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Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population

PURPOSE: BH3-like motif containing, cell death inducer (BLID) and LOC399959 are two genes associated with the single nucleotide polymorphism (SNP) rs577948, which is a susceptibility locus for high myopia in Japanese subjects. The purpose of this study was to determine if BLID and LOC399959 are asso...

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Autores principales: Zhao, Fuxin, Bai, Jian, Chen, Wei, Xue, Anquan, Li, Chaohua, Yan, Zhonghui, Chen, Hui, Lu, Fan, Hu, Yongwu, Qu, Jia, Zeng, Changqing, Zhou, Xiangtian
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956664/
https://www.ncbi.nlm.nih.gov/pubmed/21031016
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author Zhao, Fuxin
Bai, Jian
Chen, Wei
Xue, Anquan
Li, Chaohua
Yan, Zhonghui
Chen, Hui
Lu, Fan
Hu, Yongwu
Qu, Jia
Zeng, Changqing
Zhou, Xiangtian
author_facet Zhao, Fuxin
Bai, Jian
Chen, Wei
Xue, Anquan
Li, Chaohua
Yan, Zhonghui
Chen, Hui
Lu, Fan
Hu, Yongwu
Qu, Jia
Zeng, Changqing
Zhou, Xiangtian
author_sort Zhao, Fuxin
collection PubMed
description PURPOSE: BH3-like motif containing, cell death inducer (BLID) and LOC399959 are two genes associated with the single nucleotide polymorphism (SNP) rs577948, which is a susceptibility locus for high myopia in Japanese subjects. The purpose of this study was to determine if BLID and LOC399959 are associated with high myopia in Chinese Han subjects. METHODS: High myopia subjects (n=476) had a spherical refractive error of less than −6.00 D in at least one eye and/or an axial length greater than 26 mm. Genomic DNA was extracted and genotyped from peripheral blood leukocytes of high myopes and controls (n=275). Using a case-control association study of candidate regions, linkage disequilibrium blocks for 19 tag SNPs (tSNPs), including rs577948, harbored within and surrounding the BLID and LOC399959 genes were analyzed on a MassArray platform using iPlex chemistry. Each of the tSNPs had an r(2)>0.8 and minor allele frequency >10% in the Chinese Han population. Haplotype association analysis was performed on Haploview 4.1 using Chi-square (χ(2)) tests. RESULTS: None of the 19 tSNPs were statistically associated with high myopia. CONCLUSIONS: While rs577948 may be associated with high myopia in Japanese subjects, it and the other tSNPs near the BLID and LOC399959 genes are not susceptibility loci for high myopia in the Chinese Han population. Thus, associations of SNPs with high myopia as determined by Genome-Wide Association Study (GWAS) may be restricted to certain ethnic or genetically distinct populations. Without systematic replication in other populations, the results of GWAS associations should be interpreted with great caution.
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spelling pubmed-29566642010-10-28 Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population Zhao, Fuxin Bai, Jian Chen, Wei Xue, Anquan Li, Chaohua Yan, Zhonghui Chen, Hui Lu, Fan Hu, Yongwu Qu, Jia Zeng, Changqing Zhou, Xiangtian Mol Vis Research Article PURPOSE: BH3-like motif containing, cell death inducer (BLID) and LOC399959 are two genes associated with the single nucleotide polymorphism (SNP) rs577948, which is a susceptibility locus for high myopia in Japanese subjects. The purpose of this study was to determine if BLID and LOC399959 are associated with high myopia in Chinese Han subjects. METHODS: High myopia subjects (n=476) had a spherical refractive error of less than −6.00 D in at least one eye and/or an axial length greater than 26 mm. Genomic DNA was extracted and genotyped from peripheral blood leukocytes of high myopes and controls (n=275). Using a case-control association study of candidate regions, linkage disequilibrium blocks for 19 tag SNPs (tSNPs), including rs577948, harbored within and surrounding the BLID and LOC399959 genes were analyzed on a MassArray platform using iPlex chemistry. Each of the tSNPs had an r(2)>0.8 and minor allele frequency >10% in the Chinese Han population. Haplotype association analysis was performed on Haploview 4.1 using Chi-square (χ(2)) tests. RESULTS: None of the 19 tSNPs were statistically associated with high myopia. CONCLUSIONS: While rs577948 may be associated with high myopia in Japanese subjects, it and the other tSNPs near the BLID and LOC399959 genes are not susceptibility loci for high myopia in the Chinese Han population. Thus, associations of SNPs with high myopia as determined by Genome-Wide Association Study (GWAS) may be restricted to certain ethnic or genetically distinct populations. Without systematic replication in other populations, the results of GWAS associations should be interpreted with great caution. Molecular Vision 2010-10-02 /pmc/articles/PMC2956664/ /pubmed/21031016 Text en Copyright © 2010 Molecular Vision. http://creativecommons.org/licenses/by/3.0/ 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 work is properly cited.
spellingShingle Research Article
Zhao, Fuxin
Bai, Jian
Chen, Wei
Xue, Anquan
Li, Chaohua
Yan, Zhonghui
Chen, Hui
Lu, Fan
Hu, Yongwu
Qu, Jia
Zeng, Changqing
Zhou, Xiangtian
Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
title Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
title_full Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
title_fullStr Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
title_full_unstemmed Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
title_short Evaluation of BLID and LOC399959 as candidate genes for high myopia in the Chinese Han population
title_sort evaluation of blid and loc399959 as candidate genes for high myopia in the chinese han population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956664/
https://www.ncbi.nlm.nih.gov/pubmed/21031016
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