Chen Zoe Tzu-Yi, Wang I-Jong, Shih Yung-Feng, Lin Luke Long-Kung
Department of Ophthalmology, Taipei City Hospital Zhongxing Branch, Taipei, Taiwan, ROC.
Ophthalmology. 2009 Oct;116(10):1920-7. doi: 10.1016/j.ophtha.2009.03.023. Epub 2009 Jul 18.
To investigate the association of genetic polymorphisms in the dermatan sulfate proteoglycan 3 (DSPG3), lumican (LUM), and decorin (DCN) genes (component genes of the sclera) with high myopia susceptibility in Taiwanese people.
Prospective case-control study.
Hospital clinic-based samples of 120 unrelated patients with extremely high myopia were studied. One hundred thirty-seven unrelated emmetropic individuals served as controls.
Four, 8, and 4 single nucleotide polymorphism (SNPs) were genotyped within the DSPG3, lumican, and decorin genes, respectively, using direct DNA sequencing. Pairwise linkage disequilibrium, haplotype analysis, adjusted logistic regression, and multifactor dimensionality reduction (MDR) methods were used to determine significant associations.
The association of haplotypes at the lumican gene with high myopia development.
The lumican gene SNP rs3759223:T-->C demonstrated a significant association with high myopia (P = 2.83 x 10(-4)). Four lumican SNPs showed significant linkage disequilibrium and formed a haplotype block. Sliding window haplotype analyses revealed that the block consisting of rs3759223 and rs3741834 showed significant goodness of fit (global P = 1.0725 x 10(-6)). Haplotype-specific tests showed that the C-C and T-C haplotypes were associated significantly with high myopia, with odds ratios (95% confidence intervals) of 19.32 (2.55-146.54) and 0.69 (0.46-1.04), respectively. rs3759223 and rs3741834 are in a putative regulatory element of the lumican gene, which influences fibrillogenesis of scleral collagen fibers and the development of myopia. The results of an MDR analysis corroborated the single-locus association and suggested a significant 2-locus interaction model composed of SNPs rs2300588 and rs3741834 in the lumican gene.
Genetic variation in the regulatory domains of the lumican gene, where both rs3759223 and rs3741834 are located, are associated with high myopia susceptibility among the Han Chinese, making this region worthy of further investigation.
探讨硫酸皮肤素蛋白聚糖3(DSPG3)、光蛋白聚糖(LUM)和核心蛋白聚糖(DCN)基因(巩膜的组成基因)的基因多态性与台湾人群高度近视易感性的关联。
前瞻性病例对照研究。
对120例无亲缘关系的极端高度近视患者的医院门诊样本进行研究。137例无亲缘关系的正视个体作为对照。
分别采用直接DNA测序法对DSPG3、光蛋白聚糖和核心蛋白聚糖基因内的4个、8个和4个单核苷酸多态性(SNP)进行基因分型。采用成对连锁不平衡、单倍型分析、校正逻辑回归和多因素降维(MDR)方法确定显著关联。
光蛋白聚糖基因单倍型与高度近视发展的关联。
光蛋白聚糖基因SNP rs3759223:T→C与高度近视显著相关(P = 2.83×10-4)。4个光蛋白聚糖SNP显示出显著的连锁不平衡并形成一个单倍型块。滑动窗口单倍型分析显示,由rs3759223和rs3741834组成的单倍型块具有显著的拟合优度(全局P = 1.0725×10-6)。单倍型特异性检验显示,C-C和T-C单倍型分别与高度近视显著相关,优势比(95%置信区间)分别为19.32(2.55 - 146.54)和0.69(0.46 - 1.04)。rs3759223和rs3741834位于光蛋白聚糖基因的一个假定调控元件中,该元件影响巩膜胶原纤维的原纤维形成和近视的发展。MDR分析结果证实了单基因座关联,并提示由光蛋白聚糖基因中的SNP rs2300588和rs3741834组成的显著双基因座相互作用模型。
rs3759223和rs3741834所在的光蛋白聚糖基因调控域的遗传变异与汉族人群的高度近视易感性相关,该区域值得进一步研究。