Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma
| dc.contributor.author | Wiggs, Janey L. | |
| dc.contributor.author | Yaspan, Brian L. | |
| dc.contributor.author | Hauser, Michael A. | |
| dc.contributor.author | Kang, Jae H. | |
| dc.contributor.author | Allingham, R. Rand | |
| dc.contributor.author | Olson, Lana M. | |
| dc.contributor.author | Abdrabou, Wael | |
| dc.contributor.author | ETAL.. | |
| dc.date.accessioned | 2024-10-29T12:37:47Z | |
| dc.date.available | 2024-10-29T12:37:47Z | |
| dc.date.issued | 2012-04-26 | |
| dc.description | Loss of vision from glaucoma, a common cause of blindness worldwide, is due to irreversible damage to the optic nerve. Current therapies cannot prevent glaucoma-related optic nerve disease and very little is known about the underlying responsible molecular events. | |
| dc.description.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. Keywords: Optic nerve, Degeneration, Glaucoma,Genomic | |
| dc.identifier.citation | Wiggs, J. L., Yaspan, B. L., Hauser, M. A., Kang, J. H., Allingham, R. R., Olson, L. M., ... & 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. | |
| dc.identifier.doi | https://doi.org/10.1371/journal.pgen.1002654 | |
| dc.identifier.uri | https://repository.adu.ac.ae/handle/1/6879 | |
| dc.language.iso | en | |
| dc.publisher | PLOS ONE | |
| dc.title | Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma | |
| dc.type | Article |
