EFFICACY AND SAFETY OF GLUCOSAMINE SULFATE VERSUS IBUPROFEN IN PATIENTS WITH KNEE OSTEOARTHRITIS

Citation
Gx. Qiu et al., EFFICACY AND SAFETY OF GLUCOSAMINE SULFATE VERSUS IBUPROFEN IN PATIENTS WITH KNEE OSTEOARTHRITIS, Arzneimittel-Forschung, 48(5), 1998, pp. 469-474
Citations number
22
Categorie Soggetti
Pharmacology & Pharmacy","Chemistry Medicinal",Chemistry
Journal title
ISSN journal
00044172
Volume
48
Issue
5
Year of publication
1998
Pages
469 - 474
Database
ISI
SICI code
0004-4172(1998)48:5<469:EASOGS>2.0.ZU;2-Q
Abstract
A double-blind therapeutic investigation was performed on 178 Chinese patients suffering from osteoarthritis of the knee randomized into two groups, one treated for 4 weeks with glucosamine sulfate (GS, CAS 290 31-19-4, Viartril-S(R)) at the daily dose of 1,500 mg and the other wi th ibuprofen (IBU, CAS 15687-27-1) at the daily dose of 1,200 mg. Knee pain at rest, at movement and at pressure, knee swelling, improvement and therapeutic utility as well as adverse events and drop-outs were recorded after 2 and 4 weeks of treatment. The variables were recorded also after 2 weeks of treatment discontinuation in order to appreciat e the remnant therapeutic effect. Both GS and IBU significantly reduce d the symptoms of osteoarthritis with the trend of GS to be more effec tive. After 2 weeks of drug discontinuation there was a remnant therap eutic effect in both groups, with the trend to be more pronounced in t he GS group. GS was significantly better tolerated than IBU, as shown by the adverse drug reactions (6% in the patients of the GS group and 16% in the IBU group - p = 0.02) and by the drug-related drop-outs (0% of the patients in the GS group and 10% in the IBU group - p = 0.0017 ). The better tolerability of GS is explained by its mode of action, b ecause GS specifically curbs the pathogenic mechanisms of osteoarthrit is and does not inhibit the cyclo-oxygenases as the non-steroidal anti -inflammatory drugs (NSAIDs) do, with the consequent anti-inflammatory analgesic activities but also with the several adverse reactions due to this not targeted effect. The present study confirms that GS is a s elective drug for osteoarthritis, as effective on the symtoms of the d isease as NSAIDs but significantly better tolerated. For these propert ies GS seems particularly indicated in the long-term treatments needed in osteoarthritis.