HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration

Author:

DeWan Andrew12345,Liu Mugen12345,Hartman Stephen12345,Zhang Samuel Shao-Min12345,Liu David T. L.12345,Zhao Connie12345,Tam Pancy O. S.12345,Chan Wai Man12345,Lam Dennis S. C.12345,Snyder Michael12345,Barnstable Colin12345,Pang Chi Pui12345,Hoh Josephine12345

Affiliation:

1. Department of Epidemiology and Public Health, Yale University, 60 College Street, New Haven, CT 06520, USA.

2. Department of Ophthalmology and Visual Science, Yale University, 330 Cedar Street, New Haven, CT 06520, USA.

3. Department of Molecular, Cellular, and Developmental Biology, Yale University, 219 Prospect Street, New Haven, CT 06520, USA.

4. Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Hong Kong, China.

5. Genomics Resource Center, Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.

Abstract

Age-related macular degeneration (AMD), the most common cause of irreversible vision loss in individuals aged older than 50 years, is classified as either wet (neovascular) or dry (nonneovascular). Inherited variation in the complement factor H gene is a major risk factor for drusen in dry AMD. Here we report that a single-nucleotide polymorphism in the promoter region of HTRA1 , a serine protease gene on chromosome 10q26, is a major genetic risk factor for wet AMD. A whole-genome association mapping strategy was applied to a Chinese population, yielding a P value of <10 –11 . Individuals with the risk-associated genotype were estimated to have a likelihood of developing wet AMD 10 times that of individuals with the wild-type genotype.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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