American Association of Neurological Surgeons: High-Dose Omega-3 Oils used to Treat Non-Surgical Neck and Back Pain

Transcription

1 American Association of Neurological Surgeons: High-Dose Omega-3 Oils used to Treat Non-Surgical Neck and Back Pain Doctors Guide, April 20, 2005 By Cameron Johnston Investigators at the University of Pittsburgh have treated chronic pain patients with high doses of omega-3 fatty acids the ingredient found in many cold-water fish species such as salmon. The researchers say their findings suggest that this could be the answer to the adverse effects seen with nonsteroidal antiinflammatory drugs (NSAIDs), including cyclooxygenase (COX)-2 inhibitors, which have been associated with potentially catastrophic adverse effects. Dr. Joseph Maroon, neurosurgeon and specialist in degenerative spine disease at the University of Pittsburgh reported the findings April 19 th at the 73 rd meeting of the American Association of Neurological Surgeons. Patients who took high doses of omega-3 oils were impressed enough with the outcomes that they chose to continue using the oils and forego the use of NSAIDs. The 250 study patients suffered from chronic neck or back pain but were not surgical candidates, and they had been using daily doses of NSAIDs. After 75 days of taking high doses of omega-3s, 59% had stopped taking prescription drugs fro their pain. 88% said they were pleased enough with the outcomes that they planned to continue using the fish oils. No significant adverse effects were reported.

2 American Academy of Pain Management Weiner s Pain Management A Practical Guide for Clinicians Seventh Edition, 2006, pp Edited by Mark Boswell and B. Eliot Cole Changes in the modern diet are largely responsible for the increasing incidence of essential fatty acid (EFA) imbalances and deficiencies. The ratio of omega-6 to omega-3 fats has changed dramatically due to the widespread use of vegetable oils (mostly n-6 fats) in cooking and to the processing of oils to alter omega-3 fats to improve shelf life and eliminate their stronger taste (just think of the distinctive tastes of cod liver or flax oil). Historical estimates place the ratio of omega-6 to omega-3 oils at nearly 1:1 for prehistoric humans. By the turn of the century (1900), the ratio had increased to about 4:1. The current American ratio is about 25:1. The sharp rise is due to increased vegetable oil consumption: from 2 lb. per year in 1909 to 25 lb. per year in 1985! Many of the chronic inflammatory conditions that accompany EFA imbalance are currently treated with symptom-specific pharmaceutical drugs such as steroids, prednisone, aspirin, and other nonsteroidal anti-inflammatory drugs (NSAIDs), sulfasalazine, and colchicine. The problem with such drug therapies is that they prevent the formation of good anti-inflammatory eicosanoids, or they shift the production of one type of eicosanoid to another. For effective, long-term management, eicosanoid production should be modified through dietary changes (balancing dietary intake of specific fats) and controlling insulin levels in the circulation. Maintaining a proper balance between the various families of dietary fats may be one of the most important preventative measures a person can take to reduce the likelihood of developing one of the chronic diseases of modern civilization, such as diabetes, heart disease, obesity, irritable bowel syndrome, and autoimmune disease. And for patients who may already have one of these diseases, EFA testing and therapy has been demonstrated to reduce both morbidity and mortality associated with these diseases.

3 Spine Pain and Omega-3 Essential Fatty Acids Dan Murphy, DC 1 Cox enzymes convert the omega-6 fatty acid arachidonic acid into the proinflammatory pain producer prostaglandin E2 (PGE2). Cox 1 Arachidonic Acid AA 20:4n-6 Cox 2 Cox 3 Prostaglandin E2 Pain Most cox-enzyme inhibiting pain drugs known as non-steroidal antiinflammatory drugs (NSAIDs) inhibit both cox-1 and cox-2 enzymes. However, blocking the cox-1 enzyme resulted in significant bleeding problems. A study published in the New England Journal of Medicine in 1999 (1) noted that prescription NSAIDs for rheumatoid and degenerative arthritis alone conservatively accounted for a minimum of 16,500 fatal bleeding deaths per year in the US, which is the 15 th leading cause of death in the US. It was thought that if a drug could be developed that blocked only the cox-2 enzyme, there would be fewer bleeding problems / deaths while maintaining significant pain reduction. Starting in 1999, the US Food and Drug Administration (FDA) approved three such cox-2 enzyme inhibitors, Bextra, Vioxx, and Celebrex. On September 30, 2004, Merck, the maker of the cox-2 inhibiting drug Vioxx, pulled this product from the marketplace because it tripled or quadrupled the incidence of heart attacks and strokes. Bextra had already been pulled from the market for the same reason, and the FDA issued a black box warning (strongest possible warning against using the product without actually removing the drug from

4 the marketplace) against the drug Celebrex. Published accounts suggest that the drug Vioxx resulted in 56,000 fatal heart attacks / strokes in the 5 years it was on the market (see reference #2 for review). The scrutiny concerning the dangers of the cox-2 enzyme inhibiting drugs expanded to all NSAIDs, including those sold over-the-counter. An article published in 2005 notes (3): More Pain Relievers Called Into Question Study Stirs Concern About Heart Safety of Over-Counter Drugs Associated Press April 19, 2005 By Marilynn Marchione With prescription drugs Vioxx and Bextra already pulled from the market, a study has raised disturbing questions about the heart safety of over-the-counter pain relievers such as Advil, Motrin and Aleve. Those taking the drugs for at least 6 months had twice the risk of dying of a heart attack, stroke or other heart-related problem. The study was released at an American Association for Cancer Research conference in Anaheim. The findings add to the suspicion that the heart risk extends beyond the so-called COX-2 drugs Bextra, Vioxx and Celebrex to the larger family of medications known as non-steroidal anti-inflammatory drugs, or NSAIDs, which include naproxen, ibuprofen and virtually all other overthe-counter pain relievers. To the best of our knowledge, these are the first data to support putting a [black] box warning on NSAIDs, not just COX-2s said Dr. Andrew Dannenberg, a Cornell University scientist who helped do the study. The NSAID users were dying at twice the rate of the others from heart related problems. Risk was highest among ibuprofen users who were nearly three times more likely to die of cardiovascular disease than non NSAID users. 2 It is clear, that a non-drug approach to pain management is imperative. Dr. Joseph Maroon, neurosurgeon and specialist in degenerative spine disease at the University of Pittsburgh reported on such a non-drug alternative to the treatment of chronic spine pain on April 19 th at the 73 rd meeting of the American Association of

5 Neurological Surgeons. A review of his research was published the following day, and notes (4): 3 American Association of Neurological Surgeons: High-Dose Omega-3 Oils used to Treat Non-Surgical Neck and Back Pain Doctors Guide, April 20, 2005 By Cameron Johnston Investigators at the University of Pittsburgh have treated chronic pain patients with high doses of omega-3 fatty acids the ingredient found in many cold-water fish species such as salmon. The researchers say their findings suggest that this could be the answer to the adverse effects seen with nonsteroidal anti-inflammatory drugs (NSAIDs), including cyclooxygenase (COX)-2 inhibitors, which have been associated with potentially catastrophic adverse effects. Patients who took high doses of omega-3 oils were impressed enough with the outcomes that they chose to continue using the oils and forego the use of NSAIDs. The 250 study patients suffered from chronic neck or back pain but were not surgical candidates, and they had been using daily doses of NSAIDs. After 75 days of taking high doses of omega-3s, 59% had stopped taking prescription drugs for their pain. 88% said they were pleased enough with the outcomes that they planned to continue using the fish oils. No significant adverse effects were reported. This omega-3 research by Dr Maroon was published in the medical journal Surgical Neurology in April Comments from the abstract include (5): Omega-3 fatty acids (fish oil) as an anti-inflammatory: an alternative to nonsteroidal anti-inflammatory drugs for discogenic pain Department of Neurological Surgery, University of Pittsburgh Medical Center The use of NSAIDs are associated with extreme complications, including gastric ulcers, bleeding, myocardial infarction, and even deaths.

6 An alternative treatment with fewer side effects that also reduces the inflammatory response and thereby reduces pain is believed to be omega-3 EFAs found in fish oil. 4 At an average of 75 days on fish oil, 59% discontinued taking their prescription NSAIDs for pain and 88% stated they would continue to take the fish oil. There were no significant side effects reported. Our results mirror other controlled studies that compared ibuprofen and omega-3 EFAs demonstrating equivalent effect in reducing arthritic pain. Omega-3 EFA fish oil supplements appear to be a safer alternative to NSAIDs for treatment of nonsurgical neck or back pain. The ratios of the various omega-3 essential fatty acids is important (ALA/EPA/DHA plus GLA, etc.). I use those from Nutri-West along with their necessary double bond protective co-factors (Nutri-West: ). References 1) Wolfe MM, David R. Lichtenstein DR, Singh G; Gastrointestinal Toxicity of Nonsteroidal Antiinflammatory Drugs; New England Journal of Medicine; Volume 340 Number 24; June 17, 1999; pp ) Murphy D; Cox Inhibitors and the FDA; January ) Marchione M; More Pain Relievers Called Into Question: Study Stirs Concern About Heart Safety of Over-Counter Drugs; Associated Press; April 19, ) Johnston C; American Association of Neurological Surgeons: High-Dose Omega-3 Oils used to Treat Non-Surgical Neck and Back Pain; Doctors Guide, April 20, ) Maroon JC, Bost JW; Omega-3 fatty acids (fish oil) as an anti-inflammatory: an alternative to nonsteroidal anti-inflammatory drugs for discogenic pain; April 2006;65(4); pp

7 Toxic Fat Barry Sears, PhD The underlying cause of chronic disease comes from increased production of a natural fatty acid called arachidonic acid (AA), which can be incredibly toxic at high concentrations. This is the toxic fat that is key to not only understanding our obesity epidemic but also providing the linkage between obesity and chronic disease. P. 2 Classic inflammation hurts; silent inflammation slowly kills. P. 25 All forms of inflammation (including silent inflammation) are ultimately controlled by a group of hormones known as eicosanoids. It is the balance of eicosanoids in your body that is the ultimate key to wellness. All eicosanoids are ultimately derived from dietary fat, in particular the polyunsaturated essential fatty acids that must be supplied by the diet. Virtually all chronic diseases can be viewed as a consequence of a continuing imbalance of good and bad eicosanoids. P. 259 There are only three such essential fatty acids that can be made into eicosanoids: Dihomo-gamma-linolenic acid (DHGLA) Arachidonic acid (AA) Eicosapentaenoic acid (EPA) P. 19 Smoking marijuana dramatically increases appetite; it gives one the munchies. This is because of the chemical tetrahydrocannabinol or THC. The brain makes its own endocannabinoid hormones, making one dramatically more hungry, from the toxic fat arachidonic acid. P. 39 Silent inflammation causes both insulin and leptin resistance. P. 45 Sleep deprivation and stress create both insulin and leptin resistance. From AA come all the pro-inflammatory eicosanoids that in excess accelerate chronic disease. P. 77 From DHGLA come very powerful anti-inflammatory eicosanoids that accelerate cellular rejuvenation. P. 77 EPA dilutes AA concentration in cell membranes, making it difficult to make pro-inflammatory eicosanoids. P It is excess insulin that makes you fat and keeps you fat p. 87

8 The Numbers 2 TG = triglycerides HDL = high density lipoprotein (good) cholesterol If the TG/HDL ratio is greater than 4, you probably have Toxic Fat Syndrome because it means you have insulin resistance. If your fasting insulin is greater than 10 uu/ml you have increased activity of the delta-5-desaturase enzyme that is the key to the production of arachidonic acid. Ideally, fasting insulin should be less then 5 uu/ml. The lower your fasting insulin levels, the longer and better you are going to live. P. 77 The true marker of Toxic Fat Syndrome is the AA/EPA ratio. If it is greater than 10, then you have Toxic Fat Syndrome, regardless of how good you look in a bathing swimsuit. A good ratio is 3, and the ideal ratio is about 1.5. p. 78 Chronic disease people tend to have an AA/EPA ratio greater than 20. p. 78 Markers of Malignant Toxic Fat: p. 80 AA/EPA > than 15 Fasting insulin (uu/ml) > than 15 TG/HDL ratio > than 4 Dangerous Poor Good Ideal AA/EPA > Fasting Insulin > <5 TG/HDL >4 3 2 <1 AA/DHGLA < 3 Condition (p. 113) No chronic disease Overweight, obese, type 2 diabetes, heart disease, before starting any weight-loss program Chronic pain Neurological Disorders Amount of EPA + DHA Required 2.5 grams / day 5 grams / day 7.5 grams /day 10 grams / day You will also need to take at least one hundred times more EPA compared to the levels of supplemented GLA not to have problems. P. 268 The AA/DHGLA ratio will indicate where you stand in terms of the body s ability to increase cellular rejuvenation (anti-aging). P. 259 The AA/EPA ratio will tell you the extent of silent inflammation in the body. P. 258

9 1) Take a multivitamin / mineral supplement: Every Day, All People Nutri-West ( ) Core Level Health Reserve 3 per day 2) Mitochondrial Health: A) Acetyl-l-carnitine B) Alpha-lipoic acid Complete AG 3 per day C) CoQ 10 3) Increase Glutathione A) N-Acetyl Cysteine, or NAC: Complete Glutathione 2-4 per day B) Undenatured Whey Protein: Complete Whey-G 2 scoops per day 4) Take omega-3s: Complete Omega-3 Essentials capsules 3 g / day = 6 capsules per day OR Complete Hi-Potency Omege-3 liquid 1 teaspoon per day 5) Take omega-3 antioxidants Complete Omega-3 Co-Factor 3 per day 6) Take 1200 IU vitamin D3 per day Vitamin D per day New Antioxidant Shake; put into a blender: 3 Core Level Health Reserve 3 Complete AG 2-4 Complete Glutathione 3 Complete Omega-3 Co-Factors 3 Vitamin D cup of mixed frozen blueberries 3/4 cup of pomegranate juice + 1/4 cup orange juice Blend After blending add two scoops of Complete Whey-G and mix in with a fork (do Not blend). Consume all at once or divide it into thirds to consume throughout day, keep refrigerated. Take Omega-3s separate, preferably at the end of the day.