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在汉族人群中评估MYOC、ACAN、HGF和MET作为高度近视候选基因的情况。

Evaluation of MYOC, ACAN, HGF, and MET as candidate genes for high myopia in a Han Chinese population.

作者信息

Yang Xian, Liu Xiaoqi, Peng Jie, Zheng Hong, Lu Fang, Gong Bo, Zhao Guiqiu, Meng Yan, Guan Hongzai, Ning Meizhen, Yang Zhenglin, Shi Yi

机构信息

1 Department of Ophthalmology, Qingdao University School of Medicine, Affiliated Hospital of Qingdao University School of Medicine , Qingdao, China .

出版信息

Genet Test Mol Biomarkers. 2014 Jun;18(6):446-52. doi: 10.1089/gtmb.2013.0479. Epub 2014 Apr 25.

Abstract

AIM

To investigate the association between high myopia (HM) and single nucleotide polymorphisms (SNPs) in the myocilin (MYOC), hepatocyte growth factor (HGF), hepatocyte growth factor receptor (MET), and aggrecan (ACAN) genes in a Han Chinese population.

METHODS

Sixteen SNPs were genotyped by the SNaPshot method in a subject group composed of 1052 HM patients and 1070 controls. Statistical analysis was performed to determine the association between the SNPs and the susceptibility of HM.

RESULTS

Two SNPs (rs3784757 and rs1516794) in ACAN were significantly associated with HM (p=0.0334 and 0.0236, odds ratio [OR]=0.83 and 0.79, respectively). The risk haplotype CA and the protective haplotype TT, generated by rs3784757 and rs1516794, showed significant association with HM (p=0.0327 and 0.0304, OR=1.21 and 0.80, respectively). Two SNPs (rs38857 and rs10215153) in MET and one SNP (rs3784757) in ACAN showed significant association with HM (p=0.0064, 0.0113, and 0.0373; OR=4.14, 5.74 and 0.52; respectively) in the recessive model. None of the other SNPs showed significant association with HM.

CONCLUSIONS

Our results suggested that genetic variants in ACAN and MET are associated with HM. Functional roles of ACAN and MET in the development of HM need to be further investigated.

摘要

目的

在汉族人群中研究高度近视(HM)与肌纤蛋白(MYOC)、肝细胞生长因子(HGF)、肝细胞生长因子受体(MET)和聚集蛋白聚糖(ACAN)基因中的单核苷酸多态性(SNP)之间的关联。

方法

采用SNaPshot方法对由1052例高度近视患者和1070例对照组成的研究对象群体中的16个SNP进行基因分型。进行统计学分析以确定SNP与高度近视易感性之间的关联。

结果

ACAN基因中的两个SNP(rs3784757和rs1516794)与高度近视显著相关(p = 0.0334和0.0236,优势比[OR]分别为0.83和0.79)。由rs3784757和rs1516794产生的风险单倍型CA和保护性单倍型TT与高度近视显著相关(p = 0.0327和0.0304,OR分别为1.21和0.80)。MET基因中的两个SNP(rs38857和rs10215153)以及ACAN基因中的一个SNP(rs3784757)在隐性模型中与高度近视显著相关(p = 0.0064、0.0113和0.0373;OR分别为4.14、5.74和0.52)。其他SNP均未显示与高度近视有显著关联。

结论

我们的结果表明,ACAN和MET基因中的遗传变异与高度近视相关。ACAN和MET在高度近视发生发展中的功能作用需要进一步研究。

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