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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 |
Appears in Collections: | Elements Staff Publications |
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