Evidence map›Paper›PMID 35087087›Full record

ReviewNature reviews. Disease primers2022

Juvenile idiopathic arthritis.

Alberto Martini, Daniel J Lovell, Salvatore Albani, Hermine I Brunner, Kimme L Hyrich, Susan D Thompson, Nicolino Ruperto

Registry-linked trialOpen access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Disease primers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06870045 (Investigation of Validity and Reliability of Dynamic Walking Index in Childhood Rheumatic Diseases), which is not on this map. Cited by 175 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
175citing papers in PubMed, 5 pooled it
40.6field-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.

NCT06870045 recruitingnot on this mapstarted 2025, after this paper: background citation

Investigation of Validity and Reliability of Dynamic Walking Index in Childhood Rheumatic Diseases

TypeobservationalSponsorIstanbul University - CerrahpasaRan2025 to 2026Enrolled52ConditionsJuvenile Idiopathic Arthritis, Childhood Rheumatic DiseaseArmsPhysical examination, Dynamic Gait Index
3 · Its place in the literature

Who cites it

175 citing papers in PubMed, 5 syntheses or guidelines pooled it, 267 citations in OpenAlex.

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

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

7 authors at 5 institutions in 4 countries.

Alberto MartiniUniversità degli Studi di Genova, Dipartimento di Neuroscienze, Riabilitazione, Oftalmologia, Genetica e Scienze Materno-Infantili (DiNOGMI), Genova, Italy. albertomartini@gaslini.org.ORCID http://orcid.org/0000-0001-7642-1459
Daniel J LovellCincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, USA.ORCID http://orcid.org/0000-0003-1604-0130
Salvatore AlbaniTranslational Immunology Institute, Duke-NUS Medical School, SingHealth Academic Medical Center, Singapore, Singapore.
Hermine I BrunnerCincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, USA.ORCID http://orcid.org/0000-0001-9478-2987
Kimme L HyrichCentre for Epidemiology Versus Arthritis, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, UK.ORCID http://orcid.org/0000-0001-8242-9262
Susan D ThompsonDepartment of Paediatrics, University of Cincinnati College of Medicine; Center for Autoimmune Genomics and Aetiology, Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.ORCID http://orcid.org/0000-0003-4130-2796
Nicolino RupertoIRCCS Istituto Giannina Gaslini, UOSID Centro trial, Clinica Pediatrica e Reumatologia, PRINTO, Genova, Italy.ORCID http://orcid.org/0000-0001-8407-7782
Cincinnati Children's Hospital Medical Center · USIstituto Giannina Gaslini · ITSingHealth Duke-NUS Academic Medical Centre · SGUniversity of Genoa · ITUniversity of Manchester · GB

Funding

Pediatric musculOskeletal & RheumaTology Innovation COre center (PORTICO)P30AR076316 · NIAMS · CINCINNATI CHILDRENS HOSP MED CTR · PI BRUNNER, HERMINE I · 2019 to 2023
$3.4M
6 · The paper itself

Abstract

Juvenile idiopathic arthritis (JIA) is an umbrella term for arthritis of unknown origin, lasting for >6 weeks with onset before 16 years of age. JIA is the most common chronic inflammatory rheumatic condition of childhood. According to the International League Against Rheumatism (ILAR) classification, seven mutually exclusive categories of JIA exist based on disease manifestations during the first 6 months of disease. Although the ILAR classification has been useful to foster research, it has been criticized mainly as it does not distinguish those forms of chronic arthritis observed in adults and in children from those that may be unique to childhood. Hence, efforts to provide a new evidence-based classification are ongoing. Similar to arthritis observed in adults, pathogenesis involves autoimmune and autoinflammatory mechanisms. The field has witnessed a remarkable improvement in therapeutic possibilities of JIA owing to the availability of new potent drugs and the possibility to perform controlled trials with support from legislative interventions and large networks availability. The goal of drug therapy in JIA is to rapidly reduce disease activity to inactive disease or clinical remission, minimize drug side effects and achieve a quality of life comparable to that of healthy peers. As JIA can influence all aspects of a child's and their family's life, researchers increasingly recognize improvement of health-related quality of life as a key treatment goal.

Indexed as

Arthritis, JuvenileAdultChildHumansQuality of Life

Identifiers

PMID35087087
OpenAlexW4210258356

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.