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Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases

Lysosomal storage diseases (LSDs) are inherited conditions caused by impaired lysosomal function and consequent substrate storage, leading to a range of clinical manifestations, including cardiovascular disease. This may lead to significant symptoms and even cardiac failure, which is an important ca...

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Autores principales: Poletto, Edina, Pasqualim, Gabriela, Giugliani, Roberto, Matte, Ursula, Baldo, Guilherme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Genética 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687348/
https://www.ncbi.nlm.nih.gov/pubmed/31132295
http://dx.doi.org/10.1590/1678-4685-GMB-2018-0100
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author Poletto, Edina
Pasqualim, Gabriela
Giugliani, Roberto
Matte, Ursula
Baldo, Guilherme
author_facet Poletto, Edina
Pasqualim, Gabriela
Giugliani, Roberto
Matte, Ursula
Baldo, Guilherme
author_sort Poletto, Edina
collection PubMed
description Lysosomal storage diseases (LSDs) are inherited conditions caused by impaired lysosomal function and consequent substrate storage, leading to a range of clinical manifestations, including cardiovascular disease. This may lead to significant symptoms and even cardiac failure, which is an important cause of death among patients. Currently available treatments do not completely correct cardiac involvement in the LSDs. Gene therapy has been tested as a therapeutic alternative with promising results for the heart disease. In this review, we present the results of different approaches of gene therapy for LSDs, mainly in animal models, and its effects in the heart, focusing on protocols with cardiac functional analysis.
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spelling pubmed-66873482019-08-23 Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases Poletto, Edina Pasqualim, Gabriela Giugliani, Roberto Matte, Ursula Baldo, Guilherme Genet Mol Biol Articles Lysosomal storage diseases (LSDs) are inherited conditions caused by impaired lysosomal function and consequent substrate storage, leading to a range of clinical manifestations, including cardiovascular disease. This may lead to significant symptoms and even cardiac failure, which is an important cause of death among patients. Currently available treatments do not completely correct cardiac involvement in the LSDs. Gene therapy has been tested as a therapeutic alternative with promising results for the heart disease. In this review, we present the results of different approaches of gene therapy for LSDs, mainly in animal models, and its effects in the heart, focusing on protocols with cardiac functional analysis. Sociedade Brasileira de Genética 2019-05-23 2019 /pmc/articles/PMC6687348/ /pubmed/31132295 http://dx.doi.org/10.1590/1678-4685-GMB-2018-0100 Text en Copyright © 2019, Sociedade Brasileira de Genética. https://creativecommons.org/licenses/by/4.0/ License information: This is an open-access article distributed under the terms of the Creative Commons Attribution License (type CC-BY), which permits unrestricted use, distribution and reproduction in any medium, provided the original article is properly cited.
spellingShingle Articles
Poletto, Edina
Pasqualim, Gabriela
Giugliani, Roberto
Matte, Ursula
Baldo, Guilherme
Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases
title Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases
title_full Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases
title_fullStr Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases
title_full_unstemmed Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases
title_short Effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases
title_sort effects of gene therapy on cardiovascular symptoms of lysosomal storage diseases
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687348/
https://www.ncbi.nlm.nih.gov/pubmed/31132295
http://dx.doi.org/10.1590/1678-4685-GMB-2018-0100
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