Evidence map›Paper›PMID 32293539›Full record

ArticleArthritis research & therapy2020

Retrospective analysis of infliximab and adalimumab treatment in a large cohort of juvenile dermatomyositis patients.

Raquel Campanilho-Marques, Claire T Deakin, Stefania Simou, Charalampia Papadopoulou, Lucy R Wedderburn, Clarissa A Pilkington, Juvenile Dermatomyositis Research Group (JDRG)

Open access · goldAbstract read
In one paragraph

Article in Arthritis research & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Targeted Therapy for Idiopathic Inflammatory Myopathy.Journal of cachexia, sarcopenia and muscle · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Calcinosis in dermatomyositis.Current opinion in rheumatology · 2024
    Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Biological Therapies in Inflammatory Myopathies.Rambam Maimonides medical journal · 2023
    Review
  19. Review
  20. Article
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 3 institutions in 1 country.

Raquel Campanilho-MarquesInfection, Inflammation and Rheumatology Section, UCL Great Ormond Street Institute for Child Health, London, UK.
Claire T DeakinInfection, Inflammation and Rheumatology Section, UCL Great Ormond Street Institute for Child Health, London, UK.
Stefania SimouInfection, Inflammation and Rheumatology Section, UCL Great Ormond Street Institute for Child Health, London, UK.
Charalampia PapadopoulouInfection, Inflammation and Rheumatology Section, UCL Great Ormond Street Institute for Child Health, London, UK.
Lucy R WedderburnInfection, Inflammation and Rheumatology Section, UCL Great Ormond Street Institute for Child Health, London, UK.
Clarissa A PilkingtonRheumatology Section, Great Ormond Street Hospital for Children NHS Trust, Level 6 Southwood Building, Great Ormond Street, London, WC1N 3JH, UK. clarissa.pilkington@gosh.nhs.uk.
Juvenile Dermatomyositis Research Group (JDRG)
Great Ormond Street Hospital · GBUniversity College London · GBVersus Arthritis · GB

Funding

Arthritis Research UK 14518Arthritis Research UK 20164Medical Research Council MR/N003322/1Versus Arthritis 21552Wellcome Trust 085860
6 · The paper itself

Abstract

backgroundAnti-TNF treatment may be useful for the treatment of patients with refractory juvenile dermatomyositis (JDM). The aim of this study was to describe the use of infliximab and adalimumab therapy in juvenile dermatomyositis as an adjunctive treatment.

methodsSixty children recruited to the UK JDM Cohort and Biomarker Study that had received at least 3 months of anti-TNF treatment (infliximab or adalimumab) were studied. Childhood Myositis Assessment Scale (CMAS), Manual Muscle Testing (MMT8) and physician's global assessment (PGA) were recorded. Skin disease was assessed using the modified skin disease activity score (DAS). Data were analysed using Friedman's test for repeated measures analysis of variance.

resultsCompared to baseline, there were improvements at 6 and 12 months in skin disease (χ

conclusionReductions in muscle and skin disease, including calcinosis, were seen following treatment with infliximab and adalimumab.

Indexed as

AdalimumabAnti-Inflammatory AgentsCalcinosisChildChild, PreschoolDermatomyositisFemaleHumansInfliximabMaleRetrospective StudiesTreatment OutcomeTumor Necrosis Factor-alphaAdalimumabAnti-Inflammatory AgentsInfliximabTNF protein, humanTumor Necrosis Factor-alphaAdalimumabBiologic therapyInfliximabJuvenile dermatomyositisP rheumatology

Identifiers

PMID32293539
PMCPMC7161150
OpenAlexW3016067653

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.