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年龄相关性黄斑变性患者补体因子 H 相关基因拷贝数变异的相关性研究。

Association of copy number variations in complement factor H-Related genes among age-related macular degenerative subjects.

机构信息

Malaysian Research Institute on Ageing, Universiti Putra Malaysia, Serdang, Selangor DE, Malaysia.

Malaysian Research Institute on Ageing, Universiti Putra Malaysia, Serdang, Selangor DE, Malaysia.

出版信息

Kaohsiung J Med Sci. 2017 Dec;33(12):602-608. doi: 10.1016/j.kjms.2017.08.003. Epub 2017 Sep 6.

Abstract

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 < 0.05). The age-adjusted data suggests a possible increased risk of AMD disease (P < 0.05). No correlation was detected between CNVs and wet AMD for the remaining genes after we compared the frequencies of mean for that gene. An association was observed between CFH CNVs and wet AMD in the Malaysian population, however, strong evidence of a link with wet AMD was not found. Further investigative studies are needed using larger sample sizes to elucidate the role of CNVs in AMD pathogenesis.

摘要

年龄相关性黄斑变性(AMD)是最常见的不可逆转的视力丧失原因,先前的研究表明,湿性 AMD 的进展受到可改变和不可改变因素的影响。单核苷酸多态性(SNP)和拷贝数变异(CNV)与不同人群的 AMD 有关,但结果存在矛盾。我们的目的是确定马来西亚湿性 AMD 患者中补体因子 H 相关基因的 CNV。本研究纳入了 130 名湿性 AMD 患者和 120 名健康对照者。从所有受试者中提取 DNA,使用实时定量 PCR 检测 CFH、CFHR1 和 CFHR3 基因的 CNV,并比较两组之间的差异。CFH 基因与湿性 AMD 易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)。在比较该基因的平均频率后,未发现其余基因的 CNV 与湿性 AMD 之间存在相关性。在马来西亚人群中观察到 CFH CNV 与湿性 AMD 之间存在关联,但未发现与湿性 AMD 有明确关联。需要使用更大的样本量进行进一步的研究,以阐明 CNV 在 AMD 发病机制中的作用。

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