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A consensus-based framework for conducting and reporting osteoarthritis phenotype research.
van Spil, W E; Bierma-Zeinstra, S M A; Deveza, L A; Arden, N K; Bay-Jensen, A-C; Kraus, V Byers; Carlesso, L; Christensen, R; Van Der Esch, M; Kent, P; Knoop, J; Ladel, C; Little, C B; Loeser, R F; Losina, E; Mills, K; Mobasheri, A; Nelson, A E; Neogi, T; Peat, G M; Rat, A-C; Steultjens, M; Thomas, M J; Valdes, A M; Hunter, D J.
  • van Spil WE; Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, PO Box 85500, 3508 GA, Utrecht, The Netherlands. w.e.vanspil@umcutrecht.nl.
  • Bierma-Zeinstra SMA; Department of General Practice, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Deveza LA; Department of Orthopedic Surgery, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Arden NK; Department of Rheumatology, Royal North Shore Hospital and Institute of Bone and Joint Research, Kolling Institute, University of Sydney, Sydney, Australia.
  • Bay-Jensen AC; University of Oxford, Oxford, UK.
  • Kraus VB; University of Sydney, Sydney, Australia.
  • Carlesso L; Rheumatology, Nordic Bioscience, Herlev, Denmark.
  • Christensen R; School of Medicine, Duke University, Durham, USA.
  • Van Der Esch M; Université de Montréal, Montréal, Canada.
  • Kent P; Musculoskeletal Statistics Unit, The Parker Institute, Copenhagen University Hospital, Bispebjerg and Frederiksberg, Frederiksberg, Denmark.
  • Knoop J; Research Unit of Rheumatology, Department of Clinical Research, Odense University Hospital, University of Southern Denmark, Odense, Denmark.
  • Ladel C; Reade, Center of Rehabilitation and Rheumatology, Amsterdam, The Netherlands.
  • Little CB; Curtin University, Bentley, Australia.
  • Loeser RF; University of Southern Denmark, Odense, Denmark.
  • Losina E; Department of Health Sciences, VU Amsterdam, Amsterdam, The Netherlands.
  • Mills K; Merck KGaA, Darmstadt, Germany.
  • Mobasheri A; Raymond Purves Labs, Institute of Bone and Joint Research, Kolling Institute, University of Sydney, Sydney, Australia.
  • Nelson AE; Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC, USA.
  • Neogi T; Brigham and Women's Hospital, Boston, USA.
  • Peat GM; Department of Health Professions, Macquarie University, Sydney, Australia.
  • Rat AC; Research Unit of Medical Imaging, Physics and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.
  • Steultjens M; Thurston Arthritis Research Center, University of North Carolina, Chapel Hill, NC, USA.
  • Thomas MJ; School of Medicine, Boston University, Boston, USA.
  • Valdes AM; Arthritis Research UK Primary Care Centre, Research Institute for Primary Care & Health Sciences, Keele University, Staffordshire, UK.
  • Hunter DJ; Haywood Academic Rheumatology Centre, Midlands Partnership NHS Foundation Trust, Haywood Hospital, Staffordshire, UK.
Arthritis Res Ther ; 22(1): 54, 2020 03 20.
Article en En | MEDLINE | ID: mdl-32192519
ABSTRACT

BACKGROUND:

The concept of osteoarthritis (OA) heterogeneity is evolving and gaining renewed interest. According to this concept, distinct subtypes of OA need to be defined that will likely require recognition in research design and different approaches to clinical management. Although seemingly plausible, a wide range of views exist on how best to operationalize this concept. The current project aimed to provide consensus-based definitions and recommendations that together create a framework for conducting and reporting OA phenotype research.

METHODS:

A panel of 25 members with expertise in OA phenotype research was composed. First, panel members participated in an online Delphi exercise to provide a number of basic definitions and statements relating to OA phenotypes and OA phenotype research. Second, panel members provided input on a set of recommendations for reporting on OA phenotype studies.

RESULTS:

Four Delphi rounds were required to achieve sufficient agreement on 11 definitions and statements. OA phenotypes were defined as subtypes of OA that share distinct underlying pathobiological and pain mechanisms and their structural and functional consequences. Reporting recommendations pertaining to the study characteristics, study population, data collection, statistical analysis, and appraisal of OA phenotype studies were provided.

CONCLUSIONS:

This study provides a number of consensus-based definitions and recommendations relating to OA phenotypes. The resulting framework is intended to facilitate research on OA phenotypes and increase combined efforts to develop effective OA phenotype classification. Success in this endeavor will hopefully translate into more effective, differentiated OA management that will benefit a multitude of OA patients.
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Texto completo: 1 Ejes tematicos: Pesquisa_clinica Banco de datos: MEDLINE Asunto principal: Osteoartritis de la Cadera / Técnica Delphi / Osteoartritis de la Rodilla / Investigación Biomédica / Informe de Investigación Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Ejes tematicos: Pesquisa_clinica Banco de datos: MEDLINE Asunto principal: Osteoartritis de la Cadera / Técnica Delphi / Osteoartritis de la Rodilla / Investigación Biomédica / Informe de Investigación Tipo de estudio: Diagnostic_studies / Guideline Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article