Inappropriate claims from non-equivalent medications in osteoarthritis: a position paper endorsed by the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO)

被引:43
作者
Bruyere, Olivier [1 ,7 ]
Cooper, Cyrus [2 ,3 ,7 ]
Al-Daghri, Nasser M. [4 ,7 ]
Dennison, Elaine M. [3 ]
Rizzoli, Rene [5 ,6 ,7 ]
Reginster, Jean-Yves [1 ,7 ]
机构
[1] Univ Liege, Dept Publ Hlth Epidemiol & Hlth Econ, CHU Sart Tilman B23, B-4000 Liege, Belgium
[2] Univ Southampton, Southampton Gen Hosp, MRC Lifecourse Epidemiol Unit, Southampton, Hants, England
[3] Univ Oxford, NIHR Musculoskeletal Biomed Res Unit, Oxford, England
[4] King Saud Univ, Coll Sci, Biochem Dept, Prince Mutaib Chair Biomarkers Osteoporosis, Riyadh 11451, Saudi Arabia
[5] Geneva Univ Hosp, Div Bone Dis, Geneva, Switzerland
[6] Fac Med, Geneva, Switzerland
[7] WHO Collaborating Ctr Publ Hlth Aspects Musculosk, Liege, Belgium
关键词
Chondroitin sulfate; Glucosamine; Symptomatic slow-acting drugs for osteoarthritis; Knee; Osteoarthritis; CRYSTALLINE GLUCOSAMINE SULFATE; KNEE OSTEOARTHRITIS; DOUBLE-BLIND; AVOCADO/SOYBEAN UNSAPONIFIABLES; CHONDROITIN SULFATE; SYMPTOMATIC EFFICACY; HIP OSTEOARTHRITIS; GLOBAL BURDEN; TASK-FORCE; PLACEBO;
D O I
10.1007/s40520-017-0861-1
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Osteoarthritis (OA) is a progressive joint disease, that occurs frequently in the aging population and is a major cause of disability worldwide. Both glucosamine and chondroitin are biologically active molecules that are substrates for proteoglycan, an essential component of the cartilage matrix. Evidence supports the use of glucosamine and chondroitin as symptomatic slow-acting drugs for osteoarthritis (SYSADOAs) with impact on OA symptoms and disease-modifying effects in the long term. Glucosamine and chondroitin are administered in exogenous form as a sulfate salt and multiple formulations of these agents are available, both as prescription-grade products and nutritional supplements. However, while all preparations may claim to deliver a therapeutic level of glucosamine or chondroitin not all are supported by clinical evidence. Only patented crystalline glucosamine sulfate (pCGS) is shown to deliver consistently high glucosamine bioavailability and plasma concentration in humans, which corresponds to demonstrated clinical efficacy. Similarly, clinical evidence supports only the pharmaceutical-grade chondroitin sulfate. The European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO) advocates, through careful consideration of the evidence base, that judicious choice of glucosamine and chondroitin formulation is essential to maximize clinical benefit, patient adherence and satisfaction with treatment. In future, the ESCEO recommends that complex molecules with biological activity such as pCGS may be treated as "biosimilars" akin to the European Medicines Agency guidance on biological medicinal products. It seems likely that for all other complex molecules classed as SYSADOAs, the recommendation to use only formulations clearly supported by the evidence-base should apply.
引用
收藏
页码:111 / 117
页数:7
相关论文
共 60 条
[1]  
AHRQ, 2017, AHRQ PUBL, V190
[2]  
Altman Roy D, 2009, Expert Rev Clin Pharmacol, V2, P359, DOI 10.1586/ecp.09.17
[3]  
Appelboom T, 2001, SCAND J RHEUMATOL, V30, P242
[4]   Vascular and upper gastrointestinal effects of non-steroidal anti-inflammatory drugs: meta-analyses of individual participant data from randomised trials [J].
Bhala, N. ;
Emberson, J. ;
Merhi, A. ;
Abramson, S. ;
Arber, N. ;
Baron, J. A. ;
Bombardier, C. ;
Cannon, C. ;
Farkouh, M. E. ;
FitzGerald, G. A. ;
Goss, P. ;
Halls, H. ;
Hawk, E. ;
Hawkey, C. ;
Hennekens, C. ;
Hochberg, M. ;
Holland, L. E. ;
Kearney, P. M. ;
Laine, L. ;
Lanas, A. ;
Lance, P. ;
Laupacis, A. ;
Oates, J. ;
Patrono, C. ;
Schnitzer, T. J. ;
Solomon, S. ;
Tugwell, P. ;
Wilson, K. ;
Wittes, J. ;
Baigent, C. ;
Adelowo, O. ;
Aisen, P. ;
Al-Quorain, A. ;
Altman, R. ;
Bakris, G. ;
Baumgartner, H. ;
Bresee, C. ;
Carducci, M. ;
Chang, D-M. ;
Chou, C-T. ;
Clegg, D. ;
Cudkowicz, M. ;
Doody, L. ;
El Miedany, Y. ;
Falandry, C. ;
Farley, J. ;
Ford, L. ;
GarciLosa, M. ;
Gonzalez-Ortiz, M. ;
Haghighi, M. .
LANCET, 2013, 382 (9894) :769-779
[5]   Osteoarthritis: an update with relevance for clinical practice [J].
Bijlsma, Johannes W. J. ;
Berenbaum, Francis ;
Lafeber, Foris P. J. G. .
LANCET, 2011, 377 (9783) :2115-2126
[6]   Short-term efficacy of pharmacotherapeutic interventions in osteoarthritic knee pain: A meta-analysis of randomised placebo-controlled trials [J].
Bjordal, Jan Magnus ;
Klovning, Atle ;
Ljunggren, Anne Elisabeth ;
Slordal, Lars .
EUROPEAN JOURNAL OF PAIN, 2007, 11 (02) :125-138
[7]  
Blotman F, 1997, REV RHUM, V64, P825
[8]   An algorithm recommendation for the management of knee osteoarthritis in Europe and internationally: A report from a task force of the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis (ESCEO) [J].
Bruyere, Olivier ;
Cooper, Cyrus ;
Pelletier, Jean-Pierre ;
Branco, Jaime ;
Brandi, Maria Luisa ;
Guillemin, Francis ;
Hochberg, Marc C. ;
Kanis, John A. ;
Kvien, Tore K. ;
Martel-Pelletier, Johanne ;
Rizzoli, Rene ;
Silverman, Stuart ;
Reginster, Jean-Yves .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 2014, 44 (03) :253-263
[9]  
Castellsague J, 2012, DRUG SAFETY, V35, P1127, DOI 10.2165/11633470-000000000-00000
[10]   Experimental Pharmacology of Glucosamine Sulfate [J].
Chiusaroli, Riccardo ;
Piepoli, Tiziana ;
Zanelli, Tiziano ;
Ballanti, Paola ;
Lanza, Marco ;
Rovati, Lucio C. ;
Caselli, Gianfranco .
INTERNATIONAL JOURNAL OF RHEUMATOLOGY, 2011, 2011