For some years now I have sprinkled references to
inflammation throughout my articles, being convinced that the
inflammatory process was an important causative factor in all states
of dis-ease, not least because inflammation and pain are constant
companions.
Time to organize a little!
Consider the fact that the main transportation systems in our body
consist of pipe-like organs: our blood stream, our digestion,
our lungs. These pathways are lined with cells that form
membranes. The membranes in question control what stays where it is
supposed to be, and what gets to places where it shouldn't.
Simple enough so far.
When the cells that form the membranes, and
therefore the membranes themselves, become inflamed, anarchy rules.
White blood cell counts indicate inflammation, but C-reactive protein (CRP) serves
is a more accurate
marker of inflammation: levels above 2.4 mg/l suggest a
doubled risk of a coronary event.
Inflammation in the cardiovascular system causes plaque to set up in wounded arteries, and
raises homocysteine, white blood
count and CRP (C reactive protein) levels , with the
concomitant risk of clots, high blood pressure, stroke and heart attack. CRP is produced
in the liver as an inflammatory response, and is linked not only to
cardiovascular disease and stroke, but also to cancer, macular
degeneration, type 2 diabetes, and many other chronic health
problems.
Persistent
inflammation also causes
the formation of a protein called FIBRIN, which is
implicated in blood clots. A Dr. Sumi, in Japan, has recently made
the discovery that an enzyme in a food called NATTO, from
fermented soybeans, can block this process, and actually resolve
thrombi. It also decreases the viscosity of the blood, which
is good because thicker blood means higher blood pressure and more work for
the heart. It goes without saying that this enzyme cannot be used by
people with bleeding problems, and only( under the care of a health
professional if you are already on blood thinners.)
Much research implicates
inflammation in poor heart health: Dr. Giles &
colleagues (published in Am J Respir Crit Care Med
2000;162:1348-1354) examined a study conducted from 1976 to 1992 on
8900 adults, and stated "What we found was that people with an
elevated white blood count (WBC) were 40% more likely to die from coronary heart
disease after taking into account a number of traditional risk
factors".
Link between Inflammation and Disease
The study showed that patients with a WBC count over 7.6 were at
much higher risk of dying from Coronary Heart Disease, even after
adjusting for other risk factors. The new findings support a role
for inflammation as a causal factor in the pathogenesis of CHD, the
authors say. "We really don't know whether reducing white count will
lower the risk," Dr. Giles added in an interview. "That's where we
need more studies."
Interestingly, children of parents with high blood pressure are
found to have high levels of CRP. The researchers concluded "The
results of this study suggest that the offspring of parents with
hypertension may be more likely to have elevated levels of CRP, and
may therefore have an increased risk of cardiovascular disease."
(Diaz JJ, Arguelles, et al,
Arch Dis Child, 2007; 92(4): 304-8)
In 2008, the maker of the statin drug Crestor
published with great fanfare, the results of the Jupiter trial (as
Dr. Eales* says: "Know what Jupiter stands for? It
stands for Justification for the Use of Statins in Prevention: an
Intervention Trial Evaluating Rosuvastatin"),
which purported to show that Crestor "known chemically as
rosuvastatin, reduced heart attack, stroke, need for bypass or
angioplasty procedures and cardiovascular death by a surprising 45
percent over less than two years" in patients with high CRP and
normal to low LDL.
I have found a truly excellent write-up of
this trial in *
Dr. Michael Eales' blog, you can access it here, and it is a
masterly analysis of how the big drug companies can mislead us - but for
simplicity's sake here are a couple of excerpts:
-
They stopped the study right in the middle of it.
When studies are done that might put people at risk by
giving them potentially dangerous drugs, it is typical
for an outside group to take a peek at the data at
certain milestones to make sure the study medication
isn’t killing people. When this data is evaluated,
and it is found that subjects on the experimental
medicine are dying at unacceptably high rates, the study
is often halted. I’ve never seen a study halted
because the placebo group was dying at higher rates.
That really makes me wonder.
One of the negative findings in this study was that
the group on Crestor developed diabetes during the trial
at a significantly higher rate than did those on
placebo.
- let’s assume I’m taking this study at its absolute
worst. Let’s look at it in the best light
possible. If we do, we find that a small group of
unusual patients - those with low LDL-cholesterol AND
high C-reactive protein - may slightly decrease their
risk for all-cause mortality by taking a drug that costs
them almost $1,300 per year and slightly increases their
risk for developing diabetes. That’s the best spin
possible given the data from this study. Compare
that to the spin the media is giving it. (Lynn:
my emphasis)
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In fact, within the study itself, you will find that the study
leaders eliminated from consideration people with both low LDL and
low CRP, since studying them "would have been not only
infeasible in terms of statistical power and sample size but also
highly unlikely to show a benefit.”. In other words, TRULY
healthy people would not be likely to benefit at all.
This plays in to the definition of "preventive health care", which
is on the verge of becoming the new buzz phrase. Does it mean
personal accountability, watching ones diet and lifestyle, or does
it mean going to the Doctor, having tests done, and then taking
prophylactic doses of certain drugs?
More about CRP
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Controlling inflammation NATURALLY when it first
appears can lead to many
years of better health.
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Inflammation can be triggered by viruses, overweight,
food intolerances, bacteria
and even toxins entering the blood stream - here we see the
interdependence of the various systems at work.
is to change one's diet to ensure a steady supply of anti-oxidant
rich foods, high in nutritive value overall and in Omega 3 fatty
acids
Second,
make sure that you have eliminated any personal
food intolerances.
No matter how healthy the food may seem, if your
body doesn't like it, it is pro-inflammatory for you!.
Third,
ensure
that these dietary changes have modified your body's pH.
An acid pH is pro-inflammatory.
Fourth, ensure a supple
of enzymes, checking to see whether a hydrochloric acid deficiency
may be part of your problem.
Faulty digestion is pro-inflammatory.
Fifth, modify your weight and
Body Mass Index
to healthy levels.
Carrying excess weight is pro-inflammatory.Sixth,
add helpful
supplements in the number and quantity dependent on the degree of
your problem.
Nutrient deficiencies can be pro-inflammatory;
certain nutrients are anti-inflammatory
I recommend the following;
Vitamin C 500 to 2000 mg * Vitamin E (with
tocotrienols and mixed tocopherols) 400 iu* Omega 3 fatty acids * Resveratrol or Activin
* Green Tea * *
an
effective digestive enzyme * Proteolytic
enzymes * Devil's Claw*
turmeric
* bromelain * (the
herbs listed separately or in
combination.)
Inflammation can contribute to cancer
development in three ways:
- necrotic cell death ( death through
destruction) rather than apoptosis (cell death where the
mechanisms of the body tidily remove the debris). Necrosis
releases toxins into the body and promotes an inflammatory
response
- angiogenesis, or the formation of new
blood vessels to feed tumors - Chronic inflammation is closely
associated with angiogenesis, as granulation tissue requires an
extended vascular supply
- cell proliferation
caused by
inflammatory damage to DNA
In the case of the digestive tract, toxins
are re-circulated in the bloodstream, proteins incompletely digested
are recognized by the body as invaders, and the essential balance
of friendly organisms is disrupted leading to candida, IBS,
colitis, in turn disrupting the immune system.
Another way in which inflammation manifests itself
is in the painful joints that afflict so many people, whether as a
result of trauma, or age and deterioration . For years, the medical
approach to this problem has been to recommend aspirin type pain
killers, NSAIDs, or Cox 2 inhibitors, depending on the
severity of the problem.
I have written
in my Blog about the dire immediate consequences of a certain over-the-counter
pain killer, and I believe everyone
is now aware of the
consequences of taking Vioxx. However, the unintended
consequences of taking even the more seemingly benign painkillers day after
day has not been so well researched.
I was talking the other day to an old friend of my
husband, who had contacted us after 30 years of silence: he
had been a paratrooper, and having been told to "live with the pain"
of his damaged joints spent those years popping painkillers daily.
- He had suffered a heart attack
- He had been through prostate cancer.
| News flash! PAINKILLERS DEPLETE FOLIC ACID.
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Even more alarming, the February 3, 2002, issue of the British Medical
Journal carried a study on the increased risk of miscarriage among
women using non-steroidal anti-inflammatory drugs.
This Danish study involved over 1400 women . A
2003 California study confirmed this finding, coming up with an 80%
increase in risk of miscarriage where NSAIDs were used.
The importance of folic acid in pregnancy cannot
be overemphasized, and after years of proselytizing on the part of
the alternative health community is finally accepted by the
Government and the medical establishment. Remember, folic acid
depletion during pregnancy is also linked to birth defects.
A 2006
study found that inflammation leads to both weight gain AND weight
loss in older individuals, both of which can be signs of
deterioration in a persons health*
(International
Journal of Obesity (2006)
30, 1362–1367.
doi:10.1038/sj.ijo.0803306; published online 14 March 2006)
Inflammation leads to
intolerances/allergies
by the method described in this study: |
Incorrect pH balance in the body, whether caused by faulty diet or a
lack of Hydrochloric acid in the stomach, leads to
inflammation. Mineral
deficits can feed into this avenue of causality: minerals
must be provided from exterior sources, either diet or
supplementation, and their importance in controlling
inflammation stems from
adding a good multi mineral
source is therefore a recommended strategy.
Research
in the UK has connected high levels of
C-reactive protein specifically to abdominal
fat, with the inflammatory process leading
through insulin resistance to diabetes, and on
to cardiovascular disease.
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Two key
passages from a 2003 editorial by Russell Tracy
of the
Vermont College of Medicine follow:
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"First,
the data fit well with a growing
body of evidence implicating adipose tissue
in general, and visceral adiposity in
particular, as key regulators of
inflammation, coagulation, and fibrinolysis.
Adipose tissue secretes
proinflammatory cytokines and fibrinolytic
regulators such as plasminogen
activator inhibitor. Along with many
possible roles in
atherogenesis and atherosclerotic progression,
inflammatory mediators can activate
coagulation by stimulating monocytes to express tissue factor
(as can CRP itself ) and by causing disregulation in natural
anticoagulation."
"They
suggested that the role of visceral fat may be more complex than suspected,
because even people who are not
obviously overweight may still have
disproportionately too much
visceral fat, with the result of a
predisposition toward insulin
resistance and atherosclerotic disease,
possibly through inappropriate
cytokine secretion.
".
Full text here.
See also a study in RESOURCES at right
As for the respiratory pathway,
Asthma is caused by inflammation of
the airways, which results in swelling and subsequent distress.
Asthma control
is very dependent on a proper fatty acid profile.
Asthma sufferers need omega-3 fats in their
diet in the form of fish oil. Note
that
the Omega 3 fatty acid
EPA is more effective than DHA in controlling asthma and
inflammation, so make sure
your fish oil is high in that important factor.
(See
RESOURCES at right)
They also need to vastly reduce their omega-6 fat intake.
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Fatty acid balance determines one's degree of
inflammation:
if the delta5 desaturase enzymes are turned off by
insulin activity,
inflammatory cell messengers will be produced from Omega 6 fatty
acids, and anti-inflammatory ones in the Omega 3 pathway inhibited.
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Virtually
eliminating all high omega-6 fats will seem counter-intuitive to many
interested in health, as some common omega-6 foods seem healthy. For
instance, all seeds and nuts should be avoided (except walnuts and
flaxseeds, which have substantial amounts of omega-3 fats, though
omega-3 from fish oil is still far better for its high levels of EPA and
DHA). Nearly all other seeds and nuts have significant quantities of
omega-6 fats and should be eliminated from the diet (even if they are
organic), including:
- Almonds
- Pecans
- Cashews
- Peanuts
- Sunflower
seeds
- Pumpkin
seeds
- Sesame seeds
For asthmatics,
it is always beneficial to know the omega-6 content of the foods you
consume, and to eliminate those that are high in this fatty acid.
Studies published in 2004 make a connection between
eating
oily fish during pregnancy, and lower rates of asthma.
This would
confirm a protective effect from EPA and DHA. Fish STICKS,
on the other hand, fried in Omega 6 oils, had a negative effect, causing
MORE asthma in the children. Equally, studies have confirmed a
protective effect for a diet high in anti-oxidant rich fruits and
vegetables.
As more and more becomes
known of the risks of anti-inflammatory pharmaceutical drugs, it
behooves us to study and become familiar with this important health
risk, so that we can do what we need to do to protect ourselves
naturally, building health instead of compromising it further.
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