World record heart disease reversal

A quick but important note.

Track Your Plaque Members:

Keep your eyes on the Track Your Plaque Member website for details and images of our most recent huge success story. Track Your Plaque participant, Neal, dropped his score more than anyone else before.

Although reduction of heart scan score is an everyday event around here, a 51% drop in score deserves to make news!

We will post the images of Neal's heart scans on the www.cureality.com Member website in the coming days.

Dose of fish oil

Dosing for fish oil is a perennial point of confusion. However, it's quite simple.

The active ingredients in fish oil are DHA and EPA, the so-called omega-3 fatty acids. Of course, if there's anything else in your capsules, such as omega-6, omega-9, or linolenic acid, these should not count towards the sum of EPA + DHA, since they do not exert the same benefits as the omega-3s.

The basic suggested starting dose for the Track Your Plaque program is 1200 mg of EPA+DHA. This is usually provided by taking 4 x 1000 mg capsules of fish oil, providing 180 mg EPA, 120 mg DHA per capsules, for a total of 1200 mg EPA+DHA.

About a third of people, however, will require greater doses of omega-3s to reduce triglycerides, VLDL, and/or intermediate-density lipoprotein (IDL). Most people will do fine with an increase to 1800 mg EPA+DHA, usually provided by 6 x 1000 mg standard capsules. A very occasional person (about 1 in 100) will require even higher doses.

If you ever decide to change your fish oil preparation, or if you change to a more concentrated form or another form such as liquid fish oil (e.g., Carlson's), paste (e.g., Coromega), or syrup (e.g., Pharmax Frutol), then you will need to examine the label to determine the dose of EPA+DHA. If, for instance, a teaspoon of liquid fish oil provides 360 mg EPA and 240 mg DHA, that's a total of 600 mg omega-3s per teaspoon. If your EPA+DHA dose is 1200 mg per day, then two teaspoons a day should provide it. Always adding up the EPA+DHA content of whatever preparation you choose will therefore allow you to mix, match, or change your dose whenever you like.

Niacin scams

As most of you know, niacin (vitamin B3) is an important tool for many in the Track Your Plaque program.

Niacin:

--raises HDL cholesterol
--reduces small LDL
--reduces lipoprotein(a)

And it's the most potent agent we have for all three patterns, despite just being a vitamin. Niacin also reduces LDL cholesterol, VLDL, IDL, triglycerides; reduces heart attack risk dramatically either alone or in combination with other agents.

Unfortunately, some people who are either afraid of the "hot flush" side effect, or experience excessive degrees of it, have resorted to two preparations sold in stores that have none of these effects.

Most notorious is "No-flush" niacin, also known as inositol hexaniacinate. This compound is an inositol sugar molecule complexed with 6 ("hexa-") niacin molecules. Unfortunately, it exerts none of niacin's effects in the human body. No-flush niacin has no effect on HDL, small LDL, or Lp(a), nor on LDL or heart attack.

In short, no-flush niacin is a scam. It's also not cheap. I've met people who have spent hundreds of dollars on this agent before they realize that nothing is happening, including a flush.

Likewise, nicotinamide does not work. It sounds awfully close to the other name for niacin, nicotinic acid. But they are two different things. Like no-flush niacin, nicotinamide has no effect on HDL, small LDL, Lp(a), etc.

Though I've discussed this issue in past, somehow these two "supplements" seem to sneak back into people's consciousness. You walk down the health food store aisle and spy that bottle of X-brand No-flush niacin, promising all the benefits of niacin with none of the bother. Then you remember that rough night you spent a few months back when the hot flush lasted longer than usual. That's when some people end up buying this agent making extravagant--and false--promises.

For now, for all its imperfections, niacin is still a pretty darn good agent for these patterns. Remember that the best strategy to minimize the hot flush effect is to drink plenty of water. We generally recommend taking the dose at dinner along with water. If the hot flush occurs, drink two large glasses of water (total volume 16-24 oz). Nine times out of ten, the flush is gone. It also dissipates the longer you take niacin.

Media mis-information

This is an excerpt from a popular health website, EverydayHealth.com:


A Cholesterol-Busting Vitamin?
Did you know that niacin, one of the B vitamins, is also a potent cholesterol fighter? Find out how niacin can help reduce cholesterol…

Niacin is safe — except in people with chronic liver disease or certain other conditions, including diabetes and peptic ulcer. It is also inexpensive. However, it has numerous side effects. It can cause rashes and aggravate gout, diabetes, or peptic ulcers. Early in therapy, it can cause facial flushing for several minutes soon after a dose, although this response often stops after about two weeks of therapy and can be reduced by taking aspirin or ibuprofen half an hour before taking the niacin. A sustained-release preparation of niacin (Niaspan) appears to have fewer side effects, but may cause more liver function abnormalities, especially when combined with a statin.

Many people begin treatment at low doses (250 mg twice a day, for example) and, over six weeks or so, gradually build up to an amount that lowers lipid levels, anywhere from 1,000 to 2,500 mg split between two doses during the day. This gradual approach may help build tolerance to side effects such as facial flushing. Although niacin is available over the counter, you should not use it in quantities sufficient to lower cholesterol without a physician’s supervision. It is important to test liver function and levels of blood sugar and uric acid before beginning niacin therapy and during the course of treatment.


(Bold emphasis mine.)

At http://www.everydayhealth.com/publicsite/index.aspx?puid=548e8630-32d6-41dd-91a7-48e1cbac65ad&p=4




After an enticing headline, the article goes on to scare the pants off you. It also sounds like accurate information, delivered in an unbiased way, cold and straight.

If we were to use niacin this way, it would indeed be intolerable for most. Do not follow the above nonsensical advice. But that may have been the intention from the start.


Very telling are the fact that, both above and below the article were colorful advertisements for Lipitor, complete with Dr. Robert Jarvik’s (inventor of an implantable mechanical heart) soothing, professorial image.

Did they want to bait us with promising information about cholesterol and niacin, only to throw water on our fire and steer us towards something else?

That would be typical drug company marketing.

All in all, I’m grateful for the attention the media provides for health issues. Perhaps many people wouldn’t even be aware of niacin and other healthy strategies if some website, newspaper, or magazine article hadn’t talked about it.

But I do worry about bias. Was this an unbiased report? Or was it more like much of the physician-directed mail I receive, cleverly concealed propaganda from the drug manufacturers? Who wrote it? No author is listed. Could it have been ghost written by someone in the drug company itself, or an arm of the drug company? That’s a very common practice for the literature physicians receive, glossy, high-class materials paid for by drug companies, written by drug company-owned companies, but no company logo or name listed.

My point: Be skeptical of what the media tells us. There’s usually a good deal of truth in the reporting, but there’s also often just enough mis-information or slanting of content to make you behave or believe a certain way. “If niacin is this dangerous, maybe I really should take the Lipitor.”

A dirty little secret

Here's a dirty little secret many people don't know about.

If I implant a stent, I might get paid somewhere around $2000 for the heart catheterization, stent implantation, femoral artery closure device, hospitalization charges. That's not too bad.

But what if I'd like more? What if I'd like to squeeze this unsuspecting patient for more, or actually his/her insurance company?

Easy: Add on complex procedures to the basic procedure that yield more professional charges. For instance, I could perform laser angioplasty, a procedure that adds another couple thousand dollars. I might pull out the old rotational atherectomy device, a high-speed diamond tipped drill that also adds substantial professional charges. I might also use the intracoronary ultrasound device, an otherwise helpful device, but I might pull it out to use on everybody.

With the exception of ultrasound, all the "add-on" procedures were more popular in the early and mid-1990s--before they were shown in clinical studies to provide no advantage, perhaps even add to procedural risks.

Thus, a patient might undergo a heart catheterization, balloon angioplasty with stent implantation into the proximal left anterior descending coronary artery (LAD), followed by laser angioplasty of the mid-LAD, followed by intracoronary ultrasound of the vessel. Next, rotational atherectomy of the circumflex, followed by stent and ultrasound. Total charges for this 2-3 hour procedure? Somewhere around $8000 to the cardiologist. Of course, hospital charges are far more.

Ironically, patients are invariably impressed. Hearing that they went through all sort of high-tech procedures makes them grateful for receiving the benefits of the skills of their cardiologist. Of course, they would like have done as well with a far simpler procedure. Perhaps they didn't need the procedure at all.

If the excessive use of procedures and devices fails to benefit patients, why don't hospitals discourage it? Two reasons: 1) It's difficult to legislate or regulate decisions made on judgement, which can be a tough issue with many fuzzy edges, and 2) hospitals made oodles more money from the practice.

If you have a salesman in your new car lot and he outsells all his colleagues by 30-50% and makes you a couple hundred thousand a month more in sales. You've watched him at work and he's clearly good at it. But you suspect that he pushes the envelope of propriety frequently--badgering customers, add rustproofing to a little grandmother's car that will be driven 3000 miles a year, selling cars for prices far above what they would have sold for had the customer bargained more vigorously.
do you put a stop to it at the risk of pushing your star salesman away? Few would.

Only a minority of my colleagues are guilty of this despicable practice. I only know of a few who openly do it. Hopefully, you're not among their patients.

The party’s over

A good number of cardiology colleagues are vigorously bashing the outcome of the COURAGE Trial. Recall that COURAGE is the large clinical trial recently released that showed that, in people with stable angina (chest pains), people did equally well with “optimal medical therapy” as with stents.

The problem is that many of my colleagues wouldn’t know what to do in a world deprived of implanting 10 stents a day. Giving people nitroglycerin/statin drug/aspirin/beta-blocker day after day, week after week, would be an awfully dull world. All the excitement of the cath lab would be a lot more rare. We’d actually have to wait for a heart attack from some dumb smoker! All the money would disappear, too. After all, seeing a patient in the office pays, at best, $200 (and has to be stretched to cover overhead expenses like staff, malpractice insurance, and rent). Putting a stent in can pay $2000, $3000, $4000, often more. Put in several a day and—Wow! Now we’re talking money.

You can understand how upsetting it is to my colleagues who feel like the rug may be pulled out from underneath their practices and lives. Feel as sorry for them as you do for people who lose their jobs on an assembly line because of robotic technology. Or travel agents because everyone makes travel arrangements over the internet. Technology, in this information technology, marches on.

Cardiologists, cath labs, stent manufacturers, and the huge industry built around heart disease had their party. Now it’s time to clean the room and sober up. The party’s over.

The broader acceptance of “optimal medical therapy,” as lame as it is, will eventually open the door for many to demand for something even better. Ever hear of Track Your Plaque?

More on being wheat-free

Reducing or even eliminating the wheat in your diet can dramatically enhance the phenomenon of insulin resistance.

Insulin resistance is the evil process that lies behind low HDL, high triglycerides, small LDL particles, and VLDL and IDL. It’s also the process that makes us tired after meals, heightens inflammation that raises your risk of heart disease, stroke, diabetes, and caner. Insulin resistance is the culprit behind the bulge hanging over some 100,000,000 American belts.

Show me a person with a protruding abdomen and I’ll show you a bread lover, or some other form of wheat.

Why do I pick on wheat so much? Many of you among the more nutrition-minded would point out that wheat is just one group of food items among many other high-glycemic index foods, i.e., foods that yield a vigorous surge in blood sugar (glucose), followed by a sharp decline. Wheat enjoys the high-glycemic index company of corn, rice (white and brown), potatoes, among others.

I pick on wheat because, for most Americans, wheat is 90% of the high-glycemic index problem. (I’m assuming you’ve at least eliminated or dramatically reduced highly-processed sweets like candy, cookies, soft drinks, cakes, etc. That’s a no-brainer.) It’s not uncommon to have a wheat-based product with every meal, a wheat-based snack, 7 days a week. But few people have corn products (i.e., corn starch products) three times a day. Or rice three times a day.

Wheat has traded places with saturated fat sources as the chief scourge of diet. In 1985, we had dinners of spare ribs, cheeseburgers, French fries, and butter on our mashed potatoes. Hardly anybody eats that like anymore, at least amongst the web-savvy set.

Wheat has assumed the previous exalted role as chief scourge as a consequence of the low-fat consciousness of the 80s and 90s. It has since ballooned in importance in diet and, as a result, skyrocketed as a cause of obesity, insulin resistance, and coronary plaque growth.

What if you're already slender and have none of the above issues, especially small LDL particles? Then don't sweat the wheat issue.

Note: My comments on being wheat-free should not be confused with gluten sensitivity or celiac disease. These are allergies to wheat gluten that, if undiagnosed, wreak havoc on health to extremes. This phenomenon is separate and distinct from the far more prevalent issue I’m discussing.

Can you break the “Rule of 60”

In the Track Your Plaque program, we aim for conventional lipid values (LDL cholesterol, HDL cholesterol, and triglycerides) of 60—60—60, i.e., LDL 60 mg/dl, HDL 60 mg/dl or greater, triglycerides 60 mg/dl. Most participants do indeed reach these target values.

When I tell this to colleagues, they’re stunned. “You can’t possibly get those numbers in most people.” And I can sympathize with their plight. After all, they are stuck with relatively lame tools: statin drugs, the American Heart Association diet. I’d be surprised if they ever achieved 60—60—60.

But can you drop your heart scan score even if you don’t reach the 60—60—60 targets? Yes, you can. The Rule of 60 is only a guideline, a tool that helps more people achieve our goals. The Rule of 60 does not guarantee reversal (drop in heart scan score), nor does not achieving the targets completely destroy your chances.

We have had many people drop their scores even if they haven’t reached the targets. On the other hand, we’ve also had people who failed at first, only to see success once they achieved the 60 mg/dl targets.

But which one are you? That’s the problem. We possess limited capacity to predict who will or who will not drop their scores from the start. We know that there are factors that stack the odds in your favor (e.g., optimism, lack of Lp(a), ideal weight, vitamin D >50 ng/ml, etc.). We know that there are factors that make it tougher (overweight, Lp(a), pessimistic attitude, underappreciated hypertension, higher heart scan scores, etc.) But at the start, we just don’t know who truly needs to adhere to the Rule of 60. So we suggest that everyone, at least in the beginning, aim to achieve it.

I had an exception the other day. Rich did everything by the Track Your Plaque book. However, a starting low HDL of 27 only rose to 37 after one year of effort—way below our 60 mg/dl target. Yet a repeat heart scan showed 23% reduction.

Why would Rich be so successful despite a persistently very low HDL? There may be a number of reasons. One explanation could be that conventional measures of HDL fail to distinguish between what HDLs truly work and what do not. Look at ApoA1 Milano; remember this story? The people in the secluded mountain village of Limone-Sul-Garde in northern Italy have HDL cholesterols of 8-15 mg/dl yet do not experience excess vascular atherosclerosis, suggesting that what little HDL they have is super-effective.

Yes, large HDL seem to be more healthy and effective than small HDL, but perhaps there’s more to it. However, nobody has a HDL effectiveness test ready for us to use.

In the meantime, we continue to suggest that the Track Your Plaque Rule of 60 be considered as a means of making plaque reversal as likely as possible. You and your doctor can always adjust in future, depending on your heart scan score results.

Non-profit hospitals

Hospitals hide behind a veil of non-profit.

Ostensibly operating for the public good, most hospitals enjoy all the business advantages of non-profit status. This means that any profits that flow to the bottom line at the end of the year are not subject to tax. Hospitals point out that profit margins are modest, often ranging from 2-6%.

What they don’t tell you is that, regardless of non-profit status, lots of money can be paid out along the way. A hospital CEO who pays himself $4 million dollars a year can work for this non-profit organization. He can also direct the hospital in business expansion: pharmacies, extended-care facilities, medicine and medical supply distributorships. Your friendly hospital CEO, as well as his many administrators, can hold positions in hospital subsidiaries, complete with salaries and perks.

Yes, most hospitals are officially non-profit. But that’s a designation for tax purposes. It does not mean that hospitals are non-lucrative.

I believe that it’s time for hospitals to drop the façade of “Saint” in their names or other religious names—Methodist, Baptist, Jewish, All Saints’. More accurate would be something like “ABC Medical Enterprises, Inc.” That way, the public would be quicker to recognize that they are dealing with a business run by people eager to make more money.

Wheat five times a day

Terri couldn't understand why her weight wouldn't drop.

At 5'3", 208 lbs., she had the typical mid-abdominal excess weight that went with small LDL, low HDL, high triglycerides, a post-prandial (after-eating) fat clearance disorder, high blood sugar, increased c-reactive protein, and high blood pressure.

She claimed to have tried every diet and all had failed. So we reviewed her current "strict" diet:

"For breakfast, I had Shredded Wheat cereal in skim milk. No sugar, just some cinnamon and a little Splenda. For lunch, I had low-fat turkey breast sandwich--no mayonnaise--on whole wheat bread. For snacks, I had pretzels between breakfast and lunch, and a whole wheat bagel with nothing on it before dinner. For dinner, we had whole wheat pasta with tomato sauce and a salad. While we watched TV, I did have a couple of whole wheat crackers.

"I don't get it. I didn't butter anything, I didn't sneak any sweets, cakes, I didn't even touch cookies. And I love cookies!"

Did you see the pattern? I pointed out to Terri that what she was doing, in effect, was eating sugar 5 or more times a day. Many of her meals, of course, contained no sugar. All were low fat. But the excessive wheat content yielded quick conversion to sugar--glucose--immediately after ingestion.

Repeated surges of blood sugar like this trigger the excessive insulin response that yields low HDL, higher triglycerides, small LDL, etc., everything that Terri had.

Terri was skeptical when I suggested that she attempt an "experiment": Try a four week period of being entirely wheat-free. This meant more raw nuts and seeds, more lean proteins like low-fat yogurt and cottage cheese, chicken, fish, lean red meats, more vegetables and fruits.

After only two weeks, Terri dropped 5 1/2 lbs. She also reported that the mood swings she had suffered, afternoon sleepiness, and uncontrollable hunger pangs had all disappeared. The mental cloudiness that she had experienced chronically for years had lifted.

What happened was that the load of sugar from wheat products, followed by an insulin surge then a precipitous drop in sugar, and finally fogginess, irritability, and cravings for food all disappeared. With it, the entire panel of downstream phenomena (small LDL, CRP, etc.) all faded.

Though she started out intending to complete a four week trial, I believe that, having seen the light, she will continue to be wheat-free, or nearly so, for a lifetime.
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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