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  Omega 3
Battling the blues: ongoing research shows that omega-3 fatty acids help treat depression: an interview with Andrew Stoll, M.D

Saturday Evening Post, May-June, 2005 by Patrick Perry

Several years ago, Dr. Andrew Stoll, director of the Psychopharmacology Research Laboratory at Harvard Medical School-McLean Hospital, conducted a landmark study on the role of omega-3 fatty acids in bipolar disorder and came up with some surprising results. The researcher discovered that when patients with bipolar disorder consumed omega-3 from fish oil, they experienced a marked reduction in episodes of mania and depression. Extensive research continues to demonstrate that omega-3 fatty acids form the foundation of a solid, healthy diet, while also reducing the risk of heart disease, stroke, hypertension, and arthritis, among other conditions.

Depletion of the essential omega-3 fatty acids in the typical American diet is linked to chronic disease and the huge increase in the rates of depression. Researchers now speculate that the increase in depression correlates well with the progressive depletion of omega-3s in our diet throughout the 20th century. The shift from rural community life to fast-paced urban sprawl also ushered in an era of fast foods, low fiber, and foods high in saturated fats, trans-fatty acids, and excessive intake of omega-6 fatty acids.

Omega-6 fatty acids are converted by the body into a number of strongly inflammatory hormones, collectively known as eicosanoids. Prostaglandins are the most well-known class of eicosanoids. If omega-6-derived eicosanoids are produced in excess over time, the risk of developing heart disease, other inflammatory medical conditions, and, apparently, depression and bipolar disorder skyrockets.

The omega-3 fatty acid eicosapentaenoic acid (EPA) is converted into eicosanoids as well, competing directly with omega-6 fatty acids for access to the enzymes that convert these fatty acids into eicosanoids. Whichever acid wins the competition for these eicosanoid-producing enzymes depends solely on the ratio of omega-6 versus omega-3 consumption in the diet. This is crucial, because the omega-3-derived eicosanoids are largely anti-inflammatory hormones and have the role of keeping the omega-6-derived eicosanoids in check. Now, omega-6 fatty acids aren't bad, unless there is an excess over time.

Therefore, essential fats such as the omega-3s EPA and docosahexanaenoic acid (DHA) are necessary for optimal health.

Historically, scientists believe that our ancestors consumed close to a one-to-one dietary ratio of omega-3, found primarily in certain fish, to omega-6, commonly found in vegetable and seed oils. Today, researchers estimate that the ratio of omega-6 to omega-3 fatty acid consumption is somewhere between 20:1 and 50:1 in the United States, with an abundance of omega-6 over omega-3 fatty acids, which pushes us in a pro-inflammatory direction, more susceptible to heart disease, arthritis, and to illnesses related to inflammation, and perhaps depression and bipolar disorder.

To update readers about Dr. Stoll's ongoing research into the role of omega-3 fatty acids in depression, the Post spoke with the Harvard researcher and author.

Post: Do omega-3 fatty acids continue to demonstrate mood-stabilizing benefits?

Dr. Stoll: No one has replicated the findings of our original study as yet. The real story now is that there are now numerous positive studies on the benefits of omega-3 in unipolar depression, schizophrenia, borderline personality disorder, ADHD, and Huntington's disease. It seems that many disorders respond to omega-3s. Three of the four studies in depression used EPA, or EPA plus DHA, and they worked. The fourth study used pure DHA--important for developing babies, pregnant women, and nursing mothers--and it failed. People hold onto stores of DHA for a long time, so you don't need to replenish levels as often as with EPA, which is turned over constantly, by conversion into eicosanoid hormones.

Post: Does EPA have anti-inflammatory properties?

Dr. Stoll: Exactly. The anti-inflammatory action of omega-3s has been definitively shown to help prevent heart attacks, in part by reducing atherosclerosis (hardening of the arteries). Omega-3s also appear to help cut down on the need for medications to treat rheumatoid arthritis, ulcerative colitis, Crohn's disease, and a number of other medical conditions. Omega-3s may also work in osteoarthritis. Research on omega-3s is exploding-and not just in psychiatry.

Post: Are you continuing your research into the relationship between fats and mental health, particularly omega-3 fish oils in bipolar disorder?

Dr. Stoll: Yes. We published the results of our first bipolar study, and the results were very promising. We went out on a limb to do this study with no funding and with colleagues sometimes ridiculing us. But the study was logical and rational, and patients, as well as informed and open-minded physicians, liked the approach. We tried it randomly and it worked. The same pathways are activated during bipolar disorder and depression, so EPA may perform the anti-inflammatory action.

Post: Do your patients, who were part of the original study, continue to take omega-3 and experience relief from their symptoms?

Dr. Stoll: I still see some of these people. All continue to take omega-3 supplements. In my practice, I am in favor of it, so I advise people to take it--if not for the psychiatric benefits, then for the general health benefits.

Post: Is there a downside to supplementing with omega-3?

Dr. Stoll: There isn't. Some people may experience GI distress if they take a large amount of a low-quality supplement. But the highest good-quality fish oil is not rancid and has little or no taste and has no side effects. Another issue that people worry about is bleeding, because EPA inhibits platelet aggregation. But we scoured the scientific literature, and there has never been a documented case of bleeding due to omega-3 fatty acids.

We recently reviewed about 18,000 people who participated in clinical trials with omega-3s, largely in cardiology studies, and we couldn't find one instance of bleeding in any of the trials. There was no bleeding, even if used in IVs prescribed before and during cardiac surgery. I think this perception is a myth because omega-3s don't inhibit the platelets as strongly as aspirin--perhaps 60 to 70 percent as much as aspirin--and unlike aspirin, the effect is reversible.

Post: When a patient is on blood thinners, such as coumadin, should they exercise caution when supplementing with omega-3?

Dr. Stoll: In that situation, I usually recommend a lower dose, not exceeding one or two grams of EPA per day. At this dosage, there should be no effect on the action of coumadin. The unanswered question is, together are they providing too much anticoagulation? Nonetheless, there may be some minute risk of a negative interaction with anticoagulants, such as warfarin (coumadin), high-dose aspirin, or ibuprofen-like medications, based on animal data and anecdotal reports in humans.

However, large-scale controlled clinical trials with patients receiving omega-3 fatty acid supplements with either aspirin or warfarin observed no cases of bleeding even after one year of the combined treatments. It would be a shame if cardiac patients or their physicians avoided the use of omega-3 supplements out of fear. I am thoroughly convinced that the dramatic and lifesaving cardiac actions of omega-3s far outweigh the very small or nonexistent risk of bleeding.

Post: What dosage do you recommend for patients with bipolar and/or depression?

Dr. Stoll: Our omega-3-fatty-acids-inbipolar study was the first controlled study in psychiatry. We really had no way of knowing what the minimum effective dosage was, so we decided to use a moderately high dosage that had been successfully used in omega-3 studies of rheumatoid arthritis and other medical disorders. This dosage was about 10 grams per day (6.5 grams of EPA and 3.5 grams of DHA daily). Most of the newer omega-3 studies in major depression used a very low dosage of pure EPA added to partially effective or noneffective antidepressants. For example, in one small study, Dr. Malcolm Peet and colleagues from England compared one gram a day of EPA to two grams a day of EPA, and up to four grams of EPA per day. One gram of EPA did the best by far. The most recent depression study, done by a group from Taiwan, was another unipolar study where they added omega-3 to an antidepressant regimen that was not working. They used the same exact formulation that we did-nearly 10 grams of EPA plus DHA in about a 3:2 ratio--with good results.

So, the question of optimal dosage remains unanswered. Practically, I start patients on one gram of EPA per day, and go up on the dosage gradually until an effect is seen on a person's mood. I usually do not have to exceed six grams of EPA per day. The amount of omega-3 in a supplement may be calculated from the side of the bottle.

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