Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

334Citations
Citations of this article
148Readers
Mendeley users who have this article in their library.
Get full text

Abstract

We conducted a genome-wide association study for primary open-angle glaucoma (POAG) in 1,263 affected individuals (cases) and 34,877 controls from Iceland. We identified a common sequence variant at 7q31 (rs4236601[A], odds ratio (OR) = 1.36, P = 5.0 '- 10 ĝ̂'10). We then replicated the association in sample sets of 2,175 POAG cases and 2,064 controls from Sweden, the UK and Australia (combined OR = 1.18, P = 0.0015) and in 299 POAG cases and 580 unaffected controls from Hong Kong and Shantou, China (combined OR = 5.42, P = 0.0021). The risk variant identified here is located close to CAV1 and CAV2, both of which are expressed in the trabecular meshwork and retinal ganglion cells that are involved in the pathogenesis of POAG. © 2010 Nature America, Inc. All rights reserved.

Cite

CITATION STYLE

APA

Thorleifsson, G., Walters, G. B., Hewitt, A. W., Masson, G., Helgason, A., Dewan, A., … Stefansson, K. (2010). Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Nature Genetics, 42(10), 906–909. https://doi.org/10.1038/ng.661

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free