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Copy number variation in VEGF gene as a biomarker of susceptibility to age-related macular degeneration

机译: VEGF 基因的拷贝数变异作为易感年龄相关性黄斑变性的生物标志物

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Background Several studies in various populations have been conducted to determine candidate genes that could contribute to age-related macular degeneration (AMD) pathogenesis. Objective The present study was undertaken to determine the association of high temperature requirement A-1 ( HTRA1 ), vascular endothelial growth factor ( VEGF ) and very-low-density receptor ( VLDR ) genes with wet AMD subjects in Malaysia . Methods A total of 125 subjects with wet AMD and 120 subjects without AMD from the Malaysian population were selected for this study. Genomic DNA was extracted and copy number variations (CNVs) were determined using quantitative real-time Polymerase Chain Reaction (qPCR) and comparison between the two groups was done. The demographic characteristics were also recorded. Statistical analysis was carried out using software where a level of P<0.05 was considered to be statistically significant. Result Statistically significant associations of the VEGF gene were observed in mean copy differences between case and control subjects (P<0.05). The consistency of both unadjusted and age-adjusted data at Copy Number CN gain (CN=3 and CN=4) suggested that VEGF could increase the risk of wet AMD disease (P<0.05). None of CNVs of HTRA1 and VLDR genes showed associations with the wet AMD disease based on comparisons of the frequencies of mean (P>0.05). Conclusion Observations of an association between CNVs of VEGF gene and wet AMD have revealed that the CNVs of VEGF gene appears to be a possible contributor to wet AMD subjects in Malaysia.
机译:背景技术已经在各种人群中进行了一些研究,以确定可能与年龄有关的黄斑变性(AMD)发病机理的候选基因。目的研究确定高温需求A-1(HTRA1),血管内皮生长因子(VEGF)和极低密度受体(VLDR)基因与马来西亚湿性AMD患者的关系。方法从马来西亚人群中总共选择了125名湿性AMD受试者和120名无AMD受试者。提取基因组DNA,并使用定量实时聚合酶链反应(qPCR)确定拷贝数变异(CNV),并进行两组之间的比较。还记录了人口统计特征。使用软件进行统计分析,其中P <0.05的水平被认为具有统计学意义。结果在病例和对照组之间的平均拷贝数差异中观察到了VEGF基因的统计学显着关联(P <0.05)。拷贝数CN增益(CN = 3和CN = 4)下未校正和年龄校正数据的一致性表明VEGF可能增加湿性AMD疾病的风险(P <0.05)。根据平均频率的比较,HTRA1和VLDR基因的CNV均未显示与湿性AMD疾病相关(P> 0.05)。结论观察到VEGF基因的CNV与湿性AMD之间的关联,发现VEGF基因的CNV似乎是马来西亚湿性AMD患者的一个可能原因。

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