Evaluation of MYOC, ACAN, HGF, and MET as Candidate Genes for High Myopia in a Han Chinese Population

被引:14
作者
Yang, Xian [1 ]
Liu, Xiaoqi [2 ,3 ,4 ,5 ]
Peng, Jie [3 ,6 ]
Zheng, Hong [2 ,3 ]
Lu, Fang [2 ,3 ]
Gong, Bo [2 ,3 ]
Zhao, Guiqiu [1 ]
Meng, Yan [1 ]
Guan, Hongzai [1 ]
Ning, Meizhen [1 ]
Yang, Zhenglin [2 ,3 ,5 ]
Shi, Yi [2 ,3 ,4 ,5 ]
机构
[1] Qingdao Univ, Sch Med, Dept Ophthalmol, Affiliated Hosp, Qingdao 266003, Shandong, Peoples R China
[2] Sichuan Acad Med Sci, Sichuan Prov Key Lab Human Dis Gene Study, Clin Lab Dept, Chengdu 610072, Sichuan, Peoples R China
[3] Sichuan Prov Peoples Hosp, Chengdu 610072, Sichuan, Peoples R China
[4] Univ Elect Sci & Technol China, Key Lab NeuroInformat, Minist Educ, Sch Life Sci & Technol, Chengdu 610054, Peoples R China
[5] Southwest Jiaotong Univ, Sch Life Sci & Engn, Chengdu, Peoples R China
[6] Sichuan Acad Med Sci, Dept Ophthalmol, Chengdu 610072, Sichuan, Peoples R China
关键词
HEPATOCYTE GROWTH-FACTOR; OPEN-ANGLE GLAUCOMA; REFRACTIVE ERROR; CAUCASIAN POPULATION; OCULAR BIOMETRICS; RISK-FACTORS; POLYMORPHISMS; ASSOCIATION; FAMILY; SCLERA;
D O I
10.1089/gtmb.2013.0479
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:446 / 452
页数:7
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