Institute of Biological Systems and Genetics Research, Lithuanian University of Health Sciences, Tilzes 18, Kaunas, Lithuania.
Department of Ophthalmology, Lithuanian University of Health Sciences, Eiveniu 2, Kaunas, Lithuania.
Gene. 2019 Mar 1;687:151-155. doi: 10.1016/j.gene.2018.11.030. Epub 2018 Nov 17.
This study aimed to find associations between miR-328 expression in whole blood, polymorphism at 3'UTR of the PAX6 gene (paired box homeotic gene 6) and myopia.
We evaluated 451 individuals (142 individuals with low, 49 with moderate and 13 with high-degree myopia, and 247 healthy individuals). DNA and RNA were extracted from peripheral blood samples. Expression of miR-328 was assessed and genotyping of single-nucleotide polymorphisms (SNPs) of the PAX6 (rs662702) performed using the Applied Biosystems 7900HT Real-Time Polymerase Chain Reaction System.
Moderate and high degree myopia showed significant differences between TT and CT genotypes of the PAX6 gene (p < 0.001). In the myopia group, 71.4% of the subjects had the TT genotype and 28.6% had the CT genotype; meanwhile in the control group, 97.1% had the TT genotype and 2.9% had the CT genotype. The odds ratio of having moderate and/or high degree myopia for individuals with the CT genotype was 13.6 (2.865-64.55) 95% CI versus TT genotype (p = 0.001). MiR-328 results showed that ∆Ct values differed statistically significantly between the myopia and control groups. Patients with myopia in the peripheral blood cells had a higher expression of miR-328 than controls (p < 0.05).
Significant differences were detected between the PAX6 gene (rs662702) TT and CT genotypes in moderate and high degree myopia; the risk C allele increased the risk for myopia. The expression level of miR-328 in peripheral blood cells was higher in patients with myopia than controls. We did not find the association between expression of mir-328 in the peripheral blood cells and PAX6 gene (rs662702) polymorphism comparing myopia and control groups.
本研究旨在探讨全血 miR-328 表达与 PAX6 基因(配对盒基因 6)3'UTR 多态性与近视的关系。
我们评估了 451 个人(142 名低度近视者、49 名中度近视者、13 名高度近视者和 247 名健康者)。从外周血样本中提取 DNA 和 RNA。采用 Applied Biosystems 7900HT 实时聚合酶链反应系统评估 miR-328 的表达,并对 PAX6(rs662702)单核苷酸多态性(SNP)进行基因分型。
中度和高度近视者 PAX6 基因 TT 和 CT 基因型之间存在显著差异(p<0.001)。在近视组中,71.4%的受试者为 TT 基因型,28.6%为 CT 基因型;而在对照组中,97.1%为 TT 基因型,2.9%为 CT 基因型。CT 基因型个体发生中度和/或高度近视的优势比为 13.6(2.865-64.55)95%CI 与 TT 基因型(p=0.001)。miR-328 结果显示,近视组和对照组之间的∆Ct 值存在统计学差异。近视患者外周血单个核细胞中 miR-328 的表达明显高于对照组(p<0.05)。
中度和高度近视者 PAX6 基因(rs662702)TT 和 CT 基因型之间存在显著差异;C 等位基因风险增加了近视的风险。与对照组相比,近视患者外周血单个核细胞中 miR-328 的表达水平较高。我们没有发现外周血单个核细胞中 mir-328 的表达与 PAX6 基因(rs662702)多态性在近视组和对照组之间的相关性。