By: MITCHEL L. ZOLER, Family Practice News Digital Network
Major Finding: A 12-week treatment regimen of 4 g/day of a purified formulation of EPA produced a 21.5% placebo-corrected cut in triglyceride levels in patients on statin treatment who began with a triglyceride level greater than 200 mg/dL and less than 500 mg/dL.
Data Source: The ANCHOR study, which randomized 702 patients to treatment with 4-g/day purified EPA, 2-g/day purified EPA, or placebo at 97 U.S. sites.
Disclosures: ANCHOR was sponsored by Amarin, the company developing AMR101. Dr. Ballantyne said that he has been a consultant for Amarin and has consulted for, received honoraria from, and/or been a speaker for numerous other pharmaceutical companies. Dr. Brinton said that he has been a consultant to Amarin and has also consulted for and/or been a speaker for several other firms.
ORLANDO – A 12-week treatment regimen with a purified formulation of fish oil led to a greater-than-20% reduction of elevated triglyceride levels, as well as other favorable lipid changes, in a phase III, randomized, placebo-controlled trial in about 700 patients.
"AMR101, pure eicosapentaenoic acid, at both 4 g/day and 2 g/day significantly reduced triglyceride levels in statin-treated patients with optimized low-density lipoprotein cholesterol levels and persistently elevated triglyceride levels," Dr. Christie M. Ballantyne said at the annual scientific sessions of the American Heart Association. The results he reported from the ANCHOR trial came from a group of 702 patients who had high cardiovascular disease risk and were on "optimized" statin therapy, with an LDL cholesterol level of 100 mg/dL or less, but with a triglyceride level of 200-500 mg/dL.
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Although the highest dosage of AMR101 tested (4 g/day) produced an average 22% reduction in triglyceride level beyond the placebo effect after 12 weeks of treatment, the clinical benefit from this triglyceride reduction remains uncertain until results accrue from a longer-term study that has clinical end points but is only now starting, he added.
"The key issue is, What does this mean for outcomes?" said Dr. Ballantyne, professor of medicine and pediatrics and chief of the section of atherosclerosis and vascular medicine at Baylor College of Medicine in Houston. "Omega-3 fatty acids have proven safety, but the question is, What will be the event reduction? There was prior evidence for efficacy in ... JELIS [Japan EPA Lipid Intervention Study]. I think the odds are higher for this working than for many other treatments," he said in an interview. But, he acknowledged, "no one has ever done a trial on patients with elevated triglycerides."
JELIS enrolled more than 18,000 men and postmenopausal women, both with and without documented coronary artery disease, who had a total cholesterol level of at least 6.5 mmol/L (251 mg/dL), and an LDL cholesterol level of at least 4.4 mmol/L (171 mg/dL). JELIS randomized patients to treatment with either a statin alone or a statin plus 1.8 g/day eicosapentaenoic acid (EPA), purified from omega-3 fatty acids in fish oil. After an average follow-up of 4.6 years, people in the combined statin-plus-EPA group had a 2.8% incidence of a major coronary event, compared with a 3.5% rate in those who were treated with a statin only, a 19% relative risk reduction that was statistically significant (Lancet 2007;369:1090-8). According to Dr. Ballantyne and others, the JELIS result remains the only evidence documenting that treatment with EPA can reduce the incidence of coronary events, although JELIS did not specifically enroll patients with elevated triglyceride levels at baseline.
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"There is no evidence" that lowering triglycerides cuts coronary events, agreed Dr. Eliot A. Brinton, director of atherometabolic research at the Utah Foundation for Biomedical Research in Salt Lake City. "Results from five fibrate treatment trials were all suggestive that lowering triglycerides led to reduced events. And the JELIS results showed clinical benefit with fish oil and greater benefit in people who entered with high triglycerides and low levels of HDL cholesterol. The EPA [that was] used in JELIS was essentially the same drug as AMR101," a highly purified form of EPA, Dr. Brinton said in an interview. "But we won’t know what AMR101 will do for events until we do a study," added Dr. Brinton, who is on the steering committee for the AMR101 clinical trial scheduled to soon begin.
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