Miraldi Utz Virginia
a Abrahamson Pediatric Eye Institute , Cincinnati Children's Hospital Medical Center , Cincinnati , Ohio , USA .
Ophthalmic Genet. 2017 Mar-Apr;38(2):117-121. doi: 10.1080/13816810.2016.1183216. Epub 2016 May 27.
Myopia is the most common eye disorder and major cause of visual impairment worldwide. As the incidence of myopia continues to rise, the need to further understand the complex roles of molecular and environmental factors controlling variation in refractive error is of increasing importance. Tkatchenko and colleagues applied a systematic approach using a combination of gene set enrichment analysis, genome-wide association studies, and functional analysis of a murine model to identify a myopia susceptibility gene, APLP2. Differential expression of refractive error was associated with time spent reading for those with low frequency variants in this gene. This provides support for the longstanding hypothesis of gene-environment interactions in refractive error development.
近视是全球最常见的眼部疾病,也是视力损害的主要原因。随着近视发病率持续上升,进一步了解控制屈光不正变异的分子和环境因素的复杂作用变得越来越重要。特卡琴科及其同事采用了一种系统方法,结合基因集富集分析、全基因组关联研究和小鼠模型的功能分析,来确定一个近视易感基因APLP2。对于该基因低频变体携带者,屈光不正的差异表达与阅读时间有关。这为屈光不正发展中基因-环境相互作用的长期假设提供了支持。