Cohort profile: The Applied Public-Private Research enabling OsteoArthritis Clinical Headway (IMI-APPROACH) study: a 2-year, European, cohort study to describe, validate and predict phenotypes of osteoarthritis using clinical, imaging and biochemical markers.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
28 07 2020
Historique:
entrez: 30 7 2020
pubmed: 30 7 2020
medline: 20 2 2021
Statut: epublish

Résumé

The Applied Public-Private Research enabling OsteoArthritis Clinical Headway (APPROACH) consortium intends to prospectively describe in detail, preselected patients with knee osteoarthritis (OA), using conventional and novel clinical, imaging, and biochemical markers, to support OA drug development. APPROACH is a prospective cohort study including 297 patients with tibiofemoral OA, according to the American College of Rheumatology classification criteria. Patients were (pre)selected from existing cohorts using machine learning models, developed on data from the CHECK cohort, to display a high likelihood of radiographic joint space width (JSW) loss and/or knee pain progression. Selection appeared logistically feasible and baseline characteristics of the cohort demonstrated an OA population with more severe disease: age 66.5 (SD 7.1) vs 68.1 (7.7) years, min-JSW 2.5 (1.3) vs 2.1 (1.0) mm and Knee injury and Osteoarthritis Outcome Score pain 31.3 (19.7) vs 17.7 (14.6), except for age, all: p<0.001, for selected versus excluded patients, respectively. Based on the selection model, this cohort has a predicted higher chance of progression. Patients will visit the hospital again at 6, 12 and 24 months for physical examination, pain and general health questionnaires, collection of blood and urine, MRI scans, radiographs of knees and hands, CT scan of the knee, low radiation whole-body CT, HandScan, motion analysis and performance-based tests.After two years, data will show whether those patients with the highest probabilities for progression experienced disease progression as compared to those wit lower probabilities (model validation) and whether phenotypes/endotypes can be identified and predicted to facilitate targeted drug therapy. NCT03883568.

Identifiants

pubmed: 32723735
pii: bmjopen-2019-035101
doi: 10.1136/bmjopen-2019-035101
pmc: PMC7389775
doi:

Substances chimiques

Biomarkers 0

Banques de données

ClinicalTrials.gov
['NCT03883568']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e035101

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: EMvH has nothing to disclose; WEvS reports grants from The Innovative Medicines Initiative Joint Undertaking under Grant Agreement no 115770, resources of which are composed of financial contribution from the European Union’s Seventh Framework Programme (FP7/2007-2013) and EFPIA companies’ in kind contribution, during the conduct of the study; MPJ has nothing to disclose; PMJW has nothing to disclose. MK reports grants from IMI-APPROACH, grants from Dutch Arthritis Association, during the conduct of the study; other from GlaxoSmithKline, Pfizer, Merck-Serono, Kiniksa, Abbvie, outside the submitted work; ML reports grants from Inovative Medicines Initative, during the conduct of the study; FJB reports grants from Gebro Pharma, grants from BIOIBERICA, grants from AB Science, grants from Abbvie, grants from Ablynx N.V., grants from Amgen, grants from Archigen Biotech, grants from Boehringer, grants from Bristol-Myers, grants from Celgene Int., grants from Eli Lilly and Company, grants from F. Hoffmann- La Roche, grants from Galapagos, grants from Gedeon, grants from Genentech, grants from Gideal Sciences, NC, grants from Glaxosmithkline, grants from Hospira, grants from INC Research UK, grants from Inventiv Health Clinical, grants from Janssen, grants from Lilly, grants from Nichi-IKO Pharmaceutical, grants from Novartis, grants from ONO Pharma, grants from Pfizer, grants from Pharmaceutical Research, grants from Regeneron, grants from Roche, grants from SA UCB Pharma, grants from Sanofi, grants from TRB Chemedica, grants from UCB Biosciences GMBH, outside the submitted work; In addition, FJB has a patent Molecular block-matching method for gel image analysis issued, a patent Targeting A Specific Receptor On Cells With A Specific Compound For Use In The Treatment And/Or The Prevention Of Osteoarthritis And Rheumatoid Arthritis pending, a patent Genetic markers for osteoarthritis issued, a patent Method for the diagnosis of osteoarthritis issued, a patent Genetic markers for osteoarthritis pending, a patent Method for the diagnosing Arthrosis pending, a patent Method for diagnosing Arthrosis pending, a patent Method for the diagnosis of osteoarthritis pending, and a patent Anti-connexin compounds for use in the prevention and/or treatment of degenerative joint diseases. pending; IKH reports personal fees from AbbVie, grants from Pfizer, outside the submitted work; FB reports personal fees from Boehringer, Bone Therapeutics, Expanscience, Galapagos, Gilead, GSK, Merck Sereno, MSD, Nordic, Novartis, Pfizer, Regulaxis, Roche, Sandoz, Sanofi, Servier, UCB, Peptinov, TRB Chemedica, 4P Pharma, outside the submitted work; CHL reports other from Merck KGaA, during the conduct of the study; JLo has nothing to disclose; ACB-J reports non-financial support from Nordic Bioscience, personal fees from Nordic Bioscience, during the conduct of the study; AM has nothing to disclose; JLa reports personal fees and other from GlaxoSmithKline, outside the submitted work; and Current employee and shareholder of GlaxoSmithKline; JBo reports grants from Innovative Medicines Initiative (IMI-1), during the conduct of the study; and one of Lygature's other project receives part of its funding directly from Merck KgaA. This project is in the field of schistosomiasis and has no relationship whatsoever with the APPROACH project; HHW has nothing to disclose; ACAM has nothing to disclose; FPJGL has nothing to disclose.

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Auteurs

Eefje M van Helvoort (EM)

Rheumatology and Clinical Immunology, UMC Utrecht, Utrecht, The Netherlands E.M.vanHelvoort-3@umcutrecht.nl.

Willem E van Spil (WE)

Rheumatology and Clinical Immunology, UMC Utrecht, Utrecht, The Netherlands.

Mylène P Jansen (MP)

Rheumatology and Clinical Immunology, UMC Utrecht, Utrecht, The Netherlands.

Paco M J Welsing (PMJ)

Rheumatology and Clinical Immunology, UMC Utrecht, Utrecht, The Netherlands.

Margreet Kloppenburg (M)

Clinical Epidemiology, Leiden University Medical Center, Leiden, The Netherlands.
Rheumatology, Leiden Universitair Medisch Centrum, Leiden, The Netherlands.

Marieke Loef (M)

Rheumatology, Leiden Universitair Medisch Centrum, Leiden, The Netherlands.

Francisco J Blanco (FJ)

Servicio de Reumatologia, INIBIC-Hospital Universitario A Coruña, A Coruña, Spain.

Ida K Haugen (IK)

Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.

Francis Berenbaum (F)

Rheumatology, Sorbonne Université, Paris, France.

Jaume Bacardit (J)

School of Computing Science, Newcastle University, Newcastle upon Tyne, Tyne and Wear, UK.

Christoph H Ladel (CH)

Merck Serono Research, Merck KGaA, Darmstadt, Germany.

John Loughlin (J)

Musculoskeletal Research Group, Newcastle University, Newcastle upon Tyne, Tyne and Wear, UK.

Anne C Bay-Jensen (AC)

Biomarkers and Research, Nordic Bioscience, Herlev, Denmark.

Ali Mobasheri (A)

Regenarative Medicine, State Research Institute Center of Innovative Medicine, Vilnius, Lithuania.

Jonathan Larkin (J)

GlaxoSmithKline USA, Philadelphia, Pennsylvania, USA.

Janneke Boere (J)

Lygature, Utrecht, The Netherlands.

Harrie H Weinans (HH)

Rheumatology and Clinical Immunology, UMC Utrecht, Utrecht, The Netherlands.
Orthopaedics, Erasmus University Medical Center, Rotterdam, The Netherlands.

Agnes Lalande (A)

Institut de Recherches Internationales Servier, Suresnes, France.

Anne C A Marijnissen (ACA)

Rheumatology and Clinical Immunology, UMC Utrecht, Utrecht, The Netherlands.

Floris P J G Lafeber (FPJG)

Rheumatology and Clinical Immunology, UMC Utrecht, Utrecht, The Netherlands.

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