Evidence map›Paper›PMID 41291866›Full record

ReviewAdvances in rheumatology (London, England)2025

VII Brazilian Consensus guidelines for the detection and interpretation of anti-cell autoantibodies on HEp-2 cells.

Wilson de Melo Cruvinel, Paulo Luiz Carvalho Francescantônio, Wilton Ferreira Silva Santos, Fabiano de Almeida Brito, Sandra Gofinet Pasoto, Andressa Mathias, Carlos David Araújo Bichara, Diana Landoni, Trischna Martins Berger, Eliane Aparecida Rosseto Welter and 8 more

Abstract readConsensus StatementReview
In one paragraph

Review in Advances in rheumatology (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Wilson de Melo CruvinelPontifícia Universidade Católica de Goiás - School of Medical and Life Sciences, Avenida Universitária 1.440, Setor Universitário, Goiânia, GO, CEP: 74605-010, Brazil. melocruvinel@gmail.com.
Paulo Luiz Carvalho FrancescantônioPontifícia Universidade Católica de Goiás - School of Medical and Life Sciences, Avenida Universitária 1.440, Setor Universitário, Goiânia, GO, CEP: 74605-010, Brazil.
Wilton Ferreira Silva SantosEscola Superior de Ciências da Saúde do Distrito Federal (ESCS), Laboratório Sabin, Brasília, Brazil.
Fabiano de Almeida BritoUniversidade Federal de Minas Gerais, Department of Clinical Pathology, School of Medicine, Belo Horizonte, Brazil.
Sandra Gofinet PasotoReumatologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Andressa MathiasFleury Medicine and Health Laboratory, Immunology Division, São Paulo, Brazil.
Carlos David Araújo BicharaCentro Universitário Fibra, Amaral Costa Medicina Diagnóstica, Belém, Brazil.
Diana LandoniRheumatology Division, Department of Medicine, Federal University of São Paulo, São Paulo, Brazil.
Trischna Martins BergerRheumatology Division, Department of Medicine, Federal University of São Paulo, São Paulo, Brazil.
Eliane Aparecida Rosseto WelterDepartamento de Patologia Clínica e Anatomia Patológica, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Cristóvão Luis Pitangueira MangueiraFaculdade Israelita de Ciências da Saúde, Sociedade Beneficente Israelita Brasileira Hospital Albert Einstein, São Paulo, Brazil.
Eloisa BonfáReumatologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
Henrique Ataíde MarizRheumatology Department, Federal University of Pernambuco, Recife, Brazil.
Jozelia RegoFaculdade de Medicina, Universidade Federal de Goiás, Goiânia, Brazil.
Lisiane Maria Enriconi Dos AnjosUniversidade do Sul de Santa Catarina, Tubarão, Brazil.
Valeria ValimUniversidade Federal do Espírito Santo, Hospital Universitário Cassiano Antônio Moraes (HUCAM), Vitória, Brazil.
Antônio Carlos XimenesHospital Geral de Goiânia Alberto Rassi (HGG), Goiânia, Brazil.
Luis Eduardo Coelho AndradeFleury Medicine and Health Laboratory, Immunology Division, São Paulo, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303116/2022-6Conselho Nacional de Desenvolvimento Científico e Tecnológico 305242/2019-9
6 · The paper itself

Abstract

backgroundThe VII Brazilian Consensus on Autoantibodies against HEp-2 Cells (BCA/HEp-2), dedicated to the identification of autoantibodies targeting cellular constituents in HEp-2 cells, was held on October 5–6, 2023, in Goiânia (GO, Brazil), as part of the 40th Brazilian Congress of Rheumatology. MAIN BODY: Nineteen researchers and experts from universities and clinical laboratories participated in this meeting, which resulted in important advancements. Among the key updates, two new nuclear patterns were incorporated into the Brazilian classification tree: the nuclear fine speckled with mitotic plate (AC-30) and the myriad discrete speckled pattern strongly associated with antibodies to SS-A/Ro60, previously categorized as AC-4a and now recognized as AC-31. Additionally, the mitotic pattern AC-28 (mitotic chromosomal), characterized by punctate staining of chromosomes in pro- and metaphase stages without interphase cell staining, was included. Adjustments to the classification tree were made to redistribute patterns based on morphological characteristics, harmonize composite pattern designations with ICAP nomenclature, and incorporate the AC-XX group into the classification structure. Guidance was also provided to laboratory analysts on the limitations of identifying patterns with weak reactivity, recommending that reports in such cases be issued according to the appropriate level of analytical competency.

conclusionThe recommendations aimed to establish clear guidelines for laboratories and clinicians, building upon those from the V and VI Consensuses while further aligning with ICAP recommendations. This consensus marks a significant step forward in adapting ICAP guidelines to the Brazilian context, refining the classification tree and addressing practical challenges faced by the scientific and clinical community.

Indexed as

AutoantibodiesBrazilHumansAutoantibodies

Identifiers

PMID41291866
PMCPMC13488776

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.