Fish oil is not for cardiac patients

Dr. Weeks’ Comment: Seed oils heal the heart, not fish oil.

Food and Nutrition Sciences, 2013, 4; 9A, 76-85.

http://dx.doi.org/10.426/fns.2013.49A 1013 Published Online September 2013 (http://www.scirp.org/journal/fns)

Why Fish Oil Fails to Prevent or Improve CVD: A 21st Century Analysis

Brian Scott Peskin

Chief Research Scientist, The International PEO Society, Houston, USA. Email: prof-peskin@peskinpharma.com

Received June 1st, 2013; revised July 11th, 2013; accepted July 18th, 2013

Copyright © 2013 Brian Scott Peskin. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

ABSTRACT

In May 2013, The Risk and Prevention Study Collaborative Group (Italy) released a conclusive negative finding re- garding fish oil for those patients with high risk factors but no previous myocardial infarction. Fish oil failed in all measures of CVD prevention—both primary and secondary. This study was so conclusive that Eric Topol, MD, editor- in-chief of Medscape and Medscape’s Heartwire for cardiologists, issued a new directive to patients to stop taking fish oil, i.e., long-chain EFA metabolites of EPA/DHA. Fish oil’s failure is shown to be consistent with known physiology and biochemistry: there should never have been any expectation of success. To the contrary, true EFAs, linoleic acid and alpha-linolenic acid, termed Parent Essential Oils (PEOs), fulfill fish oil’s failed promise. Fish oil supplements contain supra-physiologic amounts of EPA/DHA. Recommendations are often paramount to pharmacologic overdose. Unlike fish oil, which failed to decrease 19 markers of inflammation, PEOs do decrease inflammation. The first screen- ing experiment comparing fish oil with Parent EFA oils, the seminal IOWA experiment utilizing pulse wave velocity, demonstrated unequivocally that fish oil contributes to hardening of the arteries, aging subjects by nearly 4 years (P < 0.0001). To the contrary, PEOs increase arterial compliance, making subjects’ arteries “biologically younger” (in- creased arterial compliance) by more than 11 years compared to subjects taking fish oil fish (P < 0.001).

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