首页> 外文期刊>Kaohsiung Journal of Medical Sciences >Association of copy number variations in complement factor H-Related genes among age-related macular degenerative subjects
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Association of copy number variations in complement factor H-Related genes among age-related macular degenerative subjects

机译:年龄相关性黄斑变性受试者中补体因子H相关基因拷贝数变异的关联

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摘要

Age-related macular degeneration (AMD) is the most widely recognised cause of irreversible vision loss and previous studies have suggested that the advancement of wet AMD is influenced by both modifiable and non-modifiable elements. Single nucleotide polymorphism (SNPs) and copy number of variations (CNVs) have been associated with AMD in various populations, however the results are conflicting. Our aim is to determine the CNVs of Complement Factor H-Related genes among Malaysian subjects with wet AMD. 130 patients with wet AMD and 120 healthy controls were included in this research. DNA was extracted from all subjects and CNVs of CFH , CFHR1 and CFHR3 genes; determined using quantitative real-time PCR and were compared between the two groups. A consistent association was observed between CFH gene and wet AMD susceptibility (P?
机译:年龄相关性黄斑变性(AMD)是不可逆性视力丧失的最广泛公认的原因,以前的研究表明,湿性AMD的发展受可修饰和不可修饰元素的影响。单核苷酸多态性(SNPs)和变异拷贝数(CNVs)已与AMD在各种人群中相关联,但是结果相矛盾。我们的目的是确定患有湿性AMD的马来西亚受试者中补体因子H相关基因的CNV。本研究包括130例湿性AMD患者和120例健康对照者。从所有受试者和CFH,CFHR1和CFHR3基因的CNV中提取DNA;使用实时定量PCR进行检测,并在两组之间进行比较。观察到CFH基因与湿性AMD敏感性之间存在一致的相关性(P <0.05)。年龄调整后的数据表明,AMD疾病的风险可能增加(P <0.05)。在比较了该基因的均值频率后,其余基因的CNV与湿性AMD之间未发现相关性。在马来西亚人口中观察到CFH CNV与湿性AMD之间存在关联,但是,未发现与湿性AMD相关的有力证据。需要使用更大的样本量进行进一步的调查研究,以阐明CNV在AMD发病机理中的作用。

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