Osteoarthritis
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Contents
Introduction
Primer on Osteoarthritis (OA)
Anti-Arthritic Drugs
Side Effects of Drugs
Osteoarthritis Supplementation
Protocol
1. Glucosamine Sulfate (GS)
2. Chondroitin Sulfate (CS)
3. Methylsulfonylmethane (MSM)
4. Bromelain
5. Phenylalanine (DPLA)
6. Collagen type I and II
7. Sea Cucumber
8. Cetyl Myristoluate (CMO)
9. Essential Fatty Acids
10. S-adenolsyl-methione (SAMe)
11. Antioxidants - Vitamins C , E and Others
Discussion
Introduction
Arthritis refers to inflammation of
the joint. There are various forms, including rheumatoid arthritis, an autoimmune
disorder that affects primarily young women. Osteoarthritis (OA) is a
disorder caused by the wear and tear of joint due to the natural results
of aging. OA characteristically affects middle age and elderly populations.
Over 40 million American have some form of
OA, including 80% of those over 50. The disease is more common
in men under age 45 and in women over age 45.
This Research Brief examines the current medical thinking on this common
and debilitating disease and explores alternative strategies for alleviating
osteoarthritis.
Primer on Osteoarthritis (OA)
Osteoarthritis (also known as degenerative joint disease) is the localized
degeneration of joint cartilage. It affects mainly the weight-bearing joints
(e.g. knee, hip, spine). OA results from the repetitive use of the joints
resulting in wear and tear, and from the normal results of aging without
precise etiology. This is called primary OA. Secondary OA, on the other
hand, could be the result of many factors such as sports injuries, inherited
abnormalities in joint structure, continuous repetitive use over a long
period of time, trauma, previous inflammatory disease of joints, etc.
OA is caused by the breakdown in the cellular processes that manufacture,
maintain, and repair cartilage. Cartilage covers the ends of our bones.
It is present in our joints and contains chondrocytes. Chondrocytes manufacture
proteins known as proteoglycans that consist of chondroitin and keratin
sulfate that are strung on core proteins. The proteoglycans hold joint fluid
within the joint and, in conjunction with the joint cartilage, acts as a
shock absorber for the body. Repetitive stress or trauma destroys the
proteoglycans and collagen matrix (known as glycosaminoglycans (GAG), and
inhibit the production of these substances by chondrocytes. This is how
OA starts.
OA causes achy pain in the joints, leading to limitation of movement
and loss of dexterity. Over time, osteoarthritic joints enter a vicious
cycle of progressive deterioration, as the afflicted person tends to use
the affected joints less due to pain. Symptoms generally begin in middle
age, and by age 60, most people have some degree of OA. Diagnosis is primarily
through a thorough history, physical examination, and x-ray findings, although
the correlation is not accurate. About 40% of people with the worst x-ray
classification for OA are pain-free. There is currently no reliable predictive
marker for OA.
Anti-Arthritic Drugs
Modern medicine treats OA with 3 types of drugs:
- Pain relievers, like
aspirin, that primarily act to relieve symptoms of pain.
- Non-steroidal anti-inflammatory
drugs (NSAIDs), like ibuprofen (Motrinâ), which focus on the relief
of symptomatic pain with anti-inflammatory action.
- Steroidal anti-inflammatory
drugs. While these work wonders to provide short to medium-term relief,
steroids are not recommended for long-term use.
Side Effects of Drugs
While drugs do help to relieve
symptoms of OA, they have numerous adverse side effects, from relatively
minor gastric upset, dizziness, and headaches,
to severe gastric bleeding and interference with platelet function.
In addition, virtually all drugs used to treat
OA have destructive effects on the articular cartilage lining the bones
that form the joint that the drug is supposed to help.
Analgesics, like aspirin, inhibit enzymes involved in the early stages of
chondroitin sulfate biosynthesis. NSAIDs suppress proteoglycan synthesis
by the chondrocyte. The depletion of chondrocytes further weakens the joint
and exposes it to a faster deterioration cycle. Experimental studies show
that these drugs inhibit cartilage synthesis and accelerate cartilage destruction.
Steroids are the most effective anti-inflammatory agent. However, they can
also cause extensive damage to chondrocytes in long-term use. In addition,
chronic use of strong steroids leads to conditions that mimic Cushing's
Syndrome, with a number of adverse age-accelerating consequences.
Simply put,
most drugs appear to suppress the symptoms, but accelerate the progression,
of OA.
Osteoarthritis Supplementation
Protocol
| Attention
Because of tremendous individual variation,
the use of nutritionals should therefore be personalized for your
body. One person’s nutrient can be another person’s toxin. If you
have a specific health concern and wish my personalized nutritional
recommendation, write to me by clicking here. |
The root of OA lies in the destruction of the chondrocytes.
The logical approach to solving the problem lies, therefore, in increasing
substances in the joint that have chondro-protective and chondro-regenerative
effects, at the same time reducing the inflammation caused by the degenerative
joint. Such substances reduce joint pain and inflammation without harming
the joint.
Promising natural substances that have joint protecting and repairing properties
are:
- Glucosamine
- Chondroitin Sulfate
- MSM
- Bromelain
- DLPA
-
Collagen Type I and II
- Sea
Cucumber
- CMO
-
Essential Fatty Acid
- SAMe
- Antioxidants - Vitamins C and E
1. Glucosamine Sulfate
(GS)
Glucosamine is a simple molecule composed
of glucose and an amine. It stimulates the production of glycosaminoglycan
(GAG). Without glycosaminoglycan, the collagen matrix loses its
gel-like nature and its ability to act as a shock absorber. The body's intrinsic
production of glucosamine decreases in some people as a natural result of
aging. The inability to produce glucosamine may be a major factor leading
to OA.
Several clinical studies show glucosamine is effective in the treatment
of OA. In one study, 252 patients with OA were given either 500 mg of GS
or a placebo three times a day for 4 weeks. Patients given GS showed significantly less pain after
only 4 weeks of use. Other studies support this finding.
It has been shown the longer the use of GS, the better its therapeutic
effect. In one comparative study, GS (1500 mg/day) was compared to a
common NSAID called ibuprofen (1200 mg/day). While pain scores decreased
faster in the first two weeks in the ibuprofen group, by week four the group
receiving GS had improved more than the ibuprofen group. Physicians rated
the overall responses as "good" in 44% of the GS treated patients, compared
to only 15% in the ibuprofen group.
How about side effects? In one study of 200 subjects with OA of the knee,
GS (500 mg three times a day) was compared to ibuprofen (400 mg three times
a day). Consistent with previous studies, the ibuprofen group showed faster
pain relief. By the end of the second week, the group taking GS experienced
results as good as the group taking ibuprofen. More importantly, only
6% of the GS group suffered mild adverse side effects, whereas 35% of the
ibuprofen group experienced side effects.
Long-term use of GS produces better long-term results than NSAIDs as
determined in double-blind studies conducted to compare the two. While
NSAIDs concentrate on symptomatic relief, GS appears to address the cause
of OA.
In those patients who are obese, or have peptic ulcers or are taking
diuretics, the effectiveness of GS is reduced. For these, the amount of
GS should be increased.
The improvement noted with GS lasts for a period of 6-12 weeks after the
end of treatment. GS can therefore be taken in cycles of 12 weeks on followed
by a few weeks of rest. Given the safety and excellent tolerability of GS,
it is also suitable for long-term use for those who need it.
Nutritional Supplementation consideration: 500 mg - 2000 mg per day.
2.
Chondroitin Sulfate (CS)
Chondroitin Sulfate (CS) is a mucopolysaccharide that contains a mixture
of intact or partially hydrolyzed glycosaminoglycans (GAGs). It is a
major structural component of cartilage and provides a matrix upon which
collagen, the major structural protein of ligaments and tendons, is built.
Mucopolysaccharides also add elasticity and resiliency to skin and other
connective tissue. Shark cartilage, bovine cartilage extracts, and sea cucumber
also contain GAGs. CS is composed of repeating units of derivatives of GS
with attached sugar molecules.
Studies have documented the superiority of CG for treatment of osteoarthritis
of the knee compared to NSAIDs. Clinical trials using a regimen of both
CS and GS together vs. NSAIDs are impressive. It
appears that while GS alone is better than CS alone, taking GS and CS together
offers significantly greater improvement of osteoarthritis than either used
separately. This makes sense from a logical point of view, since
glucosamine (a structural building block of chondroitin), plus chondroitin
(which stimulates the chondrocytes), should be more effective than either
one alone in speeding the regeneration and recovery of articular tissues.
One should note that despite its clinical effectiveness, the exact mechanism
of action of CS taken orally is controversial and not fully understood.
CS molecules are 50 to 300 times larger than GS, and their absorption in
the gastrointestinal tract is only 0-13% compared to 98% for GS. Because
of this, some researchers pronounced that oral administration of CS could
not have produced positive results. Yet they could not explain why patients
showed objective signs of improvement in OA after taking CS in various research
studies.
Nutritional Supplementation consideration:
100 - 500 mg per day.
3.
Methylsulfonylmethane (MSM)
When 70 year old Hollywood star James Coburn suffered from crippling arthritis
and found that traditional treatments did not help, he turned to MSM. Within
weeks, his pain subsided. Within months, he was virtually pain free. Mr.
Coburn returned to an active career and was subsequently awarded an Oscar.
Such stories, while sounding too good to be true, are real and cannot be
discarded as hoaxes.
What is MSM? MSM is also known as dimethyl sulfone. The sulfur compound
is an element found in the natural diet of all animals. Chemically speaking,
it belongs in the same family as oxygen, for in an oxygen-deprived state,
sulfur often replaces oxygen as a provider of chemical energy for the sustaining
of life. MSM is related to DMSO (dimethyl sulfoxide). It is part
of the sulfur-cycle, providing for, and recycling, the sulfur in the world.
Green vegetables such as broccoli, cauliflower, garlic, and onions are good
sources of MSM.
After ingestion, MSM gives up its sulfur to form the collagen and keratin
of the hair and nails and to form the essential amino acids methionine,
cysteine, and serum protein.
Sulfur is a critical component in maintaining normal bodily functions. It
is an essential dietary element responsible for forming disulfide bonds
between certain amino acids and helping to maintain the integrity of connective
tissues.
While MSM is commonly found in organic food, fast foods contain very little
MSM. Borderline deficiency of MSM is common among Americans.
MSM is a pain-reducing agent. It blocks the transmission of impulses in
nerve fibers that carry pain signals. It also decreases pain by altering
cross-linked collagen, resulting in less scar tissue. Studies in laboratory
animals show that in those whose diet included MSM, there was less degenerative
change of the articular joint compared to the control group.
Nutritional Supplement Consideration: 1000 mg - 4000 mg a day.
4.
Bromelain
Bromelain refers to a group of sulfur-containing enzymes that digest
protein. It comes from the pineapple plant. Bromelain was first
introduced as a therapeutic agent in 1957. Different grades are available.
For most indications, the recommended amounts in milk clotting units (mcu)
is 1,200 to 1,800 mcu. Absorption from oral ingestion peaks at 10 hours,
while detectable levels in the plasma are still apparent after 48 hours.
Bromelain's use in OA arises from its anti-inflammatory properties, which
include:
a. Inhibition of the biosynthesis of pro-inflammatory prostaglandins.
b. Fibrinolysis activity via the plasminogen-plasmin system. Bromelain breaks
down fibrin by stimulating the production of plasmin, which breaks down
fibrin, thereby preventing fibrin from producing localized swelling. Plasmin
also blocks the formation of pro-inflammatory compounds.
Bromelain's ability to reduce inflammation has been well documented
in a variety of experimental models and clinical studies.
Nutritional Supplement Consideration: 100
- 400 mg.
5.
Phenylalanine (DPLA)
DPLA is an amino acid that is a primary building block for neural transmitters
as well as pain control. A significant amount of research has been conducted
to support the use of DLPA in relief of back pain, arthritis, aches, pains,
and menstrual cramps. The DL form is especially potent in this respect.
It slows the body’s break down of endorphins. As a result the body’s internal
painkiller will have a longer half-life and therefore pain is reduced. DLPA
is also an excellent agent for the control of inflammation and enhances
the effectiveness of analgesic medication. Because a diet high in grains
and polyunsaturated oil often increase the inflammation response, the use
of Dlpaphenyl Alanine should be accompanied by a diet free from safflower
oil, sunflower oil, sugar, refined carbohydrate, and fried foods in conjunction
to enhanced the inflammatory response. DLPA
is often called nature's morphine because of its pain reduction effect.
If you have a condition known as Phenyl
Ketonurea then this nutrient is not for you. People with this
condition also know as PKU has a genetic defect that cannot break down the
DLPA. Interestingly for those people that have this problem their amino
acid tyrosine may provide some relief. Because PKU affects only a very small
percentage of the people, the majority of the people do not have this problem.
To overcome pain depression and fatigue, take 500 to 1500 mg before mealtime
can be considered.
Nutritional
Supplementation Consideration : 500 to 2000 mg.
6.
Collagen type I and II
There are over 15 types of Collagen and the predominant type of collagen
that is present in joints and cartilage is type II. Type II collagen is
derived from chicken sternum cartilage from chicks 6-8 weeks old.
It contains the greatest number of anti-inflammatory and
joints supporting proteoglycan including glucosanine sulfate. Glucosanine
a well-known nutrient has been used for 30 years to rebuild in the cartilage
in orthopedic joints. Glucosanine sulfate also has a powerful anti-inflammatory
effect and supports the joint tissue. Collagen Type II also has the advantage
and that it is much more absorbable compared to just ground cartilage. Up
to 70% of the type II collagen can be absorbed as compared to 8%. While
most people have to take anywhere from 10-15 grams of cartilage in order
to get a response Type II collagen intake can be as little as 1-3 grams.
In arthritis joints there is a selective destruction of Type II collagen
in the joint cartilage itself. Replenishment of this type II cartilage is
important. It is also important to add type I collagen to the program because
type I is found in the skin and ligaments and it works together well with
type II. It also reduces the enzymes attacks on the cartilage itself. Therefore
it has a rejuvenation effect as well as reduction and destructive chemistry
of the joints in the arthritic process.
7.
Sea Cucumber
Sea Cucumber is a marine animal indigenous to the Great Barrier Reef of
the coast of Australia. They are a source of whole food of chondroitin sulfate.
Sea cucumber is actually not a cucumber but are marine animals related to
starfishes and sea urchins. Sea Cucumber has been used by various indigenous
cultures for many centuries for treatment of many ailments, including arthritis.
They have been used in China for thousands of years as treatment of arthritis
and other inflammatory diseases including rheumatoid arthritis and ankylosing
spondilysis. It is used in osteoarthritis and has been going on for centuries.
Researchers believe the sea cucumber can improve the balance of prostaglandins.
Prostaglandins are chemicals that regulate the inflammatory process. Sea
Cucumbers also contain substances known as mucopolysaccharides and chondroitins.
Half of these are often lacking in people with arthritis and connective
tissue diseases. In addition sea cucumber provides vitamins A, B1 (thymine),
B2 (Riboflavin), B3 (niacin), and C, as well as minerals such as magnesium
and calcium and zinc.
Sea Cucumber significantly relieves joint
pains without any side effects. In particular when it is combined
with essential oils, glucosamine, sulfate and Cetyl Myristoleate. The Chinese
have known of this therapeutic effect for centuries. Clinical studies have
shown that supplements of this compound are excellent for arthritis pain
and increase joint mobility for up to 60% of the people who take it. The
amount of the relief depends on the size of the dosage. Arthritic patients
can start with 300 to 400 mg and tapering the dosage once the effects are
noticed. Because this is a natural compound
and woks it rebuild the joint it is something to be taken slowly over time
and not immediately.
8.
Cetyl Myristoluate (CMO)
CMO is an all-natural oil found in fish and sperm whale oil, dairy butter,
in a small gland in male beavers and circulating in the blood of certain
species of research mice. It has been used in the arthritis research by
the National Institute of Health in the last 25 years. CMO was discovered
by Doctors Biel and May. In their studies they learned that Swiss albino
mice that are completely immune to arthritis have a high level of CMO that
is not common in other laboratory mice. In human studies, CMO has been proven
to be just as effective if given orally. In a double blind clinical study,
431 arthritic patients was given CMO, the results show that 63% percent
who took 18grams over 2 months period had improvement of the symptoms; up
to 87% improvement. CMO and its related metabolites interrupt the inflammatory
response in the cell wall is common, including the cell wall of joints.
But the long change fatty acids become incorporated in the lipid layer of
the cell walls. They make the walls more resistance against pro-inflammatory
enzymes. Studies have shown that the effectiveness of CMO is actually superior
to over the counter prescriptions such as a non-steroid of anti-inflammatory
drugs. Because of the long chain fatty acids become part of the cell wall
structure they stay in the body longer as long as the cell does which can
be for years. CMO must be taken consistently
for approximately 2 months for it to work well. The time will allow other
companion nutrients to work. After 2 weeks some relief of symptoms
are usually noticed. A total of 180 capsules is necessary (4-6 per day)
containing 100 mg of CMO per capsule is required.
9.
Essential Fatty Acids
Fish oil contains Omega 3 fatty acids and has been found to reduce inflammation
that is associated with arthritis. Fish oils works by reducing the number
of inflammatory messenger molecules made by the body’s immune system. The
Arthritis Foundation recommends at least eating 2 fish meals a week – particularly
in fatty fish such as salmon, mackerel, and sardines. Unfortunately most
fish nowadays are polluted with mercury and extensive intake should be avoided.
High quality fish oil supplements are
probably the best source of getting the same Omega 3 on board, without the
potential toxic metal effects.
Nutritional Supplementation Consideration: 1000 - 10,000 mg of EPA/DHA
10.
S-adenolsyl-methione (SAMe)
S –Adenolsyl-Methionine also known as SAMe is a compound made from the amino
acid methionine. It has been available by prescription in Europe for years
but has been available over the counter in the U.S.A since 1996. It is a
wonderful supplement and is a fantastic nutrient for depression and chronic
fatigue syndrome, arthritis, and fibromyalgia. SAMe influences the formation
of brain chemicals and helps to preserve glutathione, the body’s most important
internal antioxidant. SAMe is also involved in the formation of myelin,
the sheath that surrounds outer part of nerve cells. As a result of this
insulation property most people, taking SAMe, notice an increase of energy,
alertness and well-being. SAMe has been used in Europe to treat depression
and arthritis for decades. It is a liver enhancer and it helps the liver
to function at its best. While it is used for all forms of arthritis it
is particularly useful in the case of osteoarthritis.
A group of researchers at the University
of Maryland, state that the use of SAMe is just as effective in the relieving
of pain in the arthritic joint as compared to a non steroidal inflammatory
drug. Furthermore there are no side effects.
Nutritional Supplementation Consideration:
100 to 400 mg a day. SAMe is an expensive nutrient because it is difficult
to produce. Alternatives to this including methionine.
11.
Antioxidants - Vitamins C , E and Others
Deficiency of vitamin C is common
among the elderly, resulting in altered cartilage synthesis and compromised
cartilage repair. Studies show that vitamin C, as with vitamin E, protects
and enhances cartilage formation. Animal studies show that cartilage erosion
is much less in animals kept on high dose of vitamin C. Vitamin E is a strong
antioxidant. Clinical trials using 600 IU of vitamin E to treat patients
with OA demonstrated significant benefits. Vitamin C and E have synergistic
effects. Together, they appear to enhance the stability of sulfated proteoglycan
in the collagen matrix.
Vitamin A, Vitamin B6, Copper, and Boron:
These are necessary for the normal production and maintenance of cartilage
structure. A deficiency in any one of these would allow accelerated joint
degeneration. Supplementation at the appropriate level would promote cartilage
repair and synthesis. Boron supplementation (6 - 9 mg a day) has been used
in the treatment of OA in Germany since the mid-1970s with impressive results
that include arthritis relief in 90% of patients in some studies.
Nutritional Supplement Consideration:
Vitamin C: 1,000 - 3,000 mg per day
Vitamin E: 400 - 800 IU per day
Vitamin A (in the form of beta-carotene): 15,000 - 25,000 IU per day
Vitamin B6: 50 - 100 mg per day
Copper: 1 - 2 mg per day
Boron: 2 - 6 mg per day
| Attention
Because of tremendous individual variation,
the use of nutritionals should therefore be personalized for your
body. Since natural compounds are weak by nature in terms of potency,
the right amount needs to be administered. This
can often mean from 2 to 5 times or more of suggested dose.
One person’s nutrient can be another person’s toxin. If you have
a specific health concern and wish my personalized nutritional recommendation,
write to me by clicking here. |
Discussion
OA is a degenerative disease that can be halted and even reversed. Traditional
drugs, while relieving symptoms of pain and discomfort, actually lead to an
acceleration of the disease.
A comprehensive strategy
to prevent or to minimize OA should include:
- Dietary Considerations: Dietary therapy primarily involves
the achievement of the ideal body weight
to reduce stress on the joint caused by the extra weight of obesity. Antioxidant
rich fruits and vegetables contain important nutrients such
as vitamin C that protect against OA. Grains shoujld be avoided.
- Natural Alternative Supplementation: Promising natural substances include Glucosamine
(500 - 2,000 mg per day), Chondroitin Sulfate (100 - 1,000 mg per day),
DLPA, SAMe, Sea Cucumber, Collagen Type I and II, Fish oil, MSM (1,000
-4,000 mg per day), and Bromelain (100 - 400 mg per day). Antioxidants
(Vitamin C 1,000 - 3,000 mg per day; Vitamin E 400 - 800 IU per day) are
valuable adjuncts. The
key is not to take any single nutrient (as large quantity of each is required)
but take a complete nutritional cocktail consisting of all of the above
to take advantage of the synergistic
effect of natural compounds working together and at the same time
avoiding any potential overdose.
- Physical Therapy: such as heat and hydrotherapy as needed.
- Drugs: can be considered as last resort if the above
fails.
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About The Author
Michael Lam, M.D.,
M.P.H., A.B.A.A.M. is a specialist in Preventive and
Anti-Aging Medicine. He is currently the Director of Medical Education at the
Academy of Anti-Aging Research, U.S.A. He received his Bachelor of Science degree
from Oregon State University, and his Doctor of Medicine degree from Loma
Linda University School of Medicine, California. He also holds a Masters of
Public Health degree and is Board Certification in Anti-aging Medicine
by the American Board of Anti-Aging Medicine. Dr. Lam pioneered the formulation
of the three clinical phases of aging as well as the concept of diagnosis and
treatment of sub-clinical age related degenerative diseases to deter the aging
process. Dr. Lam has been published extensively in this field. He is the author
of The Five Proven Secrets to Longevity (available on-line). He
also serves as editor of the Journal of Anti-Aging Research.
For More Information
For the latest anti-aging related health issues, visit Dr. Lam
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