Glucosamine sulphate
Glucosamine sulphate appears to be helpful in reducing symptoms of osteoarthritis, even better than acetaminophen.
Joint Power Rx Formulated by
Ray Sahelian, M.D.
Because
joint pain is so debilitating, glucosamine sulfate and chondroitin sulfate alone
are often not enough. This powerful joint formula includes several additional
herbal extracts and nutrients including MSM, CMO, boswellia serrata, turmeric,
cat's claw extract, grape seed extract, and sea cucumber for optimal joint
health.
Joint Power Rx Supplement has:
Glucosamine sulfate (from shellfish) - glucosamine is a popular ingredient in
many joint health products
Chondroitin sulfate - chondroitin is a popular ingredient in many joint health
products
MSM nutrient which stands for
methylsulfonylmethane
CMO complex also known as cetyl myristoleate
Boswellia serrata extract is used in Ayurvedic medicine
Turmeric is an herb that contains curcumin
Cat's claw extract comes from the Amazon jungle
Devil's claw is a plant widely used in South African
traditional medicine,
Grape seed extracts have compounds called procyanidolic
oligomers which are powerful antioxidants, perhaps much greater than vitamins C
and E.
Sea cucumbers have a number of substances that
have therapeutic value.
The effect of glucosamine sulphate on the blood levels
of cholesterol or triglycerides--a clinical study
Ugeskr Laeger. 2007 Jan 29;169(5):407-10. Østergaard K, Hviid T,
Hyllested-Winge JL. Slidgigtinstituttet A/S, Ishøj.
This study was conducted in order to determine if glucosamine sulphate taken
by patients as treatment for chronic joint pain influences the fasting blood
levels of cholesterol and triglycerides. A 3 months', post-marketing, randomised,
double-blinded, placebo-controlled, clinical trial was performed with parallel
groups of 66 patients over 40 years of age with joint pain of long duration
receiving either recommend dosage (1500 mg per day) of glucosamine sulphate or
placebo. The primary outcome measures were cholesterol levels (total
cholesterol, LDL (low density lipoprotein)-cholesterol and HDL (high density
lipoprotein)-cholesterol) and triglycerides in fasting blood (plasma levels).
Secondary outcome measures were self reported side-effects. No significant
differences between the glucosamine sulphate group and the placebo group with
respect to cholesterol and triglycerides were observed. There were no
differences between the treatment groups with respect to side-effects. This
study demonstrates that glucosamine sulphate does not significantly influence
blood levels of cholesterol or triglycerides.
Glucosamine sulphate in the treatment of knee
osteoarthritis symptoms: a randomized, double-blind, placebo-controlled study
using acetaminophen as a side comparator.
Arthritis Rheum. 2007 Feb;56(2):555-67. Rheumatology Department, Fundación
Jiménez Díaz-Capio, Madrid, Spain.
To assess the effects of the prescription formulation of glucosamine sulphate
(1,500 mg administered once daily) on the symptoms of knee osteoarthritis during
a 6-month treatment course. Three hundred eighteen patients were enrolled in
this randomized, placebo-controlled, double-blind trial in which acetaminophen,
the currently preferred medication for symptomatic treatment of osteoarthritis,
was used as a side comparator. Patients were randomly assigned to receive oral
glucosamine sulphate 1,500 mg once daily, acetaminophen 3 gm/day, or placebo.
The primary efficacy outcome measure was the change in the Lequesne index after
6 months. Secondary parameters included the Western Ontario and McMaster
Universities Osteoarthritis Index (WOMAC) and response according to the
Osteoarthritis Research Society International criteria. At baseline, the study
patients had moderately severe osteoarthritis symptoms (mean Lequesne index
approximately 11 points). Glucosamine sulphate was more effective than placebo
in improving the Lequesne score, with a final decrease of 3.1 points, versus 1.9
with placebo. The 2.7-point decrease with acetaminophen was not significantly
different from that with placebo. Similar results were observed for the WOMAC.
There were more responders to glucosamine sulphate (39%) and acetaminophen (33%)
than to placebo (21%). Safety was good, and was comparable among groups. The
findings of this study indicate that glucosamine sulphate at the oral once-daily
dosage of 1,500 mg is more effective than placebo in treating knee
osteoarthritis symptoms.
Osteoarthritic patients with high cartilage turnover
show increased responsiveness to the cartilage protecting effects of glucosamine
sulphate.
Clin Exp Rheumatol. 2004 Jan-Feb;22(1):36-42. Nordic Bioscience A/S, Herlev,
Denmark.
Glucosamine sulphate has been shown in a large double-blind, placebo-controlled
clinical trial to prevent structural damage and improve clinical symptoms of
osteoarthritis. We investigated whether early response in a newly developed
biochemical marker of collagen type II degradation (CTX-II, CartiLaps ELISA)
could reflect the long-term preservation of hyaline cartilage. Study subjects
comprised 212 knee OA patients participating in a clinical trial of the effects
of glucosamine sulphate. Disease symptoms were assessed quarterly by WOMAC
scoring and X-ray analysis was performed at baseline and after 3 years. Urine
samples were obtained at baseline and after 1, 2 and 3 years for measurement in
the CartiLaps assay. At baseline the patients had an average concentration of
urinary CTX-II of 222 ng/mmol creatinine. This was significantly above the CTX-II
levels measured in urine samples from 415 healthy controls (169). There was no
significant difference in the CTX-II response in the placebo group and the
glucosamine treated group. However, those with high cartilage turnover presented
a significant decrease in CTX-II after 12-month glucosamine treatment.
CONCLUSION: The data indicate that measurement of urinary collagen type II C-telopeptide
fragments enables the identification of OA patients with high cartilage turnover
who at the same time are most responsive to therapy with structure modifying
drugs.
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