Collapsing glomerulopathy: a review by the collapsing brazilian consortium
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , , , , , , , , , , , , |
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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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 |
format |
article |
status_str |
publishedVersion |
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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eng |
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eng |
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https://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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Frontiers in medicine |
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Frontiers in medicine |
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