Chronic Inflammation
The Epidemic Disease of
Aging
Protecting Against
Inflammatory-Related Disease
The New England
Journal of Medicine published several
studies in year 2000 [61]
showing that the blood indicators of
inflammation are strong predictive factors for
determining who will suffer a heart attack. In
the January 2001 issue of
Life Extension
magazine, we described these studies and told
members how they could protect themselves
against these inflammatory markers (such as
C-reactive protein, homocysteine and
fibrinogen).
A growing consensus amongst scientists is
that common disorders such as atherosclerosis,
colon cancer and Alzheimer’s disease are all
caused in part by a chronic inflammatory
syndrome.
Supplements used by most Life Extension
members appear to suppress these dangerous
inflammatory components of blood.
One of the inflammatory markers the
New England Journal
of Medicine identified is a protein
called fibrinogen. High fibrinogen levels can
induce a heart attack via several mechanisms,
including increased platelet aggregation,
hyper-coagulation and excessive blood
thickening. The New
England Journal of Medicine studies
showed that those with high levels of fibrinogen
were more than twice as likely to die of a heart
attack.
Another inflammatory marker reported on was
C-reactive protein. This marker indicates an
increased risk for destabilized atherosclerotic
plaque and abnormal arterial clotting. When
arterial plaque becomes destabilized, it can
burst open and block the flow of blood through a
coronary artery, resulting in an acute heart
attack. One of the
New England Journal of Medicine studies
showed that people with high levels of
C-reactive protein were almost three times as
likely to die from a heart attack.
With the availability of cytokine blood
profile tests, it is now possible to ascertain
the underlying cause of chronic inflammatory
disease. The appropriate drugs, nutrients,
dietary change(s) and/or hormones can then be
used to suppress the specific cytokines (such as
TNF-á or IL-6) that are promoting the
inflammatory cascade.
In the first addendum that appears after this
article, we discuss dietary modifications that
can also help suppress pro-inflammatory factors
in the body.
Numerous studies show that pentoxifylline
(PTX) is a potent inhibitor of TNF-a, IL-1(b),
IL-6 and other pro-inflammatory cytokines.[62-69]
A similar number of studies show that DHA fish
oil suppresses these same cytokines.[23-30,
31-32] In people suffering from a chronic
disease involving elevated levels of the
inflammatory cytokines, the daily administration
of 400 mg to 800 mg of PTX and/or 1000 mg to
2000 mg of DHA fish oil could be of enormous
benefit.
We have previously published information
showing that cytokine-suppressing nutrients such
as fish oil and nettle leaf prevent and treat a
wide range of diseases. In the second addendum
that appears at the end of this editorial, we
review studies that substantiate the potential
off-label benefits of PTX in protecting against
inflammatory cytokine-induced diseases.
What You Should Do?
The number of inflammatory-related diseases
that could be successfully treated with
cytokine-lowering therapy is staggering.
Pentoxifylline (PTX) is a cytokine-suppressing
drug that has been overlooked by most of the
medical establishment. Supplements such as fish
oil, nettle leaf, DHEA and vitamin K possess
mechanisms of suppressing inflammatory cytokines
similar to PTX. There are no side-by-side
comparisons that would enable us to
categorically state whether PTX or natural
agents (such as DHA fish oil) work better.
For those suffering from multiple
degenerative diseases, we recommend the cytokine
profile blood test. This can be done by your own
doctor or you can inquire about it by calling
1-800-208-3334. If your cytokine test reveals
excess levels of cytokines such as TNF-á and/or
IL-1b, you may consider supplements such as DHA
fish oil (1000-2000 mg/day). If you have been
taking DHA fish oil, nettle leaf extract,
vitamin K and DHEA, and blood tests show that
you still have high levels of inflammatory
cytokines, you should consider 400 mg to 800 mg
a day of pentoxifylline (PTX) or Enbrel (if you
can afford it).
We have previously published articles about
the multiple degenerative diseases caused by
chronic inflammation. The sheer volume of new
confirmatory data mandates that those seeking to
avoid age-related health catastrophes suppress
their inflammatory cytokines.
I know most members reading this column will
not have their blood tested and will instead,
use some of the supplements that have been shown
to suppress these dangerous cytokines. For most
healthy people, this should work. If you suffer
from a degenerative disease(s) associated with
chronic inflammation, I urge you to take the
Cytokine Profile or the C-reactive protein blood
test we recommend. When you get your results,
use the appropriate supplements and/or drugs to
bring your inflammatory markers down to a safe
range. This is a matter of life or death for
many aging humans!
If you have questions about this pioneering
new anti-aging protocol, call our advisors at
1-800-226-2370.
For longer life,

William Faloon
Caution: PTX should not be used in those
with bleeding disorders such as those with
recent cerebral or retinal hemorrhage
(Physicians Desk Reference, 2001). Patients
taking Coumadin should have more frequent
monitoring (once a week) of pro-thrombin
times.70, 71 Those suffering from other types of
bleeding should receive frequent physician
examinations. According to two studies, PTX
should be avoided by Parkinson’s patients.[72,
73]
It is important to note
that the body uses tumor necrosis factor-alpha
(TNF-a) to acutely fight infections. If patients
are showing any sign of infectious disease,
drugs like Enbrel (that inhibit the effects of
TNF-a) are temporarily discontinued. A new FDA
advisory states that patients should be tested
and treated for inactive tuberculosis prior to
therapy with another TNF-á inhibiting therapy (infliximab).
Since PTX, fish oil and nettle directly suppress
TNF-á, perhaps these agents should be
temporarily discontinued during the time when
one has an active infection.
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