Managing joint pain
Arthritis,
defined as �inflammation of a joint,� is a general term for
progressive joint disease marked by pain and stiffness.
The most prevalent and painful are osteoarthritis and rheumatoid
arthritis.
Osteoarthritis, characterized by the erosion of the
articulations between bones, is the most common form, and is
generally associated with aging. It
generally attacks individual joints, usually those that bear weight,
like the feet, knees, hips, and spine.
Rheumatoid arthritis is an autoimmune disease.
It is painful and crippling, causing inflammation and destruction
of joints throughout the body.
Arthritis is most commonly treated with steroidal drugs like
cortisone, and nonsteroidal anti-inflammatory drugs (NSAIDs).
They have unpleasant to dangerous side effects including nausea,
stomach irritation, stomach and duodenal ulcers, and possible kidney
damage.
As arthritis becomes more prevalent, a number of natural
approaches have appeared. In a double-blind study of patients with
osteoarthritis, patients were given either 250 mg of glucosamine
sulfate or a placebo, taken three times per day for six weeks.
Those patients who received glucosamine showed significant
alleviation and some elimination of symptoms.
In a double-blind, parallel, placebo-controlled, randomized study
involving outpatients with knee osteoarthritis, patients were given
either 400 mg of glucosamine twice a week or a placebo.
After six weeks, the patients who received glucosamine showed
150% greater improvement than the control group.
In one double-blind clinical study of patients with
osteoarthritis, patients were given 800 mg of chondroitin sulfate
per day or a placebo. The patients
who received chondroitin sulfate reported significantly reduced pain
and increased joint mobility.
In another double-blind study, a group of patients with
finger-joint osteoarthritis were given 400 mg of chondroitin three
times per day. Over the
three-year study, x-rays were taken of the finger joints at yearly
intervals. The patients
treated with chondroitin had significantly less progression of the
disease than the control group.
Boswellia serrata, an anti-inflammatory agent extracted
from the sap of a tree in India, has been traditionally used for
thousands of years. Studies
have shown that boswellia can reduce joint swelling, stiffness and
pain, improve blood supply to inflamed joints, and increase mobility
of arthritic joints.
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Red
clover (Trifolium pratense) a relatively popular herb during the
last 20 years now finds promise for menopause.
Red clover has been used as one of the best herbs in the
classification of alteratives. Alteratives
are substances that can alter the blood and lymphatic system by their cleansing
action.
How this cleansing is accomplished has never been specifically
agreed upon, but most natural practitioners refer to alteratives as
acting on the liver and the kidneys.
Red clover is one of the primary alterative herbs in many
cleansing formulas that are used for everything from acne to psoriasis.
Recently red clover has been found to contain a group of
chemicals called isoflavones, which have demonstrated estrogen-like
qualities. Isoflavones
are found in legumes such as clover, soy, lentils, chickpeas, and beans.
Due to a higher consumption of legumes in Asia, Asian
women�s blood levels of the isoflavone phytoestrogens are 20-30 times
greater than those of North American women.
Current research has shown that there are four isoflavones that
play unique and important roles: biochanin, formononetin, genistein,
and daidzein. Red
clover delivers all four of these important isoflavones.
One red clover product has been shown to reduce hot flashes
and other symptoms associated with menopause.
It was first released in 1997 in Australia, where it quickly
became the best-selling dietary supplement of natural plant estrogens
for women.
Recently, a preliminary study evaluating the effectiveness of
this product concluded it could reduce night sweats and hot flashes,
two of the most uncomfortable symptoms of menopause.
Lisa Nachtigall, Director of the Women�s Endocrine Center at
St. Elizabeth�s Medical Center in Boston, MA, demonstrated that taking
40 mg of isoflavones daily resulted in a 56% reduction in both the
intensity and the number of hot flashes and a 52% decrease in night
sweats. Reference:
Nachtigall, L.B., et al. Nonprescription
alternatives to hormone replacement therapy.
The Female Patient June 1999;24(6).
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Smokers
benefit from Pycnogenol Smoking
is a major risk factor for strokes, because smoking causes blood
platelets to aggregate or �clump� together.
Researchers from the University of Arizona, working in concert
with German researchers, investigated the ability of Pycnogenol to block
platelet aggregation. Pycnogenol is a unique mixture of
bioflavonoids and related compounds extracted from French maritime pine
bark.
Heavy smokers were enrolled in this study.
Platelet aggregation was measured two hours after each smoker
took either 500 mg of aspirin or 100 mg of Pycnogenol. Aspirin is known to reduce platelet clumping, however it also
tends to increase bleeding time. The unhealthy platelet activity was
prevented by both the aspirin and Pycnogenol.
As expected, however, the aspirin also significantly increased
bleeding time. The
Pycnogenol did not show this undesirable side effect.
In another part of this study, different intakes of Pycnogenol
were compared in smokers. It
was found that �a single, high
dose, 200 mg Pycnogenol, remained effective for over 6 days against
smoking-induced platelet aggregation.�
The researchers were enthused about the benefits of Pycnogenol
and noted that �Pycnogenol
prevented smoking-induced platelet aggregation at a lower intake and
without the adverse effect of aspirin.� Reference: Putter, M., Gortemeyer, K.H.M., Wurthwein, G., et
al. Inhibition of
smoking-induced platelet aggregation by aspirin and Pycnogenol. Thrombosis Res
1999;95:155-61.
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Surviving
a heart attack is cause for celebration, but there are still health
concerns���especially for subsequent cardiovascular events.
Italian researchers report in the prestigious journal Lancet
that omega-3 fatty acids from
fish oil reduce later risk of stroke, non-fatal heart attack, and fatal
heart events.
A total of 11,324 heart attack survivors were enrolled in this
study and assigned to take supplements of either 1 gram of omega-3 fatty
acids daily, 300 mg of vitamin E daily, both supplements, or no
supplements for three and a half years.
The supplements of omega-3 fatty acids provided statistically
significant health benefits. Long-term use of omega-3 fatty acids in heart attack survivors appears
to offer worthwhile heart protection. Reference:
GISSI-Prevenzione Investigators. Dietary
supplementation with n-3 polyunsaturated fatty acids and vitamin E after
myocardial infarction: results of the GISSI-Prevenzione trail.
Lancet 1999;354:447-55.
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