Collapsing glomerulopathy: a review by the collapsing brazilian consortium

Detalhes bibliográficos
Autor(a) principal: Almeida, Jose Bruno de
Data de Publicação: 2022
Outros Autores: Cutrim, Érico Murilo Monteiro, Neves, Precil Diego Miranda de Meneses, Campos, Marcos Adriano Garcia, Wanderley, Davi Campos, Teixeira Júnior, Antonio Augusto Lima, Muniz, Monique Pereira Rêgo, Ladchumananandasivam, Francisco Rasiah, Gomes, Orlando Vieira, Vasco, Rafael Fernandes Vanderlei, Brito, Dyego José de Araújo, Lages, Joyce Santos, Salgado-Filho, Natalino, Guedes, Felipe Leite, Magalhães, Marcelo, Araújo, Stanley de Almeida, Silva, Gyl Eanes Barros
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRN
Texto Completo: https://repositorio.ufrn.br/handle/123456789/54341
https://doi.org/10.3389/fmed.2022.846173
Resumo: Collapsing glomerulopathy (CG) is a clinicopathologic entity characterized by segmentar or global collapse of the glomerulus and hypertrophy and hyperplasia of podocytes. The Columbia classification of 2004 classified CG as a histological subtype of focal segmental glomerulosclerosis (FSGS). A growing number of studies have demonstrated a high prevalence of CG in many countries, especially among populations with a higher proportion of people with African descent. The present study is a narrative review of articles extracted from PubMed, Medline, and Scielo databases from September 1, 2020 to December 31, 2021. We have focused on populational studies (specially cross-sectional and cohort articles). CG is defined as a podocytopathy with a distinct pathogenesis characterized by strong podocyte proliferative activity. The most significant risk factors for CG include APOL1 gene mutations and infections with human immunodeficiency virus and severe acute respiratory syndrome coronavirus 2. CG typically presents with more severe symptoms and greater renal damage. The prognosis is notably worse than that of other FSGS subtypes
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spelling Almeida, Jose Bruno deCutrim, Érico Murilo MonteiroNeves, Precil Diego Miranda de MenesesCampos, Marcos Adriano GarciaWanderley, Davi CamposTeixeira Júnior, Antonio Augusto LimaMuniz, Monique Pereira RêgoLadchumananandasivam, Francisco RasiahGomes, Orlando VieiraVasco, Rafael Fernandes VanderleiBrito, Dyego José de AraújoLages, Joyce SantosSalgado-Filho, NatalinoGuedes, Felipe LeiteMagalhães, MarceloAraújo, Stanley de AlmeidaSilva, Gyl Eanes Barros2023-08-02T19:00:51Z2023-08-02T19:00:51Z2022ALMEIDA, José Bruno, et. al. Collapsing Glomerulopathy: A Review by the Collapsing Brazilian Consortium. Frontiers In Medicine, v. 9, p. 846173, 2022.DOI: https://doi.org/10.3389/fmed.2022.846173 Disponível em: https://observatorio.fm.usp.br/handle/OPI/48634 Acesso em: 27 jul. 2023https://repositorio.ufrn.br/handle/123456789/54341https://doi.org/10.3389/fmed.2022.846173Frontiers in medicinehttps://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesscollapsing glomerulopathysegmental and focal glomerulosclerosisnephrotic syndrome (NS)renal biopsypodocytesglomerulopathyCollapsing glomerulopathy: a review by the collapsing brazilian consortiuminfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleCollapsing glomerulopathy (CG) is a clinicopathologic entity characterized by segmentar or global collapse of the glomerulus and hypertrophy and hyperplasia of podocytes. The Columbia classification of 2004 classified CG as a histological subtype of focal segmental glomerulosclerosis (FSGS). A growing number of studies have demonstrated a high prevalence of CG in many countries, especially among populations with a higher proportion of people with African descent. The present study is a narrative review of articles extracted from PubMed, Medline, and Scielo databases from September 1, 2020 to December 31, 2021. We have focused on populational studies (specially cross-sectional and cohort articles). CG is defined as a podocytopathy with a distinct pathogenesis characterized by strong podocyte proliferative activity. The most significant risk factors for CG include APOL1 gene mutations and infections with human immunodeficiency virus and severe acute respiratory syndrome coronavirus 2. CG typically presents with more severe symptoms and greater renal damage. The prognosis is notably worse than that of other FSGS subtypesengreponame:Repositório Institucional da UFRNinstname:Universidade Federal do Rio Grande do Norte (UFRN)instacron:UFRNORIGINALCollapsingGlomerulopathyReview_Almeida_2022.PDFCollapsingGlomerulopathyReview_Almeida_2022.PDFapplication/pdf8694614https://repositorio.ufrn.br/bitstream/123456789/54341/1/CollapsingGlomerulopathyReview_Almeida_2022.PDF9f459b75eb34c8fb34f2e10ede7d9466MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81484https://repositorio.ufrn.br/bitstream/123456789/54341/2/license.txte9597aa2854d128fd968be5edc8a28d9MD52123456789/543412023-08-02 16:01:25.531oai:https://repositorio.ufrn.br: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Repositório de PublicaçõesPUBhttp://repositorio.ufrn.br/oai/opendoar:2023-08-02T19:01:25Repositório Institucional da UFRN - Universidade Federal do Rio Grande do Norte (UFRN)false
dc.title.pt_BR.fl_str_mv Collapsing glomerulopathy: a review by the collapsing brazilian consortium
title Collapsing glomerulopathy: a review by the collapsing brazilian consortium
spellingShingle Collapsing glomerulopathy: a review by the collapsing brazilian consortium
Almeida, Jose Bruno de
collapsing glomerulopathy
segmental and focal glomerulosclerosis
nephrotic syndrome (NS)
renal biopsy
podocytes
glomerulopathy
title_short Collapsing glomerulopathy: a review by the collapsing brazilian consortium
title_full Collapsing glomerulopathy: a review by the collapsing brazilian consortium
title_fullStr Collapsing glomerulopathy: a review by the collapsing brazilian consortium
title_full_unstemmed Collapsing glomerulopathy: a review by the collapsing brazilian consortium
title_sort Collapsing glomerulopathy: a review by the collapsing brazilian consortium
author Almeida, Jose Bruno de
author_facet Almeida, Jose Bruno de
Cutrim, Érico Murilo Monteiro
Neves, Precil Diego Miranda de Meneses
Campos, Marcos Adriano Garcia
Wanderley, Davi Campos
Teixeira Júnior, Antonio Augusto Lima
Muniz, Monique Pereira Rêgo
Ladchumananandasivam, Francisco Rasiah
Gomes, Orlando Vieira
Vasco, Rafael Fernandes Vanderlei
Brito, Dyego José de Araújo
Lages, Joyce Santos
Salgado-Filho, Natalino
Guedes, Felipe Leite
Magalhães, Marcelo
Araújo, Stanley de Almeida
Silva, Gyl Eanes Barros
author_role author
author2 Cutrim, Érico Murilo Monteiro
Neves, Precil Diego Miranda de Meneses
Campos, Marcos Adriano Garcia
Wanderley, Davi Campos
Teixeira Júnior, Antonio Augusto Lima
Muniz, Monique Pereira Rêgo
Ladchumananandasivam, Francisco Rasiah
Gomes, Orlando Vieira
Vasco, Rafael Fernandes Vanderlei
Brito, Dyego José de Araújo
Lages, Joyce Santos
Salgado-Filho, Natalino
Guedes, Felipe Leite
Magalhães, Marcelo
Araújo, Stanley de Almeida
Silva, Gyl Eanes Barros
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Almeida, Jose Bruno de
Cutrim, Érico Murilo Monteiro
Neves, Precil Diego Miranda de Meneses
Campos, Marcos Adriano Garcia
Wanderley, Davi Campos
Teixeira Júnior, Antonio Augusto Lima
Muniz, Monique Pereira Rêgo
Ladchumananandasivam, Francisco Rasiah
Gomes, Orlando Vieira
Vasco, Rafael Fernandes Vanderlei
Brito, Dyego José de Araújo
Lages, Joyce Santos
Salgado-Filho, Natalino
Guedes, Felipe Leite
Magalhães, Marcelo
Araújo, Stanley de Almeida
Silva, Gyl Eanes Barros
dc.subject.por.fl_str_mv collapsing glomerulopathy
segmental and focal glomerulosclerosis
nephrotic syndrome (NS)
renal biopsy
podocytes
glomerulopathy
topic collapsing glomerulopathy
segmental and focal glomerulosclerosis
nephrotic syndrome (NS)
renal biopsy
podocytes
glomerulopathy
description Collapsing glomerulopathy (CG) is a clinicopathologic entity characterized by segmentar or global collapse of the glomerulus and hypertrophy and hyperplasia of podocytes. The Columbia classification of 2004 classified CG as a histological subtype of focal segmental glomerulosclerosis (FSGS). A growing number of studies have demonstrated a high prevalence of CG in many countries, especially among populations with a higher proportion of people with African descent. The present study is a narrative review of articles extracted from PubMed, Medline, and Scielo databases from September 1, 2020 to December 31, 2021. We have focused on populational studies (specially cross-sectional and cohort articles). CG is defined as a podocytopathy with a distinct pathogenesis characterized by strong podocyte proliferative activity. The most significant risk factors for CG include APOL1 gene mutations and infections with human immunodeficiency virus and severe acute respiratory syndrome coronavirus 2. CG typically presents with more severe symptoms and greater renal damage. The prognosis is notably worse than that of other FSGS subtypes
publishDate 2022
dc.date.issued.fl_str_mv 2022
dc.date.accessioned.fl_str_mv 2023-08-02T19:00:51Z
dc.date.available.fl_str_mv 2023-08-02T19:00:51Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.citation.fl_str_mv ALMEIDA, José Bruno, et. al. Collapsing Glomerulopathy: A Review by the Collapsing Brazilian Consortium. Frontiers In Medicine, v. 9, p. 846173, 2022.DOI: https://doi.org/10.3389/fmed.2022.846173 Disponível em: https://observatorio.fm.usp.br/handle/OPI/48634 Acesso em: 27 jul. 2023
dc.identifier.uri.fl_str_mv https://repositorio.ufrn.br/handle/123456789/54341
dc.identifier.doi.none.fl_str_mv https://doi.org/10.3389/fmed.2022.846173
identifier_str_mv ALMEIDA, José Bruno, et. al. Collapsing Glomerulopathy: A Review by the Collapsing Brazilian Consortium. Frontiers In Medicine, v. 9, p. 846173, 2022.DOI: https://doi.org/10.3389/fmed.2022.846173 Disponível em: https://observatorio.fm.usp.br/handle/OPI/48634 Acesso em: 27 jul. 2023
url https://repositorio.ufrn.br/handle/123456789/54341
https://doi.org/10.3389/fmed.2022.846173
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dc.publisher.none.fl_str_mv Frontiers in medicine
publisher.none.fl_str_mv Frontiers in medicine
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