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Cheney Turns Omega Fatty Acid Treatments on Its Head

dannybex

Senior Member
Messages
3,564
Location
Seattle
Hi PWB

I took the Bodybio lipid tests and was impressed with Dr. Kane.

I have CFS, and was found to be low in Omega 6. I was told to supplement with both Omega 6 and 3 fats in the form of flax oil and primrose oil, unrefined Safflower or Sunflower oil (hard to find unrefined). They also recommended a low carbohydrate diet and butter.

My tests showed a build up of VLCFAs and peroxynitrates

I did not get cured of CFS, but I did notice my hair growing in more. It had thinned with the onset of CFS.

I am considering going back for another Bodybio test, if I can afford it.

Note that this test is from a blood draw. The cells they test are at the most three weeks old if I understand correctly. That means the test reflects what you have been eating or supplementing the last three weeks, not long term.

Good health to all,
PWB

Thanks for posting PWB! Always great to hear from someone who has actually had the tests done. You mentioned that it didn't cure you (and I hope no one has claimed that it is a cure) but I'm wondering (besides the hair growth), did you notice any other improvements...like in cognitive function, energy levels, exercise tolerance?

Dan

p.s. I lost a ton of hair in the last 14-15 months. Not sure if it's from arsenic toxicity, mercury, or borderline anemia -- or all -- but that's very interesting that adding the unrefined oils helped! Curious...where did you end up finding them?
 

PWB

Messages
22
Body bio test

Hello,

I took the body bio lab tests in 2001. At that time I could, with difficulty, work full time.

I had diabetes under control. Dr. Kane's Body Bio lab recommended low carbohydrate (below 18% or preferably below 15% of calories from carbohydrates) just from my lab tests (independent of blood sugar tests). So I ate less than 35 grams of carbohydrate a day (most Americans probably eat about 300 carbs a day). There was also a problem with high insulin (from high carb diets) interfering with beta oxidation in the mitochondria, resulting in very long chain fatty acid buildup (VLCFA). This also seems typical in CFS.

My diabetes continued to be in remission, and I have had years of normal blood sugars.

Ed Kane (Dr. Patricia Kane's husband) consulted for about an hour with my nutritionist (Body Bio would not talk directly with me as the patient, as they are afraid of being accused of practicing medicine without a license). I was in the room during the phone consultation on speaker phone. Ed Kane said with my lipids problems etc, it would take two to four years for a recovery.

I can't really say whether their advice would have improved my CFS as I have car accident injuries, which caused more health problems. I also had noisy neighbors who would not let me get a good night's sleep. I was not consistent in following the supplements they recommended after six months or a year. Maybe if I had followed their advice for four years, I would have recovered. They wanted me to retest after six months or a year, and I didn't have the money.

Body bio recommended to me: 4 to 1 (omega 6 to omega 3) oil, primrose oil (to get 500 mg/day of GLA) carnosine,trace minerals, succinates, pyridoxine,folate,B12, riboflavin 5 phosphate, oral electrolytes, inositol, magnesium citrate, selenium selenite, butter, raw seeds, and eggs.

They said I should avoid aspartates, and sulfur (MSM, garlice, N acetyl cysteine, methionine and sulfate endings on minerals).

I continued to work with difficulty full time and later part time. My hair grew in thicker.

I believe I should go back to the 4 to 1, or 3 to 1 ratios of Omega 6 to Omega 3 that have been recommended by Dr. Kane or Dr. Cheney. I think overall their advice was quite good. Looking back over what I know now. and what the research in CFS points to, I think their advice was mostly accurate.

The only part I'm not sure about the accuracy of the Body bio advice, is what has not been resolved yet: this disagreement over the cause and treatment of CFS. Dr. Cheney now is against high vitamin B12 and D3 supplementation. In 2001, Kane recommended high B12. Would they now? I don't know. The question really is : Is Dr. Cheney right that the body is deliberately lowering the energy level to protect from peroxinitrite buildup and heart failure? Is it dangerous to use high b12? But should we continue to supplement with zinc, selenium, colostrum as these seem ok by most CFS practitioners? I'm still trying to figure it all out.

I'm taking: goat kefir, sacc. boulardii probiotics, inosine, American biologics digestive enzymes, seacure, zinc, selenium, moderate amount of B vitamins, magnesium and a low carb hunter gatherer diet (no fruit). I'm planning on trying Artemsia Annua, and Atrium cardio (raw heart).

I hope this info helps people!
 

dannybex

Senior Member
Messages
3,564
Location
Seattle
Thanks PWB...

Yes, very helpful indeed. A little depressing about the 2-4 year recovery time, but I gotta stop dwelling on expectations and just take things day to day...

I think in her pamphlet she talked too about some people noticing a difference within six months or so, so I suppose it depends on the person, their toxicities, imbalances, etc..

Question: Did they explain why you should avoid sulfur and sulphate foods/supplements?

And did they recommend the low carbs mainly because of the diabetes, or with regards to your CFS? Interesting comments about the high-carb diet contributing to VLCFA buildup and mito dysfunction...

And finally, by eating a higher protein / fat diet, did you lose weight, gain, or just stay the same?

Thanks PWB,

Dan
 

Michael Dessin

Senior Member
Messages
608
Location
Ohio
Bacon!!

This might sound pretty nasty...Doc had me eating tons of bacon, nitrate free. Literally two pounds a day.(two packages)...when I started recovering.

My brain always felt so much clearer right after eating bacon.

My guess, is that bacon is probably pretty high in omega 6.

I did have the olive oils and other fats as well. But the bacon made me feel incredible!

Yikes!!! They call me pig for brains at the clinic sometimes :D

Mike
 

dannybex

Senior Member
Messages
3,564
Location
Seattle
That sounds great...

Sounds great to me Mike...although 2 pounds of it a day? That would be nasty. :)

Might be O-6 in the bacon, and or other fats (we do need cholesterol), but I wonder if it was the high sodium in the bacon that helped (with orthostatic intolerance or adrenal issues)...

???
 

Freddd

Senior Member
Messages
5,184
Location
Salt Lake City
I have no idea what ratio of oil components is best. Elsewhere I am familiar with folks using fish and vegetable source omega3 oils with no noticable differences. With both active b12s, methylb12 and adenosylb12 sublinguals moderately high sublingual doses in 5 star brands or injected doses of 30mg of methylb12/day in 3 or 4 sc injections, and necessary cofactors people are experiencing remyelination and both central and peripheral neurological healing. This includes at least two people reversing foot drop and loss of motor control and intermittant incontinance. This takes longer than reversing FMS/CFS symptoms.
 

Frickly

Senior Member
Messages
1,049
Location
Texas
Omega 3

My sister and husband take cod liver oil for their allergies along with some other anti inflammatory supplements and it has made a huge difference. My sister rarely has migrains which used to be a constant problem for her. I also take cod liver oil and my son takes the gel caps. I am concerned about taking extra Omega 6 since it is thought to be a pro inflammatory. I definitly don't need help in that area. My problem is, I can't afford the pill form for my son and I and I don't think I can choke down one more tsp of that fish oil. Yuk....I guess I have a sensitive stomach and need to find another form that is cheaper than my son's ProOmega gel caps. I wonder if flax seed oil would be comparable to cod liver oil?
 

Chris

Senior Member
Messages
845
Location
Victoria, BC
those fatty acids....

Hi, all; I have done a bit of checking and thinking, and remain less than totally convinced by this 3:1 or 4:1 ratio stuff, though there are real issues here. I am going to begin with what may look like a diversion, but I hope is relevant.

Caldwell Esselstyn (Prevent and Reverse Heart Disease, 2007) has been working for many years with a group of cardiac patients in bad shape, using a very low fat totally vegetarian diet based on the work of Colin Campbell (The China Study, 2005), and his patients are doing very well still, after many many years. They use no fatty acid supplements, but do take a low dose of statins. He advises against fish or fish oil. Dean Ornish has also been working with a group of cardiac patients in bad shape for many years, using a very low fat diet that does allow no-fat yogurt and egg whites, but is othewise strictly vegetarian; no statins, but 3g fish oil, plus moderate exercise and stress reduction through yoga and meditation. His patients also are doing very well, and in his most recent book (Spectrum) he gives evidence that his methods are helping reverse prostate cancer too, with further speculation that they would probably be effective in breast cancer as well, since it too is a hormonally driven cancer, though ethics prohibits the kind of control group trial used for the prostate patients. Both these doctors have documented their results with high tech imaging methods, and have published their results.

So for many, including those facing serious threat, a healthy life is possible long term without fatty acid supplements, and also with substantial omega 3 supplements. Campbell, followed by Esselstyn, are confident that the human need for both EFAs is met by vegetables. Heart disease can be partially reversed by several versions of one common theme, a low fat basically vegetarian diet; round this centre, variations are possible–a bit of non fat animal protein, a low dose of statin, fish oil supplementation, exercise or stress reduction techniques–these can be used or not as long as the basic theme is respected. The path is pretty straight but not too narrow.

I am trying to establish a paradigm based on well documented territory I know well and have lived for some five years now. Heart disease is not CFS, but Cheney has proved beyond any doubt the major role that cardiac issues play in CFS, so it is not irrelevant. Cheney said (2005, “The Heart of the Matter”) that we are all in heart failure; that term seems too dramatic–diastolic dysfunction would seem more appropriate–but it may be relevant that a recent good study (GISSI-HF) showed that while statins were of no help in heart failure, fish oil was. Since at least 50% of patients with heart failure over the age of 60 are now classified as in diastolic, i.e. they have an ejection fraction of over 50%, their condition overlaps substantially with that of most of us, including myself. Fish oil also has a long history of research showing that it helps with arrhythmias, and decreases the chances of developing atrial fibrillation (Cheney mentions in “The Heart of the Matter” and elsewhere that many CFSers have arrhythmias, and I had heart surgery, which often triggers AF, and have never developed it; I have long taken fish oil and have developed a lot of respect for it.

Another basic preliminary point: the body sees the total sum of omega 3 and omega 6 presented to it, and does not distinguish between food and supplements; discussion of fatty acid supplements should remember this.
Cheney and Patricia Kane now want us to reduce our intake of omega 3s and increase that of omega 6s. Cheney depends on his echocardiogram measurements of the quick response of the heart (specifically the IVRT interval, which measures diastolic function, and which he takes as a measure of available energy–which sounds reasonable to me) to the skin application of various substances. But this quick response test has been questioned by Rich van Konynenburg, and the results make me think that Rich probably has a point, though I have seen no detailed critique, and am not capable of mounting one myself. On these grounds, and these only as far as I know, Cheney states that omega 3s, especially fish oil, generate uniformly negative responses in CFS but not in controls (though there were only 3 of those). It is true that 3s may be more easily oxidized, a possible explanation for this result.

In Cheney’s tests Omega 6s bring a better result, and a mix of 3, 6 and 9 even better. His results show that a ratio of 3:1 of 6 to 3 brings the best results, and suggests high grade olive oil as the closest approximation to this ratio. Fish oil generates a more strongly negative response than does flax oil among the available sources of 3s. Cheney has not yet offered evidence from patient outcomes of this shift in the prevailing opinion that the DHA and EPA found in fish oil are of strong benefit to the heart in reducing atrial fibrillation and clotting, the latter of some concern to CFS, since it seems that our blood is liable to clotting. In addition, there is evidence that the reduced incidence of atrial fibrillation may be due to the way that fish oil modulates autonomic tone, which can initiate such fibrillation. It all sounds good.

Can anything account for what Cheney claims to find? I am really not up to dealing with this, but I have found one possible clue. In a study published Sept. 1992 in Cardiovasc Res, P.L. McLennan et al., using marmosets, “Dietary fat modulation of left ventricular ejection fraction in the marmoset due to enhanced filling,” both fish oil and sunflower seed oil “enhanced ventricular filling, thus providing an energy sparing promotion of diastolic relaxation.” This in comparison to groups fed either sheep fat or a low fat reference diet. We humans should respond in much the same way–marmosets are close cousins. Fish oil should improve our diastolic function.

But another study, A. O. Verkerk et al., Fish oil curtails the human action potential dome in a heterogeneous manner, published Feb 2009 in Int J Cardiology, shows that in ventricular myocites taken from explanted (i.e. removed!) hearts from patients undergoing transplantation because of cardiomyopathy (Cheney!) “Fish oil shortens the cardiac potential and may cause a loss of the dome of action potential (AP). Under conditions of increased preexisting heterogeneity in repolarization this may aggravate dispersion in action potential duration.” I don’t know exactly what this means–maybe someone could enlighten me–but it suggests that in recently dead and severely cardiomyopathic hearts fish oil can have a negative effect, diminishing available energy and increasing the chaotic and therefore energy wasting response–the irregular wall motion noted by Cheney as typical, and registered in my two most recent echocardiograms, though not present a year after my surgery (i.e. not a result of that, as the cardiologists here assumed, but a result of CFS.)

There may thus be a cause for Cheney’s finding based on the assumption that our CFS hearts really are cardiomyopathic, as Cheney insists, and as most cardiologists deny, including the two I have consulted here, as they focus on the good ejection fractions–my own was over 70% and Cheney in his recent DVD states that 80% can be found, usually coupled with irregular wall motion, also my case, due perhaps to the “heterogeneity in repolarization.” It may be the case that our cardiomyopathic hearts do respond differently to fish oil supplementation, and after discovering this study my response is shifting a bit–my first one was “no way am I going to give up the well proved benefits of EPA and DHA on this slim evidence.” Like Cort, I wish that Cheney would publish a full account of his findings, since his DVD recordings, though remarkable performances, do leave many key questions unanswered.

There is another basic thing to consider. Fish and krill oils have a well documented anti-inflammatory power, which I have used myself (fish oil in the presence of aspirin generates resolvins–there is a biotech company, Resolvyx, working on creating resolvins, and one day I suspect they will revolutionize the pharmaceutical treatment of inflammation–unfortunately, it is a privately held company–if they ever go public, I shall be buying!); this is something I have used to control occasional episodes of scleritis. It works. But that anti-inflammatory power implies also that these oils downregulate the immune system–you seldom get anything for free! So you can suppress inflammation, but.... Again, one must make a choice, and the picture is not yet totally clear–fish oil seems helpful in some autoimmune conditions.

I am not sure what I shall do about this. Remembering my first principle–look at the total food + supplement intake-- I did a quick check on a few of my regular foods (www.whfoods.com is a useful website for this), and discovered that millet has, per cup of 240 gr, about .06 gr of Omega 3, and 1.16gr Omega 6. I eat about 1/3 cup, so get .02 gr of 3 and .4 gr of 6. Oats have .05 gr omega 3 and .84 gr omega 6 per cup of 234 gr, and I guess I have about that for breakfast. So just with those I am getting 1.24 gr of omega 6. The other vegetables I eat must add some more.

I am getting very little omega 3 other than what I take as fish (only once or twice a week) and fish and krill oil. So I doubt that I am actually getting more 3 than 6 overall, and I am not going to be railroaded into switching to olive oil (sorry, Sushi!) for severa reasons: olive oil contains a fair percentage of saturated fats, and reached the big time through its participation in the “Mediterranean diet” that was given a big push by the Lyon Diet Heart Study. This took 605 subjects who had survived a first heart attack and split them into two groups; half consumed the American Heart Association version of the Mediterranean diet, with olive oil as an important source of monounsatured fat, and the other half was asked to simply eat prudently, which apparently meant that they ate a diet “comparable to what is typically consumed in the US.”

After four years those on the Med diet were 50-70% less likely to experience a further cardiac ailments. This made fish, olive oil, and other foods “heart healthy.” But there is a catch. Though they did much better than the other group, after four years 25% had “either died or experienced some new cardiovascular event.” (I take this account from Esselstyn, one of my proved heart gurus). Esselstyn does not allow any oil, and Ornish only allows fish oil supplements.

So until I get further insight or information–and I shall keep looking, since this touches me nearly at several key points-- I think I shall reduce my intake of fish and fish oil, but maintain my input of krill oil, since it includes modest amounts of omega 6 and 9 along with the EPA and DHA that seem so useful, all packaged in phospholipids and protected by astaxanthin, a very powerful antioxidant inhering in krill (OK, I am sold on the stuff, and I do own a few shares in the company that makes it!) And maybe I shall add a bit of GLA–I shall decide that when I have thought more about the Kane doctrine, which I am too fatigued to think about seriously now.

I am not suggesting this as a universal response, just my own, since I have demonstrated susceptibility to CAD despite eating and living very sensibly, and have those periodic bouts of scleritis to deal with. I am also older than most of you, I would guess–76–and that makes a difference. Part of that difference lies in two facts; there is now good and solid research showing that we humans, unlike rats or mice, do a lousy job of converting alpha-linolenic, your basic Omega 3 fatty acid, into DHA and EPA, the Omega 3s characteristic of fish and krill oil. These fishy fatty acids have clear and well researched power in improving brains and eyes and other functions, and alas the basic human weakness in producing them from vegetable forms of Omega 3–basically the alpha-linolenic found in say flax and hemp–gets worse as we age.

So as an elderly person with documented CAD I am going to stick mostly with what Ornstein has proved works, and continue taking my fish and krill, though I may add a bit of GLA (the best Omega 6, it seems). But I want to make it clear that this is not a one size fits all kind of recommendation; it depends on my particular medical history, and on my age.

More generally, it might be useful in considering how to trim one’s sails into this new breeze to step back and think about just how Cheney derived this new suggestion, and how much trust one is prepared to put upon this very individual and not fully tested methodology, and how the suggested results fit into the context of all of one’s health concerns and the totality of one’s diet. We are not made only of CFS, nor do we consume only supplements, and we all eat individually chosen diets that will contain varying amounts of those fatty acids. One size does not fit all, and in trimming our sails we should not lose sight of the goal–we are all trying to get somewhere, not sail around in circles. But Cheney is a great doc anyway.

Best wishes, Chris.
 
C

Cloud

Guest
Very Interesting Michael......My entire life I couldn't stand pork, but I have craved it for about 5 years now. I know it's not just the protein I am craving because I don't crave meat in general, just pork.

lol, "pig for brains"......well that beats the old one
 

PWB

Messages
22
Yes, very helpful indeed. A little depressing about the 2-4 year recovery time, but I gotta stop dwelling on expectations and just take things day to day...

I think in her pamphlet she talked too about some people noticing a difference within six months or so, so I suppose it depends on the person, their toxicities, imbalances, etc..

Question: Did they explain why you should avoid sulfur and sulphate foods/supplements?

And did they recommend the low carbs mainly because of the diabetes, or with regards to your CFS? Interesting comments about the high-carb diet contributing to VLCFA buildup and mito dysfunction...

And finally, by eating a higher protein / fat diet, did you lose weight, gain, or just stay the same?

Thanks PWB,

Dan


Glad to help!This is what was in the Body Bio (Dr. Kane) lab test results:

"The use of sulfur supplementation such as MSM, garlic, N acetyl cysteine, methionine and sulfate endings on minerals would further suppress the serum chloride level or the sulfation metabolism due to low uric acid and is contraindicated at this time"

I have read elsewhere that uric acid gets rid of peroxyinitrite, which builds up in CFS. That would explain the low uric acid levels.

Body bio also wrote:

"Fatty acids become either triglycerides, membrane phospholipids, or are burned (beta oxidized) for energy. Fatty acids with 18 cabons (c) and smaller are oxidized in the mitochondria (M) while fatty acids with 20 c and above are oxidized in the peroxisome (p). P are small organelles with a monolipid membrane (most are bilipid) that normally form in the cell for detoxification of xenobiotics (toxins) and very long chain fatty acids (vlcfa). In addition, P model long chain fatty acids which are metabolically required, especially the ultra PUFA DHA (they enter with 24C and exit with 22C). An increase in VLCFAs is irritating to the nervous system and indicative of weak P proliferation (PP). Increased VLCFAs and branched chain fatty acids indicate poor cellulare detoxification processes through the cytochrome P450 system, impaired production of proaglandins and unstable redox potential. Detoxifying VLCFAs (beta oxidation) is a vital function in every cell as is the healthy production of prostaglandins. Since P have a short half life (1 1/2 days), stimulating (PP) is highly desirable.

"Hormones such as DHEA, growth hormone and thyroid and nutrients such as riboflavin and manganese stimulate PP and persoxisomal rspiration. Stimulation of the betal oxidation of VLCFAs and maintaining an optimal fluidity index as well as balancing w6:w3 [omega 6 to omega 3] is highly recommended. Nutrient intervention and hormonal therapy should be guided by your healthcare practitioner

"Nervonic excessivel level avoid borage, increase beta oxidation check peroxisomal respiration excessive VLCFA very low vitamin E intake/antioxidants for now, balance EFA and FI (?) add Mn, ribofla[riboflavin b2?]"

This was followed by a list of me having high levels of fats over 23 carbons and even 26 carbons (some I think were omega 9's).

It's interesting that Dr. Cheney currently recommends DHEA and growth hormone as well . At times, I have shown B2/riboflavin deficiencies in cracked peeling lips.

I lost a lot of weight doing low carbohydrate. It the only diet which I've done which had led to long term weight loss. I highly recommend natural low carb/Paleolithic diets. I gained more weight on low fat/high carb diets recommended by mainstream doctors! I think low carb is important for people with CFS as well as in the general population. Body bio wanted me to do low carb diet for both the CFS and prevent diabetes (my blood sugars were at the top of normal when I did the Body bio lab tests).

Thanks everyone for your information and comments. It helps me to learn and feel there is hope for good health,

PWB
 

PWB

Messages
22
carbons not cabons

Glad to help!This is what was in the Body Bio (Dr. Kane) lab test

Body bio also wrote:

"Fatty acids become either triglycerides, membrane phospholipids, or are burned (beta oxidized) for energy. Fatty acids with 18 cabons (c) and smaller are oxidized in the mitochondria (M) while fatty acids with 20 c and above are oxidized in the peroxisome (p).
PWB

I made a typo, it should say "carbons" not "cabons".
 

R**

Senior Member
Messages
121
The GAPS diet is high on facts, ghee, coconut oil, meat fat (organic, pastured preferred). I cannot stand meat, but I can tolerate it with ghee in bone stock, also part of the GAPS diet.

Brian Peskin also advocated a higher 6 to 3 ratio. The Hidden Story of Cancer is his book.. I think.. he also has a site. YES essential oil pills are based on his ideas and are 2:1 ratio of 6:3.

Yasko warns against too much lipids for those with NOS+ status. I am NOS+-. I am on the GAPS diet anyway and we shall see.

Too much conflicting info out there. I would prefer to get my lipids, omegas, etc naturally. I was vegetarian for 23 years, sometimes vegan and I am not sure it was a wise move for me. It takes effort and dedication to be a balanced vegetarian (not even talking about protein here). For example, if I go back to vegetarian, I would want to use less soy products. And I am not sure that the right kind of fats are not important.
 

R**

Senior Member
Messages
121
http://www.brianpeskin.com/

He says the body need varirous ratios of omegas 6:3 in diff organs. I think I remember this can go as high as 14:1 or 15:1.

http://gapsdiet.com/
I think there is some merit to these diet: GAPS, Body Ecology, Specific Carbohydrate, Weston Price although I think any of them can box on in just like any one protocol, Yasko, Simplified methylation, etc.

My sister recovered by addressing ANS, scar tissue, lymph, energetic blocks. Not sure she would qualify for CFS/ME diagnosis, but she was bedridden for years, had severe dysautonomias, RSD, so many other diagnosis on top of that.
 

Dolche

Dolche
Messages
25
Dr. Puri on Omega Fatty Acids to fight Viral Activity

The next part of the Phoenix Rising newsletter dealt with Dr. Puri's findings.

Using LRT As An Antiviral Therapy in the U.K. by Cort Johnson



  • Cort ,

    I am trying a series of high dose vitam c 25,000 mg/ hydrogen peroxide iv treatments?

    Has anyone seen positive results???
  • Puri, B. 2006. Long chain polyunsaturated fatty acids and the path of physiology of myalgic encephalitis (chronic fatigue syndrome). Journal of Clinical Pathology
  • Puri, B. 2004. The use of eicosapentaenoic acid in the treatment of chronic fatigue syndrome. Prostaglandins, Leukotrienes, and essential fatty acids 70, 399-401.
  • Puri, B., Holmes, J., and G. Hamilton. 2004. Eicosapentaenoic acid-rich fatty acid supplementation in chronic fatigue syndrome associated with symptom remission and structural brain changes. Int J . Clin Pract 58, 297-299.
  • Puri, B. 2003. The clinical advantages of cold-pressed non-raffinated evening primrose oil over refined preparations. Medical Hypotheses 62, 116-118.
  • Puri, B., Counsel, S., Hamilton, G., Richardson, A., Horrobin, D. 2001. Eicosapentaenoic acid in treatment resistant depression associated with symptom remission, structural brain changes and reduced neuronal phospholipids turnover. IJCP 55, 56-564.

Dr. Basant Puri of Hammermith Hospital in London has published a series of short papers on the effects of fatty acid (lipid) supplementation in chronic fatigue syndrome and other diseases over the past several years. He has also published a book on CFS that outlines for the public his research and treatment plans for CFS. A pioneer in the use of NMR brain scans in CFS, he believes his (and others) findings of increased choline levels in the cerebral cortex and basal ganglia of CFS patients probably indicate a central nervous system infection is present. (see Choline on the Brain).

Dr. Puri believes these high choline levels reflect viral interference with the enzyme responsible for putting together the lipids found in our membranes. These phospholipids should have either N-6 or N-3 longchain polyunsaturated fatty acids should be attached to them. If I am reading this correctly, a polar head made up of choline, serine, or inositol should be attached at the end of these phospholipids chains.

The enzyme used to synthesize the N-6 and N-3 polyunsaturated acids (delta-6-desaturase) can, however, be inhibited by viruses. Dr. Puri believes that viral activity in the central nervous system of CFS patients leaves choline molecules that would otherwise be attached to these polyunsaturated chains free, and it is these free choline particles are being picked that by these brain scans. This, of course, also suggests that the cellular membranes in these areas may have lower than normal levels of essential fatty acids.

Interestingly, gene expression studies of infectious mononucleosis patients who came down with CFS found that over half of the genes that were overexpressed in these patients were involved in fatty acid metabolism and mitochondrial functioning. The pathogen under discussion, EBV, actually uses one of the fatty acids in our cellular membranes to replicate.

Consequences of low fatty acid levels - why is it important to have adequate levels of polyunsaturated fatty acids in our cellular membranes? It turns out that not all lipids are the same; some lipids are more apt to promote an inflammatory reaction than others. The fatty acid evening primrose oil (EPO) is rich in, for instance, y-linolenic acid, is less likely to be transformed into arachidonic acid (AA) which sits at the beginning of the inflammatory reaction.

Building up levels of good lipids that are less likely to be converted to AA could therefore lead to reduced inflammation, oxidative stress, immune activation, etc. Dr. Puri believes this could explain why EPO was reported to be helpful in rheumatoid arthritis patients. Interestingly, the y-linolenic or good fatty acid pathway appears to be inhibited in many chronic diseases including viral infections, diabetes, and cardiovascular diseases, as well as aging.

Dr. Puris protocol, then, helps CFS patients recover from the damage caused by viral activity in their central nervous system by providing the essential fatty acids the viruses inhibit; it does not bring a halt to the viral activity.



This is not, however, the end of the LRT story. Dr. Puris analyses of unrefined evening primrose oil, a source of omega 6 fatty acids, indicate that it contains substances called tripertenes are a) free radical scavengers, and b) inhibit two inflammatory enzymes called cyclo-oxygenase and neutrophil elastase. EPO supplementation, then, appears to be able to reduce inflammation in several ways; by repairing cell membrane damage, by building healthy cell membranes that are less likely to initiate the inflammatory processs when injured, by reducing free radical levels and by inhibiting the inflammatory enzymes.

The Treatment Regime - Dr. Puri uses high-dose eicosapentaeonic (EP) fatty acid supplementation in CFS (10-12 capsules of eye q; 930 mg. EPA (omega 3), 290 mg. docahexanoic acid (omega 6), 100 mg. gamma linolenic acid (omega 6) + 16 mg. Vit. E daily. The sources of these fatty acids are fish oils (omega 3s) and unrefined, cold pressed evening primrose oil (omega 6).

Treatment results - one CFS patient with high fatigue, poor sleep, muscle pain, and low mood who was almost totally confined to a wheelchair after six years of CFS began to go into remission about six to eight weeks into the program. At 16 weeks her depression score had dropped from 27 to 3 (!) and she reported that her sleep was much improved. Her muscle pain, however, was unchanged.

Comments from a group of four CFS patients after 12 weeks of therapy ranged from the startling the fogginess of the brain was gone completely and the for the first time a feeling of well being was experienced to the beneficial I am able to communicate during a relapse.

Dr. Puri also tells a remarkable story of a 20 year old who in the seven years after the appearance of his depressive symptoms, had not only not responded to anti-depressants, antipsychotics, lithium, paroxetine and hypnosis but had over time become severely suicidal. One month after starting 4 g of eicosapentoaenoic acid a day his unceasing suicidal thoughts had disappeared. Nine months later all his symptoms had disappeared, his depression rating, formerly at 32, was now zero and a brain scan indicated that substantial changes had occurred.

Like the other treatments discussed in the edition Eye Q does not appear to cure CFS but its use may help ameliorate the symptoms of CFS.

Eye Q is made by a U.K. company, Equazen. It contains high levels of omega 3 and low levels of omega 6 fatty acids (from evening primrose oil) as well as an antioxidant, vitamin E. You can learn more about Eye Q at http://www.equazen.com/default.aspx?pid=23
 
Messages
763
Location
Israel
Dr Budwig

If you are interested in this topic I would sugggest you look at Dr Johanna Budwigs cancer cure. She would take people out of hospitals in Germany on their last legs and feed them a 2:1 ratio of flax oil and quark/cottage cheese....massage them with the oil and use it as an enema....

...Dr. Budwig chose organic flaxseed oil because it is the richest source of Omega 3 essential fatty acids, as well as being well-tolerated by most people and easily assimilated. She opted to mix the oil with quark because of its high levels of sulfurated protein (cottage cheese contains similar amounts...

Amazingly, Dr. Budwig found that after only three short months on her flaxseed oil-quark combination, cancer patients began to improve. Tumors shrunk in size, patients' strength returned...
....She was even able to help the patients whose doctors had told to "go home and die." Clearly, Dr. Budwig had hit on something big in the world of cancer research!

In fact, after over 10 years of clinical research, Dr. Budwig's combination of 2 tablespoons of organic flaxseed oil combined with one quarter cup of cottage cheese has been used successfully in Europe to treat a variety of diseases in addition to cancer, including arteriosclerosis, eczema, stomach and intestinal disorders, arthritis, and strokes

I get horrible stomach pains from flax seed oil and have lactose intolerance to cow's milk. Soya also hurts my stomach. These intolerances are related to my M.E. and Dr Myhill's treatment. Before I got M.E I could eat anything and everything.
I notice cancer patients rarely have the numerous allergies and food intolerances we have. It would be great for an M.E patient to try who can tolerate those things.
 

taniaaust1

Senior Member
Messages
13,054
Location
Sth Australia
Ive found the only thing which high quality and strength fish oil capsules helped was the osteroarthritis pain I had in my back at the time. These nor cod liver oil.. never have helped any of my ME symptoms. Evening Primrose Oil didnt help me at all either.

Nowdays I just try to make sure Im getting plenty of omega 3 and omega 6 and dont worry about balances as Ive never noticed them to help anywa.