Saracaloglu Ahmet, Demiryürek Seniz, Okumus Seydi, Oztuzcu Serdar, Bozgeyik Ibrahim, Coskun Erol, Aksoy Umit, Kaydu Erdal, Erbagci Ibrahim, Gürler Bulent, Alasehirli Belgin, Demiryürek Abdullah T
1 Department of Medical Pharmacology, Faculty of Medicine, Gaziantep University , Gaziantep, Turkey .
2 Department of Physiology, Faculty of Medicine, Gaziantep University , Gaziantep, Turkey .
OMICS. 2016 May;20(5):290-5. doi: 10.1089/omi.2016.0031.
The annual economic burden of visual disorders in the United States was estimated as $139 billion. The World Health Organization has listed glaucoma in the top 10 priority eye diseases. Primary open-angle glaucoma (POAG) is a common subtype, with a lack of clinical tools for early diagnosis. The Rho GTPases belong to the Ras superfamily of proteins; the RhoA immunostaining in the optic nerve head in human glaucoma is reportedly increased. We investigated the association of polymorphisms in the Ras Homolog Family Member A, B, C, and D genes (RHOA, RHOB, RHOC, and RHOD, respectively). In a total sample of 361 unrelated subjects (179 patients with POAG and 182 age- and sex-matched healthy controls), RHOA (rs6784820, rs974495), RHOB (rs62121967), RHOC (rs11102522), and RHOD (rs61891303, rs2282502) polymorphisms were characterized by the BioMark HD dynamic array system with real-time polymerarse chain reaction. Among these candidate genetic markers and considering the Bonferroni correction, RHOA rs974495 polymorphism was significantly associated with POAG (p = 0.0011), with the TT genotype increasing the disease risk 4.9 times (95% CI 1.630-15.023). The allele and haplotype distributions of the above RHO candidate polymorphisms did not diplay a significant association. This is the first study, to the best of our knowledge, to identify a significant genotypic association between POAG and RHOA gene rs974495 polymorphism. These observations warrant replication in independent samples in the pursuit of precision medicine for rapid and early glaucoma diagnosis, and molecular targets for innovation in therapeutics of this common eye disease.
据估计,美国视觉障碍的年度经济负担为1390亿美元。世界卫生组织已将青光眼列为十大重点眼病之一。原发性开角型青光眼(POAG)是一种常见亚型,缺乏早期诊断的临床工具。Rho GTP酶属于蛋白质的Ras超家族;据报道,人类青光眼视神经头中的RhoA免疫染色增加。我们研究了Ras同源家族成员A、B、C和D基因(分别为RHOA、RHOB、RHOC和RHOD)多态性之间的关联。在总共361名无关受试者的样本中(179例POAG患者和182名年龄和性别匹配的健康对照),通过BioMark HD动态阵列系统结合实时聚合酶链反应对RHOA(rs6784820、rs974495)、RHOB(rs62121967)、RHOC(rs11102522)和RHOD(rs61891303、rs2282502)多态性进行了特征分析。在这些候选遗传标记中,并考虑到Bonferroni校正,RHOA rs974495多态性与POAG显著相关(p = 0.0011),TT基因型使疾病风险增加4.9倍(95% CI 1.630 - 15.023)。上述Rho候选多态性的等位基因和单倍型分布未显示出显著关联。据我们所知,这是第一项确定POAG与RHOA基因rs974495多态性之间存在显著基因型关联的研究。这些观察结果需要在独立样本中进行重复验证,以寻求精准医学,实现青光眼的快速早期诊断,并为这种常见眼病的治疗创新提供分子靶点。