Evidence map›Paper›PMID 31806043›Full record

ArticleArthritis research & therapy2019

Validation of prediction models of severe disease course and non-achievement of remission in juvenile idiopathic arthritis: part 1-results of the Canadian model in the Nordic cohort.

Veronika Rypdal, Jaime Guzman, Andrew Henrey, Thomas Loughin, Mia Glerup, Ellen Dalen Arnstad, Kristiina Aalto, Marite Rygg, Susan Nielsen, Troels Herlin and 5 more

Open access · goldAbstract readMulticenter StudyValidation Study
In one paragraph

Article in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 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

15 authors at 7 institutions in 5 countries.

Veronika RypdalDepartment of Pediatrics, University Hospital of North Norway, Tromsø, Norway. veronika.rypdal@unn.no.ORCID 0000-0003-3476-305X
Jaime GuzmanDepartment of Pediatrics, BC Children's Hospital and University of British Columbia, Vancouver, British Columbia, Canada.
Andrew HenreyDepartment of Statistics and Actuarial Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.
Thomas LoughinDepartment of Statistics and Actuarial Sciences, Simon Fraser University, Burnaby, British Columbia, Canada.
Mia GlerupDepartment of Pediatrics, Aarhus University Hospital, Aarhus, Denmark.
Ellen Dalen ArnstadDepartment of Clinical and Molecular Medicine, NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Kristiina AaltoDepartment of Pediatrics, Helsinki University Hospital, University of Helsinki, Helsinki, Finland.
Marite RyggDepartment of Clinical and Molecular Medicine, NTNU - Norwegian University of Science and Technology, Trondheim, Norway.
Susan NielsenDepartment of Pediatrics, Rigshospitalet Copenhagen University Hospital, Copenhagen, Denmark.
Troels HerlinDepartment of Pediatrics, Aarhus University Hospital, Aarhus, Denmark.
Anders FasthDepartment of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Lillemor BerntsonDepartment of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Martin RypdalDepartment of Mathematics and Statistics, UIT - The Arctic University of Norway, Tromsø, Norway.
Ellen NordalDepartment of Pediatrics, University Hospital of North Norway, Tromsø, Norway.
ReACCh-Out and NoSPeR Investigators
University Hospital of North Norway · NOAarhus University Hospital · DKNorwegian University of Science and Technology · NOSimon Fraser University · CAUniversity of Helsinki · FIUppsala University · SEUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundModels to predict disease course and long-term outcome based on clinical characteristics at disease onset may guide early treatment strategies in juvenile idiopathic arthritis (JIA). Before a prediction model can be recommended for use in clinical practice, it needs to be validated in a different cohort than the one used for building the model. The aim of the current study was to validate the predictive performance of the Canadian prediction model developed by Guzman et al. and the Nordic model derived from Rypdal et al. to predict severe disease course and non-achievement of remission in Nordic patients with JIA.

methodsThe Canadian and Nordic multivariable logistic regression models were evaluated in the Nordic JIA cohort for prediction of non-achievement of remission, and the data-driven outcome denoted severe disease course. A total of 440 patients in the Nordic cohort with a baseline visit and an 8-year visit were included. The Canadian prediction model was first externally validated exactly as published. Both the Nordic and Canadian models were subsequently evaluated with repeated fine-tuning of model coefficients in training sets and testing in disjoint validation sets. The predictive performances of the models were assessed with receiver operating characteristic curves and C-indices. A model with a C-index above 0.7 was considered useful for clinical prediction.

resultsThe Canadian prediction model had excellent predictive ability and was comparable in performance to the Nordic model in predicting severe disease course in the Nordic JIA cohort. The Canadian model yielded a C-index of 0.85 (IQR 0.83-0.87) for prediction of severe disease course and a C-index of 0.66 (0.63-0.68) for prediction of non-achievement of remission when applied directly. The median C-indices after fine-tuning were 0.85 (0.80-0.89) and 0.69 (0.65-0.73), respectively. Internal validation of the Nordic model for prediction of severe disease course resulted in a median C-index of 0.90 (0.86-0.92).

conclusionsExternal validation of the Canadian model and internal validation of the Nordic model with severe disease course as outcome confirm their predictive abilities. Our findings suggest that predicting long-term remission is more challenging than predicting severe disease course.

Indexed as

Logistic ModelsPredictive Value of TestsAntirheumatic AgentsArthritis, JuvenileCanadaChildChild, PreschoolFemaleHumansMaleProspective StudiesTreatment OutcomeAntirheumatic AgentsJuvenile idiopathic arthritisOutcome researchPredictionRemissionValidation

Identifiers

PMID31806043
PMCPMC6896283
OpenAlexW2993919743

What OpenQuestion holds

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LicenceCC BY
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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.