Evidence map›Paper›PMID 36376976›Full record

ArticlePediatric rheumatology online journal2022

Real-world comparison of the effects of etanercept and adalimumab on well-being in non-systemic juvenile idiopathic arthritis: a propensity score matched cohort study.

Joeri W van Straalen, Sytze de Roock, Gabriella Giancane, Alessandro Consolaro, Marite Rygg, Ellen B Nordal, Nadina Rubio-Pérez, Marija Jelusic, Jaime De Inocencio, Jelena Vojinovic and 5 more

Open access · goldAbstract read
In one paragraph

Article in Pediatric rheumatology online journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
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

15 authors at 10 institutions in 7 countries.

Joeri W van StraalenDepartment of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, P.O. box 85090, 3508 AB, Utrecht, The Netherlands. j.w.vanstraalen-2@umcutrecht.nl.ORCID http://orcid.org/0000-0002-8766-6694
Sytze de RoockDepartment of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, P.O. box 85090, 3508 AB, Utrecht, The Netherlands.
Gabriella GiancaneClinica Pediatrica E Reumatologia, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Alessandro ConsolaroClinica Pediatrica E Reumatologia, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Marite RyggDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Ellen B NordalDepartment of Pediatrics, University Hospital of North Norway, Tromsø, Norway.
Nadina Rubio-PérezDepartamento de Pediatria, Facultad de Medicina, Hospital Universitario "Dr. J. E. González", Universidad Autónoma de Nuevo León, Monterrey, Mexico.
Marija JelusicDepartment of Paediatrics, University of Zagreb School of Medicine, Zagreb, Croatia.
Jaime De InocencioDepartment of Pediatric Rheumatology, University Hospital 12 de Octubre, Madrid, Spain.
Jelena VojinovicDepartment of Pediatric Immunology and Rheumatology, Faculty of Medicine, University of Nis, Nis, Serbia.
Nico M WulffraatDepartment of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, P.O. box 85090, 3508 AB, Utrecht, The Netherlands.
Patricia C J Bruijning-VerhagenJulius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht, the Netherlands.
Nicolino RupertoUOSID Centro Trial, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
Joost F SwartDepartment of Pediatric Immunology and Rheumatology, Wilhelmina Children's Hospital, University Medical Center Utrecht, P.O. box 85090, 3508 AB, Utrecht, The Netherlands.
Paediatric Rheumatology International Trials Organisation (PRINTO)
Istituto Giannina Gaslini · ITUtrecht University · NLNorwegian University of Science and Technology · NOResearch Institute Hospital 12 de Octubre · ESUniversidad Autónoma de Nuevo León · MXUniversity Hospital of North Norway · NOUniversity Medical Center Utrecht · NLUniversity of Applied Sciences Utrecht · NLUniversity of Nis · RSUniversity of Zagreb · HR

Funding

European Union 260353ZonMw PharmachildNL 80-83600-98-21012
6 · The paper itself

Abstract

backgroundEtanercept (ETN) and adalimumab (ADA) are considered equally effective biologicals in the treatment of arthritis in juvenile idiopathic arthritis (JIA) but no studies have compared their impact on patient-reported well-being. The objective of this study was to determine whether ETN and ADA have a differential effect on patient-reported well-being in non-systemic JIA using real-world data.

methodsBiological-naive patients without a history of uveitis were selected from the international Pharmachild registry. Patients starting ETN were matched to patients starting ADA based on propensity score and outcomes were collected at time of therapy initiation and 3-12 months afterwards. Primary outcome at follow-up was the improvement in Juvenile Arthritis Multidimensional Assessment Report (JAMAR) visual analogue scale (VAS) well-being score from baseline. Secondary outcomes at follow-up were decrease in active joint count, adverse events and uveitis events. Outcomes were analyzed using linear and logistic mixed effects models.

resultsOut of 158 eligible patients, 45 ETN starters and 45 ADA starters could be propensity score matched resulting in similar VAS well-being scores at baseline. At follow-up, the median improvement in VAS well-being was 2 (interquartile range (IQR): 0.0 - 4.0) and scores were significantly better (P = 0.01) for ETN starters (median 0.0, IQR: 0.0 - 1.0) compared to ADA starters (median 1.0, IQR: 0.0 - 3.5). The estimated mean difference in VAS well-being improvement from baseline for ETN versus ADA was 0.89 (95% CI: -0.01 - 1.78; P = 0.06). The estimated mean difference in active joint count decrease was -0.36 (95% CI: -1.02 - 0.30; P = 0.28) and odds ratio for adverse events was 0.48 (95% CI: 0.16 -1.44; P = 0.19). One uveitis event was observed in the ETN group.

conclusionsBoth ETN and ADA improve well-being in non-systemic JIA. Our data might indicate a trend towards a slightly stronger effect for ETN, but larger studies are needed to confirm this given the lack of statistical significance.

Indexed as

Antirheumatic AgentsArthritis, JuvenileUveitisAdalimumabCohort StudiesEtanerceptHumansPropensity ScoreTreatment OutcomeAdalimumabAntirheumatic AgentsEtanerceptAdalimumabEpidemiologyEtanerceptJuvenile idiopathic arthritisPatient-reported outcomesPropensity score analysisReal-world data

Identifiers

PMID36376976
PMCPMC9664631
OpenAlexW4308995145

What OpenQuestion holds

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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.