Can We Identify Patients with High Risk of Osteoarthritis Progression Who Will Respond to Treatment? A Focus on Biomarkers and Frailty

被引:24
作者
Arden, Nigel [1 ,2 ]
Richette, Pascal [3 ,4 ]
Cooper, Cyrus [1 ,5 ]
Bruyere, Olivier [6 ,7 ]
Abadie, Eric [8 ]
Branco, Jaime [9 ,10 ]
Brandi, Maria Luisa [11 ]
Berenbaum, Francis [12 ,13 ]
Clerc, Cecile [14 ]
Dennison, Elaine [4 ,5 ]
Devogelaer, Jean-Pierre [15 ]
Hochberg, Marc [16 ]
D'Hooghe, Pieter [17 ]
Herrero-Beaumont, Gabriel [18 ]
Kanis, John A. [19 ]
Laslop, Andrea [20 ]
Leblanc, Veronique [21 ]
Maggi, Stefania [22 ]
Mautone, Giuseppe [23 ]
Pelletier, Jean-Pierre [24 ]
Petit-Dop, Florence [25 ]
Reiter-Niesert, Susanne [26 ]
Rizzoli, Rene [27 ,28 ]
Rovati, Lucio [29 ]
Messi, Eleonora Tajana [23 ]
Tsouderos, Yannis [25 ]
Martel-Pelletier, Johanne [24 ]
Reginster, Jean-Yves [6 ,7 ]
机构
[1] Univ Oxford, NIHR Musculoskeletal Biomed Res Unit, Oxford, England
[2] ARUK Sport Exercise & Osteoarthritis Ctr Excellen, Oxford, England
[3] Paris Diderot Univ, UFR Med, Paris, France
[4] Hop Lariboisiere, AP HP, Federat Rhumatol, F-75475 Paris, France
[5] Univ Southampton, MRC Epidemiol Resource Ctr, Southampton, Hants, England
[6] Univ Liege, Dept Publ Hlth Epidemiol & Hlth Econ, B-4000 Liege, Belgium
[7] CHU Ctr Ville, B-4000 Liege, Belgium
[8] Hop Ambroise Pare, Div Cardiol, Paris, France
[9] Univ Novade Lisboa, Fac Ciencias Med, Dept Rheumatol, CEDOC, Lisbon, Portugal
[10] Hosp Egas Moniz, EPE, CHLO, Lisbon, Portugal
[11] Univ Florence, Dept Internal Med, Florence, Italy
[12] Univ Paris 06, Hop St Antoine, AP HP, Dept Rheumatol, Paris, France
[13] Univ Paris 06, INSERM, UMR S938, Paris, France
[14] Labs Genevrier, Antibes, France
[15] Catholic Univ Louvain, St Luc Univ Hosp, Dept Rheumatol, Louvain, Belgium
[16] Univ Maryland, Sch Med, Geriatr Res Educ & Clin Ctr, Div Rheumatol & Clin Immunol,Dept Med,Maryland VA, Baltimore, MD USA
[17] Aspetar Hosp, Dept Orthopaed & Sports Med, Doha, Qatar
[18] Fdn Jimenez Diaz, Bone & Joint Res Unit, E-28040 Madrid, Spain
[19] Univ Sheffield, Sch Med, Ctr Metab Bone Dis, Sheffield, S Yorkshire, England
[20] Austrian Agcy Hlth & Food Safety AGES, Sci Off, Vienna, Austria
[21] Expansci Labs, Courbevoie, France
[22] CNR, Aging Program, Padua, Italy
[23] IBSA Inst Biochim SA, CH-6915 Pambio Noranco, Switzerland
[24] Univ Montreal Hosp Res Ctr CRCHUM, Osteoarthritis Res Unit, Notre Dame Hosp, Montreal, PQ, Canada
[25] Inst Rech Internatl Servier, Suresnes, France
[26] Fed Inst Drugs & Med Devices BfArM, Bonn, Germany
[27] Univ Hosp Geneva, Dept Rehabil & Geriatr, Serv Bone Dis, Geneva, Switzerland
[28] Fac Med Geneva, Geneva, Switzerland
[29] Rottapharm Madaus, Clin Res Unit, Monza, Italy
关键词
SYMPTOMATIC KNEE OSTEOARTHRITIS; BONE-MARROW LESIONS; HIP-OSTEOARTHRITIS; IMPLEMENTING FRAILTY; STRATIFIED MEDICINE; CLINICAL-PRACTICE; CARTILAGE VOLUME; PREVALENCE; GENE; EPIDEMIOLOGY;
D O I
10.1007/s40266-015-0276-7
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), a disease affecting different patient phenotypes, appears as an optimal candidate for personalized healthcare. The aim of the discussions of the European Society for Clinical and Economic Aspects of Osteoporosis and Osteoarthritis (ESCEO) working group was to explore the value of markers of different sources in defining different phenotypes of patients with OA. The ESCEO organized a series of meetings to explore the possibility of identifying patients who would most benefit from treatment for OA, on the basis of recent data and expert opinion. In the first meeting, patient phenotypes were identified according to the number of affected joints, biomechanical factors, and the presence of lesions in the subchondral bone. In the second meeting, summarized in the present article, the working group explored other markers involved in OA. Profiles of patients may be defined according to their level of pain, functional limitation, and presence of coexistent chronic conditions including frailty status. A considerable amount of data suggests that magnetic resonance imaging may also assist in delineating different phenotypes of patients with OA. Among multiple biochemical biomarkers identified, none is sufficiently validated and recognized to identify patients who should be treated. Considerable efforts are also being made to identify genetic and epigenetic factors involved in OA, but results are still limited. The many potential biomarkers that could be used as potential stratifiers are promising, but more research is needed to characterize and qualify the existing biomarkers and to identify new candidates.
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收藏
页码:525 / 535
页数:11
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