Acute hepatic porphyrias for the neurologist: current concepts and perspectives

Detalhes bibliográficos
Autor(a) principal: Souza,Paulo Victor Sgobbi de
Data de Publicação: 2021
Outros Autores: Badia,Bruno de Mattos Lombardi, Farias,Igor Braga, Gonçalves,Eduardo Augusto, Pinto,Wladimir Bocca Vieira de Rezende, Oliveira,Acary Souza Bulle
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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spelling 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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