Evidence map›Paper›PMID 37475055›Full record

ArticlePediatric rheumatology online journal2023

How common is remission in rheumatoid factor-positive juvenile idiopathic arthritis patients? The multicenter Pediatric Rheumatology Academy (PeRA) research group experience.

Semanur Ozdel, Hafize Emine Sönmez, Şengül Çağlayan, Özlem Akgün, Tuncay Aydın, Özge Baba, İlknur Bağrul, Gülçin Otar Yener, Kübra Öztürk, Ferhat Demir and 11 more

Abstract readMulticenter Study
In one paragraph

Article in Pediatric rheumatology online journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
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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

21 authors.

Semanur OzdelDepartment of Pediatric Rheumatology, Dr Sami Ulus Maternity and Child Health and Diseases Training and Research Hospital, Ankara, Turkey. semanurozdel@gmail.com.ORCID http://orcid.org/0000-0001-5602-4595
Hafize Emine SönmezDepartment of Pediatric Rheumatology, Faculty of Medicine, Kocaeli University, Kocaeli, Turkey.
Şengül ÇağlayanDepartment of Pediatric Rheumatology, University of Health Sciences, Umraniye Research and Training Hospital, Istanbul, Turkey.
Özlem AkgünDepartment of Pediatric Rheumatology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Tuncay AydınDepartment of Pediatric Rheumatology, Faculty of Medicine, Dokuz Eylül University, Izmir, Turkey.
Özge BabaDepartment of Pediatric Rheumatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
İlknur BağrulDepartment of Pediatric Rheumatology, Dr Sami Ulus Maternity and Child Health and Diseases Training and Research Hospital, Ankara, Turkey.
Gülçin Otar YenerDepartment of Pediatric Rheumatology, Medicalpark Hospital, Gaziantep, Turkey.
Kübra ÖztürkDepartment of Pediatric Rheumatology, Istanbul Medeniyet University, Göztepe Prof. Dr. Süleyman Yalçın City Hospital, Istanbul, Turkey.
Ferhat DemirDepartment of Pediatric Rheumatology, Acıbadem Healthcare Group, Istanbul, Turkey.
Deniz Gezgin YıldırımDepartment of Pediatric Rheumatology, Gazi University Faculty of Medicine, Ankara, Turkey.
Şerife Gül KaradağDepartment of Pediatric Rheumatology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Esra BağlanDepartment of Pediatric Rheumatology, Dr Sami Ulus Maternity and Child Health and Diseases Training and Research Hospital, Ankara, Turkey.
Mustafa ÇakanDepartment of Pediatric Rheumatology, University of Health Sciences, Umraniye Research and Training Hospital, Istanbul, Turkey.
Mukaddes KalyoncuDepartment of Pediatric Rheumatology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Balahan Bora MakayDepartment of Pediatric Rheumatology, Faculty of Medicine, Dokuz Eylül University, Izmir, Turkey.
Şevket Erbil ÜnsalDepartment of Pediatric Rheumatology, Faculty of Medicine, Dokuz Eylül University, Izmir, Turkey.
Sevcan BakkaloğluDepartment of Pediatric Rheumatology, Gazi University Faculty of Medicine, Ankara, Turkey.
Mehmet BülbülDepartment of Pediatric Rheumatology, Dr Sami Ulus Maternity and Child Health and Diseases Training and Research Hospital, Ankara, Turkey.
Betül SözeriDepartment of Pediatric Rheumatology, University of Health Sciences, Umraniye Research and Training Hospital, Istanbul, Turkey.
Nuray Aktay AyazDepartment of Pediatric Rheumatology, Faculty of Medicine, Istanbul University, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveRheumatoid factor (RF)-positive polyarthritis is the least common type of juvenile idiopathic arthritis (JIA). Functional disability in RF-positive polyarthritis patients is much more severe than in patients with other subtypes; but data on this subtype alone is limited. This study aimed to analyze clinical features, long-term follow-up, treatment response, and remission status in a large multicenter cohort of RF-positive polyarthritis patients.

methodsThis retrospective study included RF-positive polyarthritis patients that were followed up for ≥ 6 months between 2017 and 2022 by the Pediatric Rheumatology Academy (PeRA)-Research Group (RG). Data on patient demographics, clinical and laboratory characteristics were obtained from medical charts. JIA treatments and duration of treatment were also recorded. The patients were divided into 2 groups based on methotrexate (MTX) response, as follows: group 1: MTX responsive, group 2: MTX unresponsive. Clinical and laboratory findings were compared between the 2 groups.

resultsThe study included 56 (45 female and 11 male) patients. The median age at onset of RF-positive polyarthritis was 13.2 years [(interquartile range) (IQR): 9.0-15.0 years] and the median duration of follow-up was 41.5 months (IQR: 19.5-75.7 months). Symmetrical arthritis affecting the metacarpophalangeal and proximal interphalangeal joints of the hands was commonly observed. Subcutaneous MTX was the preferred initial treatment; however, it was ineffective in 39 (69.6%) of the patients. Of 25 patients followed for 24 months, 56% still had active disease at 24 months.

conclusionDuring 2 years of treatment, 44% of RF-positive polyarthritis patients have inactive disease, and they should be considered as a distinct and important clinical entity requiring aggressive and early treatment.

Indexed as

Arthritis, JuvenileRheumatologyAdolescentChildFemaleHumansMaleMethotrexateRetrospective StudiesRheumatoid FactorMethotrexateRheumatoid FactorArthritisIdiopathicJuvenileRheumatoid factor

Identifiers

PMID37475055
PMCPMC10360344

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