Evidence map›Paper›PMID 34362746›Full record

GuidelineAnnals of the rheumatic diseases2021

EULAR points to consider for conducting clinical trials and observational studies in individuals at risk of rheumatoid arthritis.

Kulveer Mankia, Heidi J Siddle, Andreas Kerschbaumer, Deshire Alpizar Rodriguez, Anca Irinel Catrina, Juan D Cañete, Andrew P Cope, Claire Immediato Daien, Kevin D Deane, Hani El Gabalawy and 10 more

Open access · bronzeAbstract readGuideline
In one paragraph

Guideline in Annals of the rheumatic diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 5 pooled it
8.7field-weighted citation impact, top 2% 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

37 citing papers in PubMed, 5 syntheses or guidelines pooled it, 65 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 17 institutions in 10 countries.

Kulveer MankiaLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK k.s.mankia@leeds.ac.uk.ORCID 0000-0002-7945-6582
Heidi J SiddleLeeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK.ORCID 0000-0002-6015-332X
Andreas KerschbaumerDepartment of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-6685-8873
Deshire Alpizar RodriguezResearch Unit, Mexican College of Rheumatology, Coyoacan, Mexico.ORCID 0000-0002-6930-0517
Anca Irinel CatrinaRheumatology Unit, -, Stockholm, Sweden.
Juan D CañeteDepartment of Rheumatology, Arthritis Unit, Hospital Clinic and IDIBAPS, Barcelona, Spain.ORCID 0000-0003-2606-0573
Andrew P CopeFaculty of Life Sciences and Medicine, Centre for Rheumatic Diseases, King's College London, London, UK.
Claire Immediato DaienDepartment of Rheumatology, CHU de Montpellier, University of Montpellier, PhyMedExp, INSERM, CNRS UMR, Montpellier, France.
Kevin D DeaneDivision of Rheumatology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Hani El GabalawyDepartment of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
Axel FinckhDivision of Rheumatology, University of Geneva, Geneva, Switzerland.ORCID 0000-0002-1210-4347
V Michael HolersDivision of Rheumatology, Department of Medicine, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado, USA.
Marios KoloumasEULAR PARE, Kilchberg, Switzerland.
Francesca OmettoRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Karim RazaCentre for Musculoskeletal Ageing Research and Research into Inflammatory Arthritis, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.ORCID 0000-0003-1570-1232
Condruta ZabalanEULAR PARE, Kilchberg, Switzerland.
Annette van der Helm-van MilDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-8572-1437
Dirkjan van SchaardenburgDepartment of Rheumatology, Academic Medical Center, Amsterdam UMC, Amsterdam, The Netherlands.
Daniel AletahaDepartment of Rheumatology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0003-2108-0030
Paul EmeryLeeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds, UK.ORCID 0000-0002-7429-8482
Medical University of Vienna · ATSanatorium Kilchberg · CHErasmus MC · NLHospital Clínic de Barcelona · ESKing's College London · GBLeeds Teaching Hospitals NHS Trust · GBNIHR Leeds Musculoskeletal Biomedical Research Unit · GBReade · NLSwedish Rheumatism Association · SEUniversité de Montpellier · FRUniversity of Birmingham · GBUniversity of Colorado Anschutz Medical Campus · USUniversity of Colorado Denver · USUniversity of Geneva · CHUniversity of Leeds · GBUniversity of Manitoba · CAUniversity of Padua · IT

Funding

Department of Health ICA-SCL-2018-04-ST2-004Medical Research Council MR/P021220/1
6 · The paper itself

Abstract

backgroundDespite growing interest, there is no guidance or consensus on how to conduct clinical trials and observational studies in populations at risk of rheumatoid arthritis (RA).

methodsAn European League Against Rheumatism (EULAR) task force formulated four research questions to be addressed by systematic literature review (SLR). The SLR results informed consensus statements. One overarching principle, 10 points to consider (PTC) and a research agenda were proposed. Task force members rated their level of agreement (1-10) for each PTC.

resultsEpidemiological and demographic characteristics should be measured in all clinical trials and studies in at-risk individuals. Different at-risk populations, identified according to clinical presentation, were defined: asymptomatic, musculoskeletal symptoms without arthritis and early clinical arthritis. Study end-points should include the development of subclinical inflammation on imaging, clinical arthritis, RA and subsequent achievement of arthritis remission. Risk factors should be assessed at baseline and re-evaluated where appropriate; they include genetic markers and autoantibody profiling and additionally clinical symptoms and subclinical inflammation on imaging in those with symptoms and/or clinical arthritis. Trials should address the effect of the intervention on risk factors, as well as progression to clinical arthritis or RA. In patients with early clinical arthritis, pharmacological intervention has the potential to prevent RA development. Participants' knowledge of their RA risk may inform their decision to participate; information should be provided using an individually tailored approach.

conclusionThese consensus statements provide data-driven guidance for rheumatologists, health professionals and investigators conducting clinical trials and observational studies in individuals at risk of RA.

Indexed as

Asymptomatic DiseasesAntirheumatic AgentsArthritis, RheumatoidClinical Trials as TopicEuropeHumansObservational Studies as TopicRheumatologyRisk FactorsSeverity of Illness IndexSocieties, MedicalAntirheumatic Agentsarthritisautoantibodiesautoimmunityrheumatoid

Identifiers

PMID34362746
PMCPMC8458095
OpenAlexW3190234011

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

None linked

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.