Evidence map›Paper›PMID 39175060›Full record

ReviewAdvances in rheumatology (London, England)2024

Inflammatory turmoil within: an exploration of autoinflammatory disease genetic underpinnings, clinical presentations, and therapeutic approaches.

Kátia Tomie Kozu, Renan Rodrigues Neves Ribeiro do Nascimento, Patrícia Pontes Aires, Rafael Alves Cordeiro, Thais Costa Lima de Moura, Flavio Roberto Sztajnbok, Ivanio Alves Pereira, Adriana Almeida de Jesus, Sandro Félix Perazzio

Abstract readReview
In one paragraph

Review in Advances in rheumatology (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. 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

9 authors.

Kátia Tomie Kozu *Universidade de Sao Paulo, Faculdade de Medicina (USP FM), Sao Paulo, Brazil.ORCID 0000-0001-8743-7827
Renan Rodrigues Neves Ribeiro do Nascimento *Universidade Federal de Sao Paulo, Escola Paulista de Medicina (Unifesp EPM), Rua Otonis, 863, Vila Clementino, São Paulo, SP, 04025-002, Brazil.ORCID 0000-0002-2638-0086
Patrícia Pontes AiresUniversidade Federal de Sao Paulo, Escola Paulista de Medicina (Unifesp EPM), Rua Otonis, 863, Vila Clementino, São Paulo, SP, 04025-002, Brazil.ORCID 0000-0002-1961-7268
Rafael Alves CordeiroUniversidade de Sao Paulo, Faculdade de Medicina (USP FM), Sao Paulo, Brazil.ORCID 0000-0002-5695-9136
Thais Costa Lima de MouraUniversidade de Sao Paulo, Faculdade de Medicina (USP FM), Sao Paulo, Brazil.ORCID 0009-0004-4103-9929
Flavio Roberto SztajnbokFederal University of Rio de Janeiro: Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0002-7301-9664
Ivanio Alves PereiraUniversidade do Sul de Santa Catarina (Unisul), Florianópolis, Brazil.ORCID 0000-0002-3910-4988
Adriana Almeida de JesusNational Institutes of Health (NIH), Bethesda, USA.ORCID 0000-0001-8966-8362
Sandro Félix PerazzioUniversidade de Sao Paulo, Faculdade de Medicina (USP FM), Sao Paulo, Brazil. sperazzio@unifesp.br.ORCID 0000-0003-1203-8287

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic autoinflammatory diseases (SAIDs) arise from dysregulated innate immune system activity, which leads to systemic inflammation. These disorders, encompassing a diverse array of genetic defects classified as inborn errors of immunity, are significant diagnostic challenges due to their genetic heterogeneity and varied clinical presentations. Although recent advances in genetic sequencing have facilitated pathogenic gene discovery, approximately 40% of SAIDs patients lack molecular diagnoses. SAIDs have distinct clinical phenotypes, and targeted therapeutic approaches are needed. This review aims to underscore the complexity and clinical significance of SAIDs, focusing on prototypical disorders grouped according to their pathophysiology as follows: (i) inflammasomopathies, characterized by excessive activation of inflammasomes, which induces notable IL-1β release; (ii) relopathies, which are monogenic disorders characterized by dysregulation within the NF-κB signaling pathway; (iii) IL-18/IL-36 signaling pathway defect-induced SAIDs, autoinflammatory conditions defined by a dysregulated balance of IL-18/IL-36 cytokine signaling, leading to uncontrolled inflammation and tissue damage, mainly in the skin; (iv) type I interferonopathies, a diverse group of disorders characterized by uncontrolled production of type I interferons (IFNs), notably interferon α, β, and ε; (v) anti-inflammatory signaling pathway impairment-induced SAIDs, a spectrum of conditions characterized by IL-10 and TGFβ anti-inflammatory pathway disruption; and (vi) miscellaneous and polygenic SAIDs. The latter group includes VEXAS syndrome, chronic recurrent multifocal osteomyelitis/chronic nonbacterial osteomyelitis, Schnitzler syndrome, and Still's disease, among others, illustrating the heterogeneity of SAIDs and the difficulty in creating a comprehensive classification. Therapeutic strategies involving targeted agents, such as JAK inhibitors, IL-1 blockers, and TNF inhibitors, are tailored to the specific disease phenotypes.

Indexed as

Hereditary Autoinflammatory DiseasesAnemia, Dyserythropoietic, CongenitalHumansImmunologic Deficiency SyndromesInflammasomesInflammationInterleukin-18Interleukin-1betaMevalonate Kinase DeficiencyNF-kappa BOsteomyelitisSchnitzler SyndromeSignal TransductionInflammasomesInterleukin-18Interleukin-1betaNF-kappa BAnti-inflammatory signaling pathway impairmentAutoinflammatory diseasesIL-18/IL-36 signaling pathway defectsInflammasomopathiesMonogenicRelopathiesType I interferonopathies

Identifiers

PMID39175060
PMCPMC13488669

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.