In the East and particularly in Russia over the last
several years, they have been researching a special analogue of
the di-peptide carnosine. This particular form is known as n-acetylcarnosine
or NAC and it has been proven to be highly efficacious in the
treatment of cataract and may also present a case for the
prevention of the same. This article is about the case for NAC and
the problems associated with senile-cataract.
Cataract is the leading cause of blindness and
accounts for about 42% of all such cases worldwide, and this is
in-spite of the availability of effective surgical treatment.
Today we have the appalling situation where more than 17 million
people around the world are blind because of cataract and 28,000
new cases are reported everyday. In developing countries, there is
simply not a sufficient number of surgeons to perform cataract
operations.
Cataract surgery is the most commonly performed
surgical procedure in people over 65-years of age, and 43% of all
visits to ophthalmologists by Medicare patients in the US
are directly associated with cataract.
Meanwhile, approximately 25% of the population over 65
(and about 50% over 80) have a serious loss of vision due to
cataract. Since this is the population that is most susceptible to
lens opacification and as this section of the population is
expected to increase dramatically, the numbers of individuals with
cataract is set to explode!
For example, the World Health Organization
anticipates that within the next 25-years, that 20% of the
population will be 65 or older. Furthermore, the single largest
growing section of the population are those over 85 and their
actual numbers are expected to quadruple in about the same period.
Such a rapidly burgeoning older population can only increase the
numbers of individuals suffering from cataract.
Of course, there is also the economic impact.
Currently 1.35 million cataract operations are performed annually
in the United States alone and Medicare estimates the
annual cost at $3.5 billion! There's no doubt about it, cataract
is a major disease.
It is also becoming apparent that it will not be
possible to eliminate the overall problems (including blindness),
caused by cataract with the current procedures. With so many
people presenting the afflictions of maturity onset cataract,
it appears not to be possible to train in-time, the necessary
numbers of surgeons required. In-fact, as-it-stands, it looks
likely that the total number of people with serious eye-disorders
because of cataract, will increase dramatically worldwide.
Surgical complications
There is another aspect to the problem that is rarely
discussed. While cataract surgery is generally recognised as being
one of the safest operations, there is a significant complication
rate. For example, in the United States 30% to 50% of all patients
having cataract extraction, develop opacification of the posterior
lens capsule within two years and require further lazer treatment.
Since the number of cataract operations is so large, even a
small percentage of complications represents a significant number
of people. Of the patients having cataract surgery, 0.8% have
retinal detachments, 0.6% to 1.3% are hospitalized for corneal
edema (or require corneal transplantation), and 0.1% present endophthalmitis.
Thus, aside from secondary cataract, about 2% of the
1.35 million (or approximately 27,000 individuals), just in the US
each year, develop serious complications as a result of
cataract surgery.
It is therefore difficult to support the argument that
cataract research is unimportant with statistics such as those
cited above. The large and growing number of people blind with
cataract and the significant complication rate, should be
sufficient reason to increase cataract research.
The considerable discomfort experienced by patients as
their vision diminishes, and the complete loss of accommodation
resulting in the removal of the lens should also be recognised.
Besides the possible complications, an artificial lens just does
not have the overall optical qualities of a natural lens.
A medical solution is required that will maintain the
transparency of the lens. Even if the development of cataract can
be delayed by 10-years, the overall benefits would be highly
significant.
The development of NAC
Innovative Vision Products
(IVP) is a US based corporation, operating in Russia (utilizing
Russian researchers and scientists), who have over the last
several-years developed and tested a unique new form of carnosine.
This form of carnosine is known as n-acetylcarnosine or
abbreviated to NAC.
NAC presents the first major leap forward in the
treatment and possible prevention of senile cataract.
As a bio-engineering company, IVP have developed a
proprietary method of producing extremely high purity NAC, that
has proven itself to be a suitable ophthalmic drug for the
non-surgical treatment of age-related cataracts. Yet it also
displays high efficacy and physiological tolerance.
NAC has a highly statistical and very significant
clinical success rate for patients within 3-12 months of
treatment. Not surprisingly, IVP has been quick to ensure that its
NAC has worldwide patents, including its use for cataract. It is
also interesting to note that NAC eye-drops are patented for use
in open-angle glaucoma, but as yet, the research for that disorder
remains unpublished. [Ed.- We are keen to report on NAC's benefit
for glaucoma as soon as it becomes available, especially as this
is an eye-disorder that is extremely difficult to treat].
Human trials
carnosine
eye-drops were used
in a clinical trial to treat 96 patients aged 60 and above. All
the patients had senile cataract in various degrees of maturity.
The duration of the disease in these patients ranged between 2 and
21 years.
Firstly, the researchers stopped the patients use of
all other anti-cataract drugs. Then the patients instilled 1 or 2
drops into each eye 3 or 4 times a day, for a period of 3 to 6
months.
The level of eyesight improvement and the change of
lens transparency was considered as an evaluation index. The
results showed that there was a pronounced effect on primary
senile cataract, the effective rate was 100% (i.e. all
patients experienced an improvement). For the more mature
senile cataract (i.e. those who had had the cataract the
longest time, in some cases more than 20-years) the effective rate
was still an extremely impressive 80%.
These are remarkable results considering that the best
that could normally be expected would be a slight improvement, a
halt to the progression and under normal (i.e. non-treated)
circumstances a continual worsening of the disease.
Importantly, it was also noted that there were no side
effects noted in any of the cases.
Another Russian study was designed to document and
quantify the changes in lens clarity over a 6 to 24 month period
for 49 volunteers. Their average age was 65 and all suffered from
senile cataract of a minimal to advanced opacification.
The patients received either a 1% solution of NAC
eye-drops or a placebo, as 2-drops twice a day into each eye. The
patients were then evaluated at 2 and 6 month periods. The tests
consisted of ophthalmoscopy (glare test), stereocinematagraphic
(slit-image) and retro-illumination (photography). A computerized
digital analysis then displayed the light scattering and absorbing
effects of the centers of each lens.
At 6-months, 88.9% of all eyes treated with NAC had an
improvement of glare sensitivity (lowest individual score was a
27% improvement, right the way up to a 100% improvement). 41.5% of
all eyes treated with NAC had a significant improvement of the transmissivity
of the lens, but perhaps most importantly 90% of the eyes treated
with NAC showed an improvement in visual acuity. Meanwhile, in the
placebo group there was little change in eye quality at 6-months
and a gradual deterioration at 12 to 24 months.
Importantly, this study also showed that at 24-months
the NAC treated group, (who already had significant improvement to
the quality of their eyesight), sustained these results with
continued use of the NAC eye-drops.
Once again, no significant side effects were noted in
any cases throughout the 2-year period.
Another interesting study also evaluated patients between the
ages of 48 and 60, who had various degrees of eyesight impairment,
but who did not have the symptoms of cataract. After a
course of treatment ranging from 2 to 6 months the conclusion was,
that the eye-drops alleviated eye-tiredness and continued to
improve eyesight (i.e. there was more clear vision). The subjects
reported that the treatment "brightened" and
"relaxed" their eyes. This is an important indicator
that the eye-drops have a value both for preventative purposes, as
well as medical applications.
At this time, it is now believed that carnosine eye-drop treatment has been applied to over one
thousand patients with senile cataract in China and Russia, (those
countries are home to the principal researchers behind the work).
Clear evidence is emerging that NAC eye-drops are a safe,
effective treatment and potential preventative against cataract.
NAC method of action
Cataract is a glycosylation problem. This
reaction occurs when proteins became cross-linked (and hence
impaired). The result of this reaction leads to the discoloration
of the eye-lens to yellow and brown, and hence the impairment of
vision. But, carnosine is known to compete on the molecule for the
glycating agent and protect cellular structures against
aldehydes. Therefore, carnosine
can slow and help to prevent proteins from becoming cross-linked,
(and in this case from becoming cataract).
NAC has been shown to be highly resistant to carnosinase,
(the natural enzyme that breaks down L-carnosine into histamine
etc.). An experiment on rabbits showed that NAC eye drops allow
themselves to be broken down into L-carnosine once inside the
eye's aqueous humor, (a process that occurs within 15 to 30
minutes after application of the eye-drops).
L-carnosine is an excellent anti-oxidant and is
particularly effective against potent free-radicals, especially
the Superoxide and the Hydroxyl. It is therefore
presumed, that the anti-oxidant role of L-carnosine (within the
aqueous humor) is a major factor, in slowing and preventing the
appearance of cataract.
However, when L-carnosine eye-drops were used
there was no presence of L-carnosine in the aqueous humor
(even after 30-minutes). This may be because L-carnosine is broken
down early into histamine etc., before it reaches the aqueous
humor. So, NAC may act as a "carrier" for L-carnosine
delivering it to where it is needed, [Ed.-see the next section of
this article for further comparisons of NAC to L-carnosine].
The powerful anti-oxidant abilities of carnosine
within the eye, and the prevention of cross-linking, helps to
explain why NAC is effective at preventing and slowing cataract,
perhaps even halting it. But it doesn't explain why NAC has been
shown to reverse cataract. But we may already know the answer.
For example, it is known that when carnosine is delivered in high doses, that it can reverse protein-aldehyde
cross-linking, (this reaction is normally very difficult to
reverse). Under these circumstances, carnosine has been shown to have a "rejuvenating" effect on
cultured cells.
Cataract develops when anti-oxidant defense is
exhausted, leading to the cross-linking of the lens crystallins,
(producing a clouded lens, and hence impaired eyesight). We can
assume that the regular use of a 1% NAC eye-drop (as used in the
clinical trials), delivers "a high-dose of carnosine
capable of reversing the lens cross-linking," and hence the
reduction and eradication of cataract.
So in conclusion, NAC eye-drops appear to act as a
universal anti-oxidant, both in the lipid phase of the cellular
lens membranes, and in the aqueous environment. NAC eye-drops
reduce and protect the crystalline lens from oxidative
stress-induced, cross-linking damage.
NAC compared to L-carnosine
We may logically ask the question; why have NAC
eye-drops been shown to have this action upon cataract, and yet
L-carnosine (which is its sister di-peptide) appears to have
little benefit? Dr. Mark Babizhayev, one of the principal Russian
researchers behind the clinical trials with NAC eye-drops gave us
this reply to that very same question:
"I believe that the application of L-carnosine
for the treatment of human cataracts is misleading. This is
because L-carnosine readily becomes a substrate for the activity
of natural peptidases (i.e. carnosinase) in the aqueous humor. So
much so, that there is no sign of L-carnosine in the
aqueous humor within 15 minutes after instillation. Furthermore, I
consider that L-carnosine eye-drops may even be harmful for eyes
because it gradually releases histamine, which, located as it
would be in the presence of the eye-lens is a very toxic agent.
However, NAC eye-drops are resistant to hydrolysis with natural
carnosinase. Therefore, NAC is the only currently known agent
which reverses and prevents human cataracts."
In conjunction with Dr. Hipkiss and Dr. Kyriazis
information, we can conclude that while some of the benefits of oral
L-carnosine may derive after carnosinase breaks down into
histamine- [Ed.- see Dr. Kyriazis interview article in this issue
for further details], that in the case of eye-drops, L-carnosine must
be avoided.
It is also interesting to note that a study by Dr.
Boldyrev et al, also concluded that the oral use of NAC was
far less likely to be broken down by carnosinase than L-carnosine
[Ed.- see Dr. Kyriazis interview in this issue for further
details].
Buyer beware!
Dr. Mark Babizhayev also makes it quite clear that
"ordinary" NAC will not be of much use in the treatment
of senile-cataract. This is because there are many synthesized
"carnosines" and their biological and medicinal activity
strongly varies and depends on the mode of their obtention.
[Ed.- see Dr. Babizhayev interview in this issue for further
details].
For example, if carnosine
is extracted from meat muscle substances, the biological and
anti-oxidant activity is very low. This is presumably due to the
contamination of the "pure" carnosine
substance by heavy metal salts and proteins and other related
impurities. It is very difficult to purify carnosine
chromatographically, as the compound chelates divalent metal ions
very heavily and the biological and anti-oxidant activities can
not be regenerated during the purification procedures.
In conclusion, there were many forms of carnosine
which were abandoned in the Russian studies because of their lack
of anti-cataract and anti-oxidant ability in the human eye.
However, IVP (in conjunction with their Japanese
partner and manufacturer), have developed a synthesized pure NAC
which has biological activity and has been well controlled and
proven in human lens studies. This is the same type that has been
used in the clinical trials.
IVP hold the proprietary knowledge to the correct and
efficient production of high-purity NAC. If the label doesn't
state it is formulated by Innovative Vision Products (IVP),
then the source of the raw material is NOT the one that the
clinical trials were conducted with. "Unknown" sources
of carnosine
eye-drops should be avoided as the material could be ineffective,
and possibly even dangerous to the human eye.
Cataract is a widespread age-related affliction and
NAC eye-drops appear to be a highly efficacious and safe treatment
for cataract. As such, I suspect that this supplement is going to
become one of the most important new discoveries, and will have a
major impact on the way that cataract is controlled.
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