Category: Blood Sugar

Enzogenol, the signature ingredient in our recently launched GenZogenol-R Healthy Aging formulation has been shown in rodent studies to lengthen telomeres by over 40% and to extend healthspan significantly as well as extend lifespan by 18% – this would equate to 15 years in humans.

We cannot assume of course that results in rodents will be duplicated in humans, however my personal philosophy has always been that when I come across an ingredient or formulation that directly targets the health of DNA and has such a significant impact on healthspan – and potentially lifespan – I am taking it!

We are working towards human clinical trials to corroborate these results, and that is a key concept with our company: we utilize third party technologies and lab tests (such as telomere length and health as well as age related methylation degradation) to corroborate the efficacy of our formulations.

GenZogenol-R targets the aging process at a DNA level

Two key animal studies:

  • In a rat study, Enzogenol LENGTHENED telomeres by more than 40%
  • In a mouse study in middle aged mice, one cohort was supplemented with Enzogenol and the other cohort was not
  • The cohort group supplemented with Enzogenol achieved an extension of healthspan as well as lifespan (18% lifespan extension which in humans would equate to 15 years)


Key GenZogenol-R Applications:

Read More:

https://www.dropbox.com/s/6hyxd3uk9ip09qs/GenZogenol-R%20Article.docx?dl=0

I am concerned about the increasing popularity of the vegan movement and vegan diets with respect to its potential impact on individuals’ health.

My personal opinion and my experience working with patients is that initially individuals who adopt a (healthy) vegan diet may realize some health benefits, however over the long term there is a significant potential that these individuals may develop nutrient deficiencies which may have profound effects on health.

From my perspective, there are a couple of considerations to this:

Firstly, every individual is biochemically and metabolically unique and a vegan diet may not be appropriate for a specific individual.  This is the same consideration with respect to any diet, whether it be low carb/high fat, vegetarian – or whatever.

The second consideration is the fact that most individuals simply do not have the knowledge and expertise to understand how to assess whether they are developing deficiencies, or how to supplement to address these deficiencies or prevent them.

I recently presented a three hour Master Class lecture to 4th year Naturopathic students at our local Naturopathic school: Boucher.

The topic of the lecture presentation covered ketosis, the ketogenic diet, intermittent fasting, time restricted feeding – but also information on the Fasting Mimicking Diet developed by Valter Longo, PhD.

If you are not familiar with the Fasting Mimicking Diet (FMD), the concept is that for a limited number of days during any month if you consume a restricted number of calories of specific types of food, it has the effect of providing a CRM (Caloric Restriction Mimetic) influence on the metabolism for the whole month.

And Longo and his colleagues have published a considerable number of studies to back up his hypothesis.

The one negative about the program is that they recommend accessing (expensive) prepared meals from a provider for the fasting days in a set up similar to Weight Watchers.

Also in the lecture presentation, I talked about some of the issues related to vegan diets (deficiencies) – and also with animal protein consumption (the primary concern being an increase in IGF-1 insulin like growth factor levels which can stimulate cell growth and division – and some ways to counteract this mechanism which I will detail in a separate article).

Today I wanted to share an article from the Daily Mail newspaper in the UK detailing Virpi Mikkonen who is a high profile poster girl for the meat-free revolution and a social media guru and how she confessed that a vegan diet ruined her health and brought on early menopause.

Also I am including some information from my Boucher lecture regarding some of the potential nutrient deficiencies associated with a vegan diet.

Individuals choose specific diets for different reasons: for ethical and environmental issues (common with the vegan community), they buy into a fad diet which has become popular – or hopefully like myself and I would presume many practitioners reading this article that have biohacked their metabolism to determine the best diet to optimize their health and quality of life.

For myself, a LCHF (low carb / high fat) / ketogenic diet works optimally: I do not stay in ketosis continuously but I have adapted my metabolism so that it can switch back and forth effortlessly between burning fat and sugars.

I am of the opinion that this metabolic flexibility is something that all individuals can benefit from, provided their metabolism and health will allow them to stay in a continuous state of ketosis to initially make this transition to being keto adapted, which takes about six weeks.

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There have been some articles circulating in the common press suggesting that skipping breakfast may be detrimental to your health – specifically CVD issues.

These articles are based upon a recently published study: the latest report from the April issue of the Journal of the American College of Cardiology: “Taken together, these studies [showing a positive association between skipping breakfast and CVD and CVD risk factors] as well as our findings underscore the importance of eating breakfast as a simple way to promote cardiovascular health and prevent cardiovascular morbidity and mortality.”

This assertion would of course seem counter-intuitive to those of us who incorporate intermittent fasting into our lifestyle.

For those of you who are practitioners, this topic may come up if some of your patient population has read any of these articles.

Peter Attia MD wrote a great rebuttal to this commentary.  

Peter hosts a great podcast and sends out a weekly newsletter article – here is his website: 

Home – Peter Attia Peter Attia explores strategies and tactics to increase lifespan, healthspan, and well-being, and optimize cognitive, physical, and emotional health. “If you want to know how to live longer, and how to live better, you should be listening to Peter. peterattiamd.com

Here is the content from his newsletter article countering the conclusions of this paper.

(as with many of these types of studies, some key issues included the fact that it was an observational study, bias, confounding factors).

Greetings –

Nota bene: I was pretty pissed off when I wrote this, but don’t let my annoyance detract from the message. Bad science is an abomination. Incompetent news reporting on bad science is worse.

You’ve probably heard that breakfast is the most important meal of the day. “What is less commonly mentioned,” writes Alex Mayyasi in The Atlantic, “is the origin of this ode to breakfast: a 1944 marketing campaign launched by General Foods, the manufacturer of Grape Nuts, to sell more cereal.”

Seventy-five years later, here’s the latest report from the April issue of the Journal of the American College of Cardiology: “Taken together, these studies [showing a positive association between skipping breakfast and CVD and CVD risk factors] as well as our findings underscore the importance of eating breakfast as a simple way to promote cardiovascular health and prevent cardiovascular morbidity and mortality.”

What were the findings? Let’s look at a few newspapers: 

  • “Want to Lower Your Risk for Heart Disease? Eat Breakfast Every Morning” (Healthline)
  • “Eating breakfast? Skipping a morning meal has higher risk of heart-related death, study says” (USA TODAY)
  • “Study: Skipping breakfast increases risk of heart disease mortality by 87 percent (FOX)”

(You may notice that all three headlines imply causality.)

Looks like General Foods was right. Time to reach for the Lucky Charms? Perhaps it’s time to put on our critical thinking cap instead. The actual study, and the media coverage of it, is a part of the Groundhog Day that is observational epidemiology (for more on the limitations of this type of research, check out Studying Studies: Part II). This was a prospective cohort study pulling data from NHANES III, looking at people who reportedly eat breakfast every day to people who never eat breakfast, and then following up with them (about 19 years later on average), tallying up the deaths from CVD and deaths from all causes.

One question to ask about the population studied is: was eating breakfast or not eating breakfast the only difference between these two groups? In other words, were there any confounding factors (for more on confounding, see Studying Studies: Part IV)? The authors reported that, “participants who never consumed breakfast were more likely to be non-Hispanic black, former smokers, heavy drinkers, unmarried, physically inactive, and with less family income, lower total energy intake, and poorer dietary quality, when compared with those who regularly ate breakfast.” Not only that, “participants who never consumed breakfast were more likely to have obesity, and higher total blood cholesterol level than those who consumed breakfast regularly.” They also had a higher reported incidence of diabetes and dyslipidemia. Read that again, please.

While the study used statistical models to “adjust for” many of these potential confounders, it’s extremely difficult (actually, it’s impossible) to accurately and appropriately adjust for what amounts to fundamentally different people. The healthy user bias (or the inverse, an unhealthy user bias) is virtually impossible to tease out of these studies (the healthy user bias is covered in more depth in Studying Studies: Part I). Not only that, you never really know what you’re not looking for. This is typically referred to as residual confounding in the literature, where other factors may be playing a role that go unmeasured by the investigators.

I haven’t even yet mentioned the misleading nature of reporting relative risk — in this case, an associated 87% (reported in the study as a hazard ratio of 1.87) — without reporting absolute risk. The question you should always ask is, 87% greater than what? To get an idea of the associated absolute risk, the number of CVD deaths in the “every day” breakfast group were 415 out of a total of 3,862 people over 16.7 years (that’s an unadjusted rate of 10.7%) while the numbers for the “never” breakfast folks were 41 CVD deaths out of a total of 336 people over 16.7 years (unadjusted rate of 12.2%). That’s an absolute difference of 1.5% over almost 17 years (annually, this is an absolute difference of 0.09%). Granted, this is before adjustment of the myriad confounders (including the biggest “risk factor” for CVD death, age, in which the “never” breakfast group was younger on average at baseline), but it gives you an idea that we’re looking at small differences even over the course of a couple of decades. This looks a lot difference on paper than an associated 87% increased risk of CVD death. (For more on absolute risk and relative risk, see Studying Studies: Part I.)

There’s more: 

  • What were the participants actually eating for breakfast? We don’t know. The investigators didn’t have information about what foods and beverages they consumed.
  • Did participants change their breakfast eating (or abstaining) habits over the course of almost 20 years? We don’t know. Information on breakfast eating was only collected at baseline.
  • Could there be errors in the classification of the causes of death in the participants? It’s possible.
  • What constitutes skipping breakfast? Was it the timing of the first meal of the day? We don’t know. Participants were asked, “How often do you eat breakfast?” but there was no definition of what that means, exactly.

What’s more likely: reported skipping breakfast was a marker for a lifestyle and environment that may have predisposed these people to a higher risk of CVD death or that skipping breakfast itself causes CVD death?

Go ahead and skip all the breakfasts you want. And please forward this to the next 10 people who tell you it’s unhealthy to do so.

– (Pissed off) Peter

For a list of all previous weekly emails, click here.

podcast | website | ama

Some recent dietary and eating pattern trends have been shown to have positive benefits on health for many individuals.

The specific trends I am referring to include: low carb diets, intermittent fasting and compressed windows of feeding (such as 8/16 hours: eating during  a period of 8 hours and fasting for 16 hours.)

The following article from Natural News highlights some of the recent studies and health benefits of intermittent fasting.

I am sure many of you may have tried intermittent fasting yourselves and have recommended it to your patients: I certainly count myself in with this group, and I have seen some significant health benefits in some patients.

In the article, it highlights a specific study done at Harvard which was published in the journal Cell Metabolism.

Here is one of the key takeaways from the study:

“Manipulating mitochondrial networks inside cells — either by dietary restriction or by genetic manipulation that mimics it — may increase lifespan and promote health, according to new research from Harvard T.H. Chan School of Public Health.”

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Genetic mutations (polymorphisms) of the MTHFR (methylenetetrahydrofolate) enzyme are common in the general population.

Estimates are that approximately 60% of the general population (including myself) possess this mutation which comes with a range of influence on such important metabolic processes as methylation* pathway impairment, the potential buildup of homocysteine levels etc.)

* For those of you who read my newsletter that are not health care practitioners here is a simple explanation of methylation from the website: Mindbodygreen:

What is methylation? Without getting too technical, methylation is the addition of a single carbon and three hydrogen atoms (called a methyl group) to another molecule. The removal of a methyl group is called demethylation. Think of billions of little on/off switches inside your body that control everything from your stress response and how your body makes energy from food, to your brain chemistry and detoxification. That’s methylation and demethylation.

Typically if the MTHFR polymorphism is negatively impacting on methylation function, one of the approaches to improve this is for the individual to supplement with 5-methyltetrahydrofolate (5-methyl THF) – which is something that I personally do.

The reason this is done is that with this polymorphism the biochemical pathway step which involves converting 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate (5-methyl THF), the primary circulatory form of folate utilized in homocysteine remethylation to methionine is impaired.  By consuming the end product – 5-methyl THF you are consuming the end product and not worrying about the impaired conversion to make the end product – 5-methyl THF.

The following article suggests that by simply supplementing with Riboflavin (Vitamin B2) that the additional Riboflavin can make the enzyme necessary for this conversion to work like normal.

Supplementing with 5-methyl THF certainly works, however many readers I am sure would agree that targeting and resolving the cause of the problem
(the enzymatic conversion of 5,10-methylenetetrahydrofolate to 5-methyltetrahydrofolate (5-methyl THF) makes more sense – rather than targeting the effect.

In addition,  5-methyl THF is typically a practitioner grade supplement which the general population would not typically have access to – and most in this population would not understand the biochemistry/biochemical pathways involved and may actually exacerbate an existing problem (for example, initiating overmethylation can disrupt neurotransmitter balance).  Also 5-methyl THF is much more expensive vs. Riboflavin, a common and accessible B vitamin.

Many comprehensive B vitamin complexes may in fact have enough Riboflavin content to meet this need, and I am of the opinion that it is always best to take balanced ratios of the B vitamins – unless there is a specific identified need for a larger amount of a specific B vitamin(s).

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Copyright (C) 2019 R. V. Lamberton & Associates All rights reserved.


A key focus in my clinical practice when I am working with clients to help them to optimize their health and resolve health issues is putting together for them a program to help them to be able to reverse their Biological Age.

Chronological vs. Biological Age

Chronological age is your age in years.
 
Biological age, also called physiological or internal age, is a measure of how well or poorly your body is functioning relative to your actual calendar age.
 
This concept would make sense to most individuals: we have all interacted with individuals who seem to be much younger – or older than their age in years.
 
We are able to assess Chronological Age via several methods: I use a technology device when I am working in person with clients which provides a comparison between Biological Age and Chronological Age.

In addition to this technology device, there are a couple of lab tests which provide information related to Biological Age vs. Chronological Age: a test to assess telomere length and health as well as a test to assess methylation function.
 

Telomeres
 
Telomeres can be described as end caps on chromosomes – a similar concept to the plastic tips on shoe laces.
 
As we age and our cells divide multiple times telomeres shorten and the shorter they get the more prone we are to chronic, degenerative disease.
 
Our lifestyle choices and situation can also impact on telomere length, for example eating poor quality food, not sleeping enough, dealing with severe stress and other factors can all have an impact of shortening telomeres.
 
 Methylation
 
Methylation is a biochemical process which happens continuously in our bodies.  As we age, our methylation function deteriorates.
 
A simple explanation of methylation is as follows:
 
“What is methylation? Without getting too technical, methylation is the addition of a single carbon and three hydrogen atoms (called a methyl group) to another molecule. The removal of a methyl group is called demethylation. Think of billions of little on/off switches inside your body that control everything from your stress response and how your body makes energy from food, to your brain chemistry and detoxification. That’s methylation and demethylation”.
 
Reversing Biological Age has the potential to extend Healthspan:
 
Healthspan vs. Lifespan
 
 Lifespan is the number of years we live: Healthspan is the duration of time we live during which we stay healthy – the maintenance of full function as nearly as possible to the end of life.
 
Recent medical advances has continuously extended lifespan, however many individuals spend differing lengths of time towards the ends of their lives dealing with poor quality of life (such as dementia, Alzheimer’s, physical challenges that significantly impact on mobility etc.)

 
Reversing Your Biological Age

If you are interested in finding out how you can reverse your Biological Age and potentially impact on your Healthspan, reach out to me:

Rob Lamberton

Phone: 778-227-4952

Email: Rob@RobLamberton.com