土耳其渗出性年龄相关性黄斑变性患者ARMS2基因的新一代测序分析。

H. Bardak, M. Gunay, Y. Ercalik, Y. Bardak, H. Ozbas, O. Bagci
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引用次数: 1

摘要

年龄相关性黄斑变性(AMD)是发达国家致盲的主要原因。这是一种复杂的疾病,有遗传和环境风险因素。为提高该病的临床管理水平,制定环境影响的风险评估和预防策略,建立更有效的治疗方法是很重要的。本研究的目的是研究土耳其渗出性AMD患者中年龄相关黄斑病变易感蛋白2 (ARMS2)基因序列。除了39名晚期渗出性AMD患者外,还包括250名可获得外显子组测序数据的健康个体作为对照组。排除有已知环境和系统性AMD危险因素病史的患者。从外周血中分离基因组DNA,并使用下一代测序技术进行分析。评估ARMS2基因的所有编码外显子。在患者和对照组中均鉴定出三种不同的ARMS2序列变异(rs10490923、rs2736911和rs10490924)。在对照组中,还检测到另外两个ARMS2基因变异(rs7088128和rs36213074)。Logistic回归分析揭示了rs10490924多态性与土耳其人群AMD之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Next-generation sequencing analysis of the ARMS2 gene in Turkish exudative age-related macular degeneration patients.
Age-related macular degeneration (AMD) is the leading cause of blindness in developed countries. It is a complex disease with both genetic and environmental risk factors. To improve clinical management of this condition, it is important to develop risk assessment and prevention strategies for environmental influences, and establish a more effective treatment approach. The aim of the present study was to investigate age-related maculopathy susceptibility protein 2 (ARMS2) gene sequences among Turkish patients with exudative AMD. In addition to 39 advanced exudative AMD patients, 250 healthy individuals for whom exome sequencing data were available were included as a control group. Patients with a history of known environmental and systemic AMD risk factors were excluded. Genomic DNA was isolated from peripheral blood and analyzed using next-generation sequencing. All coding exons of the ARMS2 gene were assessed. Three different ARMS2 sequence variations (rs10490923, rs2736911, and rs10490924) were identified in both the patient and control group. Within the control group, two further ARMS2 gene variants (rs7088128 and rs36213074) were also detected. Logistic regression analysis revealed a relationship between the rs10490924 polymorphism and AMD in the Turkish population.
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