Acute hepatic porphyrias for the neurologist: current concepts and perspectives
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Arquivos de neuro-psiquiatria (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2021000100068 |
Resumo: | ABSTRACT Background: Acute hepatic porphyrias represent an expanding group of complex inherited metabolic disorders due to inborn errors of metabolism involving heme biosynthesis. Objective: We aimed to review the main clinical and therapeutic aspects associated with acute hepatic porphyrias. Methods: The authors provided a wide non-systematic review of current concepts and recently acquired knowledge about acute hepatic porphyrias. Results: Acute neurovisceral attacks are the most common and life-threatening presentation of this group and are often considered the main clinical manifestation by clinicians during differential diagnosis and the start of proper diagnostic work-up for acute porphyrias. However, atypical presentations with central nervous system involvement, neuropsychiatric disturbances, and some subtypes with photosensitivity usually make the definite diagnosis difficult and late. Early therapeutic interventions are essential during emergency treatment and intercritical periods to avoid recurrent severe presentations. The availability of new disease-modifying therapeutic proposals based on small interfering RNA (siRNA)-based therapies, complementary to the classic intravenous glucose infusion and hemin-based treatments, emphasizes the importance of early diagnosis and genetic counseling of patients. Conclusions: This review article highlights the main biochemical, pathophysiological, clinical, and therapeutic aspects of acute hepatic porphyrias in clinical practice. |
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Acute hepatic porphyrias for the neurologist: current concepts and perspectivesNeuromuscular DiseasesPorphyriaInborn Errors of MetabolismAcute Intermittent PorphyriaHepatic PorphyriasABSTRACT Background: Acute hepatic porphyrias represent an expanding group of complex inherited metabolic disorders due to inborn errors of metabolism involving heme biosynthesis. Objective: We aimed to review the main clinical and therapeutic aspects associated with acute hepatic porphyrias. Methods: The authors provided a wide non-systematic review of current concepts and recently acquired knowledge about acute hepatic porphyrias. Results: Acute neurovisceral attacks are the most common and life-threatening presentation of this group and are often considered the main clinical manifestation by clinicians during differential diagnosis and the start of proper diagnostic work-up for acute porphyrias. However, atypical presentations with central nervous system involvement, neuropsychiatric disturbances, and some subtypes with photosensitivity usually make the definite diagnosis difficult and late. Early therapeutic interventions are essential during emergency treatment and intercritical periods to avoid recurrent severe presentations. The availability of new disease-modifying therapeutic proposals based on small interfering RNA (siRNA)-based therapies, complementary to the classic intravenous glucose infusion and hemin-based treatments, emphasizes the importance of early diagnosis and genetic counseling of patients. Conclusions: This review article highlights the main biochemical, pathophysiological, clinical, and therapeutic aspects of acute hepatic porphyrias in clinical practice.Academia Brasileira de Neurologia - ABNEURO2021-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2021000100068Arquivos de Neuro-Psiquiatria v.79 n.1 2021reponame:Arquivos de neuro-psiquiatria (Online)instname:Academia Brasileira de Neurologiainstacron:ABNEURO10.1590/0004-282x20200096info:eu-repo/semantics/openAccessSouza,Paulo Victor Sgobbi deBadia,Bruno de Mattos LombardiFarias,Igor BragaGonçalves,Eduardo AugustoPinto,Wladimir Bocca Vieira de RezendeOliveira,Acary Souza Bulleeng2021-02-24T00:00:00Zoai:scielo:S0004-282X2021000100068Revistahttp://www.scielo.br/anphttps://old.scielo.br/oai/scielo-oai.php||revista.arquivos@abneuro.org1678-42270004-282Xopendoar:2021-02-24T00:00Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologiafalse |
dc.title.none.fl_str_mv |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives |
title |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives |
spellingShingle |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives Souza,Paulo Victor Sgobbi de Neuromuscular Diseases Porphyria Inborn Errors of Metabolism Acute Intermittent Porphyria Hepatic Porphyrias |
title_short |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives |
title_full |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives |
title_fullStr |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives |
title_full_unstemmed |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives |
title_sort |
Acute hepatic porphyrias for the neurologist: current concepts and perspectives |
author |
Souza,Paulo Victor Sgobbi de |
author_facet |
Souza,Paulo Victor Sgobbi de Badia,Bruno de Mattos Lombardi Farias,Igor Braga Gonçalves,Eduardo Augusto Pinto,Wladimir Bocca Vieira de Rezende Oliveira,Acary Souza Bulle |
author_role |
author |
author2 |
Badia,Bruno de Mattos Lombardi Farias,Igor Braga Gonçalves,Eduardo Augusto Pinto,Wladimir Bocca Vieira de Rezende Oliveira,Acary Souza Bulle |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Souza,Paulo Victor Sgobbi de Badia,Bruno de Mattos Lombardi Farias,Igor Braga Gonçalves,Eduardo Augusto Pinto,Wladimir Bocca Vieira de Rezende Oliveira,Acary Souza Bulle |
dc.subject.por.fl_str_mv |
Neuromuscular Diseases Porphyria Inborn Errors of Metabolism Acute Intermittent Porphyria Hepatic Porphyrias |
topic |
Neuromuscular Diseases Porphyria Inborn Errors of Metabolism Acute Intermittent Porphyria Hepatic Porphyrias |
description |
ABSTRACT Background: Acute hepatic porphyrias represent an expanding group of complex inherited metabolic disorders due to inborn errors of metabolism involving heme biosynthesis. Objective: We aimed to review the main clinical and therapeutic aspects associated with acute hepatic porphyrias. Methods: The authors provided a wide non-systematic review of current concepts and recently acquired knowledge about acute hepatic porphyrias. Results: Acute neurovisceral attacks are the most common and life-threatening presentation of this group and are often considered the main clinical manifestation by clinicians during differential diagnosis and the start of proper diagnostic work-up for acute porphyrias. However, atypical presentations with central nervous system involvement, neuropsychiatric disturbances, and some subtypes with photosensitivity usually make the definite diagnosis difficult and late. Early therapeutic interventions are essential during emergency treatment and intercritical periods to avoid recurrent severe presentations. The availability of new disease-modifying therapeutic proposals based on small interfering RNA (siRNA)-based therapies, complementary to the classic intravenous glucose infusion and hemin-based treatments, emphasizes the importance of early diagnosis and genetic counseling of patients. Conclusions: This review article highlights the main biochemical, pathophysiological, clinical, and therapeutic aspects of acute hepatic porphyrias in clinical practice. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2021000100068 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X2021000100068 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/0004-282x20200096 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Academia Brasileira de Neurologia - ABNEURO |
publisher.none.fl_str_mv |
Academia Brasileira de Neurologia - ABNEURO |
dc.source.none.fl_str_mv |
Arquivos de Neuro-Psiquiatria v.79 n.1 2021 reponame:Arquivos de neuro-psiquiatria (Online) instname:Academia Brasileira de Neurologia instacron:ABNEURO |
instname_str |
Academia Brasileira de Neurologia |
instacron_str |
ABNEURO |
institution |
ABNEURO |
reponame_str |
Arquivos de neuro-psiquiatria (Online) |
collection |
Arquivos de neuro-psiquiatria (Online) |
repository.name.fl_str_mv |
Arquivos de neuro-psiquiatria (Online) - Academia Brasileira de Neurologia |
repository.mail.fl_str_mv |
||revista.arquivos@abneuro.org |
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