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Associations between CRYBA4 gene variants and high myopia in a Japanese population
PURPOSE: The crystallin beta A4 (CRYBA4) gene variant, rs2009066, was previously reported to be associated with high myopia in a southern Chinese population. In the present study, we investigated whether CRYBA4 variants were associated with high myopia in a Japanese population. METHODS: We recruited...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724408/ https://www.ncbi.nlm.nih.gov/pubmed/29263643 http://dx.doi.org/10.2147/OPTH.S146038 |
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author | Kawagoe, Tatsukata Ota, Masao Meguro, Akira Takeuchi, Masaki Yamane, Takahiro Shimazaki, Haruna Takeuchi, Masaru Okada, Eiichi Teshigawara, Takeshi Mizuki, Nobuhisa |
author_facet | Kawagoe, Tatsukata Ota, Masao Meguro, Akira Takeuchi, Masaki Yamane, Takahiro Shimazaki, Haruna Takeuchi, Masaru Okada, Eiichi Teshigawara, Takeshi Mizuki, Nobuhisa |
author_sort | Kawagoe, Tatsukata |
collection | PubMed |
description | PURPOSE: The crystallin beta A4 (CRYBA4) gene variant, rs2009066, was previously reported to be associated with high myopia in a southern Chinese population. In the present study, we investigated whether CRYBA4 variants were associated with high myopia in a Japanese population. METHODS: We recruited 1,063 Japanese patients with high myopia (spherical equivalent [SE] ≤−9.00 D in both eyes) and 1,009 healthy Japanese subjects (SE >−1.00 D). We genotyped rs2009066 and three tagging single-nucleotide polymorphisms (SNPs), rs16982456, rs2071861, and rs4276, in the CRYBA4 region. RESULTS: We did not find any significant association between these four SNPs and high myopia in an allele analysis. However, rs2009066 and rs2071861, which were in strong linkage disequilibrium (LD; r(2)=0.86), showed a marginal association with high myopia in the recessive genotype model of risk alleles (rs2009066 G allele: P=0.032, odds ratio [OR] =1.31; rs2071861 A allele: P=0.037, OR =1.31). Nevertheless, this association became insignificant after correcting for multiple testing (Pc >0.05). CONCLUSION: This study showed no significant association between CRYBA4 variants and high myopia in a Japanese population. Our findings did not correspond with a previous study. Further genetic studies with other populations are needed to elucidate a potential contribution of the CRYBA4 region in the development of high myopia. |
format | Online Article Text |
id | pubmed-5724408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57244082017-12-20 Associations between CRYBA4 gene variants and high myopia in a Japanese population Kawagoe, Tatsukata Ota, Masao Meguro, Akira Takeuchi, Masaki Yamane, Takahiro Shimazaki, Haruna Takeuchi, Masaru Okada, Eiichi Teshigawara, Takeshi Mizuki, Nobuhisa Clin Ophthalmol Original Research PURPOSE: The crystallin beta A4 (CRYBA4) gene variant, rs2009066, was previously reported to be associated with high myopia in a southern Chinese population. In the present study, we investigated whether CRYBA4 variants were associated with high myopia in a Japanese population. METHODS: We recruited 1,063 Japanese patients with high myopia (spherical equivalent [SE] ≤−9.00 D in both eyes) and 1,009 healthy Japanese subjects (SE >−1.00 D). We genotyped rs2009066 and three tagging single-nucleotide polymorphisms (SNPs), rs16982456, rs2071861, and rs4276, in the CRYBA4 region. RESULTS: We did not find any significant association between these four SNPs and high myopia in an allele analysis. However, rs2009066 and rs2071861, which were in strong linkage disequilibrium (LD; r(2)=0.86), showed a marginal association with high myopia in the recessive genotype model of risk alleles (rs2009066 G allele: P=0.032, odds ratio [OR] =1.31; rs2071861 A allele: P=0.037, OR =1.31). Nevertheless, this association became insignificant after correcting for multiple testing (Pc >0.05). CONCLUSION: This study showed no significant association between CRYBA4 variants and high myopia in a Japanese population. Our findings did not correspond with a previous study. Further genetic studies with other populations are needed to elucidate a potential contribution of the CRYBA4 region in the development of high myopia. Dove Medical Press 2017-12-07 /pmc/articles/PMC5724408/ /pubmed/29263643 http://dx.doi.org/10.2147/OPTH.S146038 Text en © 2017 Kawagoe et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Kawagoe, Tatsukata Ota, Masao Meguro, Akira Takeuchi, Masaki Yamane, Takahiro Shimazaki, Haruna Takeuchi, Masaru Okada, Eiichi Teshigawara, Takeshi Mizuki, Nobuhisa Associations between CRYBA4 gene variants and high myopia in a Japanese population |
title | Associations between CRYBA4 gene variants and high myopia in a Japanese population |
title_full | Associations between CRYBA4 gene variants and high myopia in a Japanese population |
title_fullStr | Associations between CRYBA4 gene variants and high myopia in a Japanese population |
title_full_unstemmed | Associations between CRYBA4 gene variants and high myopia in a Japanese population |
title_short | Associations between CRYBA4 gene variants and high myopia in a Japanese population |
title_sort | associations between cryba4 gene variants and high myopia in a japanese population |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5724408/ https://www.ncbi.nlm.nih.gov/pubmed/29263643 http://dx.doi.org/10.2147/OPTH.S146038 |
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