Fuchs Endothelial Corneal Dystrophy (FECD) is a bilateral, generally symmetric, slowly progressing disorder of the corneal endothelium that was first described by Ernst Fuchs in 1910. This debilitating disorder becomes symptomatic in the fifth or sixth decade of life, and affects 2- 4 times more women than men. Clinical presentation of FECD varies, but often includes corneal edema that results in a loss of corneal clarity, painful episodes of recurrent corneal erosions, severely impaired visual acuity, and in some cases, blindness. Although medical management of symptoms may be attempted, most patients ultimately require corneal transplantation. As a result, FECD is a leading indication for corneal transplantation in the U.S. and in other developed countries. Excessive familial aggregation in first- and second-degree relatives has been reported, and several studies suggest that FECD is a common complex genetic disease. Investigators involved in the current proposal and others in the field have independently identified loci for FECD, but no study has examined large cohorts of patients with corneal dystrophies to assess genetic contributions. In the past two years we have successfully established a multi-center consortium to delineate the genetic architecture of FECD, and have assembled a large cohort of FECD subjects that are uniformly graded for disease severity. In addition, we have successfully conducted a genome-wide association study in >1425 cases and >2525 controls. To address deficiencies in our understanding the etiologic basis of FECD, we now propose to co-ordinate the activities of this consortium, and follow up our preliminary genome-wide association study results with detailed secondary analyses that include examination of other risk factors (e.g. smoking) and genotype-phenotype correlations at interesting loci (e.g. TCF4). The dearth of biological data on corneal proteins, the growing need for engineered tissue, and the significant resources garnered by our group offer a unique opportunity to advance this field.
Fuchs Endothelial Corneal Dystrophy (FECD) is a progressive disease of eye leading to corneal edema, with rising incidence across the older age groups resulting in pain and vision loss. Reducing FECD incidence could lessen the need for surgical intervention, thus decreasing medical care and costs, and improve clinical outcomes in patients. A risk factor reliably associated with FECD is genetic predisposition; FECD has a heritability of 30-40%. The purpose of this application is to develop a better understanding of the genetic basis of FECD. In the past two years, we have jointly established a consortium for FECD genetics, and have successfully obtained National Eye Institute support for the largest genome-wide association study at the Center for Inherited Disease Research. We anticipate that this project will lead to identification of novel genes for FECD, which will assist in identifing and ideally stabilizing early disease, improve the understanding of the molecular basis of the disorder, and provide translation to effective medical therapy.
|Afshari, Natalie A; Igo Jr, Robert P; Morris, Nathan J et al. (2017) Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Nat Commun 8:14898|
|Fan, Qiao; Guo, Xiaobo; Tideman, J Willem L et al. (2016) Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium. Sci Rep 6:25853|
|Li, Yi-Ju; Minear, Mollie A; Qin, Xuejun et al. (2014) Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy. Invest Ophthalmol Vis Sci 55:4577-84|
|Cheng, Ching-Yu; Schache, Maria; Ikram, M Kamran et al. (2013) Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am J Hum Genet 93:264-77|
|Verhoeven, Virginie J M; Hysi, Pirro G; Wojciechowski, Robert et al. (2013) Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat Genet 45:314-8|
|Verhoeven, Virginie J M; Hysi, Pirro G; Saw, Seang-Mei et al. (2012) Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Hum Genet 131:1467-80|