Risks for coronary disease 2008

According to conventional thinking, there are identifiable risks for coronary disease and heart attack. These risk factors are:

* smoking
* high blood pressure
* high blood cholesterol and excessive saturated fat intake
* diabetes
* being overweight or obese
* physical inactivity

I'd agree with all the factors listed (though I would argue about the importance of high blood cholesterol and saturated fat; they are not as important as commonly made to be.)

Is the list complete?

From the unique perspectives gained in the Track Your Plaque program, I'd offer a significantly different list. Trying to stop or reduce coronary atherosclerotic plaque and heart scan scores makes you a whole lot smarter about what works and what doesn't work.

So, in addition to the risk factors listed above, I would add:

* Small LDL particles--Lots of small LDL particles is MORE important than high LDL.
* High blood pressure with exercise
* Excessive wheat intake and other processed carbohydrates--An issue of explosive importance today. Wheat creates large numbers of small LDL particles, among other adverse effects.
* Vitamin D deficiency--Among the most powerful risks I know of. It belongs at the top of the list.
* Vitamin K2 deficiency
* Low HDL cholesterol
* Blood sugar >100 mg/dl
* High triglycerides--While some argue about whether triglycerides are a risk that behaves independently of patterns like low HDL, they are neglecting the potent force of this risk. Sure, it occurs in tandem with low HDL (usually, though not always), but it is a factor that can leave you with risk even when HDL is raised to healthy levels.
* Lipoprotein(a)--It is eminently, positively crystal clear that lipoprotein(a) is a powerful risk for heart disease. The lack of a profitable treatment keeps it hidden in the shadows.
* Pessimism--Be happy, do better. Be a constantly angry, frustrated, complaining sourpuss and you are more likely to succumb to heart disease, cancer, or other undesirable fate.


These are the risk factors that we address through the Track Your Plaque program, a list that yields a far more powerful and comprehensive approach to control over coronary plaque/atherosclerosis, sufficient to achieve reversal in many (though not in all) instances.

I view the list of conventional risk factors as a "no brainer" list. Sure, smoking is a risk factor. But there are virtually no smokers in the Track Your Plaque program. If you smoke, you clearly don't care enough to engage in a high-intensity prevention program like this.

Saturated fat? Perhaps, but the battlefield of heart disease is riddled with the bodies of those who employed this as their sole strategy and failed catastrophically.

Diabetes, hypertension, and overweight all represent a continuum of risk; the solutions offered in the conventional scheme (i.e., low-fat diet, etc.) make these patterns worse, not better.

The conventional response to heart disease risk is trapped somewhere in 1973 and has not changed in over 30 years. Heart disease continues to be a growth industry for hospitals and the pharmaceutical and medical device industries. The "official" organizations continue to deliver an antiquated, outdated message.

If you want heart disease, follow the American Heart Association diet. If you want established heart disease to get worse, follow the American Heart Association diet. If you want diabetes or, if you already have diabetes or pre-diabetes, if you want it to worsen and develop organ damage (eyes, kidneys, nervous system, etc.), then follow the American Diabetes Association diet. USDA food pyramid? Loosen your belt!

The list of conventional risk factors for heart disease is woefully inadequate. If that is as far as your prevention program takes you, heart disease will not be controlled or prevented. At best, it might be slowed; at worst--and more likely--it might be accelerated.

Food sources of vitamin K2



Vitamin K2 is emerging as an exciting player in the control and possible regression of coronary atherosclerotic plaque. Only about 10% of dietary vitamin K intake is in the K2 form, the other 90% being the more common K1.

The ideal source of K2 is natto, the unpalatable, gooey, slimy mass of fermented soybeans that Japanese eat and has been held responsible for substantial decreases in osteoporosis and bone fractures of aging. Natto has an ammonia-like bouquet, in addition to its phlegmy consistency that makes it virtually inedible to anyone but native Japanese.

I say that the conversation on vitamin K2 is emerging because of a number of uncertainties: What form of vitamin K2 is best (so-called MK-4 vs. MK7 vs. MK-9, all of which vary in structure and duration of action in human blood)? What dose is required for bone benefits vs. other benefits outside of bone health? Why would humans have developed a need for a nutrient that is created through fermentation with only small quantities in meats and other non-fermented foods?

Much of the developing research on vit K2 is coming from the laboratories of Drs. Vermeer, Geleijnse, and Schurgers at the University of Maastricht in the Netherlands, along with several laboratories in Japan, the champions of K2.

MK-7 and MK-8,9,10 come from bacterial fermentation, whether in natto, cheese, or in your intestinal tract; MK-4 is naturally synthesized by animals from vitamin K1. While natto is the richest source of the MK-7 form, egg yolks and fermented cheeses are the richest sources of the MK-4 form.

Chicken contains about 8 mcg MK-4 per 3 1/2 oz serving; beef contains about 1 mcg. Egg yolks contain 31 mcg MK-4 per 3 1/2 oz serving (app. 6 raw yolks). Hard cheeses contain about 5 mcg MK-4 per 3 1/2 oz serving, about 70 mcg of MK-8,9; soft cheeses contain about 30% less. Natto contains about 1000 mcg of MK-7, 84 mcg MK-8, and no MK-4 per 3 1/2 oz serving.











Feta cheese

Thanks to the research efforts of the Dutch and Japanese groups, several phenomena surrounding vitamin K2 are clear, even well-established fact:

--Vitamin K2 supplementation (via frequent natto consumption or pharmaceutical doses of K2) substantially improves bone health. While K2 by itself exerts significant bone density/strength increasing properties in dozens of studies, when combined with other bone health-promoting agents (e.g., vitamin D3, prescription drugs like Fosamax and calcitonin), an exaggerated synergy of bone health-promoting effects develop.



--The MK-4 form of vitamin K2 is short-lived, lasting only 3-4 hours in the body. The MK-7 form, in contrast, the form in natto, lasts several days. MK-7 and MK-8-10 are extremely well absorbed, virtually complete.

--Bone health benefits have been shown for both the MK-7 and MK-4 forms.

--Coumadin (warfarin) blocks all forms of vitamin K.





Interestingly, farm-raised meats and eggs do not differ from factory farm-raised foods in K2 content. (But please do not regard this as an endorsement of factory farm foods.)

Another interesting fact: Since mammals synthesize a small quantity of Vit K2 forms from vitamin K1, then eating lots of green vegetables should provide substrate for some quantity of K2 conversion. However, work by Schurgers et al have shown that K1 absorption is poor, no more than 10%, but increases significantly when vegetables are eaten in the presence of oils. (Thus arguing that oils are meant to be part of the human diet. Does your olive oil or oil-based salad dressing represent fulfillment of some subconscious biologic imperative?)

If we believe the data of the Rotterdam Heart Study, then a threshold of 32.7 micrograms of K2 from cheese yields the reduction in cardiovascular events and aortic calcification.

It's all very, very interesting. My prediction is that abnormal (pathologic) calcium deposition will prove to be a basic process that parallels atherosclerotic plaque growth, and that manipulation of phenomena that impact on calcium depostion also impact on atherosclerotic plaque growth. Vitamins D3 and K2 provide potential potent means of at least partially normalizing these processes.

As the data matures, I am going to enjoy my gouda, Emmenthaler, Gruyere, and feta cheeses, along with a few egg yolks. I'm going to be certain to include healthy oils like olive and canola with my vegetables.


All images courtesy Wikipedia.

Copyright 2007 William Davis, MD

Track Your Plaque: Naughty or nice?



Among the many wonderful surprises we've had at Track Your Plaque this holiday season was a letter from Santa Claus himself!

It seems that Santa, like the rest of us, has been busy surfing the web for useful health information the last few months. He was struck with this curious discussion we've been having about "wheat belly" and all the unhealthy consequences of wheat products in our diet.

He writes:

"I wouldn't have believed it myself, except that my waist size has grown four inches in as many years. Sure, I'm known for my healthy girth, but now even Mrs. Claus calls me fat!

"I was open to new ideas when I came across this crazy discussion about eliminating wheat from your diet. So I said, "What have I got to lose?" Well, four weeks later and 12 lbs lighter, I'm convinced. Now comes the tough part: I've got to deliver all the toys and resist all those cookies the children put out for me. I wonder if wheat makes reindeer fat, too?

"Anyway, thanks to your program I'm back to my old weight again. Doc says my blood sugar and blood pressure are also back down to normal. Thanks, Track Your Plaque! (You'll find something extra special under the tree this year.)"

And so it goes. I'm tempted to put Santa's testimonial on our homepage, but I think that may be tooting our own horn a bit too much.

Have a wonderful holiday!

Vitamin D: Treatment for metabolic syndrome?

Metabolic syndrome is that increasingly common collection of low HDL cholesterol, high triglycerides, high blood sugar, and high pressure that now afflicts nearly 1 in 4 adults, rapidly gaining ground to 1 in 3. Beyond these surface factors, metabolic syndrome also creates small LDL particles, VLDL, intermediate-density lipoproteins (IDL), increased imperceptible inflammation measured as higher c-reactive protein, and greater blood clotting tendencies. Metabolic syndrome is usually, though not always, associated with a big tummy ("beer belly," though I call it "wheat belly").

In short, metabolic syndrome creates a metabolic mess that leads to dramatic increases in heart disease, vascular disease and stroke, and cancer. The medical community has been paying increasingly greater attention to this condition because of its booming prevalence and because of the big bucks invested in "education" by the manufacturers of the diabetes and pre-diabetes drugs, particularly makers of Actos and Avandia.

But here's a curious observation:

Replacement of vitamin D to healthy levels (we aim for 50-60 ng/ml, or 125-150 nmol/l) yields:

--Higher HDL
--Lower triglycerides
--Lower blood sugar
--Reduced c-reactive protein
--Reduced blood pressure
--Reduced small LDL
--Enhanced sensitivity to insulin

(Whether blood clotting and effects on IDL should be added to this list is uncertain.)

It's obvious: Vitamin D is proving to be a very important and powerful corrective influence on many of the facets of the metabolic syndrome. In fact, I would go as far as saying that, side by side, vitamin D yields nearly the same effect as prescription drugs Actos and Avandia--without the extravagant cost (nearly $200 per month), leg swelling, congestive heart failure and heightened heart attack risk (with Avandia), and average 8 lb weight gain. Of course, vitamin D also provides benefits beyond metabolic syndrome like facilitation of coronary plaque regression, increased bone density, reduced arthritis, and reduced risk of several cancers.

You'd think that agencies like the American Diabetes Association (ADA) would be all over vitamin D like white on rice. Yet they remain curiously quiet about the entire issue. (That should come as no surprise to anyone familiar with the behavior and politics of this organization, the same outfit that has widely propagated the ADA diet, a program that accelerates diabetes and its complications. In my view, the ADA is an embarassment.)



For a really great story and video on vitamin D that includes a terrific interview with vitamin D guru and Track Your Plaque friend, California psychiatrist Dr. John Cannell, go to What's the Real Story on Vitamin D?. While the video will yield little new to readers of The Heart Scan Blog or Track Your Plaque members, it just feels really good to see a well-made, high-class video production echoing many of the things we've been talking about these past two years.

Appetite stimulants

Ever have days when you just can't seem to get enough to eat, your stomach gnawing just a hour after a meal? We all get them, some more than others. Other days, you can be content with a few simple foods and hunger is subdued, temptation easy to control.

Why such contrasts on different days?

A major part of the reason can be the presence of appetite stimulants, factors that trigger appetite beyond rational control. The list of common appetite stimulants includes:

--Sleep deprivation--A very important factor. Lack of sleep drives tremendous appetite, and often for the wrong foods (processed carbohydrates). I personally have experienced my most shamefully indulgent days when sleep-deprived. The solution is obvious: Sleep. Another factor that is based purely on personal observation is that of waking mid-phase. In other words, waking up while you're still enjoying the deeper phases of sleep (e.g., phase 3,4, or REM). This can oddly disrupt your day and your impulse control. I usually try and time sleep to increments of 90 minutes to coincide with the average duration of the full cycle of sleep. For example, 7 1/2 hours is better than 8 hours, since the extra half hour puts your square into a deeper sleep cycle.

--Excessive caffeine--Caffeine stimulates stomach acid. This triggers the impulse to eat . . . and eat and eat.













Image courtesy Wikipedia

--Aspirin and other anti-inflammatory agents--If you take aspirin (as many of our Track Your Plaquers do), then beware of the gastritis that can develop. Like excessive caffeine, it also triggers the impulse to eat, likely a protective mechanism, since food sops up excess acid. I ask patients to take periodic breaks from aspirin, e.g., a week off every two or three months, to allow the stomach to heal. Alternatively, an occasional dose of acid-suppressing medication is a safe practice, e.g., Pepcid AC 10-20 mg; Prilosec 10-20 mg.

--Wheat-containing foods--Followers of The Heart Scan Blog know my feelings on this. Wheat is a potent appetite stimulant: Eat something containing wheat like a pretzel or whole wheat bagel, and you want more. You may want more immediately, or a little later when your blood sugar plunges after the wheat-driven insulin surge. Solution: Dump the wheat, one of the most unhealthy food groups around.

--Alcohol--Though perhaps not a direct appetite-stimulating effect, the loss of impulse-control with alcoholic drinks can lead to overindulgence, often in the worst foods. Just beware.

--Hanging around with heavy people. Remember peer pressure? It can be subliminal. People with poor eating habits provide the silent message that it's okay to yield to impulse, overeat, overindulge, and choose the wrong foods.

--Stress--Whether through cortisol stimulation or other means, stress triggers appetite in some people. If you experience this and must give in, reach for raw nuts or nuts, rather than wheat snacks or chips. The effect will be minimal, perhaps even beneficial, rather than the bloating, appetite-stimulating, fattening effect of crackers, chips, or pretzels. This may be the same phenomenon as taking prescription steroids like prednisone.

--Short dark days, long nights--In other words, winter. Though just an anecdotal observation, I am convinced that vitamin D supplementation is an effective antidote to this effect. The short, dark days just don't bother you as much, perhaps not at all, and there's no impulse for comfort foods.


How about appetite suppressants? In this list I would include 1) raw nuts--especially almonds, walnuts, pecans, and pistachios, the sort with a fibrous covering and rich in monounsaturates, 2) other sources of plentiful healthy oils, e.g, use more olive oil in your salad or add it to hummus for your veggie dip, 3) space-occupying fibers such as glucomannan, inulin (such as in Fiber Choice), and psyllium seed products. Counteracting the above appetite stimulants like sleep deprivation is, of course, important.

The coming wheat frenzy, otherwise known as the holidays, is an especially important time to be aware of these effects. Eat, drink, and be merry--but with rational impulse control not driven by subconscious appetite stimulants.

"Heart scans are experimental"

Let me warn you: This is a rant.

It is prompted by a 44-year old woman. She has a very serious lipoprotein disorder. Her family experiences heart attacks in their 40s and 50s. I asked for a heart scan. Her insurance companied denied it.

This is nothing new: heart scans, like mammograms, have not enjoyed reimbursement from most insurers despite the wealth of data and growing acceptance of this "mammogram" of the heart.

However, 10 minutes on the phone, and the "physician" (what well-meaning physician can do this kind of work for an insurance company is beyond me) advised me that, while CT heart scans for coronary calcium scoring are not covered, CT coronary angiograms are.

Now, I've been witnessing this trend ever since the big players in CT got involved in the game, namely Philips, Siemens, Toshiba, and GE. These are enormous companies with hundreds of billions of dollars in combined annual revenues. They, along with the lobbying power of cardiology organizations like the American College of Cardiology, have gotten behind CT coronary angiograms. This is most likely the explanation of why CT coronary angiograms have rather handily obtaining insurance reimbursement. Interestingly, the insurance company I was speaking to is known (notorious?) for very poor reimbursement practices.

A CT heart scan, when properly used, generates little revenue, a few hundred dollars to a scan center, barely enough to pay for a device that costs up to $2 million. However, CT coronary angiograms, in contrast, yield around $2000 per test. More importantly, they yield downstream revenues, since CT angiograms are performed as preludes to conventional heart catheterizations, angioplasty, stents, bypass surgery, etc. Now we're talking tens or hundreds of thousands of dollars revenue per test.

What puzzles me is that much of that increased cost comes out of the insurance company. Why would they support such tests if it exposes them to more costs? I'm not certain. It could be the greater pressures exerted by the big CT companies and powerful physician organizations. I seriously doubt that the insurance companies truly believe that heart scans for coronary calcium scoring are "experimental" while CT coronary angiograms are "proven." If all we did was compare the number of clinical studies that validate both tests, we'd find that the number of studies validating heart scans eclipses that of coronary angiograms several fold. Experimental? Hardly.

The smell of money by physicians eager to jump on the bandwagon of a new revenue-producing procedure is probably enough to have them lobby insurers successfully. In contrast, plain old heart scans just never garnered the kind of vigorous and vocal support, since nobody gets rich off of them.

If CT coronary angiograms are sufficiently revenue producing that my colleagues and the CT scanner manufacturers have managed to successfully lobby the health insurers, even one as financially "tight" as the one I spoke to today, well then I take that as testimony that money drives testing, as it does the behavior of hospitals, many of my colleagues, and can even force the hand of insurers.

When meat is not just meat


The edgy nutrition advocate, Mike Adams, over at NewsTarget.com came up with this scary photo tour of a processed meat product from Oscar Mayer: Mystery Meat Macrophotography: A NewsTarget PhotoTour by Mike Adams







Along with increasingly close-up photographs of this meat-product, Adams lists the ingredients in Oscar Mayer's Cotto Salami:


Beef hearts
Pork
Water
Corn syrup
Beef

Contains less than 2% of:
Salt
Sodium lactate
Flavor
Sodium phosphates
Sodium diacetate
Sodium erythorbate
Dextrose
Sodium nitrite
Soy lecithin
Potassium phosphate
Potassium chloride
Sugar


As I reconsider the role of saturated fat in diet, given the startlingly insightful discussion by Gary Taubes of Good Calories, Bad Calories, I am reminded that not all meat is meat, not all saturated fat sources are equal.

I am concerned in particular about sodium nitrite content, a color-fixer added to cured meats that caused a stir in the 1970s when data suggesting a carcinogenic effect surfaced. The public's effort to remove sodium nitrite from the food supply was vigorously opposed by the meat council and it remains in cured meats like sausage, hot dogs, and processed meats like Cotto Salami. A 2006 meta-analysis (combined analysis of studies) of 63 studies did indeed suggest that sodium nitrite was related to increased risk of gastric cancer. This argument is plausible from animal models of cancer risk, as 40 animal models have likewise suggested the same carcinogenic association.

Also, fructose? This is most likely added for sweetness. Recall that fructose heightens appetite and raises triglycerides substantially.

I personally have a natural aversion to meat. I don't like the taste, the look, smell, and the thought of what the animal went through to make it to the supermarket. But, considered from the cold, carnivorous viewpoint of the question, "Is meat okay to eat?", among the issues to consider is whether the meat has been cured or processed, and does that process include addition of sodium nitrite.

Cotto Salami and similar products are not, of course, what carnivorous humans in the wild ate. This is a processed, modified product created from factory farm animals raised in cramped conditions and fed corn and other cheap, available foods. It is not created from free-ranging animals wandering their pastures or pens, eating diets nature intended. This results in modified fat composition, not to mention hormones and antibiotics added. These are not listed on the ingredients. Wild meat does not contain fructose or color-fixers, either.

So don't mistake "meat" in your grocery store for meat. It might look and smell the same--until you look a little closer.



Copyright 2007 William Davis, MD

Don't lament no OTC mevacor

After Merck's third go at FDA approval for over-the-counter (OTC) status for its statin cholesterol drug, Mevacor (lovastatin), the FDA advisory board suggested that its request be denied. They expressed concern that too many people would not understand how the drugs would be used and that misuse would be common.

Similar sentiments were echoed by Dr. Sidney Wolfe, director of the Health Research Group at Public Citizen; the American Medical Association (though the AMA always fights anything that threatens to erode physician control over health); and the de facto spokesman for cardiologists, Dr. Steven Nissen of the Cleveland Clinic.

Although I am a supporter for tools and legislation that yield greater self-empowerment in health care to the public, there is no need to lament the failed OTC status for Mevacor. For one, Merck had no plans to reduce the price on its OTC preparation. For many people, this would have meant an increase in cost, since health insurers would surely not cover a non-prescription agent.

Second, OTC status sends the implicit message that cholesterol is the most common cause of heart disease; it is not. (Small LDL particles are the number one cause, a pattern only partially addressed by any statin drug and a pattern largely responsible for the failure of statin drugs to "cure" heart disease despite pharmaceutical manufacturer's attempts to increase doses to take up any slack in effect.)

Thirdly, you can achieve the same effect--no, a superior effect--by incorporating several simple strategies into your life. These strategies are superior to Mevacor because they do more than just reduce LDL cholesterol. You can achieve similar LDL-reducing effect to Mevacor, 20 mg, just by adding:

--2 tablespoons oat bran or ground flaxseed per day (choose flaxseed if you have sugar problems or small LDL; flaxseed contains no digestible sugars, only protein and fiber)
--Raw almonds or walnuts--at least a handful, though more is fine and will not make you fat. (It's nuts like party mixes, mixed nuts roasted in unhealthy oils, and honey-roasted nuts that make us fat, not raw.)
--Soy protein sources--probably the weakest effect of all foods listed, but a contributor that can be obtained in a variety of forms, such as tofu, soy protein powders, and soy milk.
--Other foods that reduce LDL include pectin sources (e.g., citrus rind), flavonoids (e.g., green tea); stanol esters found in butter substitute Benecol (recall that sterol-containing products like Take Control and the flood of new products on the market like HeartWise orange juice might have potential for allowing sterol esters to enter the blood, so I do NOT recommend them); and, of course, niacin.

Many of these strategies also reduce small LDL, raise HDL, reduce triglycerides, and reduce blood sugar, effects that go beyond that achieved with Mevacor. Of course, a combination strategy is not as easy as popping one pill a day, it's better for you.

I will certainly not shed any tears for Merck and its relentless efforts to gain a stronger foothold in the "transform conditions into diseases" marketing strategy, the same strategy that classifies shyness, toe fungus, and sadness into medical conditions necessitating medication. While I do generally support efforts to increase public access to strategies that increase their health care power, this one was not necessarily all good.

Members of Track Your Plaque can read the complete report, Unique nutritional strategies to Reduce cholesterol naturally on the Track Your Plaque website.



Copyright 2007 William Davis, MD

Damage control

Medical device manufacturer, Cordis, is launching a new marketing program to promote its Cypher drug-coated stent. You can view the details at www.CypherUSA.com , including the slick TV commercial that HeartHawk posted a blog about.

The campaign opens with:

When you open up your heart, you open up your life.

Lives hampered by angina. By shortness of breath. By restricted blood flow. These lives are changing. Because of a state-of-the-art advancement. One that can have a huge impact on arteries around your heart. The CYPHER® Stent. It can open up your arteries. Increase flow of blood and oxygen. And change your restricted life. To an active life worth living. Your new life is...

Life Wide Open


Direct-to-consumer drug advertising has been around for a few years. While it has increased awareness of drugs and the "conditions" they are supposed to treat, it has also highlighted the aggressive profit-motive of the drug industry. This is not health care for the needy and sick, but health care for profit.

So now we're beginning to see the emergence of direct-to-consumer (DTC) advertising for medical devices. There was also a brief, though unsuccessful, foray into DTC advertising for implantable defibrillators, of all things, by Medtronic a couple of years ago, also.

What is the purpose of Cordis' marketing effort? Is it to educate and inform the public who might unknowingly receive non-drug coated stents and be deprived of the restenosis-inhibiting advantage of a drug-coated device? Is it meant to right a systematic wrong, a failure of cardiologists to insert the technologically, biologically, and ethically superior coated stents?

I find that doubtful. A more likely motive is damage control. With some of the (both deserved and undeserved) negative press the drug-coated stents have received lately, Cordis, eager to protect their $20 billion (annual revenues, 2006) medical device franchise, came up with this DTC strategy. After viewing the smiling faces of people , elated because of their "wide open" arteries and lives, Cordis hopes to see people going to their doctors insisting on the stent that is "opening millions of lives," since, "when your arteries narrow, so does your life."

Cool, trendy, liberating. That's the message they wish to deliver. Cool music, beautiful people, flashy high-tech images. Who wouldn't want a Cypher stent?

Beyond damage control, it's a familiar marketing theme: You're slender, glamorous, and sexy if you drink Coke, you're a caring mother if you feed your children Jif peanut butter, you're health conscious and smart if you eat Total cereal . . . you're cool and know what you want from life if you insist on a Cypher stent.

I don't object to advertising. It's part of the capitalistic economic system. It drives awareness and grows businesses. I do get concerned when advertising is so slick and effective that the people who are not properly armed with information can be duped into thinking that they need something that they don't really need.

Or, for which there are powerful, viable alternatives. Even hear about "prevent the disease in the first place?"

Low expectations

The Framingham Risk Calculator is a standard method used by many physicians to predict risk for heart attack or death from heart disease over a 10-year period. Low-risk is defined as <10% risk of heart attack or cardiac death over 10 years; high-risk is defined as 20% or more over 10 years; intermediate-risk is in between.

Let's put it to the test:

Amy is a 53-year old businesswoman. She is 5 ft 4 inches, weighs 150 lbs. Her father had a heart attack in his early 50s followed by the usual list of hospital procedures including bypass surgery at age 60.

What is Amy's risk for heart attack or death from heart disease over the next 10 years? If we enter her data into the Framingham risk calculator, the following result is returned:

Information about your risk score:
Age: 53
Gender: female
Total Cholesterol: 198 mg/dL
HDL Cholesterol: 74 mg/dL
Smoker: No
Systolic Blood Pressure: 120 mm/Hg
On medication for HBP: No
Risk Score: 1% Means 1 of 100 people with this level of risk will have a heart attack in the next 10 years.


So, according to the Framingham calculation, Amy has <1% risk for heart attack or death from heart disease over the next 10 years. Most primary care physicians would, at most, prescribe a statin drug and talk about a reduction in saturated fat.

Thankfully, Amy didn't fall for that bit of conventional mis-information. She instead got a CT heart scan, principally because of her father's history. Her score: 117. At age 53, this put her into 90th percentile, in the worst 10% of scores for women in her age group (50-55). By heart scan criteria, her risk for heart attack is probably more like 4-5% per year, or approximately 40-50% over the next 10 years.

Let's do just a bit more math. If Amy hadn't known about her heart scan score and no preventive action was taken, the expected progression of her heart scan scores would likely be:

Start: 117
Year 1: 152
Year 2: 198
Year 3: 257
Year 4: 335
Year 5: 436
Year 6: 567
Year 7: 737
Year 8: 958
Year 9: 1245
Year 10: 1618

In fact, given Amy's starting heart scan score of 117, it is highly unlikely that she survives the next 10 years without heart attack or a fatal heart event. Yet the Framingham risk calculator puts Amy's risk at less than 1%. Could anything be more wrong?

The folly of the Framingham calculator was highlighted by a recent publication from the large Multi-Ethnic Study of Atherosclerosis (MESA), in which 3600 women (45-84 years), all of whom fell into the "low-risk" category by the Framingham calculator--just like Amy--were tracked over approximately 3 3/4 years. This study generated several observations:

1) 30% of the "low-risk" women had positive heart scan scores.
2) 5% of the "low-risk" women had scores of 300 or greater (very significant for a woman). 8.6% of these women experienced a cardiovascular event like heart attack or death over the period. Women with a heart scan score of 300 or greater had a 22-fold greater event risk compared to women with zero heart scan scores.
3) Women with heart scan scores of 1 to 299 had a cardiovascular event risk of approximately 5-fold greater risk over the period.


Across the U.S., 90% of women younger than 70 years old fall into the Framingham "low-risk" category. Yet this fiction is accepted as the prevailing standard, along with LDL and total cholesterol, for determination of risk in women and men.

In my view, using the Framingham risk calculator is a misguided, misleading path, one that will mis-classify a substantial number of women who could otherwise be spared from heart attack and catastrophe.

By the way, Amy is also the Track Your Plaque program record holder (by percentage drop), with a 63% drop in heart scan score over a 15 month period.
Niacin: What forms are safe?

Niacin: What forms are safe?

Niacin, or vitamin B3, remains a confusing issue for many people. It shouldn't be.

It doesn't help that most physicians and many pharmacists also do not understand the basic issues surrounding niacin. The only reason why there is any level of prevailing knowledge about niacin is that Kos Pharmaceuticals managed to "pharmaceuticalize" a niacin preparation, prescription Niaspan, that provided the revenue to fund professional "education."

Niacin can be helpful to increase HDL, reduce small LDL particles and shift them towards the more benign large particles, reduce triglycerides, and reduce lipoprotein(a).

So here's a brief description of the various forms that you will find niacin:

Immediate-release niacin--Also called crystalline niacin or just niacin. This is the original niacin that releases within minutes of ingestion. Because it releases rapidly, it triggers the most intense "hot flush." While this form of niacin works wonderfully well, is the safest, and is dirt cheap, the majority of people are simply unable to tolerate the intense flush. It also works best taken twice a day, generating two intolerable flushes per day.

Slow-release niacin--These preparations were popular in the 1980s, since the slow 12 to 24 hour pattern of release minimized the annoying hot flush. But, with prolonged use, it also became apparent that an unnaceptable frequency of liver toxicity developed. Unfortunately, this means that any niacin preparation that trickles niacin out over an extended period, including many of the slow-release preparations now sold in health food stores and pharmacies, have potential for liver toxicity. These preparations should be avoided.

6-hour release niacin--Releasing niacin more slowly than immediate-release niacin but more rapidly than slow-release niacin, 6-hour release (or what the Niaspan people call "extended-release" niacin) is nearly as effective as immediate-release niacin with approximately the same low potential for liver toxicity. It is far less liver toxic than slow-release niacin. 6-hour release niacin therefore offers the best balance between effectiveness and safety. Preparations that show this pattern of release include Niaspan ($180 per month), the poorly-named Sloniacin (about $8 per month), and Enduracin (about $7 per month) for 1000 mg per day. (Some Track Your Plaque Members have also determined that several other over-the-counter preparations have been demonstrated to share a similar pattern of release.)

Then there are the scam products that have no useful effect at all:

Flush-free or no-flush niacin--Inositol hexaniacinate, or 6 niacin molecules bound to the sugar, inositol, has no effect in humans, at least not with the dozen or so preparations that I've seen used. Nor are there any data to document the effectiveness of flush-free niacin. It's also more expensive.

Nicotinamide--This niacin derivative likewise has no effect on the usual targets for niacin treatment.

While I used to prescribe Niaspan, the ridiculous pricing and aggressive marketing really turned me off. I now advise my patients and our online followers to use only Sloniacin or Enduracin, unless you can tolerate immediate-release niacin.

Comments (52) -

  • Mikie

    4/19/2011 7:08:18 PM |

    How about this interesting source of Niacin ... drum roll please ....

    Food.

    Why the pills?  I guess to a hammer the whole world is a nail.

  • Anonymous

    4/19/2011 7:14:26 PM |

    Humans need about 20mg daily of Niacin, which can be met thru diet.
    Lipid modifying effects start to occur at levels above 1000 mg daily (sometimes not until 2000 mg).  It is essentially a type of over dose reaction.

    Tried niacin myself at only a few hundred mg daily.  Was able to tolerate the flushing, but then had the pleasure of passing 2 kidney stones.  Niacin has been given the boot ever since.

  • Anonymous

    4/19/2011 7:47:12 PM |

    Is there a relationship between niacin and kidney stones? I've had a kidney stone before and it isn't much fun.

    I tried Niacin several times, IR, Niaspan, and Enduracin. But I ended up getting heart palpitations on each. I also kinda felt weird, tired and generally lousy. And strangely enough, even though I toughed it out for several months, my HDL went down a point (at 500mg/daily -- Niaspan & Enduracin)

    Just wondering what can be done for those who are Niacin intolerant.

    And I tried the aspirin beforehand, taking with food, etc. Didn't matter in my case.

  • Anonymous

    4/19/2011 8:07:24 PM |

    Well, great...just great.  I've been taking NOW Foods Double Strength Flush-Free Niacin (500 mg) for a few months and now I'm told its for naught at best, and possibly damaging my liver.  There is a slight difference in the chemical name - Inositol Hexanicotinate.  I don't suppose that is significant?

    Anyway, I guess its back to the Sloniacin I took before.  At least that's considered safe.

    Regardless, I'm ever so grateful for this blog.  I learn something from most every post - even when it means I've been doing something wrong.

  • Daniel A. Clinton, RN, BSN

    4/19/2011 10:04:59 PM |

    I know Niacin has the power to make some numbers change, but is there any sort of credible evidence directly studying Niacin's effect on outcomes like heart attack and death? I am not comfortable inferring a benefit from alledged "cholesterol lowering."

  • Tara

    4/19/2011 10:12:41 PM |

    Good reminder post, Doc!  

    Mikie-
    I'm normally a proponent of getting your micronutrients from food, but in the case of therapeutic doses of niacin it's just not feasible.  1000mg of niacin= 19 pounds of yellowfin tuna, 17 lbs of chicken, or 500 cups of asparagus

  • Anonymous

    4/19/2011 10:45:33 PM |

    quote:
    .. but is there any sort of credible evidence directly studying Niacin's effect on outcomes like heart attack and death? I am not comfortable inferring a benefit from alleged "cholesterol lowering."

    It's interesting with niacin, even after discontinuation it seems to have an effect on mortality:

    http://www.ncbi.nlm.nih.gov/pubmed/3782631

  • Anonymous

    4/19/2011 11:09:27 PM |

    Daniel,

    It is my understanding that therapeutic doses of Niacin is VERY cardio-protective (assuming the person in question can tolerate it). Lookup the HATS, FATS & CLAS trials. Check out Dr. B G's blog for more info on this:

    http://drbganimalpharm.blogspot.com/2009/09/cardio-controversies-dr-superko-md.html

    John M.

  • Anonymous

    4/19/2011 11:16:17 PM |

    I've been taking SloNiacin at 1500 mg/day for quite some time. Recently my HDL went up to 60 mg/dl from 50. No problems with flushing or liver fuction or kidney stones. I've become interested in the use of Niacin plus bile acid binding resin (colestipol) to reduce plaque in arteries (PAD). The studies are old, 1980's and 1990's, and of limited number of patients. However on the Niaspan website they claim that Niaspan along with diet and a bile acid binding resin is FDA approved not only to slow down plaque buildup, but also to help reduce plaque that already exists. niaspan.com/heart-healthy/plaque-build-up.aspx  ...  They cite the old studies on the web page.

    I wonder if the claim is substantially true about plaque reduction and FDA approval.

  • steve

    4/19/2011 11:51:44 PM |

    interesting post.  My doctor said that Slo Niacin is less tolerated than Niaspan.  He does not care which you use.

    Separate question: what impact does Niacin have on blood sugars and homocysteine?

  • michael goroncy

    4/20/2011 12:21:50 AM |

    I have reason to treat aggressively this 'spooky' disease of the heart. The science and anecdotal experience of cardiologists (who stay on the 'cutting edge') like Dr Davis and a few others will attest to the overwhelming positive effects of NIACIN.
    I have titrated my Nicotinic Acid (OTC ..100 tabs..cost $11) up to a daily dose of 1.5gm.
    The intolerable flush I concluded is in the main...PSYCHOSOMATIC.
    At first I thought the uncomfortable feeling was unnatural and  possibly harmful but, the science convinced me that it was harmless. The tact I adopted was to enjoy the flush and look on it as a
    wonderful healing zooming through the body. The actual flush cannot harm...the liver is another story.
    Sheesh! The things you have to do to play mind games.
    The use and other add on supplements  have created excellent lipids (Iam thinking of entering them in the State Championships)
    Learn to love the flush..small discomfort-huge benefits.

  • Bobby

    4/20/2011 12:51:34 AM |

    I have been taking good old regular niacin and actually like the flush--it makes me feel like it is doing something. However, my blood glucose is somewhat elevated (104) over what I believe it should be. My doctor isn't concerned , but I'm not sure. Any feed back?

  • Dr. William Davis

    4/20/2011 2:22:21 AM |

    That's great, Tara!

    It would be a great episode of Man vs. Food.

  • Dr. William Davis

    4/20/2011 2:23:55 AM |

    A discussion of the downsides of niacin, even when done properly, sounds like it might be of help to many people.

    I'l put it on the "to-do" list.

  • Dymphna

    4/20/2011 2:29:15 AM |

    Did anyone have nausea with higher levels of niacin? I've tried it but it makes me somewhat sick-feeling.

    Any ideas?

  • Anonymous

    4/20/2011 12:09:20 PM |

    I'd second the notion to avoid real-slow release niacin...I looked in the mirror to see someone with yellow skin when taking some.

    So what are the available 6 hour release brands?

    And what about pomegranate extracts to help clear plaque buildup?

  • Renfrew

    4/20/2011 12:37:06 PM |

    Good thread.
    I am taking a form of niacin that has 1000 mg of Niacin plus 20 mg of Laropiprant. The Laropiprant is a prostaglandin inhibitor and prevents flushes.
    The brand name is "Tredaptive".

    My LDL Cholesterol went from 160 to 120 within 1 month. Trigs from 75 to 55.

    I combine the tablet with 500 mg of milk-thistle (for liver protection) and have not had any increase in liver enzymes.

    That is really a workable compromise and easy to take as one tablet a day.

    Not sure if this is available in the US though, I am living in Germany.

  • Anonymous

    4/20/2011 1:06:25 PM |

    I'd be interested in knowing more about the twice-a-day recommendation. I've been taking my immediate-release 2gm/day dose once a day for a couple of years now. (Yes, I get the flush--and my liver numbers are good.)  Dr Davis seems to be saying to take (in my case) 1gm every 12 hours?  Is this easier on the liver?

  • Anonymous

    4/20/2011 1:22:59 PM |

    Too many adverse effects from taking Niacin.  It's not worth the risk.

  • Anonymous

    4/20/2011 2:52:24 PM |

    I would like to hear the author's opinions on the best forms of excersise for heart health.

  • Dr. William Davis

    4/20/2011 3:17:43 PM |

    Hi, Renfrew-

    I believe you have earlier access to this preparation than we do.

    This may an interesting, though prescription, possibility for those who have intolerable flushes.

  • Dr. William Davis

    4/20/2011 3:19:36 PM |

    Re: comments about the potential dangers of niacin.

    We always have to weight the risks vs. benefits. If I have, for instance, a 45-year survivor of sudden cardiac death with 3 stents who I meet with BMI 23.0 and a lipoprotein(a) of 450 nmol/L, then niacin is a small price to pay.

    Every situation is unique.

  • Anonymous

    4/20/2011 4:45:00 PM |

    In regards to the risks - can you direct me to research on that. A personal friend of mine had been on a research program in the past for a major pharma in northern Illinois. What they were trying to do was find exactly how niacin works so the process could be synthesized and patented. The project was not successful. In laying the groundwork for the project he had to look at past use of it in the treatment for heart disease. Older docs he interviewed had used up to 3 grams a day with no adverse effects to their patients. Used as a drug, my friend feels it is the safest non diet way to control Tri's and raise HDL. Personally I have take 2 grams a day for well over a year. No harmful effects, blood work normal.
    Without statins, tri - 151, HDL - 32
    With Crestor 10mg tri 80 to 100, HDL 45.
    With 2 gram niacin - Tri 52, HDL 80.
    I take regular niacin. After a while, you will experience almost no flushing. Your body will acclimate.
    I tout the use of it because it seems a lot of docs have forgotten it's usefulness. Keep up the info when you can.

  • Anonymous

    4/20/2011 4:59:05 PM |

    I've taken immediate-release niacin since 2003 and the only time I developed elevated liver enzymes was when I split a 4 gram daily dose into three divided doses.  I can take 1 gram three times a day with no problems, or up to 2.5 grams twice a day with no problems.  However, HDL elevation seems to plateau at 3 grams a day.

    Once in the last 3 years my doctor took me off niacin for 3 weeks to perform an NMR lipoprotein test.  With carbohydrate consumption under 70 grams a day and fat intake of 67%, my LDL particle count was over 2,000 and over 75% of them were small and dense.

    Niacin is the only way for me to reduce my small, dense LDL to a safer level.  Diet and exercise is not enough.  I suppose this explains why every male (except for me) has a major heart attack or stroke by the age of 50.

  • Anonymous

    4/20/2011 5:04:31 PM |

    One reason aspirin blocks only part of the flush is that the flush is produced by two separate mechanisms.  The most well known is the release of PGD2 from mast cells.  The other, which is rarely mentioned, is the release of serotonin from platelets.  Serotonin antagonists completely block the flushing due that mechanism (see "Niacin-induced “flush” Involves Release of PGD2 from Mast Cells and Serotonin from Platelets: Evidence from Human Cells In Vitro and an Animal Model", Dean Papaliodis,2008, American Society for Pharmacology and Experimental Therapeutics"

  • Sara

    4/20/2011 7:42:08 PM |

    I think niacin and metformin are 2 of the most powerful and safest drugs for metabolic syndrome.

  • pjnoir

    4/20/2011 9:39:57 PM |

    High doses of Niacin will increase blood sugars - I'll take my chances with Chloresterol (mind is low enough) then mess with my sugars.

  • pjnoir

    4/20/2011 10:07:25 PM |

    *mine    not mind  
    Sara- since blood sugars go up- how can it be a good choice to improve metabolism?

  • Might-o'chondri-AL

    4/20/2011 11:00:14 PM |

    ? Anyone with input on the supposed benefit of taking Niacin every other day, instead of daily ?
    Someone brought it up once in an old niacin post of this blog, but nobody else seemed to know about that dosing.

  • Christi

    4/21/2011 12:16:02 AM |

    You could also add Protandim to your daily regimen. Pubmed.gov studies have shown Protandim to be extremely helpful in heart disease. It reduces Oxidative Stress and inflammation in the cells. www.dailylifesource.com

  • christi

    4/21/2011 12:18:13 AM |

    You should also add Protandim to your daily regimen. I first was exposed to this product on the ABC Primetime news investigative report. Pubmed.gov has published peer reviewed studies that show Protandim is very effective with heart disease. Check out the ABC news program here: www.dailylifesource.com

  • Anonymous

    4/21/2011 3:18:08 AM |

    Christi:

    I looked up on Wikipedia the supplement Protandim you mentioned. I am familiar with 4 of the 5 ingredients it contains and while the 4 have a good reputation, I am not impressed with the overall product. Most of the studies were conducted in an animal model. If I was looking to raise my endogenous antioxidant levels (SOD, catalase & glutathione) like Protandim claims, I would take GliSODin instead...probably in the form of Life Extension brand Endothelial Defense. I am sure Endothelial Defense is more cost effective and a has meaningful doses of better researched ingredients.

    Pjnoir:

    While it is true that Niacin can raise fasting glucose a few points, this can be more than made up for with a better diet and exercise. In fact, niacin might actually increase insulin sensitivity. Niacin is also extremely cardio protective. The HATS trial showed that Simvastatin+niacin reduced CHD events 89% less than the placebo group.

    John M.

  • Anonymous

    4/21/2011 6:42:52 AM |

    Kenneth....
    After a long period of utterly fruitless treatment with flush-free niacin as high as 4 grams a day, I started good old fashioned immediate release niacin.

    The flushing is manageable. The key is in slowly titrating up to your target dose. I think I went up maybe 50 mg a day every two weeks. I've been at 500 mg twice a day for months. I only get bad flushing when I let myself get dehydrated or indulge in sugar or other pro-inflammatory foods ie fast food or chips, things you shouldn't be eating anyway.

    There is some evidence that flavanoids can mitigate the flush, and I've had good luck with 600 mg or so of quercetin taken with my fish oil half an hour or so before the niacin. Baby aspirin helps, as does celebrex when I happen to take it for aches. I haven't been able to escalate the dose as I started getting muscle pains and fatigue even though my liver panels didn't indicate any problem. Everyone has different reactions, but don't write off niacin until you've given it a fair shot.  

    I will also tell you that Niaspan is NOT in fact flush-free either. I tried it for a short while and found that it simply delayed the flushing. The product literature says as much. The strategy is simply to put off the flushing until you're already asleep, and you pay hundreds of dollars more for that dubious benefit.

  • Hans Keer

    4/21/2011 10:07:15 AM |

    Why pills? Meat, vegetables and fruit deliver all the B3 you need.

  • Anonymous

    4/21/2011 12:36:50 PM |

    Even though I'm pre-diabetic, I've never experienced blood sugar elevation with niacin.

    The tolerance to the flushing develops with continuous use.  Although I've never tried it, every other day dosing may result in a more pronounced flushing effect.

    I've also used quercetin concurrently with niacin and have noticed a decrease in flushing.  I'm very fair-skinned and still experience flushing after all these years.

  • Anonymous

    4/21/2011 12:50:54 PM |

    What would be interesting if people who are using Niacin here tell us, what effect it had on their respective Cholesterol levels (HDL, LDL, Trigs).
    And if they had any issues with increasing liver enzymes or higher bloodsuger.

  • Kent

    4/21/2011 3:16:42 PM |

    Just an observation on the (Niaspan or intermediate release verses the imediate release.  I found Niaspan along with other LP(a) supplements (fish oil, Coq10, Pauling Protocol, low wheat) to work much better than the Intermediate release niacin. My LP(a) started at 198 and dropped to 45 with Naiaspan included in the regimen. I switched to imediate release and it went up to 150. I switched back to Niaspan and the LP(a) dropped back down. Has anyone else experienced this phenomena?

  • Leshme

    4/22/2011 2:30:31 AM |

    Since I began taking 1,000mg of regular niacin/day, my blood platelet count has hovered around 120,000. I have read online that niacin may cause a reduction in blood platelets. Can anyone comment?

  • Anonymous

    4/22/2011 6:52:39 AM |

    I use immediate release Niacin 2 grams a day.  Have used as much as 4 grams a day.

    I find that if I take any other supplements with plenty of fluid/food - usually a glass of tomato juice and a glass of water - and then wait for about 15 minutes before taking the niacin, I don't get a flush except maybe once a month and only slightly.  I use capsules and pull them slightly apart so that I can seperate them before swallowing, otherwise I might get a flush at some random time in the future when the capsules finally break open.  When I used to use tablets, I would chew them up so I wouldn't get a random flush at some future point.

  • Anonymous

    4/22/2011 3:26:02 PM |

    I took Niaspan for almost six months.  My physician started me off at 700mg and I ended up at 1000mg by the time I was taken off of it.  My blood work was somewhat better but nothing spectacular and it sure wasn't good enough for me to endure the extreme flushing I experienced three or four times a week. My whole body turned a dark apple red and I experienced extreme itching over every square inch of my body at once for thrity to forty-five minutes, as if I had millions of ants crawling on me.  I've read comments about how people enjoy this experience and I cannot begin to comprehend that as it was like being tortured to me.  I would scratch myself so much that I tore my skin.  Flushing took place even after taking aspirin and eating yogurt thirty minutes to an hour prior to taking it. You can have your niacin.  I'll stick to my Crestor.

  • Anonymous

    4/22/2011 5:08:25 PM |

    Dr. William Davis said...

        A discussion of the downsides of niacin, even when done properly, sounds like it might be of help to many people.

        I'l put it on the "to-do" list.
    .................

    I scheduled a general checkup in a few weeks, which I'm going to request a purines test, since I've read Niacin might affect gout sufferers.

    I've not been diagnosed with gout, but as it runs in my family, and I've also read that even though females get it less - that changes after (menopause, which I've started).

    Paternal grandfather suffered from diagnosed gout for years - he had many stomach bleeds from gout meds, so was taken off them. His last gout attack landed him in the hospital: Normal diet, IVF @ 125cc/hr, Foley output at end of day: ZERO.

    Younger brother's first gout attack  in late 30's (has one kidney, which probably hastened things). Mother also thinks she had one gout attack after over-indulging on a roast too many days in a row - she recognized her toe as looking like granddaddy's (not her father).

    So I'll play it safe and wait to see that my hormone situation didn't trigger high purine levels before starting slowly on SloNiacin.

    Please consider including Gout/Niacin info in your article Dr. Davis, and correct any mis-info I might have misinterpreted. I'll ask my GP if he orders liver functions with checkups at my age.

    Shreela

  • Jim (formerly anonymous)

    4/22/2011 11:53:16 PM |

    A Different Anonymous said...

        What would be interesting if people who are using Niacin here tell us, what effect it had on their respective Cholesterol levels (HDL, LDL, Trigs).
        And if they had any issues with increasing liver enzymes or higher bloodsuger.

        April 21, 2011

    I gave my results much earlier.

    I think that people here fail to understand that the very first successful Cholesterol lowering "drug" was niacin, plain old drugstore type.

    Evidently, the first American drug trial of Niacin was run by William Parsons Jr. MD in 1955 who was then a Resident at Mayo clinic. The actual use of Niacin was pioneered by the Canadians, and Parsons heard about it from a visiting Canadian Physician.

    There is therefore well over a half a century of use of Niacin for cholesterol control.

    Many MD's did't like it, because it is an unregulated non-prescription substance. Now there is a prescription form which is very expensive and well promoted with big bucks and drug representatives to push it.

    Dr. Parsons became less of a researcher and more of a clinician in later years. He has published a book "Cholesterol Control Without Diet : The Niacin Solution" which I suggest that you look at (library) or buy, if you are interested in the use of Niacin for cholesterol control.ISBN 0966256875 $14.95. 276 pages.

    With the expensive prescription Niaspan, now made and sold and marketed by Abbott Laboratories,the classical resistance of MD's to use this treatment is falling. No vitamin supplement firm could do this level of marketing for a cheap generic pill.

    From page 196:
    "Since the 1996 edition, there have been no more significant reports of liver problems with niacin. ...... and yet there are still no more than the 18 cases we listed here, 5 of them questionable."

    He also discusses the studies designed to make Niacin look bad, and Statins look good.

    It can be said that there is considerable confusion as to how Statins actually work. The first theory was cholesterol lowering. As evidence for inflammation to be a more dominant mechanism for CHD, there are now more reports that Statins have anti-inflammatory properties. But after all of the millions and millions of dollars spent on Statin R&D, the exact behavior of Statins is still not understood in detail.

    In fact, there were no real good theories for the painkilling behavior of Aspirin until sometime in about the 1960's or later.

    There are tons of information about Niacin out there, you have to go look for them, or buy the books. Well, you can just ask somebody to feed the information to you. That still works as a labor saving device.

  • Anonymous

    4/23/2011 2:23:35 PM |

    Thank you for the reminder to check into my "Now" brand Niacin.  

    Now claims sustained release formula on the bottle but there is nothing in the ingredients to suggest any coating or binding.  Regardless, I have been taking 2grms for a long time last thing at night along with my 2.7grms omega3 and 20mg crestor. Trigs and LDL were well controlled with this combo but my HDL was still only 45.  Then I switched back to eating meat(saturated fat), lowered my grain intake and last blood test HDL was 67.  the down side was my LDL went up 10%

    Regarding the Flush. If I awake after a few hrs into my sleep, often I will feel the flush/itchy skin.  Small price to pay for 90% reduction in a heart attack.

    Trev

  • Anonymous

    4/23/2011 2:45:06 PM |

    http://www.scribd.com/doc/50437/Niacin#fullscreen:off

    excellent summary of Niacin types and explanation  for liver toxicity.
    Trev

  • jbuch

    4/26/2011 2:51:35 PM |

    Excellent article on the Pharmacists knowledge of the different forms of niacin.

    Inspired me to do some more digging and I found this excellent webpage which is a baseline discussion of the ARBITER 6 Trial, with excellent comments on Niacin myths and factoids.

    http://www.theheart.org/article/1022265.do

    In particular, look at the readers comments, evidently almost exclusively MD, numbers 34 to about 57. It is here that some of the common myths and factoids are noted, mostly with literature citations rather than unsubstantiated claims.

    Below is one example.
    ---------------------------

    Niacin Dissolution Rates
    I recently came across an interesting paper on the dissolution rates of various niacin formulations. Niaspan was best in terms of slow dissolution, followed by Enduracin and Slo-niacin. For those interested:

    Poon, Ivy O., Chow, Diana S.-L., Liang, Dong
    Dissolution profiles of nonprescription extended-release niacin and inositol niacinate products
    Am J Health Syst Pharm 2006 63: 2128-2134
    ------------------------

  • Susan

    5/8/2011 7:20:26 AM |

    You might want to take a closer look at Protandim, it's not a simple product and takes a bit of time to take in what it really does in the body. There is proof that it  raises SOD in a human peer-reviewed study. Protandim is proven to increase catalase, glutathione, and a number of other endogenous antioxidants in addition to increasing SOD. The science is there, but how I really know it works is through what it has done for me and quite a number of people I know who have had notable improvements in their health. There is nothing wrong with glisodin, but it isn't in the same class as Protandim.  Protandim is proven to work through the activation of the Nrf2 transcription factor, up-regulating the antioxidant response gene sequence that causes the body to produce it's own native antioxidant products in every cell of the body. This site explains more about it and has links to supportive science:  www.radicalresults.net

  • yves

    5/11/2011 12:37:31 AM |

    Any insight as to whether Nicotinamide may be effective for those with fungal infections?
    http://www.wellnessresources.com/studies/niacinamide_helps_combat_candida_albicans/

  • georgepds

    5/20/2011 4:40:12 PM |

    "Why pills? Meat, vegetables and fruit deliver all the B3 you need."

    Because you would have to eat too much to get a clinical benefit

    You need 1000 to 2000 mg, 4 oz of chicken gets only 14 mg.. so, for the clinical benefit, you'd have to eat ~400 oz of chicken, or about 25 pounds of chicken a day.. just a  tad too much chiken for me


    http://www.whfoods.com/genpage.php?tname=nutrient&dbid=83

  • Ken Levin

    6/5/2011 11:00:23 PM |

    Hi Dr Davis, I'm a new Track Your Plaque member and noticed two new studies claiming niacin was not helpful in reducing the incidence of heart attack. One study compared Zocor with and without  niaspan (summarized in New York Times about a week ago)  and one studied niacin (not sure which form, heard about the study through a physician)  alone.   Do these studies change your recommendations about niacin for Track Your Plaque members?  Thanks in advance and thank you for your Track your Plaque program.

  • Jonathan

    6/6/2011 5:03:29 PM |

    All I could find around here locally was slow release niacin (capsule shaped tablet).  I pop two 500mg and chew them.  I get a real nice flush.

  • Jesse

    6/24/2011 4:42:46 PM |

    Dr Davis, can you comment on the studies mentioned by Ken Levin above? I would be interested to know the specifics about them, and if they hold nay water.

    Thanks

  • M2

    7/2/2011 6:17:01 PM |

    Dr. Davis, very interested in a response to the niacin studies referenced by Ken and Jesse above.

    Thanks!

Loading