Kalantan Hatem, Kondkar Altaf A, Sultan Tahira, Azad Taif A, Alsabaani Nasser A, AlQahtani Masoud Ali, Almummar Abdulrahman, Liu Yuato, Abu-Amero Khaled K
Glaucoma Research Chair, Department of Ophthalmology, College of Medicine, King Saud University, Riyadh, 11411, Saudi Arabia.
Ophthalmology Department, College of Medicine, King Khalid University, P.O. Box 641, Abha, 61421, Saudi Arabia.
BMC Res Notes. 2017 Nov 29;10(1):652. doi: 10.1186/s13104-017-2996-8.
Polymorphism rs13334190 in the zinc finger protein 469 gene has been suggested to predispose toward a "thin" cornea, which then becomes keratoconic or is directly pathogenic. Thus, we genotyped polymorphism rs13334190 in 127 unrelated keratoconus cases and 168 control subjects from Saudi Arabia using Taq-Man assay.
The genotype frequency distribution did not deviate significantly from the Hardy-Weinberg equilibrium (p > 0.05). Overall, both the genotype and allele frequencies were not significantly different between cases and controls. A minor allele frequency of 0.068 was comparable to the aggregate rates ranging from 0.060 to 0.086 observed in other populations. Binary logistic regression analysis was performed to ascertain the effects of age, gender and genotype on the likelihood of having keratoconus. The analysis indicated that increased age was statistically significant (p = 0.000) and that females have a 2.19-fold increased risk (p = 0.018) of developing keratoconus. The genotype frequencies did not differ between the sporadic or familial keratoconus cases. Polymorphism rs13334190 is not an independent risk factor for keratoconus in the Saudi cohort.
锌指蛋白469基因中的rs13334190多态性被认为易导致角膜“变薄”,进而发展为圆锥角膜或直接致病。因此,我们采用Taq-Man分析法对来自沙特阿拉伯的127例无关圆锥角膜患者和168例对照者的rs13334190多态性进行基因分型。
基因型频率分布未显著偏离哈迪-温伯格平衡(p>0.05)。总体而言,病例组和对照组之间的基因型和等位基因频率均无显著差异。0.068的次要等位基因频率与在其他人群中观察到的0.060至0.086的总发生率相当。进行二元逻辑回归分析以确定年龄、性别和基因型对患圆锥角膜可能性的影响。分析表明,年龄增长具有统计学意义(p = 0.000),女性患圆锥角膜的风险增加2.19倍(p = 0.018)。散发性或家族性圆锥角膜病例之间的基因型频率没有差异。在沙特队列中,rs13334190多态性不是圆锥角膜的独立危险因素。