Category: Blood Sugar

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

The Dangers of Drinking Sodas

Great article from Organic Lifestyle Magazine on the dangers of drinking soda drinks:

“Soda is proven to be addictive and consumption has been clinically linked to increased blood pressure, high blood sugar, weight gain, kidney disease, heart disease, diabetes, depression, asthma, headaches, ear infections, joint and muscle problems, developmental delays, ADHD, heavy metal toxicity, yeast infections, urinary tract infections, candidiasis, other increased pathogenic activity, increased PMS symptoms, brain damage, liver toxicity, tooth decay, acne, mood swings, decreased fertility in men and women, and so much more!

In other words, drinking soda feeds infections, disrupts the gut microbiome and the metabolic processes, degrades cells, causes chronic illness, exacerbates virtually all chronic illness symptoms, and rapidly ages the body.”

Read More:

https://www.organiclifestylemagazine.com/if-you-drink-soda-its-probably-the-worst-thing-you-do-to-yourself-even-worse-than-smoking

One of the most dramatic and effective therapeutic modalities for targeting a spectrum of chronic, degenerative diseases – as well as potentially having a direct impact on quality of life/healthspan is now starting to gain some traction in North America.

Used for many years as a therapeutic intervention for serious health issues by the medical community in countries such as Japan, hydrogen therapy is now starting to gain attention in the naturopathic/integrative and functional medicine communities.

Just this past week I was contacted by two local clinics here in Vancouver inquiring about whether I had knowledge about H2 therapy (I do) – and whether I knew where to access a new patent pending H2 tablet product which is becoming very widely used in the U.S. (I do know the contacts for accessing this product).

Six months ago I had the good fortune to meet with one of the co-inventors of this new patent pending tablet technology, to learn more about the product and the research behind it – and as well I have been personally taking the product for some six months now.

So as I do with many interesting therapeutic modalities which may have an impact on disease processes and health, I took a deep dive into the literature to understand more about H2 therapy – and the published research is very impressive:

Why You Should Know About H2 Therapy – and Why You Should Consider Prescribing It To Your Patients
Here is a summary and some links to further published articles on H2 therapy if you have an interest in investigating it further:

From an article from the website H2fx.com:

Research shows molecular hydrogen has the potential to exhibits these effects:

  • Anti-Inflammatory Effects 13
  • Smallest, most bioavailable molecule in existence 14
  • Selective antioxidant 15
  • Participates in Gene Expression 16
  • Anti-Allergic Effects 17
  • Anti-Cellular Death 18
  • Anti-Aging 19
  • Reduces aches and pains 20
  • Protective to skin 21
  • Cardioprotective 22
  • Increases Metabolism 23
  • Increases Body’s Antioxidants (Nrf2 activator) 24
  • Decreases Muscle Fatigue 25
  • Reduces Lactate Levels 26
  • Anti-Diabetic Effects (type 1 and 2) Type 1, 27 Type 2, 28
  • Anticancer 29
  • Improves Cognitive Function 30
  • Protects DNA & RNA 31
  • Anti-Tumor Effects 32
  • Cytotoxic Protection 33
  • Neuroprotective 34
  • Radiation Protection 35
  • With zero toxic effects 36

Based on scientific studies/evidence, hydrogen gas therapy has the potential to benefit:

Alzheimer’s 37, arthritis 38, rheumatoid arthritis 39, Type 1 diabetes 40, Type 2 diabetes 41, Parkinson’s 42, COPD 43, asthma 44, heart disease 45, kidney disease 46, stroke 47, cancer 48, tumors 49, ALS 50, dementia 51, psoriasis 52, dermatitis 53, IBS 54, hemorrhagic shock 55, Crohn’s 56, fatty liver disease 57, liver cirrhosis 58, pancreatitis 59, cardiac arrest 60, neuropathy 61, Multiple Sclerosis 62, Hepatitis B 63, atherosclerosis 64, cataracts 65, hypertension 66, gum disease 67, traumatic brain injury 68, sepsis 69, subarachnoid hemorrhage (aneurysms) 70, infant lung disease 71, metabolic syndrome 72, lymphoma 73, retinitis 74, painful bladder syndrome 75, osteosclerosis 76, osteoarthritis 77, osteoporosis 78, glaucoma 79, pulmonary hypertension 80, pulmonary fibrosis 81, autism 82, depression 83, bipolar disorder 84, anxiety 85, schizophrenia 86, inflammation 87, muscle fatigue 88, increased ATP production 89, soft tissue injuries 90, pain 91, wounds 92, burns 93, seasonal allergies 94, autoimmune disorders 95, insulin resistance 96, hearing loss 97, ulcers 98, radiation damage 99, sleep apnea 100to name just a few as there are studies on over 170 human disease models

If you have an interest in finding out how you can access the H2 tablet product for yourself and/or your patients, reach out to me as I am working directly with the company to make this exciting product available to health care practitioners.

In the near future – within the next five years or so there will be a paradigm shift in how health care practitioners across the spectrum – including allopathic MD’s will be able to help their patients mitigate one of the key identified degenerative processes associated with aging.

What I am referring to is the pending availability of compounds referred to as “senolytics” – compounds developed to target senescent cells (referred to as “zombie cells” in the popular literature).

I suggest that the allopathic MD community will be very much involved in this treatment modality due to the fact that big pharma and the biotech industry are actively engaged in the development of pharmaceutical, prescription drugs for this application.  In fact there are currently trials going on which are testing senolytic drugs and early results should be available later this year.

So let me give you some background and context on why this concept of senolytic compounds is perceived to be such a significant development to target the deterioration associated with the aging process:

Senescent Cells: What Are They?

From the FightAging.org website:

(great free weekly newsletter on the latest developments in the antiaging research community)
The evidence of the past decades, and particularly the past seven years, strongly supports the idea that the accumulation of senescent cells is a root cause of aging. Cells become senescent in large numbers day in and day out, a normal end of life state for somatic cells that have reached the Hayflick limit. Cells also become senescent as the result of damage, or a toxic environment, and there is ever more of that with advancing age. Near all of these cells are destroyed quite quickly after they enter a senescent state, but enough linger to ensure that a few percent of all cells are senescent in old age. These problem cells secrete a potent mix of signals that induces chronic inflammation, degrades tissue structure, and alters the behavior of normal cells for the worse.

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Image from Life Extension Foundation

There has been an explosion of published research in the medical literature the last several years (over 8,000 citations in PubMed just on the search term AMPK) documenting the wide ranging significance of this endogenously produced enzyme on our health.

The Dangers of Reduced AMPK

With reduced AMPK signaling, a range of damaging conditions begins to take over a previously healthy body, often leading to an early death.

These damaging conditions include:

  • Increased belly fat,47,48
  • Chronic inflammation,7,47,48
  • Elevated blood sugar,47-50
  • Insulin resistance,7,47-50
  • High cholesterol and triglycerides,47,48
  • Decreased numbers and function of mitochondria,7,47,48
  • Increased accumulations of abnormal or damaged proteins in our cells that lead to neurodegeneration.7,51

To date, experiments have shown that increased AMPK activation is associated with:

Extended life span by as much as 2030% in animals,7,22,106

Improved glucose uptake in cells, lowering blood sugar,58,69,70

Inhibiting excess fat synthesis and increased burning of stored fat,17,71

Reduction of blood triglycerides,72

Decreased liver fat accumulation and fat-related chronic inflammation,63

Increased numbers of new, healthy mitochondria.62-64,69

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Robert (Rob) Lamberton