Genetics of Age-Related Macular Degeneration: Current Concepts, Future Directions

被引:71
|
作者
DeAngelis, Margaret M. [2 ,3 ]
Silveira, Alexandra C. [2 ]
Carr, Elizabeth A. [3 ]
Kim, Ivana K. [1 ]
机构
[1] Harvard Univ, Massachusetts Eye & Ear Infirm, Retina Serv, Dept Ophthalmol,Med Sch, Boston, MA 02114 USA
[2] Harvard Univ, Massachusetts Eye & Ear Infirm, Ocular Mol Genet Inst, Dept Ophthalmol,Med Sch, Boston, MA 02114 USA
[3] Univ Utah, John A Moran Eye Ctr, Salt Lake City, UT USA
关键词
ARMS2/HTRA1; CFH; choroidal neovascularization; complement; geographic atrophy; susceptibility; COMPLEMENT FACTOR-H; HEMOLYTIC-UREMIC SYNDROME; STARGARDT-DISEASE GENE; APOLIPOPROTEIN-E GENE; BEAVER DAM EYE; POLYPOIDAL CHOROIDAL VASCULOPATHY; MANGANESE SUPEROXIDE-DISMUTASE; FAMILIAL ALZHEIMERS-DISEASE; GENOME-WIDE ASSOCIATION; CASE-CONTROL SAMPLES;
D O I
10.3109/08820538.2011.577129
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Age-related macular degeneration (AMD) is a progressive degenerative disease which leads to blindness, affecting the quality of life of millions of Americans. More than 1.75 million individuals in the United States are affected by the advanced form of AMD. The etiological pathway of AMD is not yet fully understood, but there is a clear genetic influence on disease risk. To date, the 1q32 (CFH) and 10q26 (PLEKHA1/ARMS2/HTRA1) loci are the most strongly associated with disease; however, the variation in these genomic regions alone is unable to predict disease development with high accuracy. Therefore, current genetic studies are aimed at identifying new genes associated with AMD and their modifiers, with the goal of discovering diagnostic or prognostic biomarkers. Moreover, these studies provide the foundation for further investigation into the pathophysiology of AMD by utilizing a systems-biology-based approach to elucidate underlying mechanistic pathways.
引用
收藏
页码:77 / 93
页数:17
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