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Seven New Loci Associated with Age-Related Macular Degeneration

Age-related macular degeneration (AMD) is a common cause of blindness in older individuals. To accelerate understanding of AMD biology and help design new therapies, we executed a collaborative genomewide association study, examining >17,100 advanced AMD cases and >60,000 controls of European...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739472/
https://www.ncbi.nlm.nih.gov/pubmed/23455636
http://dx.doi.org/10.1038/ng.2578
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description Age-related macular degeneration (AMD) is a common cause of blindness in older individuals. To accelerate understanding of AMD biology and help design new therapies, we executed a collaborative genomewide association study, examining >17,100 advanced AMD cases and >60,000 controls of European and Asian ancestry. We identified 19 genomic loci associated with AMD with p<5×10(−8) and enriched for genes involved in regulation of complement activity, lipid metabolism, extracellular matrix remodeling and angiogenesis. Our results include 7 loci reaching p<5×10(−8) for the first time, near the genes COL8A1/FILIP1L, IER3/DDR1, SLC16A8, TGFBR1, RAD51B, ADAMTS9/MIR548A2, and B3GALTL. A genetic risk score combining SNPs from all loci displayed similar good ability to distinguish cases and controls in all samples examined. Our findings provide new directions for biological, genetic and therapeutic studies of AMD.
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spelling pubmed-37394722013-10-01 Seven New Loci Associated with Age-Related Macular Degeneration Nat Genet Article Age-related macular degeneration (AMD) is a common cause of blindness in older individuals. To accelerate understanding of AMD biology and help design new therapies, we executed a collaborative genomewide association study, examining >17,100 advanced AMD cases and >60,000 controls of European and Asian ancestry. We identified 19 genomic loci associated with AMD with p<5×10(−8) and enriched for genes involved in regulation of complement activity, lipid metabolism, extracellular matrix remodeling and angiogenesis. Our results include 7 loci reaching p<5×10(−8) for the first time, near the genes COL8A1/FILIP1L, IER3/DDR1, SLC16A8, TGFBR1, RAD51B, ADAMTS9/MIR548A2, and B3GALTL. A genetic risk score combining SNPs from all loci displayed similar good ability to distinguish cases and controls in all samples examined. Our findings provide new directions for biological, genetic and therapeutic studies of AMD. 2013-03-03 2013-04 /pmc/articles/PMC3739472/ /pubmed/23455636 http://dx.doi.org/10.1038/ng.2578 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Seven New Loci Associated with Age-Related Macular Degeneration
title Seven New Loci Associated with Age-Related Macular Degeneration
title_full Seven New Loci Associated with Age-Related Macular Degeneration
title_fullStr Seven New Loci Associated with Age-Related Macular Degeneration
title_full_unstemmed Seven New Loci Associated with Age-Related Macular Degeneration
title_short Seven New Loci Associated with Age-Related Macular Degeneration
title_sort seven new loci associated with age-related macular degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3739472/
https://www.ncbi.nlm.nih.gov/pubmed/23455636
http://dx.doi.org/10.1038/ng.2578
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