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.
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.
|Geerlings, Maartje J; Kersten, Eveline; Groenewoud, Joannes M M et al. (2018) Geographic distribution of rare variants associated with age-related macular degeneration. Mol Vis 24:75-82|
|Marouli, Eirini (see original citation for additional authors) (2017) Rare and low-frequency coding variants alter human adult height. Nature 542:186-190|
|Schulz, Heidi L; Grassmann, Felix; Kellner, Ulrich et al. (2017) Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs. Invest Ophthalmol Vis Sci 58:394-403|
|Persad, Patrice J; Heid, Iris M; Weeks, Daniel E et al. (2017) Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Invest Ophthalmol Vis Sci 58:4027-4038|
|Grassmann, Felix; Kiel, Christina; Zimmermann, Martina E et al. (2017) Genetic pleiotropy between age-related macular degeneration and 16 complex diseases and traits. Genome Med 9:29|
|Sardell, Rebecca J; Persad, Patrice J; Pan, Samuel S et al. (2016) Progression Rate From Intermediate to Advanced Age-Related Macular Degeneration Is Correlated With the Number of Risk Alleles at the CFH Locus. Invest Ophthalmol Vis Sci 57:6107-6115|
|Cooke Bailey, Jessica N; Hoffman, Joshua D; Sardell, Rebecca J et al. (2016) The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review. J Clin Med 5:|
|Fritsche, Lars G; Igl, Wilmar; Bailey, Jessica N Cooke et al. (2016) A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Nat Genet 48:134-43|
|Grassmann, Felix; Cantsilieris, Stuart; Schulz-Kuhnt, Anja-Sabrina et al. (2016) Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD). J Neuroinflammation 13:81|
|Cuellar-Partida, Gabriel; Craig, Jamie E; Burdon, Kathryn P et al. (2016) Assessment of polygenic effects links primary open-angle glaucoma and age-related macular degeneration. Sci Rep 6:26885|
Showing the most recent 10 out of 12 publications