Evidence map›Paper›PMID 32065273›Full record

ArticlePediatric radiology2020

Autoinflammatory diseases in childhood, part 2: polygenic syndromes.

María Navallas, Emilio J Inarejos Clemente, Estíbaliz Iglesias, Mónica Rebollo-Polo, Joan Calzada Hernández, Oscar M Navarro

Abstract read
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In one paragraph

Article in Pediatric radiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 13% 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, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Cutaneous vasculitis in autoinflammatory diseases.The Journal of dermatology · 2024
    Review
  4. Review
  5. New insights on multigenic autoinflammatory diseases.Therapeutic advances in musculoskeletal disease · 2022
    Review
  6. Review
  7. Article
  8. Article
  9. Notch Signaling Regulation in Autoinflammatory Diseases.International journal of molecular sciences · 2020
    Review
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

6 authors at 2 institutions in 2 countries.

María NavallasDepartment of Radiology, Hospital Sant Joan de Déu, Passeig Sant Joan de Déu, 2, 08950 Esplugues de Llobregat, Barcelona, Spain. mnavallas@gmail.com.ORCID 0000-0001-7971-1152
Emilio J Inarejos ClementeDepartment of Radiology, Hospital Sant Joan de Déu, Passeig Sant Joan de Déu, 2, 08950 Esplugues de Llobregat, Barcelona, Spain.
Estíbaliz IglesiasDepartment of Rheumatology, Hospital Sant Joan de Déu, Barcelona, Spain.
Mónica Rebollo-PoloDepartment of Radiology, Hospital Sant Joan de Déu, Passeig Sant Joan de Déu, 2, 08950 Esplugues de Llobregat, Barcelona, Spain.
Joan Calzada HernándezDepartment of Rheumatology, Hospital Sant Joan de Déu, Barcelona, Spain.
Oscar M NavarroDepartment of Medical Imaging, University of Toronto, Toronto, ON, Canada.
Hospital Sant Joan de Déu Barcelona · ESUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoinflammatory diseases are a family of disorders characterized by aberrant stimulation of inflammatory pathways without involvement of antigen-directed autoimmunity. They can be further divided in monogenic and polygenic types. Those without an identified genetic mutation are known as polygenic and include systemic-onset juvenile idiopathic arthritis, idiopathic recurrent acute pericarditis, Behçet syndrome, chronic recurrent multifocal osteomyelitis and inflammatory bowel disease among others. Autoinflammatory diseases are characterized by recurrent flares or persistent systemic inflammation and fever, as well as lymphadenopathy and cutaneous, abdominal, thoracic and articular symptoms. Although these syndromes can mimic infections clinically, the inflammatory lesions in autoinflammatory disorders are aseptic. However, because of their infrequency, varied and nonspecific presentation, and the new genetic identification, diagnosis is usually delayed. In this article, which is Part 2 of a two-part series, the authors review the main polygenic autoinflammatory diseases that can be seen in childhood, with special emphasis wherever applicable on imaging features that may help establish the correct diagnosis. However, the major role of imaging is to delineate organ involvement and disease extent.

Indexed as

AdolescentChildChild, PreschoolDiagnostic ImagingFemaleHereditary Autoinflammatory DiseasesHumansInfantMaleMultifactorial InheritanceSyndromeAcute recurrent pericarditisAutoinflammatory diseasesBehçet syndromeChildrenChronic recurrent multifocal osteomyelitisInflammatory bowel diseaseSystemic-onset juvenile idiopathic arthritis

Identifiers

PMID32065273
OpenAlexW3008620558

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.