Dr. Susie Rockway on conjugated linoleic acid (CLA)

I’m fascinated by the perspectives that nutritionists (free-thinking ones, at least), food scientists, and biochemists bring on nutrition and nutritional supplements.

A few months ago, I met a fascinating nutritionist/biochemist named Susie Rockway, PhD. Dr. Rockway brings a world of experience in the world of nutritional supplements, clinical trials with supplements, and their development. She has special expertise in conjugated linoleic acid (CLA), having been among the scientists who initially developed CLA as a supplement. We are also exploring CLA as a possible addition to the Track Your Plaque program and wanted to get Dr. Rockway’s perspectives.

So I asked Dr. Rockway if she’d answer a few questions for us.






TYP: Dr. Rockway, we understand that you are particularly excited about the prospects of CLA for FAT loss and perhaps for regression of atherosclerosis. Can you tell us about the origins of your interest in CLA and why you're so enthusiastic?

Dr. Rockway: I have been fascinated with this unique fatty acid since the early 1990’s when CLA was first being discussed as nature’s most potent anti-carcinogen. I was then working in the granting/funding section of the National Dairy Council and saw this molecule as truly one of the future functional fats that would likely benefit people (next to omega-3’s!)

I think the benefits of CLA have just begun to be investigated—animal studies are extraordinary for showing fat reduction, lean mass (muscle) increases, immune enhancements, blood glucose normalization, anti-inflammatory properties and plaque reduction!

Human data to date is very encouraging for fat reduction. As a nutritionist seeing the massive increase in abdominal fat (stomach fat) in the world population and the direct relationship to cardiovascular disease, I see CLA as a great supplement to take to help this. Of course eating lots of vegetables, fruit, lean protein and whole grain products is also a must for maximizing good health.

I am studying the impact of CLA in reducing muscle loss in aging women—a condition known as sarcopenia. As we lose muscle with age, we lose strength, falls increase, we become frailer, and eventually many of us lose our independence. Along with the muscle atrophy, most people gain fat—never a good thing! So, if CLA can reduce fat and increase muscle, our bodies are more likely to withstand the hurdles that life throws at us much more efficiently.

So, how can you not be excited about this very bioactive molecule?




TYP: What are your specific areas of interest in nutrition and health?

Dr. Rockway: I strive to understand the role of bioactive molecules that can be taken to improve the aging process and enhance health.

As a trained nutritional biochemist, we tend to look at cell metabolism in a very ideal sense: what we learned in our biochemistry texts years ago where all substrates, proteins, enzymes, etc. are made exactly when we need them, where all cells behave as they should.

Unfortunately, little research has been devoted to understanding the changes in metabolism as we age. Do we still produce everything as efficiently as when we were 20? I suspect not. So, I think we need a little help, and supplements are a key to getting there.

Two nutrients that I think are emerging as “super nutrients” are the fatty acids found in fish oil (EPA and DHA) and vitamin D. Where we know these two nutrients are essential for life, we are seeing that they play a huge role in the QUALITY of life. Mood, depression, PMS, wound healing, bone growth, atherosclerosis, and arthritis are clinical areas where we see a direct benefit with doses of omega-3 and Vitamin D that are probably much greater than the RDA. Our current requirements for nutrients are really based on fixing deficiencies and not maximizing health, and maximizing health is where I’m at.

Thus, I am very interested molecules like CLA as mentioned above, and other bioactive ingredients such as plant derived ingredients (phytochemicals) called flavonoids that may well help explain why people who have diets high in fruits and vegetables are less likely to have certain cancers and heart disease. Reducing oxidative stress through foods that provide these active molecules (think colored fruits and veggies) is a new and exciting area of research.



TYP:The big "diet experiment" in America has clearly steered people in the wrong direction, usually by 50 or more pounds. As a scientist in nutrition, what are your thoughts?

Dr. Rockway: The American Heart Association was keen 20 years ago to promote the low-fat diet for all Americans as the key way to reduce cholesterol levels and decrease chance of heart disease, the number one killer of men and women. However, I must admit the nutritional community bought into this one, too. Unfortunately, the general public took this message to reduce percent fat in their diet (and they did a bit), but increased overall calories instead—and a large portion of the increased calories was from simple carbohydrates. I’m convinced that this in itself has been part of the huge rise in obesity…we simply eat more food and it’s not the healthy kind of food either.

When you increase sugar intake beyond what you burn off, you will store some of it as glycogen in the liver and muscles, but you will convert most of the excess into fat—and that we can store very efficiently! The fat that is made in the liver is sent to the blood as VLDL’s which are the precursor to the class of lipids called low density lipoproteins (LDL) that are the “lethal” type of cholesterol circulating in our blood.

So, Americans now have to listen to a new message that they need to eat more fruits and vegetables in hopes they will cut down on fast foods—tending to be high in fat (saturated particularly), low in fiber and low in nutrients and other high calorie dense foods. We nutritionists have our work cut out for us, that’s for sure.



TYP: We are especially excited that nutritionists are assuming a leading role in shining light on the confusion in diet and nutrition that has characterized the last 40 years. Do you have a sense for the emerging important issues for the next 10 years?

Dr. Rockway: Certainly, the scientists in the nutritional field are well aware of the problems facing this nation—it’s in fixing them that we fall short!

We aren’t very well coordinated to get a single message out, nor do we all agree on what that message should be. I feel that people need to eat healthy MOST OF THE TIME, exercise all of the time, and take supplements that have clear evidence of benefit. Lots of my colleagues would not concur with supplement use. Our bodies were designed to move a lot and eat a lot…we just do the latter now and are paying the price!

One emerging and very exciting area that we have to teach Americans is that all fat is not bad. The different types of fat—omega-6 vs. omega-3, are where we need to focus our education.

Decreasing the corn oil we pour on everything needs to go out the window! Consume olive oil and eat fish or take fish oil supplements—we simply have tons and tons of research showing the benefits of reducing the ratio of omega-6 to omega-3. Did you know that cattle that are grass fed actually have less omega-6 in their tissues and more CLA? But most cattle are fed corn-based diets, so we have perturbed their natural selection of food and their fat composition.

See, it all comes back to CLA!


TYP: Thanks, Susie!




Susie Rockway, Ph.D., C.N.S.

Dr. Susie Rockway is an experienced scientist with accomplishments in both the academic and food and supplement industry business directing science/technology research. Her background includes faculty appointments at the graduate level in teaching and research at Rush University Medical Center and industrial experience managing basic and applied research studies.

Dr. Rockway received her Ph.D. in Nutritional Sciences, Biochemistry from the University of Arizona. Dr. Rockway has authored several publications in journals such as the Physiological Genomics, Journal of Nutrition, the Journal of Food Science, International Archives of Occupational and Environmental Health and has published chapters on nutrition on inflammatory bowel diseases. She is a member of the American Society for Nutrition, American Oil Chemists Society, the Institute of Food Technology, American College of Nutrition and is a Certified Nutrition Specialist.

We're also proud to add Dr. Rockway to our panel of Track Your Plaque Experts.

Comments (7) -

  • Perplexed

    10/5/2007 7:36:00 PM |

    Excellent! At 62 years old I'm one who followed a <10% fat diet fo 11 months and developrd a pot belly that still amazes me.
    I began following the TYP program 4 weeks ago but have been unable to reduce the abdominal fat.
    How long did it take Dr. Davis to see results after he stopped the Ornish diet?

  • Dr. Davis

    10/6/2007 12:13:00 AM |

    Within days, though weight was lost gradually, since it was a lesson I learned slowly back then.

  • ShuffleUp

    11/26/2007 3:11:00 PM |

    I've only done the non-wheat diet that TYP advocates for a couple weeks and my stomach is visibly thinner to not only me but others that know me and see me regularly.  The thing that amazes me more is that I am not hungry either.  I've cut out most grains as well but I eat 4 tbsp's of oat bran (2 in the morning and 2 at night).  I think on a low(er) carb diet you will notice that you will lose some glycogen in the beginning which will show up in less weight on the scale as well.  I've probably dropped a good 5 lbs. in that time period. My skinfold measurements have changed very slightly but if you are losing more VAT then this won't show up in the skinfolds as much.

  • Anonymous

    1/26/2008 3:33:00 PM |

    Regarding CLA as a supplement to aid in weight loss and other promoted benefits; any thoughts on what would be the recommended dosage and are there differences in the capsules available on the market?
    Thanks in advance -

  • Dr. Davis

    1/27/2008 2:09:00 AM |

    I'll answer for Susie.

    I've had experience (as has Susie) with the Intellitrim brand (www.beneomega.com, the same source as the PharmaOmega high-potency fish oil) and the Tonalin brand, which is distributed by a number of retailers, including Vitamin Shoppe.

    The dose that has been most widely explored in clinical trials and appears to yield weight-loss effects is 3000 mg per day.

  • Anonymous

    11/17/2009 11:40:54 AM |

    It was extremely interesting for me to read this blog. Thanks for it. I like such topics and anything connected to this matter. I definitely want to read more soon.

  • buy jeans

    11/3/2010 7:34:51 PM |

    I think the benefits of CLA have just begun to be investigated—animal studies are extraordinary for showing fat reduction, lean mass (muscle) increases, immune enhancements, blood glucose normalization, anti-inflammatory properties and plaque reduction!

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Vitamin D disappointment ahead

Vitamin D disappointment ahead

Anyone following the Track Your Plaque conversation know that we are rabid fans of normalizing blood vitamin D blood levels (25-OH-vitamin D3).

A wonderful report on vitamin D was aired this morning on the NBC Today show. The interviewed guests did a good job of describing the health effects of vitamin D, thought the focus was on some new data on the use of vitamin D for breast and prostate cancer.

I learned that shiitake mushrooms have some vitamin D--I didn't know that! (They contain 260 units per 4 mushrooms.)

Unfortunately, the closing comments from the guests, among whom was nutritionist and author, Joy Bauer,MS, was that you should get vitamin D from your multivitamin or your calcium with vit D.

That is absolutely wrong. When you check blood levels of vitamin D, as we do in everybody we see, you quickly learn what works and what doesn't.

Vitamin D in multivitamins is very poorly absorbed, if at all. Likewise, about 90% of the D in most calcium preparations is not absorbed. The vast majority of tablet or powder preparations, such as those in calcium tablets, are not absorbed to any significant extent. Take all you want and you remain vit D-deficient with osteoporosis, growing coronary plaque, low HDL, and exposed to risk for prostate and colon cancer.

If you take vitamin D in supplement form, it must--MUST--be in an oil-based capsule. The tablets are simply much too poorly and erratically absorbed to be reliable. There's nothing more frustrating to take, for instance, 4000 units of vitamin D in tablet form, only to have a blood level of 12 ng/ml--severe deficiency. Take the same 4000 unit dose in capsule form and blood level skyrockets to 58 ng/ml. And it's no more expensive.

One other thing: If you want to waste time and money, take the prescription vitamin D prescribed by many doctors. This is vitamin D2, also known as "ergocalciferol". Why use the synthetic vitamin D2 when D3 is the form your body needs? Because the D2 is patent-protectable and profitable to the drug manufacturer, similar to using Premarin (horse estrogens) when human preparations would suffice--or be superior. I saw a woman today taking 50,000 of prescription D2 once per week. Her blood level of 25-OH-vitamin D3? 17 ng/ml--severe deficiency. Don't waste your time with this garbage.

Comments (9) -

  • Ortcloud

    6/5/2007 4:50:00 PM |

    I am often disappointed with "experts" that you see being interviewed on tv. It makes you wonder where they get these people. Do you think they would ever interview you if you offered? Maybe you could get on their list of experts to refer to.

  • Anonymous

    6/5/2007 5:13:00 PM |

    Dr. Davis, Thank you for this posting!  My vitamin D levels were tested in early April at 17.  I have been taking citrical with vit. D.  From your post, this sounds like a bad idea!  Can you recommend a good brand of oil-based D3 capsules?  Also, how long should it take for my vit. D levels to normalize?  Thank you!

  • Dr. Davis

    6/5/2007 8:20:00 PM |

    Ortcloud--
    Thanks for the vote of confidence.

  • Dr. Davis

    6/5/2007 8:21:00 PM |

    We've used Carlson's and Vitamin Shoppe's 2000 unit vitamin D3 (cholecalciferol) capsules with great results. It takes about 4 weeks to fully reflect the dose.

  • Anonymous

    6/30/2007 12:34:00 PM |

    How about co-administering an oil along with a powdered vitamin D tablet or capsule? I would be curious to see absorption rates using this method vs. oil-based vitamin D.

    Also does this low absorption apply to all fat soluble vitamins? In other words, must vitamin A, E, and K also be in an oil or oil-based to maintain optimal bioavailability? Thanks.

  • Dr. Davis

    6/30/2007 1:51:00 PM |

    Including oil with a powder form of D does enhance absorption though in my experience it remains erratic.

    I'm uncertain about the E and A, though I suspect the same remains true. I would really like to know how important this phenomenon is with K2, but I am not unaware of any real data, nor do I have sufficient experience to say at this point. With time.

  • Anonymous

    8/13/2007 12:51:00 PM |

    After taking Prescription Vitamin D ( oil ) capsule for
    3 month my levels were up to 50.
    Now I am taking 1ooooIU's daily and my levels are down to 29. Does fish oil capsule interfere with the asboprtion of Vitamin D?
       Maria

  • Dr. Davis

    8/13/2007 2:51:00 PM |

    Hi, Maria--

    No, in fact fish oil should do the opposite and can increase D absorption. It might therefore be variation in your preparation.

  • Doug

    4/7/2009 6:21:00 PM |

    I live in Canada and am on a perpetual 50,000 iu/week dose of Vitamin D due to low blood levels.

    AFAIK only D2 is available in Canada, and the endo dismissed any negative comparison with D3.

    What can I do ?

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Emmer, einkorn, and agribusiness

Emmer, einkorn, and agribusiness

10,000 years ago, Neolithic humans did not obtain wheat products from the bagel shop, grocery store, or Krispy Kreme. They obtained wheat by locating a nearby wild-growing field of wild emmer or einkorn wheat grass, then harvesting it with their stone sickles.

Neolithic humans, such as the Natufians of the Fertile Crescent, carried their freshly-cut wheat home, then ground it by hand using homemade mortar and pestle. As yeast-raised bread was still some 5000 years in the future, emmer and einkorn wheat was not used to bake bread, but was consumed as a porridge in bowls. Einkorn has the simplest genetic code of 14 chromosomes, while emmer has 28 chromosomes.

A third variety of wheat appeared on the scene around 9000 years ago, a natural hybridization between emmer and goat grass, yielding the 42-chromosome Triticum aestivum species. Egyptians learned how to cause wheat to rise around 3000 BC, yielding bread, rather than the unleavened flatbreads of their predecessors.

From the original three basic varieties of wheat available to Neolithic man, over the past 30 years wheat has exploded to over 25,000 varieties. Where did the other 24,997+ strains come from?

In the 1980s, thousands of new wheat strains arose from hybridization experiments, many of them conducted in Mexico. Then, in the late 1980s, genetic engineering quietly got underway in which geneticists inserted or deleted single genes, mostly designed to generate specific characteristics, such as height, yield per acre, drought resistance, but especially resistance to various pesticides and weed killers. The fruits of these efforts were introduced into the market in 1994. Most of the genetically modified foods were thought to be only minor modifications of the unmodified original and thus no safety testing in animals or humans was conducted.

We now have many thousands of wheat strains that are different in important ways from original emmer, einkorn, and Triticum aestivum wheat. Interestingly, it has been suggested that einkorn wheat fails to provoke the same immune response characteristic of celiac disease provoked by modern wheat gluten, suggesting a different amino acid structure in gluten proteins. Another difference: Emmer wheat is up to 40% protein, compared to around 12% protein for modern wheat.

In other words, the wheat of earlier agricultural humans, including the wheat of Biblical times, is NOT the wheat of 2010. Modern wheat is quite a different thing with differing numbers of chromosomes, different genes due to human manipulation, varying gluten protein composition, perhaps other differences.

Somewhere in the shuffle and genetic sleight-of-hand that has occurred over the last 30 years, wheat changed. What might have been the "staff of life" has now become the cause of an incredible array of diseases of "wheat" intolerance.

Comments (32) -

  • Anonymous

    5/21/2010 8:38:44 AM |

    I guess the scientists can once again manipulate wheat sorts to a form that may benefit us folks who love toast at breakfast.

  • Anne

    5/21/2010 11:24:05 AM |

    "Emmer wheat is 40% protein, compared to around 12% protein for modern wheat."

    Is that supposed to be 12% for emmer wheat and 40% for modern wheat?

    In Italy Emmer wheat is called faro. Is the ancient emmer wheat the same thing as what is grown today or have we "improved" it?

    There are some ancient grains unrelated to wheat that are used by people with celiac disease. Amaranth and teff are two examples. Indian rice grass used by native Americans is sold under the name Montina.

    All grains raise my blood glucose.

  • arnoud

    5/21/2010 11:47:28 AM |

    Very interesting post. Even when buying supposedly 'unprocessed' foods at the grocery store, we need to keep in mind that there may be little 'natural' about some/many of those foods.   The processing may be in the modified genetics...

    Are the original emmer and einkorn still available somewhere?

  • Meredith

    5/21/2010 12:31:50 PM |

    An absolutely fascinating history!  Is it possible to obtain ungenetically modified Einkorn wheat today?

  • Ned Kock

    5/21/2010 2:56:57 PM |

    Fascinating analysis. This may explain why many people whose ancestors consumed wheat in great quantities do not tolerate wheat well. This happens even though it may not take that long for a food-related trait to evolve (as little as 396 years may be enough):

    http://healthcorrelator.blogspot.com/2010/01/how-long-does-it-take-for-food-related.html

  • Kathryn

    5/21/2010 3:55:52 PM |

    I love this info.

    But on occasion i wish you would quote your source.  I belong to a health forum where we use stuff like this, but without an original source i can't do much with it.  

    Not to be critical.  I so appreciate all that you take time to share here.

  • shel

    5/21/2010 10:20:28 PM |

    brilliant. thanks for this.

  • shel

    5/21/2010 10:24:15 PM |

    ...incidentally, can you put a search box on this blog?

  • Dr. William Davis

    5/22/2010 12:46:08 AM |

    Hi, Anne--

    No, the emmer is unusually rich in protein.

    Makes you wonder if there is a lesson in that observation. The protein--gluten--differs in structure, also.

  • Dr. William Davis

    5/22/2010 12:47:13 AM |

    Meredith--

    I am looking!

    It would be an interesting experiment to consume emmer alongside modern wheat and see what happens. Some people claim that einkorn can be consumed by celiacs safely.

  • Anonymous

    5/22/2010 12:59:17 AM |

    Interesting and thought provoking post. As another commenter said, I do really wish you would quote the source of your information.

  • Kurt N.

    5/22/2010 2:06:28 AM |

    Do you have a reference for the protein content of emmer?  I've heard it was pretty high, but 40% seems off the scale.

  • Anne

    5/22/2010 3:50:13 AM |

    Oops, the high percentage I was thinking of was the percentage of the protein that is gluten.

  • Dr. William Davis

    5/22/2010 12:57:41 PM |

    Source for emmer wheat protein composition:

    Avivi L. High grain protein content in wild tetraploid wheat, Triticum dicoccoides. In Fifth International Wheat Genetics Symposium, New Delhi, India 1978, Feb 23-28;372-80.

    Dr. Shewry of the UK is a great resource:

    Wheat. J Exp Botany 2009; 60(6):1537-53.

  • billye

    5/22/2010 5:05:31 PM |

    Hi Dr. Davis,

    More confusing information for the evolutionary life style advocate to deal with.  This is my simple clarifying statement.  Since wheat in any form, regardless of chromosome content, is not a health supporting evolutionary food, due to the fact that we did not evolved to eat it, should we not avoid it like the plague?  After all, it along with high fructose, and high starch vegetables and fruits are the main cause of most if not all of the diseases of the metabolic syndrome.

    Billy E
    Nephropal.com

  • Anonymous

    5/22/2010 9:35:37 PM |

    Source for organically grown emmer:  http://www.bluebirdgrainfarms.com/

  • Santiago

    5/23/2010 12:40:46 AM |

    Something similar most happen with the corn we eat here (Colombia), as it causes very little blood sugar raise no where close to what you describe when you talk about corn bread

  • Stan Ness

    5/23/2010 8:05:20 AM |

    Great post on einkorn and emmer you have provided here. Thanks for sharing.  I've been following the research on einkorn for some time now.  More and more, I see that einkorn has many health benefits that our modern wheat lacks.  You are right on when you call it a "genetic slight-of-hand".  Well said!  I found some research about antioxidants in einkorn grain and thought you may also find it interesting.  There's a lot too this stuff!

  • Dr. William Davis

    5/23/2010 2:10:40 PM |

    Thanks for the lead anonymous.

  • Dr. William Davis

    5/23/2010 2:11:16 PM |

    Stan--

    I've perused your Einkorn Blog. Great stuff!

  • billye

    5/23/2010 3:43:47 PM |

    I perused Bluebird farms.com as a commenter recommended.  Emmer, einkorn etc, a grain by any other name is still a grain.  One of Bluebird farms offerings says it all. "we offer a variety of gift baskets and boxes filled with fresh milled whole grains and local artisanal honey and syrup."  This is great for those of you that wish to raise your blood sugar and prompt diabetes type 2 along with any number of metabolic syndrome diseases, including Celiac disease.

    Billy E
    Nephropal.com

  • Miki

    5/23/2010 5:26:38 PM |

    It does seems the diploid and tetraploid varieties of wheat are less potent as far as gluten poisoning is concerned: "Mapping of gluten T-cell epitopes in the bread wheat ancestors: implications for celiac disease." (http://www.ncbi.nlm.nih.gov/pubmed/15685550?dopt=AbstractPlus&holding=f1000,f1000m,isrctn). A quote from the conclusions: "we found that the fragments identical or equivalent to the immunodominant 33mer fragment are encoded by alpha-gliadin genes on the wheat chromosome 6D and thus absent from gluten of diploid einkorn (AA) and even certain cultivars of the tetraploid (AABB) pasta wheat".

  • Anonymous

    5/24/2010 1:35:10 AM |

    I have some kind of sensitivity to wheat. After reading this post I've been looking arround and found in wikipedia some info saying Durum wheat doesn't cause alergui reaction either.
    Maybe this is why I have so strong reactions to beer, bread and pizza, but I seem to be able to eat pasta with out any problems.
    Maybe this explains a bit of the italian heart health thing, probably most of the wheat they eat is of a healthier kind.

  • Cherry

    5/24/2010 8:20:21 AM |

    Love your blog, not only for your thorough much needed nutritional correlates to CAD, but also your gutsy willingness to expose the truth around big pharma, and greed influencing the practice of medicine.  
    Here in France, Einhorn( Triticum monococcum) has been cultivated since the 9 th millennium BC in a small area of Haute Provence. It is called petit epeautre and it is truly delicious!  It has very little gluten.
    There is much regulation in the cultivation in order to protect the genetic purity of this ancient grain.  Like wines it has a AOC (appelation d'origine controlee)  Petitepeautre.com has wonderful information also in english. Each September there is a petit epeautre festival.  It is one grain I allow myself to enjoy occasionally.

  • Dr. William Davis

    5/24/2010 10:39:46 PM |

    Great find, Miki!

    Thanks for the lead.

  • Dr. William Davis

    5/24/2010 10:53:49 PM |

    Hi, Cherry--

    Thank you for pointing me towards the French source.

    While I knew that there was some einkorn or emmer grown in Italy, some in the Middle East, and very little in the U.S., I had difficulty locating it in France.

    It would be interesting to compare the various sources.

  • Anonymous

    7/21/2010 7:29:47 AM |

    As someone (a celiac) who is EXTREMELY interested in introducing ancient and potentially benign wheat ancestors into my diet, I am very curious as to how someone like myself might be expected to react to emmer.  (And by the way, I'm pending reception of some einkorn I've already ordered to see if I can tolerate it.)

    In any case, success stories will be warmly welcomed.  Failure stories not so much, but I would appreciate you please tell them, nevertheless.  The pain is necessary, and it is for all of us to share for our common edification.

  • David Isaak

    8/1/2010 11:16:22 PM |

    Well, I expect a whole host of bricks to come hurtling my way when I say this, but I'm  a low-carber...and one of the things I eat quite frequently is seitan. That's essentially pure wheat gluten (which has long been a staple in Asian cuisines).

    I avoid most grains (other than flaxseed), but I don't avoid grain proteins. I sometimes wonder if all the wheat problems people report are really from the gluten proteins. Funny those problems weren't reported in China over all those centuries...

  • Fredo

    8/3/2010 9:41:19 AM |

    i`m not sure if this was posted here before, but i guess it fits good into the context:

    http://www.einkorn.com/toxicity-of-einkorn-gluten/

  • Principal Quattrano

    10/3/2010 4:58:07 AM |

    I used to eat a lot of seitan myself, before I had to give up wheat.

    I have heard a great many suggestions as to what celiacs can or ought to be able to eat, but very little evidence that such things are truly safe for one who reacts to gluten. A lot of common knowledge is based on nothing but oft-repeated rumors.

    Before giving up gluten, I purchased some farro in an Italian grocery. It was regular wheat. Emmer was not available. Perhaps it is in Italy.

  • Anonymous

    12/22/2010 4:58:51 AM |

    Dr Davis,
    I would like to know your thoughts on Ezekiel bread.  I thought it was better since it's a pure protein and sprouted.  

    I would really appreciate your feedback.

    thanks,
    tina

  • Henry North London 2.0

    2/25/2011 12:12:39 AM |

    I've just come across Kamut flour

    http://www.kamut.com/en/origin.html

    This is a tetraploid wheat high in selenium.  Ive bought a couple of lbs of flour to try it out.

    Im hoping that this will restore bread to my diet as I find modern pappy breads made by the CBP really awful,on my digestion and this wheat has higher protein.

    Its much like emmer in that its tetraploid and has been called everything from King Tut wheat to Noahs Flood wheat.

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Heart disease prevention for the helpless, ignorant, or non-compliant

Heart disease prevention for the helpless, ignorant, or non-compliant

The media outlets are gushing with the "research"/marketing spinoff of the JUPITER trial, an analysis conducted by Dr. Erica Spatz of Yale University, that suggests that statin use should be expanded to many millions more Americans.

USA Today: Study: 11M more should get statins

MedPage: JUPITER Findings Could Boost Statin Use by 20%

Health Day: Millions More Americans Might Be Placed on Statins

WebMD: More May Benefit From Cholesterol Drugs: Study Shows More Would Qualify for Statin Treatment if Levels of C-Reactive Protein Are Considered


You may recall that the JUPITER trial (discussed previously in a Heart Scan Blog post) studied the cardiovascular event risk in people with "normal" LDL cholesterols (calculated, of course, not measured) of 130 mg/dl or less, along with increased c-reactive protein, a crude inflammatory measure, of 2.0 mg/dl or greater. A 54% (relative) reduction in cardiovascular events occured in the group taking Crestor 20 mg per day.

What I see is a confluence of events that have brought us to the "statin drugs are necessary for everybody" mentality:

--The low-fat diet advice of the last 40 years has increased non-fat or low-fat foods that increase LDL, since removing fat from the diet provokes small LDL particle production and increases the inflammatory measure, c-reactive protein (CRP).

--The proliferation of "healthy whole grains" in the diet have also caused an enormous boom in small LDL particles, which is interpreted to the uninformed as "high cholesterol." It has also provoked CRP substantially.

--The advice to reduce salt intake has brought a broad re-emergence of iodine deficiency. When thyroid hormone production flags due to lack of iodine, LDL cholesterol (both large and small) increase.

--Our lives, which are increasingly conducted indoors, have worsened the already substantial vitamin D deficiency. While deficiency of vitamin D primarily reduces HDL cholesterol and increases triglycerides, it can also cause an increase in small LDL and a large increase in CRP.


In other words, a collection of events have converged to provide the appearance of high LDL cholesterol and high CRP. This creates the appearance of a "need" for statin drugs. The JUPITER trial now exploits both the LDL-reducing and CRP-decreasing effects of statins.

I view the foisting of Crestor via the JUPITER argument on the public as taking full advantage of the helpless situation many Americans find themselves in: Reduce fat intake, eat more healthy whole grains and . . . cholesterol and CRP skyrocket! "You need Crestor! See, I told you it was genetic," says the doctor after attending the nice AstraZeneca-sponsored drug dinner.

The notion of using a drug like Crestor to suppress inflammatory patterns is absurd. There are far better, easier, cheaper ways to achieve this goal, along with dramatic reduction in cardiovascular risk. But, to the ignorant, the helpless, or non-compliant with real change in diet and lifestyle, then Crestor does serve a purpose.

I can only hope that the excessive pushing of statin drugs on the public will sooner or later trigger a revolt.

Comments (9) -

  • Anonymous

    1/20/2009 6:16:00 PM |

    Before going on a low carb diet, my total cholesterol was 245. Doc wanted me to take statins, I said no. So I went on a Low carb diet. After 5 months of keeping the carbs <50 mg daily, my total cholesterol went down to 164. That's all you need to know about this "high cholesterol" scam.

  • renegadediabetic

    1/20/2009 8:24:00 PM |

    After JUPITER, they should be restricting statin presecriptions to those with high inflammation who don't want to give up their inflammatory diet & lifestyle.  When Crestor was tested for lowering cholesterol, they found that is was NOT shown to prevent heart attacks, per the fine print on Crestor ads.  When it preformed better when targeting inflammation, that shoud tell you what the real culprit is.

    The greedy drug companies don't want to lose their cholesterol revenues.  They only want to increase sales.

  • Paul Kelly

    1/20/2009 8:57:00 PM |

    Why am I not surprised at the media coverage of this story?

    A little off topic - but a quick question regarding fish oil gelcaps. I read where fish oil goes from being beneficial to hurtful when it becomes oxidized. Are we better off with gelcaps or liquid? Are the gelcaps protective to prevent the fish oil from becoming rancid?

    Thanks!

    Paul

  • vin

    1/21/2009 9:39:00 AM |

    Crestor is the last statin drug developed and one which is still patented. As far as I know there are no other statins being developed; at least not for lowering LDL levels.  So I guess they will push Crestor as long as they can to recover costs and rake in the profits the company had exepected.

    Once the patent ends then they will stop pushing. Just have to wait.

  • Olga

    1/21/2009 2:57:00 PM |

    Hi Dr. Davis:

    I would like you to fo a post about iodine.  I am a 42 year old mother of two.  To make a long story short, I was misdiagnosed with a thyroid neoplasm which resulted in a hemithyroidectomy following my second pregnancy.  After 5 years of ill health, I figured out on my own that I had a goiter and that high levels of iodine supplementation was required to regain my health.  I was told to eliminate salt from my diet 20 year prior because of a high incidence of heart disease in my family, despite the fact that I have low blood pressure. I am currently seeing a doctor who is helping me stabilize my thyroid function.  The reason I am writing to you is that I also have familial hypercholesterolemia.  Thanks to your program, my HDL and triglycerides are excellent.  Is it possible that the LDL will also come down if I can get my iodine into an optimal range?  Thanks for all the great information.

  • Quelle

    1/21/2009 10:11:00 PM |

    "The proliferation of "healthy whole grains" in the diet have also caused an enormous boom in small LDL particles, which is interpreted to the uninformed as "high cholesterol." It has also provoked CRP substantially"

    Which studies are you talking about in this paragraph?

  • Ricardo Carvalho

    1/21/2009 10:52:00 PM |

    I think this cartoon explains the "logic" behind all this "health" industry - http://www.naturalnews.com/023014.html

  • JPB

    1/22/2009 11:08:00 PM |

    The scary thing here is that there are parts of the medical care industry who are pushing for mandatory testing/drugs/etc. in exchange for lower "health" insurance rates (i.e. "preventative care").  
    I think that we need to preserve free choice for individuals.  I don't know exactly how to ensure this, but I do know that I don't want to be forced into mandatory lipid testing and/or treatment!  Anyone have any ideas on this?

  • Trinkwasser

    1/23/2009 11:49:00 AM |

    Same story here. trigs 380 HDL 25 LDL 165 so I was put on a Healthy High Carb Low Fat Diet, which put my LDL up to 200. The simvastatin reduced this to 75 without greatly affecting the dangerous components.

    Reducing my carbs until my BG no longer spiked (60 - 100g carefully spread through the day) has given me trigs 39 HDL 47 LDL 105

    Now my previous doctor died "unexpectedly" which is a good indication of his competence level, blamed me for not complying with the diet and failed to notice I was actually diabetic.

    My current docs are obviously singing off the same hymn sheet as many of you in the "Blogosphere", their main problem is being forced to follow outmoded protocols. She wasn't fussed by my LDL being over 100 in view of the improvement in the other lipids and though she was a bit wary of my latest experiment of eating more saturated fats which put my HDL up to 55 and brought my LDL down to 93 she can't argue with the result!

    Next experiment will be to drop the statin and see what my unmedicated lipids look like now the insulin resistance has been kicked into touch.

    The big problem here in the UK is accountants, who decree no test strips for Type 2s, TChol instead of Full Lipid Panel and no possibility of a CRP test. Hey they have to cut back somewhere in order to afford all the statins . . .

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Non-profit hospitals

Non-profit hospitals

Take a look at your local hospital and you're likely to notice several curious things:

1) It is likely non-profit, meaning it enjoys a non-profit status with the Internal Revenue Service and enjoys the tax benefits of not paying taxes on profits. This provides an advantage to tax-protected hospitals. 70% or more of hospitals in the U.S. are "non-profit."

2) Non-profit or no, many hospitals operate under the guise of a religious affiliation, e.g., St. Mary's Hospital, Trinity Hospital, All Saints', Jewish Hospital, etc.

3) Executives in non-profit hospitals can make capitalistic salaries. One CEO of a Milwaukee hospital took home $3.7 million dollars in salary last year. That's not including the very substantial perks and business interests in the spin-off businesses the hospital owns, including pharmacies, drug and medical device disitributors, even a venture capital division. "Non-profit" does not have to mean that executives within the operation can't benefit handsomely.

That same hospital system spends over $10 million dollars in a year in local marketing for TV ads, print advertising, etc. Ads are slick and professionally produced.

Make no bones about it: These are "non-profit" for tax purposes only . They are for-profit in every other sense of the phrase, including rich rewards for the insiders.

Guess how those fat executive salaries and large marketing budgets are paid for? That's right: the 12-inch incision in your chest; the four stents, defibrillator, and repeated nuclear stress tests; the revolving door of hospitalization after hospitalization that typifies the "heart patient" experience.

See the hospital for what it is: In the 21st century, it is no longer a charitable operation worthy of your volunteer time and donations. It is a business no different than Home Depot, IBM, or--Enron. Yes, they do perform needed services, as well. But the perverse equation that often determines who needs hospitalization and who doesn't, who needs a heart procedure and who doesn't, is not always based on necessity but on financial return. Just ask the CEO.
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Melatonin for high blood pressure?

Melatonin for high blood pressure?

Melatonin is fascinating stuff.

In addition to its use as a sleep aid, melatonin exerts possible effects on cardiovascular parameters, including anti-oxidative action on LDL, reduction in sympathetic (adrenaline-driven) tone, and reduction in blood pressure.

Several studies document the blood pressure-reducing effect of melatonin:

Daily nighttime melatonin reduces blood pressure in male patients with essential hypertension.

Melatonin reduces night blood pressure in patients with nocturnal hypertension.

Prolonged melatonin administration decreases nocturnal blood pressure in women.

Blood pressure-lowering effect of melatonin in type 1 diabetes.


But blood pressure may be increased when melatonin is added to nifedipine, a calcium channel blocker:

Cardiovascular effects of melatonin in hypertensive patients well controlled by nifedipine: a 24-hour study.


Effects on BP tend to be modest, on the order of 5-8 mmHg reduction in systolic, half that in diastolic.

But don't pooh-pooh such small reductions, however, as small reductions exert mani-fold larger reductions in cardiovascular events like heart attack and stroke. NIH-sponsored NHANES data (see JNC VII), for example, document a doubling of risk for each increment of BP of 20/10. The Camelot Study demonstrated a reduction in cardiovascular events from 23% in placebo subjects to 16.7% in subjects taking amlodipine (Norvasc) with a 5 mm reduction in systolic pressure, 2 mmHg drop in diastolic pressure. Small changes, big benefits.

Many people take melatonin at bedtime and are disappointed with the effects. However, a much better way is to take melatonin several hours before bedtime, e.g., take at 7 pm to fall asleep at 10 pm. Don't think of melatonin as a sleeping pill; think of it as a sleep hormone, something that simply prepares your body for sleep by slowing heart rate, reducing body temperature, and reducing blood pressure. (You may need to modify the interval between taking melatonin and sleep, since individual responsiveness varies quite a bit.)

I also favor the sustained-release preparations, e.g., 5 mg sustained-release. Immediate-release, while it exerts a more rapid onset of sleep, allows you to wake up prematurely, The sustained-release preparations last longer and allow longer sleep.

The dose varies with age, with 1 mg effective in people younger than 40 years, higher doses of 3, 5, even 10 or 12 mg in older people. Sustained-release preparations also should be taken in slightly higher doses.

The only side-effect I've seen with melatonin is vivid, colorful dreams. Perhaps that's a plus!

Comments (15) -

  • Jeanne Shepard

    5/10/2008 2:27:00 PM |

    I've hears that you can take melatonin too long, that is build up a tolerance.
    Any thoughts? I prefer it to other sleep aides, otherwise.

  • Anonymous

    5/10/2008 9:15:00 PM |

    After reading the article, I'm going to give melatonin a try.  Bought a bottle of 1mg tablets.

  • Michael

    5/10/2008 11:09:00 PM |

    I don't know if I have a weird body or something, but melatonin doesn't agree with me at all. It makes me a tiny bit groggy when I take it, but it turns me into a zombie the next day. Even small doses, like 1-2grams, basically makes me feel like I didn't sleep at all that night, and I feel crummy all day.

  • Jenny

    5/11/2008 11:33:00 AM |

    Dr. Davis,

    I have taken melantonin for many years and it helps me not only sleep, but get back to sleep if I wake up in the middle of the night.

    I've found a huge difference in the effectiveness of various company's pills. Trader Joe's for example, don't work for me at all. Schiff work very well.

    I was told years ago to take 1/4 of a pill for best results, and that is what I do. That works better than a larger amount for me.

  • Anne

    5/12/2008 1:10:00 AM |

    I have found melatonin to be very helpful. I go to sleep easily and I stay asleep. After I had bypass 8years ago, I was unable to sleep more than an 4-6 hours without Ambien. 8 months ago I started taking melatonin. It did not work right away, but after a few weeks I started to sleep very well and I have not had to restort to Ambien since. I take 3mg.

    I take 25mg metoprolol, a Beta blockers and found out that BB's decrease melatonin. Found this info through the internet, not my doctor.  

    My BP has been well controlled, even at night so I never checked to see if it went lower with melatonin.

  • Jeanne Shepard

    5/12/2008 3:24:00 AM |

    Jenny,

    Have you ever been told that you can't take it for a long period of time?
    I'd like to keep taking it, but was told not to.

    Jeanne

  • JohnN

    5/15/2008 2:01:00 AM |

    I have been taking melatonin for years and credit it with restorative sleep and general good health.
    Even so, my success rate is only about 70%. I discover that the amount of melatonin (in the blood) for a good night sleep (the desired effect) is a very small fraction of the oral dose that you can take. The difference is how the body (liver) metabolizes the substance. You really have to experiment to find the right dose for yourself; more is not better.
    For someone to try it for the very first time start at .1-.2 mg (a very small chunk of the tablet) and modify the dose accordingly.
    Do not think of it the same way as Ambien. It's best function is to ease you into sleep.
    Good luck.

  • Ann Theresa

    9/27/2008 1:59:00 PM |

    I am so hot at night that when I sleep, I wake up because of it.  I started taking my blood pressure upon waking and found it to be high.  160 or so over  90-95. I could feel the way my body felt. My blood pressure during the day is usually 115-120 over 70.  I knew I was peri menepausal, so the hormone thing was very suspect. After a lot of research, I decided to start taking 3 mg Melatonin. I checked with my doctor and he was catching up with me on his computer as we spoke.It was funny!  But anyway....I have been on these for about 3-4 weeks now and find that although I'm still warm when sleeping,  I am in a deeper sleep. My blood pressure now upon waking is about 123-125 over 82-83.  I have seen a significant improvement in lower blood pressure.  I will add that I have been walking daily and started taking a B complex also before bed.  I take my melatonin just before bedtime.  I have never had any problems with falling asleep. So the timing of use should be adjusted for when you need it.  I would much rather take this hormone than take the blood pressure medicine my doctor was so fast to offer.

  • Anonymous

    11/10/2008 7:54:00 PM |

    I swear by melatonin, and recommend the 5mg time release.  For me, it works best if I take it about 30 minutes before bedtime.  The time release eliminates the problems with waking up too early.

    The only time I have problems with feeling groggy is when I don't get enough sleep.  If you take it at midnight, then get up at 5 am, you're going to feel it.  If I know I'm not going to get at least 7-8 hours of sleep, I will skip the melatonin that night so I don't feel groggy.

    I have seen extreme differences in brands, so I think there is something to the comments about the quality of different manufacturers.

    I've never been told not to take it over long periods, but then I didn't ask a doctor about it.  I've noticed a slight tolerance if you take it all the time, so I sometimes will stop taking it for a while to break that cycle.

  • Improve Health Heart

    4/10/2009 3:43:00 PM |

    Hello.

    Your post looks quite interesting.. I never knew that Melatonin is a substance which has such uses.. I had heard of the term anywhere in any book but never took much interest in it..

    But your post spills out quite knowledgeable information definitely this much that it will hold my attention for a long long time..

    I also have a great interest in Heart related issue's and I have created a blog myself for it..

    I hope my posts will also help you gain some info..

  • Jonathan Byron

    4/22/2009 2:44:00 PM |

    There is some interesting research that suggests that melatonin is one factor that reduces insulin secretion at night.

  • TedHutchinson

    9/6/2009 6:26:07 PM |

    Oxidized-LDL and Fe3+
    /Ascorbic Acid-Induced Oxidative
    Modifications and Phosphatidylserine Exposure in Human
    Platelets are Reduced by Melatonin

    Abstract.
    Low-density lipoprotein (LDL) modifications and platelet activation are major risk factors for cardiovascular diseases. When platelets are exposed to oxidative stress, they become activated. Oxidized LDL (ox-LDL) and metal-catalysed oxidation systems such as Fe3+/ascorbic acid increase free radical production.
    We wanted to verify whether melatonin has a protective effect against oxidative modifications and phosphatidylserine externalization in platelets induced by ox-LDL and Fe3+/ascorbic acid.....snip.... These data suggest that melatonin may protect platelets from iron overload-induced and ox-LDL-induced
    oxidative modifications and also from the triggering signals of apoptosis activation, possibly due to its scavenger effect on toxic free radicals.

    The full text of both abstract and paper are the link above.

  • Serg

    7/21/2010 5:52:26 PM |

    This article regarding Melatonin for high blood pressure? is very interesting and useful, blood pressure may affect your sexual activity, and this not only happen to older people as I used to believed, young people can also be affected so you may need  to buy viagra to help yourself on those situations.

  • buy jeans

    11/3/2010 4:54:14 PM |

    I also favor the sustained-release preparations, e.g., 5 mg sustained-release. Immediate-release, while it exerts a more rapid onset of sleep, allows you to wake up prematurely, The sustained-release preparations last longer and allow longer sleep.

  • mike

    2/22/2011 11:37:17 AM |

    One such remedy that has gained popularity in recent years is melatonin. Melatonin is a growth hormone naturally produced by the pineal gland in your brain. Melatonin hormones are secreted at night or in the dark and helps regulate the sleeping cycle. It is believed that melatonin may help the body know when it is time to go to sleep and when it's time to wake up. These days, melatonin can be taken in pill form to treat everything from jet lag to insomnia. However, like with all medications, there is the potential for serious melatonin side effects if take with other medications.

    Reference:
    melatonin usage consider your age

    melatonin side effects

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Confessions of a former drug company patsy
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