The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1177/09612033211054397 http://hdl.handle.net/11449/231543 |
Resumo: | Objective: To evaluate if the 2019-European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) criteria at diagnosis of childhood-onset systemic lupus erythematosus (cSLE) are associated with higher rates of early damage scored by Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index (SDI). Methods: This retrospective multicenter study included 670 cSLE patients with ≤5 years of disease duration. All patients fulfilled both 2019-EULAR/ACR and 1997-ACR classification criteria. Total score of 2019-EULAR/ACR criteria and each of its specific domains were assessed at diagnosis as predictors of damage accrual at the last visit, according to the presence of any organ damage (defined by SDI ≥ 1). Results: Median disease duration was 2.8 (IQR 1.8–3.8) years and 200 (29.9%) patients had at least one organ damage (SDI ≥ 1). The most frequent domains were neuropsychiatric (12%), renal (7%), and musculoskeletal (6%). There was a higher frequency of renal (58% vs 43%, p = 0.0004) and neuropsychiatric domain (21% vs 7%, p < 0.0001) of 2019-EULAR/ACR criteria in patients with damage (SDI ≥ 1) compared to those without damage (SDI = 0). Patients scoring renal or neuropsychiatric domains of the 2019-EULAR/ACR criteria at diagnosis were associated with renal damage (odds ratio 9.701, 95% confidence interval 3.773–24.941, p < 0.001) or neuropsychiatric damage (OR 9.480, 95% CI 5.481–16.399, p<0.0001) at latest visit, respectively. cSLE patients with positive anti-dsDNA at diagnosis were also associated with renal damage by the latest visit (OR 2.438, 95% CI 1.114–5.3381, p = 0.021). Constitutional, hematologic, mucocutaneous, serosal, and musculoskeletal domains and specific criteria as well as other immunologic criteria were not associated with damage accrual. Median of SLEDAI-2K was significantly higher in patients with global damage (19.5 (2–51) vs 14 (0–51), p<0.001). 2019-EULAR/ACR score >25 was associated with more overall (SDI ≥ 1) (38% vs 25%, p = 0.0002) and renal damage (11% vs 5%, p = 0.023). Conclusions: The 2019-EULAR/ACR criteria at diagnosis were associated with a higher rate of early damage in cSLE patients, especially for renal and neuropsychiatric damage. Of note, damage was particularly associated with high disease activity at diagnosis and 2019-EULAR/ACR score >25. |
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The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients2019-EULAR/ACR criteriaChildhood systemic lupus erythematosusdisease damageorgan damageSLICC/ACR Damage IndexObjective: To evaluate if the 2019-European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) criteria at diagnosis of childhood-onset systemic lupus erythematosus (cSLE) are associated with higher rates of early damage scored by Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index (SDI). Methods: This retrospective multicenter study included 670 cSLE patients with ≤5 years of disease duration. All patients fulfilled both 2019-EULAR/ACR and 1997-ACR classification criteria. Total score of 2019-EULAR/ACR criteria and each of its specific domains were assessed at diagnosis as predictors of damage accrual at the last visit, according to the presence of any organ damage (defined by SDI ≥ 1). Results: Median disease duration was 2.8 (IQR 1.8–3.8) years and 200 (29.9%) patients had at least one organ damage (SDI ≥ 1). The most frequent domains were neuropsychiatric (12%), renal (7%), and musculoskeletal (6%). There was a higher frequency of renal (58% vs 43%, p = 0.0004) and neuropsychiatric domain (21% vs 7%, p < 0.0001) of 2019-EULAR/ACR criteria in patients with damage (SDI ≥ 1) compared to those without damage (SDI = 0). Patients scoring renal or neuropsychiatric domains of the 2019-EULAR/ACR criteria at diagnosis were associated with renal damage (odds ratio 9.701, 95% confidence interval 3.773–24.941, p < 0.001) or neuropsychiatric damage (OR 9.480, 95% CI 5.481–16.399, p<0.0001) at latest visit, respectively. cSLE patients with positive anti-dsDNA at diagnosis were also associated with renal damage by the latest visit (OR 2.438, 95% CI 1.114–5.3381, p = 0.021). Constitutional, hematologic, mucocutaneous, serosal, and musculoskeletal domains and specific criteria as well as other immunologic criteria were not associated with damage accrual. Median of SLEDAI-2K was significantly higher in patients with global damage (19.5 (2–51) vs 14 (0–51), p<0.001). 2019-EULAR/ACR score >25 was associated with more overall (SDI ≥ 1) (38% vs 25%, p = 0.0002) and renal damage (11% vs 5%, p = 0.023). Conclusions: The 2019-EULAR/ACR criteria at diagnosis were associated with a higher rate of early damage in cSLE patients, especially for renal and neuropsychiatric damage. Of note, damage was particularly associated with high disease activity at diagnosis and 2019-EULAR/ACR score >25.Pediatric Rheumatology Unit Children’s Institute Hospital das Clinicas HCFMUSP Faculdade de Medicina Universidade de Sao PauloDivision of Rheumatology Hospital das Clinicas HCFMUSP Faculdade de Medicina Universidade de Sao PauloPediatric Rheumatology Unit Universidade Federal de Sao PauloPediatric Rheumatology Division Sao Paulo State University (UNESP)Pediatric Rheumatology Unit Janeiro Federal University (IPPMG-UFRJ)Pediatric Rheumatology Unit Hospital da Criança de Brasília Jose AlencarPost-graduation Program in Medical Science and Rheumatology Unit University of BrasiliaPediatric Rheumatology Unit Ribeirao Preto Medical School University of Sao PauloPediatric Rheumatology Unit Hospital Geral de FortalezaPediatric Rheumatology Unit University of Campinas (UNICAMP)Pediatric Rheumatology Unit Pedro Ernesto University HospitalPediatric Rheumatology Unit Irmandade da Santa Casa de Misericórdia de Sao PauloRheumatology Division - Universidade Federal do Rio de Janeiro Hospital Universitário Clementino Fraga FilhoPediatric Rheumatology Unit Federal University of ParáPediatric Rheumatology Unit Federal University of BahiaPediatric Rheumatology Unit Hospital Menino JesusPediatric Rheumatology Unit Federal University of PernambucoPediatric Rheumatology Unit Federal University of Mato Grosso do SulPediatric Rheumatology Division Sao Paulo State University (UNESP)Universidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Universidade Estadual Paulista (UNESP)Universidade Federal do Rio de Janeiro (UFRJ)Hospital da Criança de Brasília Jose AlencarUniversity of BrasiliaHospital Geral de FortalezaUniversidade Estadual de Campinas (UNICAMP)Pedro Ernesto University HospitalIrmandade da Santa Casa de Misericórdia de Sao PauloUniversidade Federal do Pará (UFPA)Universidade Federal da Bahia (UFBA)Hospital Menino JesusUniversidade Federal de Pernambuco (UFPE)Federal University of Mato Grosso do SulPitta, Ana CSilva, Clovis AInsfrán, Carlos EPasoto, Sandra GTrindade, Vitor CNovak, Glaucia VSakamoto, Ana PTerreri, Maria TPereira, Rosa MRMagalhães, Claudia S [UNESP]Fonseca, Adriana RIslabão, Aline GAssad, Ana PLBuscatti, Izabel MElias, Adriana MPiotto, Daniela PFerriani, Virginia PCarvalho, Luciana MRabelo Junior, Carlos NMarini, RobertoSztajnbok, Flavio RSacchetti, Silvana BBica, Blanca EMoraes, Ana JRobazzi, Teresa CLotufo, SimoneCavalcanti, Andre SNaka, Erica NCarneiro-Sampaio, MagdaBonfá, EloisaAikawa, Nadia E2022-04-29T08:46:03Z2022-04-29T08:46:03Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1177/09612033211054397Lupus.1477-09620961-2033http://hdl.handle.net/11449/23154310.1177/096120332110543972-s2.0-85118236557Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengLupusinfo:eu-repo/semantics/openAccess2024-09-30T17:35:27Zoai:repositorio.unesp.br:11449/231543Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-30T17:35:27Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients |
title |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients |
spellingShingle |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients Pitta, Ana C 2019-EULAR/ACR criteria Childhood systemic lupus erythematosus disease damage organ damage SLICC/ACR Damage Index |
title_short |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients |
title_full |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients |
title_fullStr |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients |
title_full_unstemmed |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients |
title_sort |
The new 2019-EULAR/ACR classification criteria specific domains at diagnosis can predict damage accrual in 670 childhood-onset systemic lupus erythematosus patients |
author |
Pitta, Ana C |
author_facet |
Pitta, Ana C Silva, Clovis A Insfrán, Carlos E Pasoto, Sandra G Trindade, Vitor C Novak, Glaucia V Sakamoto, Ana P Terreri, Maria T Pereira, Rosa MR Magalhães, Claudia S [UNESP] Fonseca, Adriana R Islabão, Aline G Assad, Ana PL Buscatti, Izabel M Elias, Adriana M Piotto, Daniela P Ferriani, Virginia P Carvalho, Luciana M Rabelo Junior, Carlos N Marini, Roberto Sztajnbok, Flavio R Sacchetti, Silvana B Bica, Blanca E Moraes, Ana J Robazzi, Teresa C Lotufo, Simone Cavalcanti, Andre S Naka, Erica N Carneiro-Sampaio, Magda Bonfá, Eloisa Aikawa, Nadia E |
author_role |
author |
author2 |
Silva, Clovis A Insfrán, Carlos E Pasoto, Sandra G Trindade, Vitor C Novak, Glaucia V Sakamoto, Ana P Terreri, Maria T Pereira, Rosa MR Magalhães, Claudia S [UNESP] Fonseca, Adriana R Islabão, Aline G Assad, Ana PL Buscatti, Izabel M Elias, Adriana M Piotto, Daniela P Ferriani, Virginia P Carvalho, Luciana M Rabelo Junior, Carlos N Marini, Roberto Sztajnbok, Flavio R Sacchetti, Silvana B Bica, Blanca E Moraes, Ana J Robazzi, Teresa C Lotufo, Simone Cavalcanti, Andre S Naka, Erica N Carneiro-Sampaio, Magda Bonfá, Eloisa Aikawa, Nadia E |
author2_role |
author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) Universidade Federal de São Paulo (UNIFESP) Universidade Estadual Paulista (UNESP) Universidade Federal do Rio de Janeiro (UFRJ) Hospital da Criança de Brasília Jose Alencar University of Brasilia Hospital Geral de Fortaleza Universidade Estadual de Campinas (UNICAMP) Pedro Ernesto University Hospital Irmandade da Santa Casa de Misericórdia de Sao Paulo Universidade Federal do Pará (UFPA) Universidade Federal da Bahia (UFBA) Hospital Menino Jesus Universidade Federal de Pernambuco (UFPE) Federal University of Mato Grosso do Sul |
dc.contributor.author.fl_str_mv |
Pitta, Ana C Silva, Clovis A Insfrán, Carlos E Pasoto, Sandra G Trindade, Vitor C Novak, Glaucia V Sakamoto, Ana P Terreri, Maria T Pereira, Rosa MR Magalhães, Claudia S [UNESP] Fonseca, Adriana R Islabão, Aline G Assad, Ana PL Buscatti, Izabel M Elias, Adriana M Piotto, Daniela P Ferriani, Virginia P Carvalho, Luciana M Rabelo Junior, Carlos N Marini, Roberto Sztajnbok, Flavio R Sacchetti, Silvana B Bica, Blanca E Moraes, Ana J Robazzi, Teresa C Lotufo, Simone Cavalcanti, Andre S Naka, Erica N Carneiro-Sampaio, Magda Bonfá, Eloisa Aikawa, Nadia E |
dc.subject.por.fl_str_mv |
2019-EULAR/ACR criteria Childhood systemic lupus erythematosus disease damage organ damage SLICC/ACR Damage Index |
topic |
2019-EULAR/ACR criteria Childhood systemic lupus erythematosus disease damage organ damage SLICC/ACR Damage Index |
description |
Objective: To evaluate if the 2019-European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) criteria at diagnosis of childhood-onset systemic lupus erythematosus (cSLE) are associated with higher rates of early damage scored by Systemic Lupus International Collaborating Clinics/American College of Rheumatology (SLICC/ACR) Damage Index (SDI). Methods: This retrospective multicenter study included 670 cSLE patients with ≤5 years of disease duration. All patients fulfilled both 2019-EULAR/ACR and 1997-ACR classification criteria. Total score of 2019-EULAR/ACR criteria and each of its specific domains were assessed at diagnosis as predictors of damage accrual at the last visit, according to the presence of any organ damage (defined by SDI ≥ 1). Results: Median disease duration was 2.8 (IQR 1.8–3.8) years and 200 (29.9%) patients had at least one organ damage (SDI ≥ 1). The most frequent domains were neuropsychiatric (12%), renal (7%), and musculoskeletal (6%). There was a higher frequency of renal (58% vs 43%, p = 0.0004) and neuropsychiatric domain (21% vs 7%, p < 0.0001) of 2019-EULAR/ACR criteria in patients with damage (SDI ≥ 1) compared to those without damage (SDI = 0). Patients scoring renal or neuropsychiatric domains of the 2019-EULAR/ACR criteria at diagnosis were associated with renal damage (odds ratio 9.701, 95% confidence interval 3.773–24.941, p < 0.001) or neuropsychiatric damage (OR 9.480, 95% CI 5.481–16.399, p<0.0001) at latest visit, respectively. cSLE patients with positive anti-dsDNA at diagnosis were also associated with renal damage by the latest visit (OR 2.438, 95% CI 1.114–5.3381, p = 0.021). Constitutional, hematologic, mucocutaneous, serosal, and musculoskeletal domains and specific criteria as well as other immunologic criteria were not associated with damage accrual. Median of SLEDAI-2K was significantly higher in patients with global damage (19.5 (2–51) vs 14 (0–51), p<0.001). 2019-EULAR/ACR score >25 was associated with more overall (SDI ≥ 1) (38% vs 25%, p = 0.0002) and renal damage (11% vs 5%, p = 0.023). Conclusions: The 2019-EULAR/ACR criteria at diagnosis were associated with a higher rate of early damage in cSLE patients, especially for renal and neuropsychiatric damage. Of note, damage was particularly associated with high disease activity at diagnosis and 2019-EULAR/ACR score >25. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-01-01 2022-04-29T08:46:03Z 2022-04-29T08:46:03Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1177/09612033211054397 Lupus. 1477-0962 0961-2033 http://hdl.handle.net/11449/231543 10.1177/09612033211054397 2-s2.0-85118236557 |
url |
http://dx.doi.org/10.1177/09612033211054397 http://hdl.handle.net/11449/231543 |
identifier_str_mv |
Lupus. 1477-0962 0961-2033 10.1177/09612033211054397 2-s2.0-85118236557 |
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eng |
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eng |
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Lupus |
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openAccess |
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Universidade Estadual Paulista (UNESP) |
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Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
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