Literature DB >> 19271029

Glucosamine/chondroitin/primorine combination therapy for osteoarthritis.

Beth Anne Fox1, Mary M Stephens.   

Abstract

Osteoarthritis (OA) is the most common arthritis affecting the aging population. This degenerative disease can cause significant pain and functional disability in affected individuals. Despite advances in the retardation of rheumatoid arthritis with disease-modifying agents, comparable oral agents have been relatively unavailable for OA. The mainstays of therapy continue to be acetaminophen and nonsteroidal antiinflammatory medications to manage symptoms. Unfortunately, these medications can precipitate severe adverse events in some patients or may be contraindicated, leaving few choices remaining to control pain and suffering. Glucosamine sulfate and chondroitin sulfate have been evaluated in many studies as agents to relieve pain, improve functional activity, and slow disease progression in OA especially of the hip and knee. Studies have reported conflicting results regarding improvement in the pain and disability associated with OA with the use of glucosamine and chondroitin as single agents; however, when improvement has been demonstrated, the formulation has primarily been glucosamine sulfate combined with chondroitin sulfate. Recently, as a result of information implicating the role of reactive oxygen species and oxidative cellular stress reactions on the onset of neurodegenerative and inflammatory disorders, it has been theorized that medications that could control or alter these reactions might improve or prevent the onset of these conditions. Primorine is a combination of products thought to alter these biochemical oxidative byproducts. Based on current evidence, the use of a combination product of glucosamine sulfate and chondroitin sulfate seems to have the greatest potential as a therapeutic intervention for patients at increased risk from the adverse events of accepted current oral therapies. The use of primorine and its combination of products as an intervention in OA has theoretical advantages but its benefits are unproven. A new product, relamine, is a combination of these three formulations. While no studies have evaluated glucosamine sulfate, chondroitin sulfate and primorine in a single product, it may be an option for those who wish to try an alternate therapy for OA, as there appears to be a low risk for serious adverse events. Copyright 2009 Prous Science, S.A.U. or its licensors. All rights reserved.

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Year:  2009        PMID: 19271029     DOI: 10.1358/dot.2009.45.1.1314053

Source DB:  PubMed          Journal:  Drugs Today (Barc)        ISSN: 1699-3993            Impact factor:   2.245


  6 in total

1.  Shikonin inhibits inflammation and chondrocyte apoptosis by regulation of the PI3K/Akt signaling pathway in a rat model of osteoarthritis.

Authors:  Daijie Fu; Xifu Shang; Zhe Ni; Guoguang Shi
Journal:  Exp Ther Med       Date:  2016-08-31       Impact factor: 2.447

Review 2.  Green tea polyphenol epigallocatechin 3-gallate in arthritis: progress and promise.

Authors:  Salahuddin Ahmed
Journal:  Arthritis Res Ther       Date:  2010-04-28       Impact factor: 5.156

3.  Down-regulation of IL-6, IL-8, TNF-α and IL-1β by glucosamine in HaCaT cells, but not in the presence of TNF-α

Authors:  Kun Park; Ji-Hye Lee; Ho-Chan Cho; Sun-Young Cho; Jae-We Cho
Journal:  Oncol Lett       Date:  2010-03-01       Impact factor: 2.967

4.  The effects of different molecular weight chondroitin-4-sulfates in chondrocyte pellet culture.

Authors:  Shu-Rui Yang; Sydney Peng; Chao-Yin Ko; I-Ming Chu
Journal:  Cytotechnology       Date:  2014-10-05       Impact factor: 2.058

5.  The human pharmacokinetics of oral ingestion of glucosamine and chondroitin sulfate taken separately or in combination.

Authors:  C G Jackson; A H Plaas; J D Sandy; C Hua; S Kim-Rolands; J G Barnhill; C L Harris; D O Clegg
Journal:  Osteoarthritis Cartilage       Date:  2009-11-10       Impact factor: 6.576

Review 6.  Intra-articular injections for the treatment of osteoarthritis: focus on the clinical use of hyaluronic acid.

Authors:  Tommaso Iannitti; Daniele Lodi; Beniamino Palmieri
Journal:  Drugs R D       Date:  2011
  6 in total

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