Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10451/54399 |
Resumo: | © 2022 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
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Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative reviewABCC2/MRP2Dubin-Johnson syndromeRotor syndromeSLCO1B1/OATP1B1SLCO1B3/OATP1B3Conjugated hyperbilirubinemia© 2022 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.Bilirubin, a breakdown product of heme, is normally glucuronidated and excreted by the liver into bile. Failure of this system can lead to a buildup of conjugated bilirubin in the blood, resulting in jaundice. Hyperbilirubinemia is an important clinical sign that needs to be investigated under a stepwise evaluation. Inherited non-hemolytic conjugated hyperbilirubinemic conditions include Dubin-Johnson syndrome (caused by mutations affecting ABCC2 gene) and Rotor syndrome (caused by the simultaneous presence of mutations in SLCO1B1 and SLCO1B3 genes). Although classically viewed as benign conditions requiring no treatment, they lately gained an increased interest since recent studies suggested that mutations in the responsible genes leading to hyperbilirubinemia, as well as minor genetic variants, may result in an increased susceptibility to drug toxicity. This article provides a comprehensive review on the pathophysiology of Dubin-Johnson and Rotor syndromes, presenting the current knowledge concerning the molecular details and basis of these conditions.WileyRepositório da Universidade de LisboaMorais, Mariana BMachado, Mariana2022-09-09T10:44:43Z20222022-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10451/54399engUnited European Gastroenterol J. 2022 Jul 202050-640610.1002/ueg2.122792050-6414info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-08T17:00:20Zoai:repositorio.ul.pt:10451/54399Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T22:04:59.267951Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review |
title |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review |
spellingShingle |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review Morais, Mariana B ABCC2/MRP2 Dubin-Johnson syndrome Rotor syndrome SLCO1B1/OATP1B1 SLCO1B3/OATP1B3 Conjugated hyperbilirubinemia |
title_short |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review |
title_full |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review |
title_fullStr |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review |
title_full_unstemmed |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review |
title_sort |
Benign inheritable disorders of bilirubin metabolism manifested by conjugated hyperbilirubinemia: a narrative review |
author |
Morais, Mariana B |
author_facet |
Morais, Mariana B Machado, Mariana |
author_role |
author |
author2 |
Machado, Mariana |
author2_role |
author |
dc.contributor.none.fl_str_mv |
Repositório da Universidade de Lisboa |
dc.contributor.author.fl_str_mv |
Morais, Mariana B Machado, Mariana |
dc.subject.por.fl_str_mv |
ABCC2/MRP2 Dubin-Johnson syndrome Rotor syndrome SLCO1B1/OATP1B1 SLCO1B3/OATP1B3 Conjugated hyperbilirubinemia |
topic |
ABCC2/MRP2 Dubin-Johnson syndrome Rotor syndrome SLCO1B1/OATP1B1 SLCO1B3/OATP1B3 Conjugated hyperbilirubinemia |
description |
© 2022 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09-09T10:44:43Z 2022 2022-01-01T00:00:00Z |
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.uri.fl_str_mv |
http://hdl.handle.net/10451/54399 |
url |
http://hdl.handle.net/10451/54399 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
United European Gastroenterol J. 2022 Jul 20 2050-6406 10.1002/ueg2.12279 2050-6414 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Wiley |
publisher.none.fl_str_mv |
Wiley |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799134601401073664 |