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GWAS Study

Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.

Wiggs JL, Yaspan BL, Hauser MA et al.

22570617 PubMed ID
GWAS Study Type
6633 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WJ
Wiggs JL
YB
Yaspan BL
HM
Hauser MA
KJ
Kang JH
AR
Allingham RR
OL
Olson LM
AW
Abdrabou W
FB
Fan BJ
WD
Wang DY
BW
Brodeur W
BD
Budenz DL
CJ
Caprioli J
CA
Crenshaw A
CK
Crooks K
DE
Delbono E
DK
Doheny KF
FD
Friedman DS
GD
Gaasterland D
GT
Gaasterland T
LC
Laurie C
LR
Lee RK
LP
Lichter PR
LS
Loomis S
LY
Liu Y
MF
Medeiros FA
MC
McCarty C
MD
Mirel D
MS
Moroi SE
MD
Musch DC
RA
Realini A
RF
Rozsa FW
SJ
Schuman JS
SK
Scott K
SK
Singh K
SJ
Stein JD
TE
Trager EH
VP
Vanveldhuisen P
VD
Vollrath D
WG
Wollstein G
YS
Yoneyama S
ZK
Zhang K
WR
Weinreb RN
EJ
Ernst J
KM
Kellis M
MT
Masuda T
ZD
Zack D
RJ
Richards JE
PM
Pericak-Vance M
PL
Pasquale LR
HJ
Haines JL
Chapter II

Abstract

Summary of the research findings

Optic nerve degeneration caused by glaucoma is a leading cause of blindness worldwide. Patients affected by the normal-pressure form of glaucoma are more likely to harbor risk alleles for glaucoma-related optic nerve disease. We have performed a meta-analysis of two independent genome-wide association studies for primary open angle glaucoma (POAG) followed by a normal-pressure glaucoma (NPG, defined by intraocular pressure (IOP) less than 22 mmHg) subgroup analysis. The single-nucleotide polymorphisms that showed the most significant associations were tested for association with a second form of glaucoma, exfoliation-syndrome glaucoma. The overall meta-analysis of the GLAUGEN and NEIGHBOR dataset results (3,146 cases and 3,487 controls) identified significant associations between two loci and POAG: the CDKN2BAS region on 9p21 (rs2157719 [G], OR = 0.69 [95%CI 0.63-0.75], p = 1.86×10⁻¹⁸), and the SIX1/SIX6 region on chromosome 14q23 (rs10483727 [A], OR = 1.32 [95%CI 1.21-1.43], p = 3.87×10⁻¹¹). In sub-group analysis two loci were significantly associated with NPG: 9p21 containing the CDKN2BAS gene (rs2157719 [G], OR = 0.58 [95% CI 0.50-0.67], p = 1.17×10⁻¹²) and a probable regulatory region on 8q22 (rs284489 [G], OR = 0.62 [95% CI 0.53-0.72], p = 8.88×10⁻¹⁰). Both NPG loci were also nominally associated with a second type of glaucoma, exfoliation syndrome glaucoma (rs2157719 [G], OR = 0.59 [95% CI 0.41-0.87], p = 0.004 and rs284489 [G], OR = 0.76 [95% CI 0.54-1.06], p = 0.021), suggesting that these loci might contribute more generally to optic nerve degeneration in glaucoma. Because both loci influence transforming growth factor beta (TGF-beta) signaling, we performed a genomic pathway analysis that showed an association between the TGF-beta pathway and NPG (permuted p = 0.009). These results suggest that neuro-protective therapies targeting TGF-beta signaling could be effective for multiple forms of glaucoma.

3,146 European ancestry cases, 3,487 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

6633
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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