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DOI 10.1371/journal.pgen.1002654

Медицинская библиотека · PLoS genetics · 2012

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

Wiggs Janey L, Yaspan Brian L, Hauser Michael A, Kang Jae H, Allingham R Rand, Olson Lana M, Abdrabou Wael, Fan Bao J, Wang Dan Y, Brodeur Wendy, Budenz Donald L, Caprioli Joseph, Crenshaw Andrew, Crooks Kristy, Delbono Elizabeth, Doheny Kimberly F, Friedman David S, Gaasterland Douglas, Gaasterland Terry, Laurie Cathy, Lee Richard K, Lichter Paul R, Loomis Stephanie, Liu Yutao, Medeiros Felipe A, McCarty Cathy, Mirel Daniel, Moroi Sayoko E, Musch David C, Realini Anthony, Rozsa Frank W, Schuman Joel S, Scott Kathleen, Singh Kuldev, Stein Joshua D, Trager Edward H, Vanveldhuisen Paul, Vollrath Douglas, Wollstein Gadi, Yoneyama Sachiko, Zhang Kang, Weinreb Robert N, Ernst Jason, Kellis Manolis, Masuda Tomohiro, Zack Don, Richards Julia E, Pericak-Vance Margaret, Pasquale Louis R, Haines Jonathan L

СтатьяМетаанализПоддержка NIH: внешняя программаПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: Wiggs Janey L, Yaspan Brian L, Hauser Michael A, Kang Jae H, Allingham R Rand, Olson Lana M, Abdrabou Wael, Fan Bao J, Wang Dan Y, Brodeur Wendy, Budenz Donald L, Caprioli Joseph, Crenshaw Andrew, Crooks Kristy, Delbono Elizabeth, Doheny Kimberly F, Friedman David S, Gaasterland Douglas, Gaasterland Terry, Laurie Cathy, Lee Richard K, Lichter Paul R, Loomis Stephanie, Liu Yutao, Medeiros Felipe A, McCarty Cathy, Mirel Daniel, Moroi Sayoko E, Musch David C, Realini Anthony, Rozsa Frank W, Schuman Joel S, Scott Kathleen, Singh Kuldev, Stein Joshua D, Trager Edward H, Vanveldhuisen Paul, Vollrath Douglas, Wollstein Gadi, Yoneyama Sachiko, Zhang Kang, Weinreb Robert N, Ernst Jason, Kellis Manolis, Masuda Tomohiro, Zack Don, Richards Julia E, Pericak-Vance Margaret, Pasquale Louis R, Haines Jonathan L. Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.. PLoS genetics. 2012. DOI: 10.1371/journal.pgen.1002654.

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