Differentiation of patented crystalline glucosamine sulfate from other glucosamine preparations will optimize osteoarthritis treatment.


Journal

International journal of rheumatic diseases
ISSN: 1756-185X
Titre abrégé: Int J Rheum Dis
Pays: England
ID NLM: 101474930

Informations de publication

Date de publication:
Mar 2019
Historique:
pubmed: 24 3 2017
medline: 30 7 2019
entrez: 24 3 2017
Statut: ppublish

Résumé

Symptomatic slow-acting drugs for osteoarthritis (SYSADOAs) are recommended for the medium- to long-term management of knee osteoarthritis (OA) due to their abilities to control pain, improve function and delay joint structural changes. Among SYSADOAs, evidence is greatest for the patented crystalline glucosamine sulfate (pCGS) formulation (Mylan). Glucosamine is widely available as glucosamine sulfate (GS) and glucosamine hydrochloride (GH) preparations that vary substantially in molecular form, pharmaceutical formulation and dose regimen. Only pCGS is given as a highly bioavailable once-daily dose (1500 mg), which consistently delivers the plasma levels of around 10 μmol/L required to inhibit interleukin-1-induced expression of genes involved in the pathophysiology of joint inflammation and tissue destruction. Careful consideration of the evidence base reveals that only pCGS reliably provides a moderate effect size on pain that is higher than paracetamol and equivalent to non-steroidal anti-inflammatory drugs (NSAIDs), while non-crystalline GS and GH fail to reach statistical significance for pain reduction. Chronic administration of pCGS has disease-modifying effects, with a reduction in need for total joint replacement lasting for 5 years after treatment cessation. Pharmacoeconomic studies of pCGS demonstrate long-term reduction in additional pain analgesia and NSAIDs, with a 50% reduction in costs of other OA medication and healthcare consultations. Consequently, pCGS is the logical choice, with demonstrated medium-term control of pain and lasting impact on disease progression. Physician and patient education on the differentiation of pCGS from other glucosamine formulations will help to improve treatment selection, increase treatment adherence, and optimize clinical benefit in OA.

Identifiants

pubmed: 28332780
doi: 10.1111/1756-185X.13068
doi:

Substances chimiques

Antirheumatic Agents 0
Glucosamine N08U5BOQ1K

Types de publication

Editorial Review

Langues

eng

Pagination

376-385

Subventions

Organisme : Bristol Myers Squibb
Organisme : Ebewee Pharma
Organisme : SMB
Organisme : Nutraveris
Organisme : Galapagos
Organisme : Negma
Organisme : Roche
Organisme : Teijin
Organisme : Theramex
Organisme : Merckle
Organisme : Zodiac
Organisme : Medical Research Council
ID : MC_U147585824
Pays : United Kingdom
Organisme : Chiltern
Organisme : Alliance for Better Bone Health
Organisme : GlaxoSmithKline (GSK)
Organisme : Takeda
Organisme : Servier
Organisme : Will Pharma
Organisme : UCB
Organisme : Medtronic
Organisme : Danone
Organisme : Medical Research Council
ID : G0400491
Pays : United Kingdom
Organisme : Wyeth
Organisme : Medical Research Council
ID : MC_U147585819
Pays : United Kingdom
Organisme : Boehringer
Organisme : Organon
Organisme : Medical Research Council
ID : MC_UU_12011/1
Pays : United Kingdom
Organisme : Novartis
Organisme : Amgen
Organisme : Teva
Organisme : Asahi Kasei
Organisme : Medical Research Council
ID : MC_UP_A620_1014
Pays : United Kingdom
Organisme : Merck
Organisme : NPS
Organisme : Genevrier
Organisme : Eli Lilly
Organisme : Nycomed
Organisme : Therabel
Organisme : Analis
Organisme : ESCEO asbl, Belgium
Organisme : Pfizer
Organisme : Endocyte
Organisme : Medical Research Council
ID : MC_U147585827
Pays : United Kingdom
Organisme : NovoNordisk
Organisme : Rottapharm
Organisme : IBSA
Organisme : Merck Sharp and Dohme (MSD)

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2017 Asia Pacific League of Associations for Rheumatology and John Wiley & Sons Australia, Ltd.

Auteurs

Sukit Saengnipanthkul (S)

Department of Orthopedics, Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand.

Saranatra Waikakul (S)

Department of Orthopedics, Siriraj Hospital, Mahidol University, Bangkok, Thailand.

Sattaya Rojanasthien (S)

Department of Orthopedics, Faculty of Medicine, Chiangmai University, Chiangmai, Thailand.

Kitti Totemchokchyakarn (K)

Division of Allergy, Immunology and Rheumatology, Department of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Attarit Srinkapaibulaya (A)

Department of Rehabilitation, Faculty of Medicine, King Chulalongkorn Memorial Hospital, Chulalongkorn University, Bangkok, Thailand.

Tai Cheh Chin (T)

Orthopedic Department, Ara Damansara Medical Center Sdn Bhd, Selangor, Malaysia.

Nguyen Mai Hong (N)

Department of Rheumatology, Bach Mai Hospital, Hanoi, Vietnam.

Olivier Bruyère (O)

Department of Public Health, Epidemiology and Health Economics, University of Liège, Liège, Belgium.

Cyrus Cooper (C)

MRC Lifecourse Epidemiology Unit, University of Southampton, Southampton, UK.
NIHR Musculoskeletal Biomedical Research Unit, University of Oxford, Oxford, UK.

Jean-Yves Reginster (JY)

Department of Public Health, Epidemiology and Health Economics, University of Liège, Liège, Belgium.

Myat Lwin (M)

Orthopedic Unit, Yangon Orthopedic Hospital, Yangon, Myanmar.

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Classifications MeSH