Literature DB >> 27044882

Association of IGF1 and IGF1R gene polymorphisms with high myopia in a Han Chinese population.

Pu Wang1, Xiaoqi Liu2, Zimeng Ye2,3, Bo Gong2, Yin Yang4, Dingding Zhang2, Xuemei Wu2, Hong Zheng2, Yuanfeng Li2, Zhenglin Yang2,3, Yi Shi2,3.   

Abstract

OBJECTIVES: Insulin-like growth factor 1 (IGF1) and insulin-like growth factor 1 receptor (IGF1R) have been shown to influence the development of form-deprivation myopia. However, genetic association between these two genes and high myopia remains inconsistent in different studies. This study was conducted to investigate the association between IGF1and IGF1R and high myopia in a Han Chinese population.
METHODS: Fourteen single nucleotide polymorphisms (SNPs) in the IGF1 and IGF1R genes were genotyped by SNaPshot method in a Han Chinese subject group composed of 1244 high myopia patients and 1380 controls. The genotyping data was analyzed by χ2 test and the linkage disequilibrium block structure was examined by Haploview software.
RESULTS: There were no statistically significant differences in the allele frequencies of IGF1 and IGF1R SNPs and genotypes between patients and controls after Bonferroni multiple-correction (p > 0.05). However, the G allele of rs35766 in the IGF1 gene showed a protective effect for high myopia (p = 0.015, corrected p = 0.21, odds ratio [OR] = 0.77, 95% CI = 0.70-0.97). The carriers of rs35766GG and rs35766GG+AG genotypes displayed a decreased risk of high myopia compared with rs35766AA carriers (p = 0.012, OR = 0.65, 95% CI = 0.47-0.91; p = 0.019, OR = 0.68, 95% CI = 0.50-0.94, respectively).
CONCLUSIONS: Genetic variants in the IGF1 and IGF1R genes might not be associated with high myopia in Han Chinese. Further studies are needed to verify the possible function of IGF1 and IGF1R in the development of myopia.

Entities:  

Keywords:  High myopia; IGF1; IGF1R; single nucleotide polymorphisms

Mesh:

Substances:

Year:  2016        PMID: 27044882     DOI: 10.3109/13816810.2016.1145699

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  5 in total

1.  Abnormal resting-state functional network centrality in patients with high myopia: evidence from a voxel-wise degree centrality analysis.

Authors:  Yu-Xiang Hu; Jun-Rong He; Bo Yang; Xin Huang; Yu-Ping Li; Fu-Qing Zhou; Xiao-Xuan Xu; Yu-Lin Zhong; Jun Wang; Xiao-Rong Wu
Journal:  Int J Ophthalmol       Date:  2018-11-18       Impact factor: 1.779

2.  Next-Generation Sequencing Screening of 43 Families with Non-Syndromic Early-Onset High Myopia: A Clinical and Genetic Study.

Authors:  Eva González-Iglesias; Ana López-Vázquez; Susana Noval; María Nieves-Moreno; María Granados-Fernández; Natalia Arruti; Irene Rosa-Pérez; Marta Pacio-Míguez; Victoria E F Montaño; Patricia Rodríguez-Solana; Angela Del Pozo; Fernando Santos-Simarro; Elena Vallespín
Journal:  Int J Mol Sci       Date:  2022-04-11       Impact factor: 6.208

3.  Association of IGF1 single-nucleotide polymorphisms with myopia in Chinese children.

Authors:  Tianyu Cheng; Jingjing Wang; Shuyu Xiong; Bo Zhang; Qiangqiang Li; Xun Xu; Xiangui He
Journal:  PeerJ       Date:  2020-01-27       Impact factor: 2.984

4.  The G allele of the IGF1 rs2162679 SNP is a potential protective factor for any myopia: Updated systematic review and meta-analysis.

Authors:  Bo Meng; Kang Wang; Yingxiang Huang; Yanling Wang
Journal:  PLoS One       Date:  2022-07-21       Impact factor: 3.752

Review 5.  Insight into the molecular genetics of myopia.

Authors:  Jiali Li; Qingjiong Zhang
Journal:  Mol Vis       Date:  2017-12-31       Impact factor: 2.367

  5 in total

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