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Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma
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 associati...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343074/ https://www.ncbi.nlm.nih.gov/pubmed/22570617 http://dx.doi.org/10.1371/journal.pgen.1002654 |
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author | 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. |
author_facet | 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. |
author_sort | Wiggs, Janey L. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3343074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-33430742012-05-08 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. PLoS Genet Research Article 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. Public Library of Science 2012-04-26 /pmc/articles/PMC3343074/ /pubmed/22570617 http://dx.doi.org/10.1371/journal.pgen.1002654 Text en Wiggs et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article 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 |
title | Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma |
title_full | Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma |
title_fullStr | Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma |
title_full_unstemmed | Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma |
title_short | Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma |
title_sort | common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3343074/ https://www.ncbi.nlm.nih.gov/pubmed/22570617 http://dx.doi.org/10.1371/journal.pgen.1002654 |
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