Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pgen.1002654
Title: Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
Authors: Wiggs J.L.
Yaspan B.L.
Hauser M.A. 
Kang J.H.
Allingham R.R. 
Olson L.M.
Abdrabou W.
Fan B.J.
Wang D.Y.
Brodeur W.
Budenz D.L.
Caprioli J.
Crenshaw A.
Crooks K.
DelBono E.
Doheny K.F.
Friedman D.S.
Gaasterland D.
Gaasterland T.
Laurie C.
Lee R.K.
Lichter P.R.
Loomis S.
Liu Y.
Medeiros F.A.
McCarty C.
Mirel D.
Moroi S.E.
Musch D.C.
Realini A.
Rozsa F.W.
Schuman J.S.
Scott K.
Singh K.
Stein J.D.
Trager E.H.
VanVeldhuisen P.
Vollrath D.
Wollstein G.
Yoneyama S.
Zhang K.
Weinreb R.N.
Ernst J.
Kellis M.
Masuda T.
Zack D.
Richards J.E.
Pericak-Vance M.
Pasquale L.R.
Haines J.L.
Keywords: animal experiment
animal model
animal tissue
article
CDKN2BAS gene
chromosome 14q
chromosome 8q
chromosome 9p
controlled study
disease association
disease classification
DNA sequence
exfoliation syndrome
gene
gene expression profiling
gene function
gene location
gene locus
genetic association
genetic identification
genetic susceptibility
genetic variability
human
intraocular pressure
LRP12 gene
major clinical study
mouse
nerve degeneration
nonhuman
open angle glaucoma
optic nerve disease
signal transduction
single nucleotide polymorphism
ZFPM2 gene
allele
chromosome 8
chromosome 9
exfoliation syndrome
genetic association
genetics
meta analysis
metabolism
nerve degeneration
optic nerve
pathology
ANRIL long non coding RNA, human
ANRIL long non-coding RNA, human
homeodomain protein
SIX1 protein, human
transforming growth factor beta
untranslated RNA
Alleles
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Exfoliation Syndrome
Genome-Wide Association Study
Glaucoma, Open-Angle
Homeodomain Proteins
Humans
Nerve Degeneration
Optic Nerve
Polymorphism, Single Nucleotide
RNA, Untranslated
Transforming Growth Factor beta
Issue Date: 2012
Citation: Wiggs J.L., Yaspan B.L., Hauser M.A., Kang J.H., Allingham R.R., Olson L.M., Abdrabou W., Fan B.J., Wang D.Y., Brodeur W., Budenz D.L., Caprioli J., Crenshaw A., Crooks K., DelBono E., Doheny K.F., Friedman D.S., Gaasterland D., Gaasterland T., Laurie C., Lee R.K., Lichter P.R., Loomis S., Liu Y., Medeiros F.A., McCarty C., Mirel D., Moroi S.E., Musch D.C., Realini A., Rozsa F.W., Schuman J.S., Scott K., Singh K., Stein J.D., Trager E.H., VanVeldhuisen P., Vollrath D., Wollstein G., Yoneyama S., Zhang K., Weinreb R.N., Ernst J., Kellis M., Masuda T., Zack D., Richards J.E., Pericak-Vance M., Pasquale L.R., Haines J.L. (2012). Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. PLoS Genetics 8 (4) : e1002654. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pgen.1002654
Rights: Attribution 4.0 International
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. © 2012 Wiggs et al.
Source Title: PLoS Genetics
URI: https://scholarbank.nus.edu.sg/handle/10635/161641
ISSN: 15537390
DOI: 10.1371/journal.pgen.1002654
Rights: Attribution 4.0 International
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