Evidence map›Paper›PMID 31209708›Full record

ArticleClinical rheumatology2019

Disease presentation of 1312 childhood-onset systemic lupus erythematosus: influence of ethnicity.

Fernanda J Fiorot, Aline G Islabão, Rosa M Pereira, Maria T Terreri, Claudia Saad-Magalhães, Glaucia V Novak, Beatriz C Molinari, Ana P Sakamoto, Nadia E Aikawa, Lucia M Campos and 25 more

Open access · greenAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Clinical rheumatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Lupus Nephritis in Children: Novel Perspectives.Medicina (Kaunas, Lithuania) · 2023
    Review
  7. Recent advances in immunotherapies for lupus nephritis.Pediatric nephrology (Berlin, Germany) · 2023
    Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. The Roles of Orphan G Protein-Coupled Receptors in Autoimmune Diseases.Clinical reviews in allergy & immunology · 2021
    Review
  13. Review
  14. 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

35 authors at 15 institutions in 1 country.

Fernanda J FiorotPediatric Rheumatology Unit, Children's Institute, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Av. Dr. Eneas Carvalho Aguiar, 647 - Cerqueira César, Sao Paulo, SP, 05403-000, Brazil.
Aline G IslabãoPediatric Rheumatology Unit, Hospital Jose Alencar, Brasilia, Brazil.
Rosa M PereiraDivision of Rheumatology Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil.
Maria T TerreriPediatric Rheumatology Unit, Universidade Federal de Sao Paulo, Sao Paulo, Brazil.
Claudia Saad-MagalhãesPediatric Rheumatology Division, Sao Paulo State University (UNESP), Botucatu, Brazil.
Glaucia V NovakPediatric Rheumatology Unit, Children's Institute, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Av. Dr. Eneas Carvalho Aguiar, 647 - Cerqueira César, Sao Paulo, SP, 05403-000, Brazil.
Beatriz C MolinariPediatric Rheumatology Unit, Children's Institute, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Av. Dr. Eneas Carvalho Aguiar, 647 - Cerqueira César, Sao Paulo, SP, 05403-000, Brazil.
Ana P SakamotoPediatric Rheumatology Unit, Universidade Federal de Sao Paulo, Sao Paulo, Brazil.
Nadia E AikawaPediatric Rheumatology Unit, Children's Institute, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Av. Dr. Eneas Carvalho Aguiar, 647 - Cerqueira César, Sao Paulo, SP, 05403-000, Brazil.
Lucia M CamposPediatric Rheumatology Unit, Children's Institute, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Av. Dr. Eneas Carvalho Aguiar, 647 - Cerqueira César, Sao Paulo, SP, 05403-000, Brazil.
Octavio A PeracchiPediatric Rheumatology Unit, Universidade Federal de Sao Paulo, Sao Paulo, Brazil.
Simone AppenzellerPediatric Rheumatology Unit, University of Campinas (UNICAMP), Campinas, Brazil.
Virgínia P FerrianiPediatric Rheumatology Unit, Ribeirao Preto Medical School - University of Sao Paulo, Ribeirão Preto, Brazil.
Marco F SilvaPediatric Rheumatology Unit, Hospital Geral de Fortaleza, Fortaleza, Brazil.
Adriana R FonsecaPediatric Rheumatology Unit, Rio de Janeiro Federal University (IPPMG-UFRJ), Rio de Janeiro, Brazil.
Flávio R SztajnbokPediatric Rheumatology Unit, Pedro Ernesto University Hospital, Rio de Janeiro, Brazil.
Luciana B PaimPediatric Rheumatology Unit, Albert Sabin Children's Hospital, Fortaleza, Brazil.
Melissa M FragaPediatric Rheumatology Unit, Hospital Darcy Vargas, Sao Paulo, Brazil.
Eunice M OkudaPediatric Rheumatology Unit, Irmandade da Santa Casa de Misericórdia de Sao Paulo, Sao Paulo, Brazil.
Blanca E BicaRheumatology Division - Universidade Federal do Rio de Janeiro, Hospital Universitário Clementino Fraga Filho, Rio de Janeiro, Brazil.
Evaldo G SenaPediatric Rheumatology Unit, Lauro Vanderley University Hospital, João Pessoa, Brazil.
Ana J MoraesPediatric Rheumatology Unit, Federal University of Pará, Belém, Brazil.
Ana M RolimPediatric Rheumatology Unit, Obras Sociais Irmã Dulce, Salvador, Brazil.
Paulo F SpellingPediatric Rheumatology Unit, Hospital Evangélico de Curitiba, Curitiba, Brazil.
Iloite M ScheibelPediatric Rheumatology Unit, Hospital Criança Conceição, Porto Alegre, Brazil.
André S CavalcantiPediatric Rheumatology Unit, Federal University of Pernambuco, Recife, Brazil.
Erica N MatosPediatric Rheumatology Unit, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
Teresa C RobazziPediatric Rheumatology Unit, Federal University of Bahia, Salvador, Brazil.
Luciano J GuimarãesPediatric Rheumatology Unit, University of Brasilia, Brasília, Brazil.
Flávia P SantosPediatric Rheumatology Unit, Federal University of Minas Gerais, Belo Horizonte, Brazil.
Valeria C RamosPediatric Rheumatology Unit, Pontifícia Catholic University of Sorocaba, São Paulo, Brazil.
Magda Carneiro-SampaioPediatric Rheumatology Unit, Children's Institute, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Av. Dr. Eneas Carvalho Aguiar, 647 - Cerqueira César, Sao Paulo, SP, 05403-000, Brazil.
Eloisa BonfáDivision of Rheumatology Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Brazil.
Clovis A SilvaPediatric Rheumatology Unit, Children's Institute, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Av. Dr. Eneas Carvalho Aguiar, 647 - Cerqueira César, Sao Paulo, SP, 05403-000, Brazil. clovisaasilva@gmail.com.ORCID http://orcid.org/0000-0001-9250-6508
Brazilian Childhood-onset Systemic Lupus Erythematosus Group
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversidade Federal do Rio de Janeiro · BRHospital Universitário Evangélico de Curitiba · BRUniversidade Federal de Mato Grosso do Sul · BRUniversidade Federal de Minas Gerais · BRUniversidade Federal do Pará · BRClinics Hospital of Ribeirão Preto · BRHospital Infantil Albert Sabin · BRHospital Universitário Pedro Ernesto · BRIrmandade da Santa Casa de Misericórdia de São Paulo · BRUniversidade de São Paulo · BRUniversidade Estadual de Campinas (UNICAMP) · BRUniversidade Estadual Paulista (Unesp) · BRUniversidade Federal da Bahia · BRUniversidade Federal de Pernambuco · BR

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303422/2015-7Fundação de Amparo à Pesquisa do Estado de São Paulo 2015/03756-4
6 · The paper itself

Abstract

objectiveTo evaluate the influence of ethnicity in presentation of childhood-onset systemic lupus erythematosus (cSLE) patients.

methodsThis multicenter study included cSLE patients (American College of Rheumatology criteria) followed in 27 Pediatric Rheumatology services of Brazil. Ethnicities were classified in four groups according to the parents' and all four grandparents' self-reported ethnicity. The statistical analysis was performed using the Bonferroni's correction (p < 0.0027).

resultsAccording to ethnic groups, 1537 cSLE patients were classified in Caucasian (n = 786), African-Latin American (n = 526), Asian (n = 8), and others/unknown (n = 217). Comparisons between 1312 African-Latin American and Caucasian revealed similar median age at cSLE diagnosis [12.2(2.6-18) vs. 12.1(0.3-18) years, p = 0.234], time interval to diagnosis [0.25(0-12) vs. 0.3(0-10) years, p = 0.034], and SLEDAI-2K score [14(0-55) vs. 14(0-63), p = 0.781] in both groups. The mean number of diagnostic criteria according to SLICC (6.47 ± 1.911 vs. 5.81 ± 1.631, p < 0.0001) and frequencies of maculopapular lupus rash (8% vs. 3%, p < 0.0001), palate oral ulcers (17% vs. 11%, p = 0.001), tongue oral ulcers (4% vs. 1%, p = 0.001), and nonscarring alopecia (29% vs. 16%, p < 0.0001) were significantly higher in African-Latin American, whereas malar rash (45% vs. 58%, p < 0.0001) was more frequent in Caucasian. The presence of anti-phospholipid antibody (23% vs. 12%, p < 0.0001), low complement levels (58% vs. 41%, p < 0.0001), and isolated direct Coombs test (10% vs. 5%, p = 0.001) was also significantly higher in the former group.

conclusionsOur study demonstrated that disease presentation severity of African-Latin American cSLE patients is comparable with Caucasian. Mucocutaneous manifestations and autoantibodies profile were the only distinctive features of the former group. The unique mixed background of Brazilian patients probably minimized race diversity spectrum of these patients. Key Points • Our study demonstrated that disease presentation severity of African-Latin American cSLE patients is comparable with Caucasian. • Mucocutaneous manifestations and autoantibodies profile were the only distinctive features of African-Latin American cSLE patients. • African-Latin American cSLE patients had more often anti-phospholipid antibodies and hypocomplementemia. • The unique mixed background of Brazilian patients probably minimized race diversity spectrum of these patients.

Indexed as

AdolescentAge of OnsetAmerican Indian or Alaska NativeAntibodies, AntiphospholipidAsian PeopleBlack PeopleBrazilChildChild, PreschoolEthnicityFemaleHumansInfantLupus Erythematosus, SystemicMaleRetrospective StudiesAntibodies, AntiphospholipidAnti-phospholipid antibodyChildhood-onset systemic lupus erythematosusEthnicityRace

Identifiers

PMID31209708
OpenAlexW2950789411

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.