on therapy that fills the gap statins leave behind.
How does Vascepa actually lower Triglyceride levels?
If you’ve ever asked yourself, “How can a fish-oil pill change my blood fat numbers?” the answer lies in biology. Vascepa works through several connected processes inside your body.
Studies show that omega-3 fatty acids like EPA reduce how much fat your liver makes. They cut down production of very-low-density lipoproteins (VLDL), the type that carries triglycerides in your blood. When VLDL drops, triglycerides fall. At the same time, EPA helps shift LDL particles from small and dense to larger and more stable forms. Larger particles are less likely to sneak into artery walls, reducing damage over time.
The ANCHOR trial confirmed these effects. Patients already on statins who added Vascepa saw triglycerides fall sharply, even when their starting levels were between 200 and 500 mg/dL. Importantly, their LDL cholesterol stayed the same or improved, proving that Vascepa doesn’t trigger the LDL rise seen with DHA-containing products.
Vascepa also affects inflammation and oxidative stress. It becomes part of your cell membranes, making them more resilient. Inside the arteries, this means plaques become firmer and less likely to rupture. A ruptured plaque can block blood flow and cause a heart attack, so stability matters a lot.
The EVAPORATE trial gave real-world proof of this. Patients on statins with an average triglyceride level near 259 mg/dL were studied for 18 months. Those who took Vascepa had a 17% reduction in soft plaque volume, while those on placebo saw plaque growth more than double. That difference shows Vascepa doesn’t just change lab results, it changes artery health itself.
These findings explain why Vascepa lowers triglycerides and helps at many levels. It cuts liver fat production, improves the size and quality of lipoproteins, stabilizes arterial plaques, and calms inflammation all at once.
Does Vascepa really protect the heart beyond lowering triglycerides?
Many people wonder whether Vascepa’s benefits stop at the lab report or actually extend to preventing heart attacks and strokes. The evidence says yes.
The REDUCE-IT study was the most influential of all. It enrolled 8,179 patients who were already on statins. Their triglycerides ranged from 135 to 499 mg/dL, and their LDL cholesterol stayed between 41 and 100 mg/dL. They were randomly assigned to receive either Vascepa 4 grams per day or a placebo, and they were followed for almost five years.
Results were eye-opening. The combined risk of heart-related death, heart attack, stroke, unstable angina, or revascularization occurred in 17.2% of Vascepa users versus 22.0% in the placebo group. That means a 25% relative risk reduction. Death, heart attack, and stroke alone also dropped significantly, showing clear cardiovascular protection.
However, another trial, STRENGTH, seemed to challenge those results. It studied 13,078 patients taking a mix of EPA and DHA omega-3s versus a corn-oil placebo. The outcome showed no difference between the two groups, and the study was stopped early. That raised questions: could DHA reduce EPA’s benefits? Did the mineral-oil placebo used in REDUCE-IT make Vascepa look better by making the placebo group slightly worse?
While debates continued, most experts leaned toward Vascepa’s benefits being genuine. Other studies supported it. The earlier Japanese JELIS trial, which tested pure EPA in 18,645 patients on statins, also showed a 19% drop in major cardiovascular events. That consistency matters because it shows EPA itself, not the placebo choice, drives heart protection.
So even though not every study agreed, the weight of evidence favors Vascepa. The majority of research demonstrates real reductions in cardiovascular events beyond what would be expected from triglyceride lowering alone.
Safety concerns with Vascepa
Like all medicines, Vascepa has side effects that need attention. They are generally mild, but some can be serious.
Heart rhythm and bleeding risks
In REDUCE-IT, more people taking Vascepa experienced atrial fibrillation or flutter, 3.1% versus 2.1% in the placebo group. Atrial fibrillation causes an irregular heartbeat that sometimes leads to blood clots or strokes. Doctors usually monitor heart rhythm more closely in patients with a history of arrhythmias before starting Vascepa.
Serious bleeding events were also slightly higher among Vascepa users. The difference was small and not statistically significant, but it highlights the need for caution when patients already take blood thinners or antiplatelet drugs.
Trial controversies and comparisons
Safety discussions often overlap with debates about the clinical trials themselves. In REDUCE-IT, the mineral-oil placebo slightly raised LDL cholesterol and inflammation markers in the placebo group. Critics argued this could exaggerate Vascepa’s benefits.
Later, STRENGTH used corn oil as a placebo and found no benefit with an EPA + DHA mix. This led to speculation that DHA might interfere with EPA’s protective effects. Regulators, including the FDA and the European Medicines Agency, reviewed all data and concluded that the placebo differences explained only a small part of the outcome gap. Still, researchers continue to study these details to refine the science.
Accessibility and cost factors
For years, cost limited Vascepa’s use because the branded version was expensive. When key patents expired, generic icosapent ethyl entered the market. This change lowered the price and improved access for patients who need extra cardiovascular protection.
At the same time, it created a complex market, since multiple companies now produce the same medicine.
Comparison with other omega-3 products
Unlike fish-oil blends that contain DHA, Vascepa’s pure EPA profile avoids raising LDL cholesterol. That makes it safer for people who already struggle with high LDL or who have a history of heart disease. Many over-the-counter omega-3s can’t offer that reassurance. Vascepa’s cleaner profile gives doctors confidence when prescribing it for patients already at cardiovascular risk.
What makes vascepa different from ordinary fish oil supplements?
You might ask, “Can’t I just take regular fish oil instead?” It’s a fair question, but the difference is big. Over-the-counter fish oils usually mix EPA and DHA in various ratios and often contain impurities or inconsistent dosages. They also aren’t tested or approved to prevent cardiovascular events.
Vascepa, on the other hand, is highly purified, prescription-grade EPA in a stable ethyl-ester form. It undergoes strict manufacturing standards and has proven clinical trial data behind it. The dosage used in studies, 4 grams per day, can’t be matched by standard supplement capsules. This means the benefits seen in trials apply to Vascepa, not to generic fish oil pills from the store shelf.
Takeaway
- Vascepa (icosapent ethyl) is a purified EPA-only omega-3 drug approved to lower cardiovascular risk and triglycerides.
- It works by reducing liver fat production, lowering VLDL, improving lipoprotein structure, and stabilizing artery plaques.
- Large trials like REDUCE-IT show it cuts heart attack, stroke, and cardiovascular death rates even when patients already take statins.
- Minor side effects include a slightly higher chance of atrial fibrillation and bleeding, so monitoring is important.
- Compared with DHA-containing fish oils, Vascepa does not raise LDL cholesterol, giving it a cleaner safety profile.
- Generic versions now make it more affordable and accessible, allowing more patients to benefit.
Was this article helpful?
References
- Huston, J., Schaffner, H., Cox, A., Sperry, A., Mcgee, S., Lor, P., Langley, L., Skrable, B., Ashchi, M., Bisharat, M., Gore, A., Jones, T., Sutton, D., Sheikh-Ali, M., Berner, J., & Goldfaden, R. (2023). A critical review of icosapent ethyl in cardiovascular risk reduction. American Journal of Cardiovascular Drugs, 1–14. Advance online publication. https://doi.org/10.1007/s40256-023-00583-8
- Curfman, G., & Shehada, E. (2021). Icosapent ethyl: Scientific and legal controversies. Open Heart, 8(1), e001616. https://doi.org/10.1136/openhrt-2021-001616
- Gupta, A., & Alkhalil, M. (2023). The emerging role of icosapent ethyl in patients with cardiovascular disease: Mechanistic insights and future applications. Journal of Clinical Medicine, 12(11), 3758. https://doi.org/10.3390/jcm12113758
- Sutariya, B., Montenegro, D. M., Chukwu, M., Ehsan, P., Aburumman, R. N., Muthanna, S. I., Menon, S. R., Vithani, V., & Penumetcha, S. S. (2022). Emphasis on icosapent ethyl for cardiovascular risk reduction: A systematic review. Cureus, 14(12), e32346. https://doi.org/10.7759/cureus.32346
- Budoff, M. J., Bhatt, D. L., Kinninger, A., Lakshmanan, S., Muhlestein, J. B., Le, V. T., May, H. T., Shaikh, K., Shekar, C., Roy, S. K., … & EVAPORATE Study Group. (2020). Effect of icosapent ethyl on progression of coronary atherosclerosis in patients with elevated triglycerides on statin therapy: Final results of the EVAPORATE trial. European Heart Journal, 41(40), 3925–3932. https://doi.org/10.1093/eurheartj/ehaa652
- Yokoyama, M., Origasa, H., Matsuzaki, M., Matsuzawa, Y., Saito, Y., Ishikawa, Y., Oikawa, S., Sasaki, J., Hishida, H., Itakura, H., Kita, T., Kitabatake, A., Nakaya, N., Sakata, T., Shimada, K., Shirato, K., & Japan EPA Lipid Intervention Study (JELIS) Investigators. (2007). Effects of eicosapentaenoic acid on major coronary events in hypercholesterolaemic patients (JELIS): A randomised open-label, blinded endpoint analysis. The Lancet, 369(9567), 1090–1098.
