Precision medicine for lysosomal disorders

Detalhes bibliográficos
Autor(a) principal: Vairo, Filippo Pinto e
Data de Publicação: 2020
Outros Autores: Málaga, Diana Elizabeth Rojas, Kubaski, Francyne, Souza, Carolina Fischinger Moura de, Poswar, Fabiano de Oliveira, Baldo, Guilherme, Giugliani, Roberto
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/214122
Resumo: Precision medicine (PM) is an emerging approach for disease treatment and preventionthat accounts for the individual variability in the genes, environment, and lifestyle of each person.Lysosomal diseases (LDs) are a group of genetic metabolic disorders that include approximately70 monogenic conditions caused by a defect in lysosomal function. LDs may result from primarylysosomal enzyme deficiencies or impairments in membrane-associated proteins, lysosomal enzymeactivators, or modifiers that affect lysosomal function. LDs are heterogeneous disorders, and thephenotype of the affected individual depends on the type of substrate and where it accumulates,which may be impacted by the type of genetic change and residual enzymatic activity. LDs areindividually rare, with a combined incidence of approximately 1:4000 individuals. Specific therapiesare already available for several LDs, and many more are in development. Early identification mayenable disease course prediction and a specific intervention, which is very important for clinicaloutcome. Driven by advances in omics technology, PM aims to provide the most appropriatemanagement for each patient based on the disease susceptibility or treatment response predictionsfor specific subgroups. In this review, we focused on the emerging diagnostic technologies that mayhelp to optimize the management of each LD patient and the therapeutic options available, as well asin clinical developments that enable customized approaches to be selected for each subject, accordingto the principles of PM.
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spelling Vairo, Filippo Pinto eMálaga, Diana Elizabeth RojasKubaski, FrancyneSouza, Carolina Fischinger Moura dePoswar, Fabiano de OliveiraBaldo, GuilhermeGiugliani, Roberto2020-10-14T03:48:36Z20202218-273Xhttp://hdl.handle.net/10183/214122001117489Precision medicine (PM) is an emerging approach for disease treatment and preventionthat accounts for the individual variability in the genes, environment, and lifestyle of each person.Lysosomal diseases (LDs) are a group of genetic metabolic disorders that include approximately70 monogenic conditions caused by a defect in lysosomal function. LDs may result from primarylysosomal enzyme deficiencies or impairments in membrane-associated proteins, lysosomal enzymeactivators, or modifiers that affect lysosomal function. LDs are heterogeneous disorders, and thephenotype of the affected individual depends on the type of substrate and where it accumulates,which may be impacted by the type of genetic change and residual enzymatic activity. LDs areindividually rare, with a combined incidence of approximately 1:4000 individuals. Specific therapiesare already available for several LDs, and many more are in development. Early identification mayenable disease course prediction and a specific intervention, which is very important for clinicaloutcome. Driven by advances in omics technology, PM aims to provide the most appropriatemanagement for each patient based on the disease susceptibility or treatment response predictionsfor specific subgroups. In this review, we focused on the emerging diagnostic technologies that mayhelp to optimize the management of each LD patient and the therapeutic options available, as well asin clinical developments that enable customized approaches to be selected for each subject, accordingto the principles of PM.application/pdfengBiomolecules. Basel. Vol. 10, no. 8 (Aug. 2020), 1110, p. 1-26Doenças por armazenamento dos lisossomosErros inatos do metabolismoMedicina de precisãoTerapia de reposição de enzimasTerapia genéticaLysosomal diseasesPrecision medicineEnzyme replacement therapyPharmacological chaperonesGene therapyPrecision medicine for lysosomal disordersEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001117489.pdf.txt001117489.pdf.txtExtracted Texttext/plain83404http://www.lume.ufrgs.br/bitstream/10183/214122/2/001117489.pdf.txt19b04ccf6fc178a97ded815be42b4104MD52ORIGINAL001117489.pdfTexto completo (inglês)application/pdf371552http://www.lume.ufrgs.br/bitstream/10183/214122/1/001117489.pdf8f4cc36e8c80fc3339ca5f408ab0a453MD5110183/2141222023-08-09 03:47:51.216803oai:www.lume.ufrgs.br:10183/214122Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2023-08-09T06:47:51Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Precision medicine for lysosomal disorders
title Precision medicine for lysosomal disorders
spellingShingle Precision medicine for lysosomal disorders
Vairo, Filippo Pinto e
Doenças por armazenamento dos lisossomos
Erros inatos do metabolismo
Medicina de precisão
Terapia de reposição de enzimas
Terapia genética
Lysosomal diseases
Precision medicine
Enzyme replacement therapy
Pharmacological chaperones
Gene therapy
title_short Precision medicine for lysosomal disorders
title_full Precision medicine for lysosomal disorders
title_fullStr Precision medicine for lysosomal disorders
title_full_unstemmed Precision medicine for lysosomal disorders
title_sort Precision medicine for lysosomal disorders
author Vairo, Filippo Pinto e
author_facet Vairo, Filippo Pinto e
Málaga, Diana Elizabeth Rojas
Kubaski, Francyne
Souza, Carolina Fischinger Moura de
Poswar, Fabiano de Oliveira
Baldo, Guilherme
Giugliani, Roberto
author_role author
author2 Málaga, Diana Elizabeth Rojas
Kubaski, Francyne
Souza, Carolina Fischinger Moura de
Poswar, Fabiano de Oliveira
Baldo, Guilherme
Giugliani, Roberto
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Vairo, Filippo Pinto e
Málaga, Diana Elizabeth Rojas
Kubaski, Francyne
Souza, Carolina Fischinger Moura de
Poswar, Fabiano de Oliveira
Baldo, Guilherme
Giugliani, Roberto
dc.subject.por.fl_str_mv Doenças por armazenamento dos lisossomos
Erros inatos do metabolismo
Medicina de precisão
Terapia de reposição de enzimas
Terapia genética
topic Doenças por armazenamento dos lisossomos
Erros inatos do metabolismo
Medicina de precisão
Terapia de reposição de enzimas
Terapia genética
Lysosomal diseases
Precision medicine
Enzyme replacement therapy
Pharmacological chaperones
Gene therapy
dc.subject.eng.fl_str_mv Lysosomal diseases
Precision medicine
Enzyme replacement therapy
Pharmacological chaperones
Gene therapy
description Precision medicine (PM) is an emerging approach for disease treatment and preventionthat accounts for the individual variability in the genes, environment, and lifestyle of each person.Lysosomal diseases (LDs) are a group of genetic metabolic disorders that include approximately70 monogenic conditions caused by a defect in lysosomal function. LDs may result from primarylysosomal enzyme deficiencies or impairments in membrane-associated proteins, lysosomal enzymeactivators, or modifiers that affect lysosomal function. LDs are heterogeneous disorders, and thephenotype of the affected individual depends on the type of substrate and where it accumulates,which may be impacted by the type of genetic change and residual enzymatic activity. LDs areindividually rare, with a combined incidence of approximately 1:4000 individuals. Specific therapiesare already available for several LDs, and many more are in development. Early identification mayenable disease course prediction and a specific intervention, which is very important for clinicaloutcome. Driven by advances in omics technology, PM aims to provide the most appropriatemanagement for each patient based on the disease susceptibility or treatment response predictionsfor specific subgroups. In this review, we focused on the emerging diagnostic technologies that mayhelp to optimize the management of each LD patient and the therapeutic options available, as well asin clinical developments that enable customized approaches to be selected for each subject, accordingto the principles of PM.
publishDate 2020
dc.date.accessioned.fl_str_mv 2020-10-14T03:48:36Z
dc.date.issued.fl_str_mv 2020
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Biomolecules. Basel. Vol. 10, no. 8 (Aug. 2020), 1110, p. 1-26
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reponame_str Repositório Institucional da UFRGS
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