Back to Search Start Over

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

Authors :
Wiggs JL
Yaspan BL
Hauser MA
Kang JH
Allingham RR
Olson LM
Abdrabou W
Fan BJ
Wang DY
Brodeur W
Budenz DL
Caprioli J
Crenshaw A
Crooks K
Delbono E
Doheny KF
Friedman DS
Gaasterland D
Gaasterland T
Laurie C
Lee RK
Lichter PR
Loomis S
Liu Y
Medeiros FA
McCarty C
Mirel D
Moroi SE
Musch DC
Realini A
Rozsa FW
Schuman JS
Scott K
Singh K
Stein JD
Trager EH
Vanveldhuisen P
Vollrath D
Wollstein G
Yoneyama S
Zhang K
Weinreb RN
Ernst J
Kellis M
Masuda T
Zack D
Richards JE
Pericak-Vance M
Pasquale LR
Haines JL
Source :
PLoS genetics [PLoS Genet] 2012; Vol. 8 (4), pp. e1002654. Date of Electronic Publication: 2012 Apr 26.
Publication Year :
2012

Abstract

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.<br />Competing Interests: The authors have declared that no competing interests exist.

Details

Language :
English
ISSN :
1553-7404
Volume :
8
Issue :
4
Database :
MEDLINE
Journal :
PLoS genetics
Publication Type :
Academic Journal
Accession number :
22570617
Full Text :
https://doi.org/10.1371/journal.pgen.1002654