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Genetics and age-related macular degeneration: a practical review for the clinician

Age-related macular degeneration is a complex disease, with both genetic and environmental risk factors interacting in unknown ways. Currently, 52 gene variants within 34 loci have been significantly associated with age-related macular degeneration. Two well-studied major genes are complement factor...

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Autores principales: Schwartz, Stephen G, Hampton, Blake M, Kovach, Jaclyn L, Brantley, Milam A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938141/
https://www.ncbi.nlm.nih.gov/pubmed/27445455
http://dx.doi.org/10.2147/OPTH.S109723
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author Schwartz, Stephen G
Hampton, Blake M
Kovach, Jaclyn L
Brantley, Milam A
author_facet Schwartz, Stephen G
Hampton, Blake M
Kovach, Jaclyn L
Brantley, Milam A
author_sort Schwartz, Stephen G
collection PubMed
description Age-related macular degeneration is a complex disease, with both genetic and environmental risk factors interacting in unknown ways. Currently, 52 gene variants within 34 loci have been significantly associated with age-related macular degeneration. Two well-studied major genes are complement factor H (CFH) and age-related maculopathy susceptibility 2 (ARMS2). There exist several commercially available tests that are proposed to stratify patients into high-risk and low-risk groups, as well as predict response to nutritional supplementation. However, at present, the bulk of the available peer-reviewed evidence suggests that genetic testing is more useful as a research tool than for clinical management of patients.
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spelling pubmed-49381412016-07-21 Genetics and age-related macular degeneration: a practical review for the clinician Schwartz, Stephen G Hampton, Blake M Kovach, Jaclyn L Brantley, Milam A Clin Ophthalmol Review Age-related macular degeneration is a complex disease, with both genetic and environmental risk factors interacting in unknown ways. Currently, 52 gene variants within 34 loci have been significantly associated with age-related macular degeneration. Two well-studied major genes are complement factor H (CFH) and age-related maculopathy susceptibility 2 (ARMS2). There exist several commercially available tests that are proposed to stratify patients into high-risk and low-risk groups, as well as predict response to nutritional supplementation. However, at present, the bulk of the available peer-reviewed evidence suggests that genetic testing is more useful as a research tool than for clinical management of patients. Dove Medical Press 2016-07-04 /pmc/articles/PMC4938141/ /pubmed/27445455 http://dx.doi.org/10.2147/OPTH.S109723 Text en © 2016 Schwartz et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Schwartz, Stephen G
Hampton, Blake M
Kovach, Jaclyn L
Brantley, Milam A
Genetics and age-related macular degeneration: a practical review for the clinician
title Genetics and age-related macular degeneration: a practical review for the clinician
title_full Genetics and age-related macular degeneration: a practical review for the clinician
title_fullStr Genetics and age-related macular degeneration: a practical review for the clinician
title_full_unstemmed Genetics and age-related macular degeneration: a practical review for the clinician
title_short Genetics and age-related macular degeneration: a practical review for the clinician
title_sort genetics and age-related macular degeneration: a practical review for the clinician
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4938141/
https://www.ncbi.nlm.nih.gov/pubmed/27445455
http://dx.doi.org/10.2147/OPTH.S109723
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