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11/12/21

This article was previously published December 27, 2020, and has been updated with new information.

In this interview, Tucker Goodrich and I discuss what will be the topic of my next book, namely linoleic acid (LA), which I believe is likely the leading contributing cause of virtually all chronic diseases we've encountered over the last century. Unfortunately, this is a topic that most clinicians and health care practitioners who focus on natural medicine have only a superficial understanding of.

Goodrich has a business background as a stockbroker and asset manager, and developed an IT risk management system used by two of the largest hedge funds in the world. A string of health crises in his late 30s and early 40s prompted him to apply his research and troubleshooting skills to medical research.

As noted by Goodrich, "It was a very upsetting time in my life and medical professionals really weren't any help at all in trying to figure out what caused things." After a lot of reading and researching, he decided to cut out seed oils from his diet, and in just two days, his 16-year-long bout with irritable bowel disease started to dramatically improve.

"I started immediately feeling better," he says. He also lost a significant amount of weight over the next two months. After that, he stopped eating carbs and realized he must have had a severe case of gluten intolerance.

"Being an engineer by trade, I did a lot of experimenting. What can I eat? What brings back the symptoms? What do I have to avoid to keep the symptoms away? And it was a transformation that made everybody I worked with comment on what a difference they saw in me. It was a very quick change," he says.

Avoiding Omega-6 Fats Is Key for Good Health

While considered an essential fat, when consumed in excessive amounts, which over 99% of people do, LA (an omega-6 polyunsaturated fat or PUFA) acts as a metabolic poison.

Most clinicians who value nutritional interventions to optimize health understand that vegetable oils, which are loaded with omega-6 PUFA, are something to be avoided. What most fail to appreciate is that even if you eliminate the vegetable oils and avoid them like the plague, you may still be missing the mark.

Chances are you're still getting too much of this dangerous fat from supposedly healthy food sources such as olive oil and chicken (which are fed LA-rich grains).

Another common mistake is to simply increase the amount of omega-3 that you eat. Many are now aware that the omega-3 to omega-6 ratio is very important, and should be about equal, but simply increasing omega-3 can be a dangerous strategy. You really need to minimize the omega-6. As explained by Goodrich:

"The ratio is not really what's important. What's important is avoiding the omega-6 fats. There are disease models, like age-related macular degeneration (AMD), where that's starting to be clearly understood, and you can find papers saying explicitly that the important intervention that prevents AMD from progressing is reduction of omega-6 fats, and you can't prevent it by increasing your omega-3 fats.

I've got papers that show, in animal models, very nasty outcomes, such as liver failure, with a lower omega-6 to omega-3 ratio, but high absolute levels of both fats still allows pathology to progress."

LA Is a Primary Contributor to Chronic Disease

When we talk about omega-6, we're really referring to LA. They're largely synonymous, as LA makes up the bulk — about 60% to 80% — of omega-6 and is the primary contributor to disease. Broadly speaking, there are three types of fats:

  • Saturated fats, which have a full complement of hydrogen atoms
  • Monounsaturated fats, which are missing a single hydrogen atom
  • PUFAs, which are missing multiple hydrogen atoms

The missing hydrogen atoms make PUFAs highly susceptible to oxidation, which means the fat breaks down into harmful metabolites. OXLAMS (oxidized LA metabolites) are what have a profoundly negative impact on human health. While excess sugar is certainly bad for your health and should be limited to 25 grams per day or less, it doesn't oxidize like LA does so it's nowhere near as damaging.

Over the last century, thanks to fatally flawed research suggesting saturated animal fat caused heart disease, the LA in the human diet has dramatically increased, from about 2 to 3 grams a day 150 years ago, to 30 or 40 grams a day. Goodrich cites research showing LA used to make up 1% to 3% of the energy in the human diet and now it makes up 15% to 20%.

In my mind, this radical change has had the most catastrophic impact on human health in the history of the human race, as it is the complete opposite of what you need for optimal health. This dietary change has undoubtedly killed millions, probably hundreds of millions, prematurely and still continues to do so because people don't understand this.

"I'm a speed reader and I love reading medical journals … but what nobody's really done is connect all the dots. There are a lot of people who understand little sections of [the science], but they haven't gone on to coalesce everything into a common explanation for these pathologies across different disease states.

I think that's what I've been able to do, and I think that's the key insight that makes this message really compelling," Goodrich says.

On a side note, do not confuse LA with conjugated linoleic acid (CLA). While most think CLA and LA are interchangeable, they're not. CLA has many potent health benefits and will not cause the problems that LA does.

How Excess LA Consumption Damages Your Health

At a molecular level, excess LA consumption damages your metabolism and impedes your body's ability to generate energy in your mitochondria. There is a particular fat only located in your mitochondria — most of it is found in the inner mitochondrial membrane — called cardiolipin.

Cardiolipin is made up of four fatty acids, unlike triglycerides which have three, but the individual fats can vary. Examples include LA, palmitic acid and the fatty acids found in fish oil, DHA and EPA. Each of these have a different effect on mitochondrial function, and depending on the organ, the mitochondria work better with particular kinds of fatty acids.

For example, your heart preferentially builds cardiolipin with LA, while your brain dislikes LA and preferentially builds cardiolipin in the mitochondria with fats like DHA. Goodrich further explains:

"To give you an idea of how important this is, 20% of the fat in your entire body is contained in cardiolipin. So, for anybody who doesn't understand mitochondria, mitochondria are what distinguish us from bacteria. It's what allows us to be a multi-cellular creature. They are what produce the energy in your body, what's known as ATP, which is a chemical carrier of energy.

To give you an example of how important it is, cyanide, which we all know is highly toxic, breaks your mitochondria, and that's why it kills you so fast. It prevents mitochondrial respiration and therefore your entire body shuts down almost instantly.

So, [mitochondria are] something we want to take good care of because they're everywhere, in almost every tissue except for red blood cells … There are studies showing that cardiolipin is directly controlled by dietary intake of fats. That is, to an extent, true. Obviously, different tissues build cardiolipin in the mitochondria out of different fats.

But they can vary that composition in fairly short order through changing the diet in rat models, like in the order of weeks. So, you can see changes pretty quickly. I notice things happening in days. What's unique about LA is that it is very susceptible to oxidation when it is in the cardiolipin molecule.

Two LAs that are adjacent to each other can oxidize each other. They're also attached to proteins in the mitochondria that contain iron, and that iron can catalyze the oxidation of cardiolipin. This is a pretty fundamental process in the body."

Oxidation of Cardiolipin Controls Autophagy

Oxidation of cardiolipin is one of the things that controls autophagy. In other words, it's one of the signals that your body uses when there's something wrong with a cell, triggering the destruction and rebuilding of that cell. Your cells know that they're broken when they have too many damaged mitochondria, and the process that controls this is largely the oxidation of omega-6 fats contained within cardiolipin.

So, by altering the composition of cardiolipin in your mitochondria to one that's richer in omega-6 fats, you make it far more susceptible to oxidative damage. Goodrich cites research showing that when the LA in cardiolipin is replaced with oleic acid, another fat found in olive oil, the cardiolipin molecules become highly resistant to oxidative damage.

"That is basically what I think we need to go back to," he says. "We evolved with low levels of LA in our diet and therefore in our cardiolipin. One of the neatest papers I've ever seen looking at this, something that encapsulated this whole model that I'm talking about, fed rats either a regular high carbohydrate diet, or they added PUFAs to their diet.

Just adding the omega-6 fats to the diet caused the mice to become diabetic. They became insulin resistant, leptin resistant, obese, and the differences are pretty stark between the fat mice and the skinny mice on the high carbohydrate rat diet …

The high-PUFA diet caused a breakdown in the cardiolipin content in the mitochondria in their hearts. So just adding seed oils caused heart damage through a change in the cardiolipin composition."

As mentioned, the primary problem is the OXLAMS, the oxidized byproducts. One of them is 4HNE, which is relatively easy to measure. Studies have shown there's a definite correlation between elevated levels of 4HNE and heart failure. LA is broken down into 4HNE even faster when the oil is heated, which is why cardiologists recommend avoiding fried foods.

OXLAMS Trigger Cancer

Heart disease isn't the only condition triggered by excessive LA intake and the subsequent OXLAMS produced. It also plays a significant role in cancer. As noted by Goodrich, to induce cancer in animal models, you actually have to feed them seed oils. "So, this is a really fundamental process that we're talking about here," he says.

As I mentioned above, animals typically develop cancer once the LA in their diet reaches 4% to 10% of their energy intake, depending on the cancer. In the breast cancer model, cancer incidents increase once 4% of calories are in the form of seed oils.

Disturbingly, most Americans get approximately 8% of their calories from seed oils. "So, we're way over what these thresholds in the lab would suggest is a safe level of these fats based on the laboratory work in animals," Goodrich says, adding:

"We've got this huge disconnect between what the lab science tells us we should be doing and what our dietary guidelines tell us we should be doing. The scientists are saying, 'Oh, look, it's poison. It causes all the chronic diseases,' and the government's saying, 'Eat lots of it.' That's not a good thing."

4HNE is a mutagen, in other words, a toxin that causes DNA damage. One of the primary genes it damages is the P53 anticancer gene. Mutations in the P53 gene are found in 15% of cancers, making it one of the most common. As noted by Goodrich, "P53 is literally a cancer prevention gene. It's how your body regulates cancer. You can all draw your own conclusions about the wisdom of eating something that can cause that to break."

On a side note, one of the major jobs of glutathione is to detoxify 4HNE. You can often tell that you have excess 4HNE if your glutathione levels are low, as this means it's being used up detoxifying 4HNE.

LA and Obesity

High-LA diets also cause obesity. "If you feed mice lots of saturated fat, they don't get fat and they don't get sick. It's only when you increase the LA in the diet from 1% to 8% that they become obese," Goodrich says. Now, mice and rats are not exactly like humans, so how do we know all of this applies to us? Goodrich explains:

"What Alheim and Ramston observed is that, back in 2006, there was a drug introduced called Rimonabant, which was an anti-obesity drug. It was a bit of a miracle drug. I want to quote this exactly because it's so important to understand the effects that this drug had on humans.

'Large randomized trials with Rimonabant have demonstrated efficacy in treatment of overweight and obese individuals with weight loss significantly greater than a reduced calorie diet alone.

In addition, multiple other cardiometabolic parameters were improved in the treatment groups, including increased levels of HDL, reduced triglycerides, reduced weight circumference, improved insulin sensitivity, decreased insulin levels. And in diabetic patients, improvements in HBA1C.'

This paper was released in 2007. Unfortunately, Rimonabant had a side effect that it caused people to want to kill themselves. So, it was withdrawn from the market and it largely killed research for several years into that area.

But what Alheim did in 2012 was demonstrate that the mechanism behind Rimonabant is to block the metabolism of seed oils into the chemicals in your body and the endocannabinoid system that cause overeating. My experience when I stopped eating seed oils was that I forgot to eat carbohydrates.

The effect of Rimonabant in these mouse models is to make them crave carbohydrates and to stimulate them to eat sweet foods and carbohydrates. Everybody's familiar with this effect. It's called the munchies. And it's what you get after you smoke pot, because the endocannabinoid system is the system that marijuana affects and the chemical that Rimonabant blocks is your body's homologue to the THC in marijuana.

So essentially what we've done to ourselves is given ourselves a chronic case of the munchies, which is blocked by this unfortunately very harmful drug. This is as open and closed a case for causation as you're going to find in the medical literature.

We have a human drug that treats this, and as I just read, it treats all these different aspects of this disease. And it works through this one pathway that we have a clear demonstration of in animal models. In this case, the drug is completely pointless because the dietary fix is well known and is simple."

Increased LA Also Increases Your Risk of Sunburn

So, to summarize, the dramatic increase in LA — and the oxidative end products that cause the damage — is the primary cause behind the increase in chronic diseases such as obesity, diabetes, heart disease and cancer.

Simply lowering your LA intake to what your great-great grandparents used to eat, you can essentially eliminate almost every single one of the diseases that are now prematurely killing us.

Interestingly enough, there's even evidence showing eliminating seed oils from your diet will dramatically reduce your risk of sunburn, which is something Goodrich experienced first-hand. "Susceptibility to UV radiation damage is controlled by how much PUFAs are in your diet," he says. "It's like a dial. They can control how fast it happens, and how fast you get skin cancer."

Seed Oils Raise Risk of ARDS and COVID-19

Considering the metabolic and mitochondrial damage caused by LA, there's reason to suspect LA may also play a role in COVID-19, as some white blood cells convert LA into leukotoxin. Essentially, LA contributes to the inflammatory domino effect that eventually kills. Goodrich explains:

"Yes. That's certainly what the conclusion that I drew. I did an enormous post on this, looking at the effects of LA in SARS COV-2 and SARS in general. SARS is a severe acute respiratory syndrome. SARS kills you by giving you acute respiratory distress syndrome (ARDS).

ARDS can be caused by lots of different things, not just these viruses. You can get it from influenza. You can get it from inhaling acid into your lungs. What's fascinating is the human literature is quite clear that you can induce ARDS through feeding seed oils.

Very sick people who can't eat are fed intravenously. It's called total parenteral nutrition (TPN). Generally, this is used through a product called Intralipid, which is made out of soybean oil and sugar. When you start to understand all this stuff, it's just mind boggling. Doctors did an experiment after they noticed that a lot of their patients who came into the ICU and got TPN then subsequently got ARDS.

So, they started playing with what they were feeding them, and what they discovered was this soybean oil formula increased the patient's rate of getting ARDS. The fatality rate from ARDS is 30% to 60%. Feeding seed oils increased the rate of ARDS by seven times."

As explained by Goodrich, the key toxin that produces the symptoms of ARDS is called leukotoxin, and leukotoxin is made from LA by white blood cells to kill pathogens. It's toxic enough to where if you inject high-enough amounts of it into animals, it kills them in minutes. Leukocytes incubated with LA convert all of the LA into this toxin until there's none left, so, a major part of the disease process in ARDS is the conversion of LA into leukotoxin. That is what ends up killing patients.

"It is often noted in the popular press that what kills people is this cytokine storm. What I'm describing is the mechanism of the cytokine storm. Leukotoxin is uniquely what causes the symptoms of ARDS, as has been clearly demonstrated in the animal models," Goodrich says. "So, it seems to me that a sensible thing to do would be [to] change your diet. Why wouldn't you want to do that?"

How LA Triggers Heart Disease

Goodrich also explains how high LA levels cause heart disease. One of the first things that happens in atherosclerosis is your macrophages, another type of leukocyte, turns into a foam cell, essentially a macrophage stuffed with fat and cholesterol. Atherosclerotic plaque is basically dead macrophages and other types of cells loaded with cholesterol and fat. This is why heart disease is blamed on dietary cholesterol and fat.

However, researchers have found that in order for foam cells to form, the LDL must be modified through oxidation, and seed oils do just this. Seed oils cause the LDL to oxidize, thereby forming foam cells. LDL in and of itself does not initiate atherosclerosis. LDL's susceptibility to this oxidative process is controlled by the LA content of your diet.

"That's a result that's been repeated several times, so subsequently, the definition of an atherogenic lipid in your blood is one that contains oxidized omega-6 fats. That's the definition," Goodrich says.

"The standard explanation of why you get heart disease and why it progresses the way it does is because the omega-6 fats in your blood get oxidized and become toxic, and progress you all the way through atherosclerosis until it finally kills you.

That's the standard explanation for what causes heart disease. I can't tell you how many cardiologists I have talked to who don't understand that that's what the medical literature says is causing this disease.

Now, it's worse if you're also on a high carbohydrate diet. A ketogenic diet is somewhat protective against the negative effects of this, but I can't stress enough that this is the standard explanation for cardiovascular disease in the medical literature — that seed oils oxidize and that's what causes the pathology."

Understanding Olive Oil

As mentioned, olive oil also contains LA, but it also has other healthy fats. This makes olive oil a bit tricky. The main fat in olive oil is oleic acid, which is one of your body's favorite fats. Your body actually makes it, which is why it's not considered an essential fat. Oleic acid is much more resistant to oxidation than LA, which is why olive oil is a pretty decent cooking oil.

According to Goodrich, oleic acid is protective against both cardiolipin oxidation and LDL oxidation. Interestingly, oleic acid can also replace LA in LDL. Other fats, such as palmitic acid, cannot do that. The problem with olive oil is that it also has a fair amount of LA.

"The percentages that I've seen quoted in literature range from 2%, which is awesome, to 22%, which is not good," Goodrich says. The other problem is the olive oil market is hugely corrupt and fraught with fraud. Many olive oils are cut with cheaper seed oils, which raises the LA content.

So, in summary, if you're using olive oil, I strongly recommend keeping close track of your total LA intake. Anything over 10 grams a day is likely to be problematic (although the exact cutoff is still unknown, so this is merely an educated guess).

If you really want to be on the safe side, consider cutting LA down to 2 or 3 grams per day, to match what our ancestors used to get before all of these chronic health conditions became widespread. If olive oil puts you over the limit, consider cooking with tallow or lard instead. Beef tallow is 46% oleic acid and lard is 36% oleic acid.

High-LA Sources to Avoid

As Goodrich suggests, if you want to protect your health, you'd be wise to avoid all concentrated sources of LA. Top sources include chips fried in vegetable oil, commercial salad dressings, virtually all processed foods and any fried fast food, such as french fries.

"What amazes me is people who go to all these measures and I'll hold up my girlfriend as an example. She was a vegan when we got together, had a farm and grew organic food and went to extremes to avoid toxins in food and then went home and cooked with seed oils," Goodrich says.

"There are so many people who are like this, who are genuinely trying to do their best to have a healthy diet and then they're chugging down LA that turns into a metabolic toxin in your body, and they wonder why they can't lose weight.

By the way, after I told her, what I just said here: Avoid seed oils, avoid refined carbohydrates, eat animal food and animal fats, she lost 56 pounds in two and a half months and her autoimmune disease, fibromyalgia, went into complete remission."

The Importance of Carnosine

Beef, even conventional grain-finished beef, has low LA. Grass fed beef has higher DHA and CLA, which makes it a healthier option. Beef is also the primary source of carnosine, which has been shown to be anti-atherogenic.

Carnosine is also a mitochondrial stimulant, a sacrificial scavenger of advanced lipooxidation end products (ALEs), which is very similar to advanced glycation end products (AGEs). AGEs is another name for HNE and all the other reactive oxygen species generated from oxidizing LA.

Carnosine is the most effective scavenger for HNE. Carbonylation of proteins is basically the process through which proteins in your body get damaged and become ineffective. HNE damages 24% of the proteins in your cells, so carnosine can go a long way toward warding off this cellular damage. As explained by Goodrich:

"In heart failure, Alzheimer's and in AMD, one of the things they see is an inability of the cell to produce enough energy. The mitochondria are getting damaged. HNE does that damage. It damages 24% of the proteins in the cell, primarily around energy production.

One of the worst cancers is glioblastoma, a brain cancer. A researcher up in Boston, [Thomas Seyfried], decided to try and figure out why the mitochondria are getting damaged in glioblastoma, and found they all have oxidized cardiolipin. Every single cancer cell he looked at had damaged cardiolipin in it.

One of the ways your cells produce energy is they basically ferment glucose into pyruvate outside of the mitochondria This is a perfectly normal part of metabolism and they produce something called pyruvate. A molecule called pyruvate dehydrogenase takes pyruvate into the mitochondria and converts it to acetyl-CoA so the mitochondria can burn it very efficiently for fuel.

Well, one of the things HNE does is it breaks pyruvate dehydrogenase, and they see this in Alzheimer's where their cells are no longer able to produce enough energy. This is why your cells are dying in Alzheimer's. The beta amyloid plaques in Alzheimer's disease are induced by HNE. There's a great model that came out of Harvard a couple of years ago showing that.

And in cancer, if you can't get pyruvate out of the cell, out of the cytosol, the part of the cell surrounding the mitochondria, it has to ferment there and turn it into energy, which is what we call the Warburg effect, where you start shifting over to this damaged primitive fuel system. The evidence seems to be that that's because you've broken your mitochondria.

Even the critical, the most important part of the mitochondria, complex 5ADP synthase — which is what takes all the energy coming from your mitochondria and turns it into ATP, which is what fuels the rest of your body — is damaged by HNE. This is a huge issue. There's no more fundamental problem in aging and health than protein damage."

Take Control of Your Health by Lowering Your LA Intake

As you can see, the evidence strongly suggests excessive LA is driving all the killer diseases today. The solution is simple though. Just lower your LA intake. There's an easy way to do this. You don't have to send all your food out for analysis. Simply use an online nutritional calculator such as Chronometer to calculate your daily intake.

Chronometer will tell you how much omega-6 you're getting from your food down to the 10th of a gram, and you can assume 90% of that is LA. Again, anything over 10 grams is likely to cause problems. Since there's no downside to limiting your LA, you'll want to keep it as low as possible, which you do by avoiding high-LA foods.

Keep in mind you'll never be able to get to zero, and you wouldn't want to do that either. So, just what should you eat to keep your LA intake low? Goodrich summarizes his own diet:

"I eat mostly beef. I eat vegetables. I cook mostly in butter. I eat a little bit of fruit. I eat occasional grains. Occasionally I'll have corn, a little bit of rice and potatoes. I'm mostly on a cyclical keto diet. Once you fix your metabolic system, then you can go back and forth a lot easier and I don't see any reason to be on strict keto long term. I think [cyclical keto] is healthier.

They looked at a ketogenic diet in rodents and found they were protected. The reason they were protected is because they were able to burn HNE as fuel. But if you add a little bit more insulin into the system, then it turns off fat-burning and HNE goes out of the mitochondria and does more damage."

This is yet another reason for working out in a fasted state, which Goodrich also recommends. "I think working on a fasted state is one of the most important health things that you can do, without question," he says. Goodrich also points out that the reason a strict ketogenic diet can cause liver failure is due to the omega-6 fats in the diet. It's crucial to make sure the fats you eat are actually healthy.

Goodrich is currently in the process of writing a book about this, as am I, in which all of this information will be laid out in even greater detail. In the meantime, you can learn more by visiting Goodrich's blog, Yelling-Stop, or follow him on Twitter. In closing:

"I can't say anything that you haven't already said in this talk, honestly," Goodrich says. "You want to eat like your ancestors ate because your ancestors were healthier and they were not eating industrial seed oils. They were not eating industrial processed carbs in high quantities.

They were making sure that they got lots of animal meat and animal fat and they were getting exercise. I mean, it doesn't really matter what kind of exercise you're doing, just as long as you're doing it.

I think I have helped many people in many different ways by telling people this. And it's typically a short conversation, like my girlfriend who cured her autoimmune disease, fibromyalgia. She'd been in constant pain for almost 30 years and it went away in a couple of weeks. I mean, that's amazing, and it's so simple to do.

This is, I believe, the fundamental problem with our modern health — this issue of LA. There are lots of other things that play into it. There's no doubt about that, but that's the fundamental thing. If you fix that, you can get away with doing a lot of other things that aren't exactly optimal, but still be healthy."



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A recent study published in the New England Journal of Medicine1 discovered that the rate of cardiovascular events and death were lower in the group of individuals who used a salt substitute with potassium than in those who used regular salt. The salt substitute was 75% sodium chloride and 25% potassium chloride.

In the interview above with James DiNicolantonio, PharmD., we discuss how salt has been vilified in the past several decades and the possible impact this had on the development of chronic diseases, including high blood pressure and obesity. The interview was in 2017, just after the publication of his book “The Salt Fix: Why the Experts Got It All Wrong — and How Eating More Might Save Your Life.”

In today's culture, most people think of salt as seasoning for their food. But historically, salt was necessary for the preservation of food and was inextricably intertwined with trade.2 Salt was highly valued, and the word salary is actually derived from the word salt.

It was used as a method of currency and was crucially important economically to many cultures. According to historians, salt played a prominent role in the exploration of the Pacific Northwest in America, was used by the British as a leverage tool in the American Revolution and played a key role in defeating civilian and military morale in the South in the Civil War.

DiNicolantonio first became interested in salt when he was working as a community pharmacist.3 His patients were complaining of new symptoms after their physician put them on a low-salt diet for their high blood pressure. The symptoms included muscle fatigue, heart palpitations, muscle spasms and cramps.

He advised his patients to talk with their doctors and ask more questions about the necessity for using a low-salt diet. He also encouraged them to request a serum sodium blood test to determine if they had low salt levels.

His patients found that after adding salt back into their diet the symptoms disappeared. DiNicolantonio believed this was a real indication that low salt diets were not “panning out in the real world.”4

Potassium Salt Substitute Lowered Cardiovascular Events

The original “Dietary Approaches to Stop Hypertension” (DASH), was published in 1997 in the New England Journal of Medicine.5 The researchers enrolled 459 adults who had blood pressure of less than 160/95. After eating a control diet low in fruits and vegetables and dairy products for three weeks, they were randomly assigned to one of three diets.

One group of participants ate a diet rich in fruits and vegetables, the second ate the control diet and the third ate a combination of the two. The researchers concluded, “A diet rich in fruits, vegetables and low-fat dairy foods and with reduced saturated and total fat can substantially lower blood pressure.”6 At the time of publication, national guidelines also recommended a low-salt diet.

The intervention diet had a salt content of approximately 3 grams per day, with higher levels of potassium, magnesium and calcium. The researchers wrote, “Nonetheless, known diet-related determinants of blood pressure (sodium chloride, body weight and alcohol) could not have accounted for the reductions in blood pressure, because changes in these potential confounders were small and similar for all the diets.”7

In other words, they found that low-salt diets we're likely not responsible for the reductions in blood pressure that were found in those eating a whole-food diet. But later they wrote it was “noteworthy” that reductions happened with a “sodium intake of approximately 3 grams per day and consumption of two or fewer alcoholic drinks per day.”8 Twenty years later the diet is still considered an important advance in nutritional science. According to one paper:9

“It emphasizes foods rich in protein, fiber, potassium, magnesium, and calcium, such as fruits and vegetables, beans, nuts, whole grains, and low-fat dairy. It also limits foods high in saturated fat and sugar. DASH is not a reduced-sodium diet, but its effect is enhanced by also lowering sodium intake.”

Yet it has been the salt consumption in the DASH diet that has received the greatest attention. The recent data are from the Salt Substitute and Stroke Study10 which sought to determine if using a salt substitute that contained 75% sodium and 25% potassium could have an effect on the rate of major cardiovascular events, stroke and death.

While the endpoint of the DASH diet was to measure blood pressure reduction in a small number of participants, the Salt Substitute study involved people in 600 villages across rural China and used endpoint measurements that clearly had an impact on health.

The researchers chose participants who were 60 years old and older and had high blood pressure. Others were chosen because they had a history of stroke. The researchers randomly assigned villages to use a salt substitute or regular salt11 and followed up for a mean of 4.74 years.12

Those consuming the salt substitute had a lower rate of stroke, major cardiovascular events and death. The rate of hyperkalemia, or high levels of potassium in the blood, was only slightly higher in those using a salt substitute.13 While these results are encouraging, the researchers did not measure whether the participants were first deficient in potassium, also crucial for cardiovascular health.

Low-Salt Recommendations Likely Does More Harm

The original studies linking a low salt diet to high blood pressure began in the 1940s with Dr. Lewis Dahl. At the time of his death, he was chief of staff at the Hospital of Medical Research Center, Brookhaven National Laboratory, New York. In 1956 he concluded that a high-salt diet was an important factor in high blood pressure.14

In my interview with DiNicolantonio, he referred to Dahl as “the Ancel Keys of salt,”15 in reference to the way Keys’ and Dahl’s studies were structured.16,17 The method behind Keys’ study was seriously flawed, with the biggest flaw being that Keys cherry-picked the countries he used to support his hypothesis.

According to DiNicolantonio, Dahl did virtually the same thing as he chose five populations from which he would draw a linear line from high blood pressure to salt intake. DiNicolantonio commented:18

"I don't know what was in the water in the 1950s, but these doctors seemed to pick just five or six populations that fit their hypothesis, plot it out and show the association basically finding what they wanted to find."

DiNicolantonio continued by describing the 1988 Intersalt study19 in which 52 populations were evaluated for the relationship between urinary electrolyte excretion and blood pressure measurements. Included in the 52 populations were four primitive cultures that did not consume salt.

An analysis of the data showed that when the four tribal populations are included in the total, the overall results show that salt reduction can help lower blood pressure. However, it is important to note that while those populations did not eat salt, they had a diet with high levels of potassium and magnesium. The people group also exercised more, drank no alcohol and ate no foods with processed sugar.

When that group was removed from the data, it demonstrated that the lower levels of salt did not have a positive effect on blood pressure. One of the reasons this may happen is because when salt is cut from the body, insulin resistance rises.

The combination of Dahl’s study and the DASH study lay the blame for high blood pressure, diabetes and kidney disease on salt. DiNicolantonio commented on the relationship between the study funding sources and the results:20

“When you look at the data and look at studies that didn't have any conflicts with the food industry … There was one systematic review published a few years ago and it literally showed the opposite results.

The studies that didn't have any conflicts, basically 80% showed that sugar is associated with obesity and gaining weight. And of course 80% of the studies that had conflicts with the industry showed exactly the opposite, which literally goes to show you that absolutely conflicts with the sugar industry and food industry can affect scientific results. That's what was going on here.”

Conditions That Require Greater Attention to Sodium Levels

One of the best ways I have found to affect my mitochondrial health is through a cyclical ketogenic diet. When some people first begin this switch to ketosis, they can develop something called “keto flu.” This is often a transitory combination of symptoms that include nausea, fatigue and headaches.21

DiNicolantonio describes the process of how going into ketosis can deplete your body of salt, and thus result in some of these symptoms. He explains that your salt levels directly control levels of magnesium and calcium.22

As carbohydrates are cut from the diet, it reduces the amount of insulin in the body, raises glucagon and produces negatively charged ketone bodies. Each of these processes play a role in lowering sodium levels. DiNicolantonio also points out that there are certain subpopulations of people who are more salt sensitive, such as those with:

  • High aldosterone levels — This hormone helps the body retain salt by reducing the amount excreted in the kidneys.23 At the same time it causes the body to remove more magnesium.24 This can happen with a benign tumor-secreting aldosterone.
  • Cushing's syndrome — In this disorder, your body makes too much cortisol. This can mimic the actions of aldosterone and cause the body to keep too much sodium and excrete more potassium.25
  • Liddle’s Syndrome — In this rare condition people retain too much salt.26

A healthy body has a “salt thermostat”27 that helps control how much salt you should be eating. It basically is about listening to your own salt cravings. However, as DiNicolantonio describes, there are health conditions that contribute to poor sodium absorption or sodium loss. Those include:

  • Bowel diseases — People with ulcerative colitis, celiac disease and irritable bowel syndrome do not absorb salt well. Individuals who have had surgical intervention in their gut may also have poor salt absorption. This could include those who have had bariatric surgery or had part of their intestines removed from cancer.
  • Adrenal insufficiency — This is also called Addison's disease and happens when the adrenal glands do not make enough cortisol.28 DiNicolantonio spoke of a paper published in JAMA in the 1940s describing a child who was eating a lot of salt to the point where the parents hospitalized the child. The child ended up dying a few days later from salt loss. People with adrenal insufficiency do not absorb sodium well.
  • Hypothyroidism — Thyroid hormones help control metabolism and the kidneys’ ability to resorb salt.29 People with some type of thyroid dysfunction may need more salt.
  • Sleep apnea — People with sleep apnea may be losing twice the amount of salt at night, which is why they're often up during the night to urinate. The interruption in breathing can cause blood to enter the thorax, which increases central blood pressure. This tricks the body into thinking there is an overload of salt and causes the kidneys to excrete more salt and thus more urine during the night.
  • Kidney diseases — Individuals with polycystic kidney disease, glomerulonephritis and interstitial damage to the tubules can negatively affect salt loss, leaving higher levels of sodium in the body.

Low Sodium Level Impacts Exercise Performance

DiNicolantonio calls salt “the sixth factor in fitness.”30 He described how Ancel Keys discovered the benefits of salt for individuals who exercise. In the 1940s Keys demonstrated that individuals who work out in the heat without adequate amounts of salt have a 10-fold increase in the potential risk of heat stroke.

As people are looking for ways to improve blood circulation, DiNicolantonio believes that taking a bit of salt before exercise is one of the best ways to improve performance and reduce the risk of dehydration. Before working out he takes a half-teaspoon of salt with enough lemon juice to cover the taste of the salt and 2 ounces of water. He uses this approximately 20 minutes before working out.

The benefits are that you immediately begin increasing blood volume, circulation and reducing heart rate. People who have adequate sodium levels also release more heat because salt is a good vasodilator and allows heat to escape the body. As the heat dissipates during exercise it reduces your core body temperature.

Overtraining syndrome is a challenge faced by many athletes. The literature describes it as a “maladapted response to excessive exercise without adequate rest, resulting in perturbations of multiple body systems coupled with mood changes.”31 DiNicolantonio describes the effect salt has on overtraining syndrome:32

“Overtraining syndrome is literally salt deficiency in the tissues. When your muscles are just losing salt it's why you get muscle spasms, and twitches and if you just add salt back to the diet you can completely eliminate overtraining syndrome.”

Consider Your Salt Intake

As DiNicolantonio points out, our ancestors ate much more salt than we do, potentially up to 10 times more than we consume today.33 From a historical perspective it's important to note that society did not suffer from the chronic diseases that are also common today. He believes that the rise in high blood pressure, diabetes and obesity parallels lower salt diets and may have been a contributor to the development of these diseases.

In his research DiNicolantonio finds that the average American consumes about 3,400 milligrams of sodium each day. He does not believe that a person with healthy kidneys can consume too much salt, since the kidneys will flush out the excess amount.

It's crucial to consider the source of your sodium since sea salt from the modern oceans contains modern-day pollutants,34 like plastics and traces of heavy metals when compared to Himalayan Sea salt or Redmond salt from ancient oceans.

DiNicolantonio also points out that it’s important to get enough salt each day because a sodium deficiency can reduce vitamin C absorption, which indirectly affects bone health and strength due to the resultant vitamin C deficiency.35 The chloride in salt is also a necessary part of hydrochloric acid, which is a component of how food is broken down in the stomach.

One factor in lower amounts of hydrochloric acid in the gut, which contributes to acid reflux and gastroesophageal reflux disease, is there may not be enough salt to produce enough hydrochloric acid. Simply normalizing your salt intake is a classic example of how simple strategies have a considerable impact on health and wellness.



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New York pulmonologist Dr. Pierre Kory, an unapologetic champion of evidence-based medicine, has had remarkable success treating patients with ivermectin and other therapies during the pandemic. His efforts to get the word out on this treatment protocol as part of the Front Line COVID-19 Critical Care Working Group (FLCCC) have largely been stifled by censorship, ridicule and colleagues — brainwashed by the official narrative — unwilling to accept the science.

Kory spoke with Dr. Chris Martenson, host of the Peak Prosperity podcast, about his incredible experiences over the last nearly two years.1 On December 8, 2020, Kory testified to the Senate Committee on Homeland Security and Governmental Affairs, which held a hearing on “Early Outpatient Treatment: An Essential Part of a COVID-19 Solution.”

He called on the NIH, CDC and FDA to review the expansive data on ivermectin to prevent COVID-19, keep those with early symptoms from progressing and help critically ill patients recover.2,3 As he told Martenson, due to their promising results, he believed early on that “the pandemic has been solved,” until he realized that those in power weren’t open to hearing what he had to say.

Despite his impassioned pleas and astonishing science to back them up, the treatment not only was ignored by the Senate committee but promptly eviscerated.4 Now, he feels his colleagues in the health care field are living in one of two worlds — by either not following the data or putting patients first because they’re afraid of losing their job or status, or by risking everything to put patients first. He’s become estranged from many colleagues who he says “don’t get it.”

There Is Treatment Available for Viruses

Kory’s eyes have been opened to the reality that many people only hear or believe what public health officials tell them, whether it’s because they’re overworked and don’t have time to delve into the real data or because they’re following with blind trust. Many of Kory’s colleagues have gone along with those they believe to be authoritative experts, even when their guidance defies logic and commonsense. Kory’s trust in the “experts,” however, started to erode the more that he learned.

One of Kory’s role models is Dr. Paul Marik, a critical care doctor at Sentara Norfolk General Hospital in East Virginia, who is renowned for his work in creating the “Marik Cocktail,” which significantly reduces death rates from sepsis using inexpensive, safe, generic medications.5

Marik was one of a small group of critical care physicians who formed FLCCC, which developed a highly effective COVID-19 treatment protocol known as MATH+.6 Marik is so in tune with science that if he reads a new study and has questions, he’ll contact the first author on the paper to get direct answers.

Right off the bat, the MATH+ protocol led to high survival rates. Out of more than 100 hospitalized COVID-19 patients treated with the MATH+ protocol by mid-April 2020, only two died. Both were in their 80s and had advanced chronic medical conditions.7

After several tweaks and updates, the prophylaxis and early outpatient treatment protocol is now known as I-MASK+8 while the hospital treatment has been renamed I-MATH+,9 due to the addition of ivermectin.

Kory is now a public face of FLCCC, and he’s forged a global network of colleagues who are willing to adapt to new information in any way they can to help patients. One of Kory’s biggest revelations involved the treatment of viruses — specifically, the fact that there are dozens of treatment options available, about 90% of which are repurposed, cost pennies and are readily available:10

“I went into this pandemic believing what I’ve been taught my whole career, which is that there is no specific antiviral therapy … I mean, you get a cold, you just rest … and now here I am 18 months later — oh my gosh — there are literally two dozen compounds and now we have trial evidence showing pretty profound large magnitude benefits, either in the duration of symptoms, the duration of viral transmission, hospitalization and death.

We have a number of molecules that actually reduce mortality in what’s turned out to be a deadly viral disease. This isn’t the common cold, we’re clear on that.

I went from, there’s nothing to do for a virus to now, anytime I have a cold going forward, or any of my children, or any other virus that comes at us, we already have a whole armory of stuff that we can employ. And that data for those — which are best, which should be employed — is only going to increase.”

Giving Patients Agency Over Their Own Health

Marteson said that, since learning about accessible treatment options, “I feel like I have agency in my own health that I didn’t have before.”11 Kory mentions natural options like curcumin and nigella sativa, or black cumin, which he would have laughed off years ago, but now realizes they have multiple mechanisms by which they fight viruses:12

“Reading about something like curcumin or nigella sativa, which if someone told me a year ago to take something like nigella sativa — black cumin seed — it would save your life in a viral disease, I would have literally burst out laughing … but when you look, there’s literally 10 years of lots of little trials and studies that have evaluated and defined multiple mechanisms of black cumin seed — immunomodulatory, anti-inflammatory, antiviral.

So you have all of these building blocks, and then you have this trial from Pakistan — large randomized controlled trial with really large magnitude benefits — of literally nigella sativa and honey. And then you find out about honey. Honey also has pleotropic properties.”

Kory is driven to share what he’s learned with as many people as possible, because he believes that everyone should feel empowered to stay healthy, similar to what I have long advised — to take control of your health. He told Marteson:13

“It’s so satisfying because now we have agency, and so many people have agency by learning this knowledge of things that are readily available, cheap, don’t need a prescription, that you can actually treat yourself with very safe compounds. Not only is that agency so satisfying, but boy does it seem critical for the future. Is this going to be the last viral pandemic?”

His index case with ivermectin — the first person with COVID-19 whom he treated with the drug — is also etched in his memory. The patient — a “slightly older, slightly overweight” woman — was two weeks into COVID-19 and still having fevers and night sweats, so still quite sick. He treated her with ivermectin and she woke up in the morning feeling great:14

“Literally I saw what could only be described as a phenomenal response to a medication. So when we talk about data that we use, I’m sorry but I was sold right there on the first dose. First patient, first dose. And then I had repeated experiences.”

COVID-19 Is Highly Treatable

Fear has dominated the pandemic, but both Martenson and Kory say there’s no need to walk around in fear. As a lung and ICU expert, Kory is a master at treating acute illnesses which, he says, “is all about trajectories.” “When we make rounds on patients, we see them every day, we’re following their course … in an ICU, I have to be very knowledgeable about their minute-to-minute, or sometimes hour-to-hour trajectory,” he said.15

He teaches medicine also, and he teaches his trainees to study trajectories in their patients. When the trajectory worsens, especially in critical illness, therapies must be instituted but, he says, when “I see a trajectory on the improvement, I always say just stand back. They’re getting better, they’re going to continue to get better …”16

In the case of his index patient with ivermectin, she was on a steady trajectory, but it rapidly improved upon administration of ivermectin — a pattern he sees regularly with the drug. The ability to get a sense of this pattern recognition is what makes the difference between an expert and nonexpert in critical care medicine, Kory says.

“The longer you’re in medicine, the better you get at that and you can see which medicines are working.” In this case, ivermectin is one that quickly stood out from the rest. Especially if you’re an expert at trajectories, patterns and diseases, as Kory is, “you can figure things out much quicker than a massive, multicentered, double-blinded, randomized controlled trial.”17

If there were one thing that Kory could share, it’s that he wants everyone to know that COVID-19 is a highly treatable disease:18

“I want everybody to know how treatable this is … I’m not that worried about it for me, my friends, my family, my colleagues. I’m not worried about it for those who follow the FLCCC and our protocols because we know that they’re effective.

And I just hope that umbrella of reassurance and protection, which is to say there are effective treatments which will save your life and prevent the need for hospitalization, I just hope that number grows. But me personally, I’m not that bothered by COVID. As you know, I actually got COVID. It was a relatively mild case and so I also have natural immunity in my camp.”

Early treatment, however, is essential. One of his friends became ill with COVID-19 and made the mistake of thinking he had a cold. He didn’t contact Kory until he’d been sick for seven or eight days and by that time, he said, “I had to pull out all the stops for him. I really had to use every tool in my arsenal to keep him out of the hospital.” So if you have COVID-19, the sooner you implement the treatment protocol, the better.

There’s a War Against Truth

The successful treatment of COVID-19 using ivermectin and other therapies is being actively suppressed. Few, for instance, have heard about the astonishing success in Uttar Pradesh, India, which embraced large-scale prophylactic and therapeutic use of ivermectin for COVID-19 patients, close contacts of patients and health care workers.19

They’ve since had a COVID-19 positivity rate of almost zero, marking a major public health achievement that Kory believes should be a model for the world. Even the World Health Organization praised Uttar Pradesh for their excellent public health measures, which included sending people out to villages to conduct rapid COVID-19 tests and, if positive, treat patients and close contacts with ivermectin.

WHO, however, did not mention ivermectin as part of Uttar Pradesh’s success story.20 Kory now calls the FLCCC an “army,” because “they’re actively fighting a war”:21

“They’re challenging the pharmacists. They’re talking to their doctors. They’re writing to pharmacy boards … I don’t think war is an overstatement here. There’s a war on truth. There’s a war on free discourse and sharing of opinions. One of the catastrophic things is the way they branded misinformation on the level of a felony. Someone who has an opinion that differs from the agency’s is automatically medical misinformation.

It’s treated as though it’s a scourge of society that needs to be extinguished. I think people are fighting back against that. It’s nice to hear the army and the tribe is growing and most important is, I think we’re helping people. We’re arming people with agency and the ability to navigate a pretty confusing world.”

FLCCC’s I-MASK+ protocol can be downloaded in full,22 giving you step-by-step instructions on how to prevent and treat the early symptoms of COVID-19. FLCCC also has protocols for at-home prevention and early treatment, called I-MASS, which involves ivermectin, vitamin D3, a multivitamin and a digital thermometer to watch your body temperature in the prevention phase and ivermectin, melatonin, aspirin and antiseptic mouthwash for early at-home treatment.

Household or close contacts of COVID-19 patients may take ivermectin (18 milligrams, then repeat the dose in 48 hours) for post-exposure prevention.23 FLCCC also has a management protocol — I-RECOVER24 — for long-haul COVID-19 syndrome. The protocols are translated into 23 different languages to provide widespread, free access to this lifesaving information, including how to get ivermectin.25

FLCCC remains hopeful that ivermectin will be formally adopted into national or international COVID-19 treatment guidelines in the near future.



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When you have become immune to malaria after having contracted the disease, it seems that the body uses a more efficient protection than if you have been vaccinated against the deadly disease. The researchers believe the new findings may be used to improve existing malaria vaccines.

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Chronic inflammation caused by obesity may trigger the development of cells that break down bone tissue, including the bone that holds teeth in place, according to new research that sought to improve understanding of the connection between obesity and gum disease. The study, completed in an animal model and published in October in the Journal of Dental Research, found that excessive inflammation resulting from obesity raises the number of myeloid-derived suppressor cells (MDSC), a group of immune cells that increase during illness to regulate immune function. MDSCs, which originate in the bone marrow, develop into a range of different cell types, including osteoclasts (a cell that breaks down bone tissue).

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Clotting problems and resulting complications are common in COVID-19 patients. Researchers have now shown that a member of the anticoagulant group of drugs not only has a beneficial effect on survival of COVID-19 patients, but also influences the duration of active infection with the SARS-CoV-2 coronavirus.

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Breast cancers that have an overactive PI3K enzyme tend to be more aggressive and to spread and divide more like stem cells. But a new study uncovers a surprising relationship between PI3K activity and mutations in the PIK3CA gene that codes for the enzyme.

from Top Health News -- ScienceDaily https://ift.tt/2YHfZLL

New study results demonstrate that unstable housing and homelessness is associated with a two-fold greater chance of being re-infected with SARS-CoV-2 compared to those who are securely housed. The research indicates that unstable housing was the only demographical factor associated with re-infection despite the presence of antibodies from the first infection.

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