Evidence map›Paper›PMID 30878974›Full record

ArticleAnnals of the rheumatic diseases2019

Synovial cellular and molecular signatures stratify clinical response to csDMARD therapy and predict radiographic progression in early rheumatoid arthritis patients.

Frances Humby, Myles Lewis, Nandhini Ramamoorthi, Jason A Hackney, Michael R Barnes, Michele Bombardieri, A Francesca Setiadi, Stephen Kelly, Fabiola Bene, Maria DiCicco and 15 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Annals of the rheumatic diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 177 papers.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed
28.2field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

177 citing papers in PubMed, 312 citations in OpenAlex.

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117 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 8 institutions in 4 countries.

Frances Humby *Centre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.ORCID 0000-0003-1280-9133
Myles Lewis *Centre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.ORCID 0000-0001-9365-5345
Nandhini Ramamoorthi *Biomarker Discovery OMNI, Genentech Inc, South San Francisco, California, USA.
Jason A Hackney *Bioinformatics and Computational Biology, Genentech Inc, South San Francisco, California, USA.
Michael R BarnesCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Michele BombardieriCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
A Francesca SetiadiBiomarker Discovery OMNI, Genentech Inc, South San Francisco, California, USA.
Stephen KellyCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Fabiola BeneCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Maria DiCiccoCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Sudeh RiahiCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Vidalba RocherCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Nora NgCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Ilias LazarouCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Rebecca HandsCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK.
Désirée van der HeijdeDepartment of Rheumatology, Leiden University Medical Center, Leiden, Netherlands.ORCID 0000-0002-5781-158X
Robert B M LandewéAmsterdam Rheumatology Center, AMC, Amsterdam, Netherlands.
Annette van der Helm-van MilDepartment of Rheumatology, Leiden University Medical Center, Leiden, Netherlands.
Alberto CauliUniversita degli Studi di Cagliari, Cagliari, Italy.
Iain McInnesInstitute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Christopher Dominic BuckleyUniversity of Birmingham, Birmingham, UK.
Ernest H ChoyInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.
Peter C TaylorNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Kennedy Institute of Rheumatology, Oxford, UK.ORCID 0000-0001-7766-6167
Michael J TownsendBiomarker Discovery OMNI, Genentech Inc, South San Francisco, California, USA c.pitzalis@qmul.ac.uk townsend.michael@gene.com.
Costantino PitzalisCentre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Barts & The London School of Medicine & Dentistry, Queen Mary University of London, London, UK c.pitzalis@qmul.ac.uk townsend.michael@gene.com.ORCID 0000-0003-1326-5051
Queen Mary University of London · GBLeiden University Medical Center · NLCardiff University · GBGene Therapy Laboratory · FRUniversity of Birmingham · GBUniversity of Cagliari · ITUniversity of Glasgow · GBZuyderland Medisch Centrum · NL

Funding

Arthritis Research UK 20670Medical Research Council G0800648Medical Research Council MR/K015346/1
6 · The paper itself

Abstract

objectivesTo unravel the hierarchy of cellular/molecular pathways in the disease tissue of early, treatment-naïve rheumatoid arthritis (RA) patients and determine their relationship with clinical phenotypes and treatment response/outcomes longitudinally.

methods144 consecutive treatment-naïve early RA patients (<12 months symptoms duration) underwent ultrasound-guided synovial biopsy before and 6 months after disease-modifying antirheumatic drug (DMARD) initiation. Synovial biopsies were analysed for cellular (immunohistology) and molecular (NanoString) characteristics and results compared with clinical and imaging outcomes. Differential gene expression analysis and logistic regression were applied to define variables correlating with treatment response and predicting radiographic progression.

resultsCellular and molecular analyses of synovial tissue demonstrated for the first time in early RA the presence of three pathology groups: (1)

conclusionsWe demonstrate at disease presentation, prior to pathology modulation by therapy, the presence of specific cellular/molecular synovial signatures that delineate disease severity/progression and therapeutic response and may pave the way to more precise definition of RA taxonomy, therapeutic targeting and improved outcomes.

Indexed as

AdultAgedAntirheumatic AgentsArthritis, RheumatoidBiomarkersBiopsyDisease ProgressionFemaleGene Expression RegulationHumansLongitudinal StudiesMaleMiddle AgedPhenotypePrognosisRadiographyAntirheumatic AgentsBiomarkersdmards (synthetic)early rheumatoid arthritisinflammationsynovitis

Identifiers

PMID30878974
PMCPMC6579551
OpenAlexW2920823803

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.