CFS and ME Flashcards

1
Q

CFS and ME

A

CFS = chronic fatigue syndrome. ME = myalgic encephalomyelitis. CFS and ME are terms often used interchangeably though ME is sometimes defined as CFS + inflammation.

  • Characterised by long-term physical and cognitive fatigue, not alleviated by rest.
  • Other symptoms include post-exertional malaise, muscle and joint pain, unrefreshing sleep, flu-like symptoms with sore throat and tender lymph nodes, mood disturbances.
  • While mitochondrial dysfunction is recognised as a key player, there are a number of proposed contributing factors.

CFS and ME are not diagnoses — they are clinical pictures. The role of healthcare practitioners is to identify the underlying mechanisms and contributing factors.

  • Both are characterised by fatigue but in ME there is also an inflammatory process:

‒ CFS = poor energy delivery mechanisms. ‒ ME = CFS plus inflammation.

  • Inflammation occurs when the immune system is active i.e., chronic infection, allergy and / or autoimmunity.
  • Poor energy delivery systems can result in myriad symptoms

Chronic stress effectively ‘kicks’ mitochondria unrelentingly but:

  • Eventually mitochondria will fatigue either because they run out of raw materials and / or there is no proper ‘shut down’ during sleep for healing and repair.
  • If they become unable to respond to the unrelenting adrenaline kick, it results in the clinical picture of chronic fatigue syndrome.
  • If the immune system lacks energy, then it cannot deal with an infection efficiently so the infection may become chronic.
  • The above mechanisms result in the clinical picture of myalgic encephalomyelitis
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2
Q

CFS and ME aetiologies

A

Proposed aetiologies:

  • Infectious organisms — in particular EBV (high antibody titres in patients with symptoms indicative of CFS). Other: Human herpes virus-6, Borrelia burgdorferi (Lyme’s).
  • Immunological — e.g., increased cytokines, NK cell abnormalities, decreased CD8 suppressor cells. Imbalances that collectively suggest chronic, low level activation of the immune system.
  • Abnormal HPAA functioning — association with hypocortisolism.
  • Mitochondrial dysfunction and high oxidative stress — associated with ↓ GPO and SOD. Also low melatonin (sleep dysregulation). Consider polymorphisms in antioxidant or detox pathways
  • Serotonin studies have concluded:

‒ Increased 5-HT autoimmune activity is associated with activation of inflammatory pathways and increased bacterial translocation. A reduction in 5 HT neurons has been noted.

‒ Proposed upregulation of the serotonin transporter (5-HTT) in astrocytes, reducing extracellular serotonin (5-HT) levels.

  • A breakdown in the bidirectional communication between the brain and the gut mediated by bacteria and their metabolites. CFS / ME are commonly associated with GI symptoms
  • Findings in relation to intestinal health and CFS:

– High relative abundance of bacterial species such as clostridium and ruminococcus in CFS / ME; decreased faecalibacterium abundance.

– Metabolic endotoxaemia as a driver for CFS / ME.

  • Microbes that cause dysbiosis can alter the immune system and disregulate mitochondrial function.

Further, CNS manifestations are thought to relate in part to increases in neurotoxic ammonia and D-lactic acid-producing gut bacteria

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3
Q

Natural approach to CFS / ME — avoid

A
  • Caffeine (coffee, tea, chocolate, energy drinks). Temporarily counters fatigue, but the effect is short-lived and places strain on the adrenal glands exacerbating an already fatigued body.
  • Sugar — an immune system depressant. Destabilises blood glucose causing peaks and troughs in energy.
  • Artificial sweeteners — interact with sweet receptors to trigger insulin release (destabilise blood glucose). Aspartame contains excitotoxins (e.g., aspartates) and methanol, which converts to formic acid — a neurotoxin. Can worsen neurological symptoms.
  • Alcohol — worsening of symptoms, depletes body of nutrients.
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4
Q

Natural approach to CFS / ME — include

A
  • Good quantities of essential fatty acids:

– Omega-3 is especially important for the activity of the mitochondrial membrane. EPA — anti-inflammatory properties and increases mitochondrial growth, size and distribution. DHA — essential for the structure of ETC complexes.

– Most notable benefits observed are improvements in cognitive function and reduction in relapse frequency.

  • Sufficient protein to allow for immune cell restoration and function.
  • Individualised immune support (e.g., anti-microbials, vitamin C etc.)
    and GI support (e.g., digestive bitters, pro and prebiotics etc.)
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5
Q

Nutritional ketosis in CFS / ME

A

Nutritional ketosis in CFS / ME — considered a beneficial dietary strategy for supporting mitochondrial function.

  • Total carbohydrate intake < 50 g / day (or whatever is needed to get into ketosis).
  • Moderate protein intake, around 1.5 g / kg bodyweight per day.
  • Fuel as ketones come from fat AND the fermentation of fibre in the large bowel to short chain fatty acids.
  • Typical macronutrient ratio — 75% fat, 20% protein, 5% carbohydrate.
  • Changes the body’s primary fuel source from glucose to ketones.
  • Ketones enter the mitochondria of body tissues for ATP production.
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6
Q

Benefits of a ketogenic diet

A
  • While excess levels of mitochondrial ROS (mtROS) are associated with mitochondrial dysfunction, low concentrations of mtROS can act as signalling molecules, upregulating mitochondrial capacity and antioxidant defence — known as mitohormesis.
  • Ketosis causes a significant shift in energy metabolism increasing reliance on mitochondrial respiration ― this induces mitohormesis.
  • Further, in addition to their role as energy substrates, ketones (especially β-hydroxybutyrate) act as signalling molecules increasing expression of antioxidant enzyme systems.
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7
Q

Liquorice Glycyrrhiza glabra 1‒2 tsp powder daily.

A
  • Suboptimal HPAA function and low cortisol is a common feature of CFS / ME. Liquorice is an adrenal cortex restorative, supporting cortisol production and ↓ fatigue.
  • Anti-inflammatory activity — research indicates inhibitory effects on ROS-induced tissue inflammation and the COX, LOX and NF-κB inflammatory pathways.
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8
Q

Astragalus Astragalus membranaceus

2.5‒3.5 g dry herb

A
  • An adaptogen and tonic indicated for debility and CFS.
  • Regulatory effect on immune function; supports aspects of innate immunity while promoting Th1 / Th2 balance.
  • Reduces abnormal cytokine production.
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9
Q

Poor energy delivery to the body:

A
  • Physical fatigue, poor stamina.
  • Post-exertional malaise (akin to over-training in athletes).
  • Loss of muscle power — muscles heavily rely on ATP!
  • Muscle pain — because of an early switch into anaerobic metabolism with production of lactic acid.
  • Variable blurred vision — the ciliary body muscles required for focusing tire easily.
  • Subnormal core temperature
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10
Q

Poor energy delivery to the brain

A
  • Mental fatigue with brain fog — the brain weighs 2% of body weight but consumes 20% of total energy.
  • Light and noise intolerance.
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11
Q

Mental symptoms which inhibit energy expenditure

A
  • Low mood.
  • Feeling stressed.
  • Procrastination.
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12
Q

Poor energy delivery to the heart

A
  • Hypotension — in severe cases this manifests with orthostatic intolerance and POTS.
  • Angina described as ‘atypical’ (from lactic acid)
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13
Q

Poor energy delivery to the immune system

A
  • Susceptibility to infection, unable to run a good fever.
  • Slow healing and repair
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14
Q

Naturapatic approach to CFS and ME

A

To improve energy delivery mechanisms, all aspects must be addressed. They must also be addressed in the correct order.

  1. Fuel in the tank (paleo-ketogenic diet, basic package of nutritional supplements and good gut function).
  2. Mitochondrial engine — servicing and repair (quality and quantity of sleep).
  3. The control mechanisms:
  • Thyroid accelerator pedal.
  • Adrenal gear box.
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15
Q

Fuel in the tank — paleo-ketogenic diet (PK Diet)

A

Fuel in the tank — paleo-ketogenic diet (PK Diet):

  • Mitochondria evolved to use ketones from fat and fibre for energy.
  • Increases expression of energy-producing genes — energy output is increased.
  • Decreases inflammatory end-products and the toxic load on the mitochondria

Avoid gluten and all dairy except butter (almost 100% fat).

  • Gluten — Non-coeliac wheat sensitivity (NCWS), identified in a subset of individuals with CFS / ME, is linked with increased intestinal permeability and systemic immune activation.
  • Other grains are permitted so long as ketosis is maintained — this is why a ketone breath meter is so helpful.
  • Dairy — at least 30% of people are allergic; lactose may be fermented; milk protein contains growth promoters (risk for cancer); high Ca / Mg ratio which induces Mg deficiency, increased risk of osteoporosis; milk protein increases blood viscosity
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16
Q

How to determine you are in ketosis

A

How to determine you are in ketosis — three types of ketones: * Beta-hydroxybutyric acid — is present in the blood

and can be measured in the blood — this is the most accurate measure, but testing strips are expensive.

  • Acetoacetate — is excreted in the urine. Testing is cheap and easy with urine keto-stix but as the body becomes more efficient at matching ketone production to demand, urine tests may show false negatives.
  • Acetone — is exhaled and can be measured with breath testing. This can easily be tested after every meal to ensure you have not overdone the carbohydrates
  • When sufficiently low in carbs, expect to blow 2–6 (ppm) of ketones.
  • However, the body will always use sugar in preference to ketones.

So ANY amount of ketones in the breath means you are in ketosis.

17
Q

Very high ketones (up to 10 ppm)

A

Very high ketones (up to 10 ppm) may occur because:

  • When stressed, an outpouring of adrenaline stimulates fat burning.
  • Fasting — even on a PK diet you consume some carbohydrates! With fasting you get ALL your calories from fat, so ketones are higher. This illustrates the point that even in mild ketosis you will be using some sugars as a fuel — that is fine!
  • Over-dosing with thyroid hormones may cause high levels
17
Q

How to determine you are in ketosis — false positives

A
  • The mechanism used to measure ketones is the same as that for measuring alcohol. You may see a positive if you have consumed any alcohol in the past 24 hours (depending on how much!)
  • If you have SIBO, this too produces alcohol.
  • Any products containing alcohol may give a positive result e.g., an alcohol wipe to clean the mouthpiece.
  • The meter measures parts per million — it is very sensitive!

Only a tiny amount of contaminant can upset the result.

  • Many household cleaners contain volatile organic compounds which may register on the meter!
18
Q

How to determine you are in ketosis — false negatives

A

How to determine you are in ketosis — false negatives: * Eating or drinking anything other than water

in the preceding 20 minutes may affect the test e.g., a sip of coffee can = a negative reading.

  • Breath ketone levels may not align with blood levels and urine ketones, which does not matter. It is not unusual to see ketones present on a breath test, but the urine test is negative.
  • With time, the body gets better at matching energy demands to delivery, so less ketones are ‘wasted’ through urinary losses.
  • Note — being in ketosis is NOT dangerous and is not the same as ketoacidosis.
19
Q

Mitochondrial engine

A

Mitochondrial engine — raw materials that mitochondria need daily for enzyme systems to work:

  • CoQ10 100‒300 mg.
  • Magnesium 300 mg (absorption enhanced by vit. D 10,000iu / day).
  • Niacinamide 1500 mg daily.
  • Acetyl L-carnitine 500‒2,000 mg (vegetarians and vegans are often deficient).
  • Vitamin B12 1‒5 mg daily.
  • D-ribose 5‒15 g daily — but has to be part of the PK diet carb count — it is a sugar! Use as a rescue remedy to shorten recovery time if the patient has overdone his / her activity
20
Q

Factors that inhibit mitochondrial function

A
21
Q

The control mechanisms

A

The control mechanisms — balance the thyroid (accelerator pedal) and adrenal glands (gear box).

  • The thyroid and adrenal glands allow energy delivery to be matched closely with energy demands.
  • They are also essential for circadian rhythms.

Tests of thyroid function are essential for two reasons:

  • First to exclude an overactive thyroid.
  • Secondly to see if there is a need for thyroid support, e.g., a trial of thyroid glandulars.

The thyroid, adrenals and circadian rhythm:

  • Light (sunshine is best) switches off melatonin production.
  • Darkness triggers melatonin production from the suprachiasmatic nuclei in the pineal gland, following signalling from the retina.
  • As melatonin rises TSH production is stimulated — spiking at 12am.
  • The thyroid gland increases output of T4 which spikes at 4am.T4 is converted to T3 which spikes at 5am.T3 stimulates the adrenals and so adrenal hormones, including cortisol and DHEA, spike at 6‒7am; this wakes you up
22
Q

Assuming the fuel and engines are correct

A
  • The average core temperature reflects thyroid function.
  • The fluctuations reflect adrenal function
23
Q

Correcting temperatures — adrenals

A

Correcting temperatures — adrenals:

  • See earlier adrenal support. Or glandulars, e.g.:
  • If the core temperature wobbles by more than 0.6 degrees (i.e.,

0.3 above and below average) adrenal glandulars may be needed. Alternatively, adrenal herbs / nutrients can be implemented here.

  • Start with a glandular such as adrenavive II (cortex only) on rising.
  • Increase by one capsule every two weeks.
  • Monitor with core temps and ‘how do you feel’.
  • Most need adrenavive II 2‒6 daily (or adrenavive II 1‒3 daily).
  • With time, some further benefit from adrenavive I (whole adrenal — cortex and medulla).