Evidence map›Paper›PMID 31680207›Full record

ReviewRheumatology international2020

Biologic therapy in the idiopathic inflammatory myopathies.

Thomas Khoo, Vidya Limaye

Abstract readReview
PubMed Publisher
In one paragraph

Review in Rheumatology international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. [Dermatomyositis and juvenile dermatomyositis].Zeitschrift fur Rheumatologie · 2023
    Review
  7. Article
  8. Juvenile Dermatomyositis: New Clues to Diagnosis and Therapy.Current treatment options in rheumatology · 2021
    Article
  9. Article
  10. 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

2 authors at 2 institutions in 1 country.

Thomas KhooCentral Adelaide Local Health Network, Adelaide, Australia.ORCID http://orcid.org/0000-0003-1122-3384
Vidya LimayeRheumatology Unit, Royal Adelaide Hospital, Adelaide, Australia. vidya.limaye@sa.gov.au.ORCID http://orcid.org/0000-0002-8142-9532
Royal Adelaide Hospital · AUWomen's and Children's Health Network · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The idiopathic inflammatory myopathies (IIM) are a group of autoimmune diseases resulting from inflammation of muscle and manifesting as weakness, though a range of extra-muscular manifestations are observed. These are often correlated closely with disease subtype and the presence of myositis-specific/myositis-associated antibodies. IIM are notoriously difficult to treat and often refractory to glucocorticoid therapy and synthetic immunosuppressants. Both the innate and adaptive immune systems are implicated in the pathogenesis of IIM. A growing understanding of the key cytokines as well as the cell-mediated and antibody effectors of disease has identified multiple potential targets for biologic therapy. The most widely used of these is B-cell depletion via rituximab though the tumour necrosis factor inhibitors and other biologic therapies used in diseases such as rheumatoid arthritis, systemic lupus erythematosus and multiple sclerosis have also been trialled. This review summarises the literature thus far on biologic therapy in IIM, highlighting both the significant trials that influence current treatment regimens and also the continuing need for further research to inform more effective therapies.

Indexed as

AbataceptAlemtuzumabAntibodies, Monoclonal, HumanizedAntirheumatic AgentsBasiliximabBiological ProductsDermatomyositisHumansImmunologic FactorsImmunosuppressive AgentsMyositisMyositis, Inclusion BodyPolymyositisRituximabTumor Necrosis Factor InhibitorsAbataceptAlemtuzumabAntibodies, Monoclonal, HumanizedAntirheumatic AgentsBasiliximabBiological ProductsImmunologic FactorsImmunosuppressive AgentsRituximabsifalimumabtocilizumabTumor Necrosis Factor InhibitorsBiologicsEtanerceptIdiopathic inflammatory myopathiesInfliximabRituximab

Identifiers

PMID31680207
OpenAlexW2989003994

What OpenQuestion holds

Textmetadata
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.