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Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies
Successful sequencing of the human genome and evolving functional knowledge of gene products has taken genomic medicine to the forefront, soon combining broadly with traditional diagnostics, therapeutics, and prognostics in patients. Recent years have witnessed an extraordinary leap in our understan...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334564/ https://www.ncbi.nlm.nih.gov/pubmed/35911417 http://dx.doi.org/10.3389/fmed.2022.906482 |
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author | Panikker, Priyalakshmi Roy, Shomereeta Ghosh, Anuprita Poornachandra, B. Ghosh, Arkasubhra |
author_facet | Panikker, Priyalakshmi Roy, Shomereeta Ghosh, Anuprita Poornachandra, B. Ghosh, Arkasubhra |
author_sort | Panikker, Priyalakshmi |
collection | PubMed |
description | Successful sequencing of the human genome and evolving functional knowledge of gene products has taken genomic medicine to the forefront, soon combining broadly with traditional diagnostics, therapeutics, and prognostics in patients. Recent years have witnessed an extraordinary leap in our understanding of ocular diseases and their respective genetic underpinnings. As we are entering the age of genomic medicine, rapid advances in genome sequencing, gene delivery, genome surgery, and computational genomics enable an ever-increasing capacity to provide a precise and robust diagnosis of diseases and the development of targeted treatment strategies. Inherited retinal diseases are a major source of blindness around the world where a large number of causative genes have been identified, paving the way for personalized diagnostics in the clinic. Developments in functional genetics and gene transfer techniques has also led to the first FDA approval of gene therapy for LCA, a childhood blindness. Many such retinal diseases are the focus of various clinical trials, making clinical diagnoses of retinal diseases, their underlying genetics and the studies of natural history important. Here, we review methodologies for identifying new genes and variants associated with various ocular disorders and the complexities associated with them. Thereafter we discuss briefly, various retinal diseases and the application of genomic technologies in their diagnosis. We also discuss the strategies, challenges, and potential of gene therapy for the treatment of inherited and acquired retinal diseases. Additionally, we discuss the translational aspects of gene therapy, the important vector types and considerations for human trials that may help advance personalized therapeutics in ophthalmology. Retinal disease research has led the application of precision diagnostics and precision therapies; therefore, this review provides a general understanding of the current status of precision medicine in ophthalmology. |
format | Online Article Text |
id | pubmed-9334564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93345642022-07-30 Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies Panikker, Priyalakshmi Roy, Shomereeta Ghosh, Anuprita Poornachandra, B. Ghosh, Arkasubhra Front Med (Lausanne) Medicine Successful sequencing of the human genome and evolving functional knowledge of gene products has taken genomic medicine to the forefront, soon combining broadly with traditional diagnostics, therapeutics, and prognostics in patients. Recent years have witnessed an extraordinary leap in our understanding of ocular diseases and their respective genetic underpinnings. As we are entering the age of genomic medicine, rapid advances in genome sequencing, gene delivery, genome surgery, and computational genomics enable an ever-increasing capacity to provide a precise and robust diagnosis of diseases and the development of targeted treatment strategies. Inherited retinal diseases are a major source of blindness around the world where a large number of causative genes have been identified, paving the way for personalized diagnostics in the clinic. Developments in functional genetics and gene transfer techniques has also led to the first FDA approval of gene therapy for LCA, a childhood blindness. Many such retinal diseases are the focus of various clinical trials, making clinical diagnoses of retinal diseases, their underlying genetics and the studies of natural history important. Here, we review methodologies for identifying new genes and variants associated with various ocular disorders and the complexities associated with them. Thereafter we discuss briefly, various retinal diseases and the application of genomic technologies in their diagnosis. We also discuss the strategies, challenges, and potential of gene therapy for the treatment of inherited and acquired retinal diseases. Additionally, we discuss the translational aspects of gene therapy, the important vector types and considerations for human trials that may help advance personalized therapeutics in ophthalmology. Retinal disease research has led the application of precision diagnostics and precision therapies; therefore, this review provides a general understanding of the current status of precision medicine in ophthalmology. Frontiers Media S.A. 2022-07-15 /pmc/articles/PMC9334564/ /pubmed/35911417 http://dx.doi.org/10.3389/fmed.2022.906482 Text en Copyright © 2022 Panikker, Roy, Ghosh, Poornachandra and Ghosh. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Panikker, Priyalakshmi Roy, Shomereeta Ghosh, Anuprita Poornachandra, B. Ghosh, Arkasubhra Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies |
title | Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies |
title_full | Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies |
title_fullStr | Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies |
title_full_unstemmed | Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies |
title_short | Advancing precision medicines for ocular disorders: Diagnostic genomics to tailored therapies |
title_sort | advancing precision medicines for ocular disorders: diagnostic genomics to tailored therapies |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334564/ https://www.ncbi.nlm.nih.gov/pubmed/35911417 http://dx.doi.org/10.3389/fmed.2022.906482 |
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