Grant Detail
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Advancing Genetics Through the AMDgene Consortium
1 April 2012 - 31 March 2015
NATIONAL EYE INSTITUTE
Total Funding: $ 397,302
DESCRIPTION (provided by applicant): Age-related macular degeneration (AMD) is the most common cause of severe vision loss among individuals over age 50 in the U.S. with millions of individuals around the world suffering severe vision loss. The influence of genetic variation on AMD is strong and through recent technological advances the genetic etiology of risk for AMD is being deconstructed. Independent studies have identified and confirmed variations in multiple genes that strongly affect risk to AMD, including CFH, HTRA1/ARMS2, C2/CFB, and C3 explaining a significant portion of the genetic risk for AMD. Initial efforts at genome-wide association studies have identified and/or confirmed several additional loci of more modest individual effect (CFI, LIPC, TIMP3), with many more loci providing suggestive associations. However, a substantial portion of the genetic architecture remains unexplained and detailed examination of effects specific to subtypes of AMD have been lacking. To address these deficiencies very large sample sizes of well characterized cases and controls and families are needed. Over the past year we have formed the AMDgene consortium to combine both samples and expertise. The initial goal of the consortium was a meta-analysis of existing GWAS data in a combined dataset of over 9,000 cases and 49,000 controls. Preliminary findings have identified new genome-wide significant loci. We have chosen an approach that maintains the primary data at each site, which promotes continued engagement by all participating sites, is cost and time efficient, and avoids potential consent, ethics, and privacy issues of sharing data collected under a wide variety of informed consent. The primary goal of this proposal is to support the AMDgene consortium effort through the following specific aims (1) Coordinate the activities of the AMDgene Consortium;(2) Add new datasets and augment current datasets;(3) Perform detailed meta-analyses on existing and new datasets;and (4) Perform detailed secondary analyses on these data. PUBLIC HEALTH RELEVANCE: Age-related macular degeneration (AMD) is the most common cause of severe vision loss among elderly individuals. Variations in multiple genes strongly affect risk to AMD but a substantial portion of the genetic architecture remains unexplained. The AMDgene international consortium was formed to aggregate existing genome-wide genotype data and to perform detailed meta-analyses to further understand the genetic underpinnings of AMD.
Scientific Context
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Related Grants
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1.
PERICAK-VANCE, MARGARET A.
Genomic Architecture of Progression and Treatment Response in AMD
15 June 2000 - 31 July 2016
NATIONAL EYE INSTITUTE
Total Funding: $ 7,341,637
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2.
Pericak-Vance, Margaret A
UNIFYING GENETICS EPIDEMIOLOGY OF MACULAR DEGENERATION
15 June 2000 - 31 May 2005
NATIONAL EYE INSTITUTE
Total Funding: $ 3,478,367
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3.
HAINES, JONATHAN L.
15 August 2011 - 31 July 2015
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
Total Funding: $ 1,868,230
Related Publications
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1.
2005Jonathan L Haines; Michael A Hauser; Silke Schmidt; William K Scott; Lana M Olson; Paul Gallins; Kylee L Spencer; Shu Ying Kwan; Maher Noureddine; John R Gilbert; et al.
Complement factor H variant increases the risk of age-related macular degeneration.
Science (New York, N.Y.) 2005;308(5720):419-21. -
2.
2011Lintje Ho; Redmer van Leeuwen; Jacqueline C M Witteman; Cornelia M van Duijn; André G Uitterlinden; Albert Hofman; Paulus T V M de Jong; Johannes R Vingerling; Caroline C W Klaver
Archives of ophthalmology 2011;129(6):758-66. -
3.
2006Silke Schmidt; Michael A Hauser; William K Scott; Eric A Postel; Anita Agarwal; Paul Gallins; Frank Wong; Yu Sarah Chen; Kylee Spencer; Nathalie Schnetz-Boutaud; et al.
American journal of human genetics 2006;78(5):852-64.
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