Evidence map›Paper›PMID 39334496›Full record

ReviewAdvances in rheumatology (London, England)2024

Rare diseases: What rheumatologists need to know?

Renan Rodrigues Neves Ribeiro do Nascimento, Daniela Gerent Petry Piotto, Eutilia Andrade Medeiros Freire, Fabricio de Souza Neves, Flavio Roberto Sztajnbok, Blanca Elena Rios Gomes Bica, Frederico Augusto Gurgel Pinheiro, Katia Tomie Kozu, Ivanio Alves Pereira, Valderilio Feijo Azevedo and 6 more

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Renan Rodrigues Neves Ribeiro do NascimentoUniversidade Federal de Sao Paulo - Escola Paulista de Medicina, Rua Botucatu, 740, 3º andar, São Paulo, SP, 04023-062, Brazil.
Daniela Gerent Petry PiottoUniversidade Federal de Sao Paulo - Escola Paulista de Medicina, Rua Botucatu, 740, 3º andar, São Paulo, SP, 04023-062, Brazil.
Eutilia Andrade Medeiros FreireParaiba Federal University (Universidade Federal da Paraiba), João Pessoa, Brazil.
Fabricio de Souza NevesFederal University of Santa Catarina (Universidade Federal de Santa Catarina), Florianópolis, Brazil.
Flavio Roberto SztajnbokFederal University of Rio de Janeiro (Universidade Federal do Rio de Janeiro), Rio de Janeiro, Brazil.
Blanca Elena Rios Gomes BicaFederal University of Rio de Janeiro (Universidade Federal do Rio de Janeiro), Rio de Janeiro, Brazil.
Frederico Augusto Gurgel PinheiroUniversidade Federal de Sao Paulo - Escola Paulista de Medicina, Rua Botucatu, 740, 3º andar, São Paulo, SP, 04023-062, Brazil.
Katia Tomie KozuUSP FM (Universidade de Sao Paulo Faculdade de Medicina), Pacaembu, Brazil.
Ivanio Alves PereiraUnisul (Universidade do Sul de Santa Catarina), Tubarão, Brazil.
Valderilio Feijo AzevedoFederal University of Parana (Universidade Federal do Parana), Curitiba, Brazil.
Rafael Alves CordeiroUSP FM (Universidade de Sao Paulo Faculdade de Medicina), Pacaembu, Brazil.
Henrique Ayres Mayrink GiardiniUSP FM (Universidade de Sao Paulo Faculdade de Medicina), Pacaembu, Brazil.
Marco Túlio Muniz FrancoFederal University of Amapá (Universidade Federal do Amapa), Macapá, Brazil.
Margarida de Fátima Fernandes CarvalhoState University of Londrina (Universidade Estadual de Londrina), Londrina, Brazil.
Nilton Salles Rosa-NetoUNISA (Universidade de Santo Amaro), São Paulo, Brazil.
Sandro Félix PerazzioUniversidade Federal de Sao Paulo - Escola Paulista de Medicina, Rua Botucatu, 740, 3º andar, São Paulo, SP, 04023-062, Brazil. sperazzio@yahoo.com.br.ORCID 0000-0003-1203-8287

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the terms "rare diseases" (RD) and "orphan diseases" (OD) are often used interchangeably, specific nuances in definitions should be noted to avoid misconception. RD are characterized by a low prevalence within the population, whereas OD are those inadequately recognized or even neglected by the medical community and drug companies. Despite their rarity, as our ability on discovering novel clinical phenotypes and improving diagnostic tools expand, RD will continue posing a real challenge for rheumatologists. Over the last decade, there has been a growing interest on elucidating mechanisms of rare autoimmune and autoinflammatory rheumatic diseases, allowing a better understanding of the role played by immune dysregulation on granulomatous, histiocytic, and hypereosinophilic disorders, just to name a few. This initiative enabled the rise of innovative targeted therapies for rheumatic RD. In this review, we explore the state-of-the art of rare RD and the critical role played by rheumatologists in healthcare. We also describe the challenges rheumatologists may face in the coming decades.

Indexed as

Rare DiseasesRheumatic DiseasesHumansRheumatologistsRheumatologyOrphan diseasesRare diseasesRheumatic diseases

Identifiers

PMID39334496
PMCPMC13488650

What Socratic 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 Socratic graph.