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GWAS Study

A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci.

Scheetz TE, Fingert JH, Wang K et al.

23536807 PubMed ID
GWAS Study Type
797 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ST
Scheetz TE
FJ
Fingert JH
WK
Wang K
KM
Kuehn MH
KK
Knudtson KL
AW
Alward WL
BH
Boldt HC
RS
Russell SR
FJ
Folk JC
CT
Casavant TL
BT
Braun TA
CA
Clark AF
SE
Stone EM
SV
Sheffield VC
Chapter II

Abstract

Summary of the research findings

Glaucoma and age-related macular degeneration (AMD) are the two leading causes of visual loss in the United States. We utilized a novel study design to perform a genome-wide association for both primary open angle glaucoma (POAG) and AMD. This study design utilized a two-stage process for hypothesis generation and validation, in which each disease cohort was utilized as a control for the other. A total of 400 POAG patients and 400 AMD patients were ascertained and genotyped at 500,000 loci. This study identified a novel association of complement component 7 (C7) to POAG. Additionally, an association of central corneal thickness, a known risk factor for POAG, was found to be associated with ribophorin II (RPN2). Linked monogenic loci for POAG and AMD were also evaluated for evidence of association, none of which were found to be significantly associated. However, several yielded putative associations requiring validation. Our data suggest that POAG is more genetically complex than AMD, with no common risk alleles of large effect.

200 cases, 197 controls

Chapter III

Study Statistics

Key metrics and study information

797
Total Participants
GWAS
Study Type
Yes
Replicated
200 cases, 200 controls
Replication Participants
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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