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CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration

机译:CYP4F2(rs2108622)基因多态性与年龄相关性黄斑变性

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摘要

Background. Age-related macular degeneration is the leading cause of blindness in elderly individuals where aetiology and pathophysiology of age-related macular degeneration are not absolutely clear. Purpose. To determine the frequency of the genotype of rs2108622 in patients with early and exudative age-related macular degeneration. Methods. The study enrolled 190 patients with early age-related macular degeneration, 181 patients with exudative age-related macular degeneration (eAMD), and a random sample of 210 subjects from the general population (control group). The genotyping of rs2108622 was carried out using the real-time polymerase chain reaction method. Results. The analysis of rs2108622 gene polymorphism did not reveal any differences in the distribution of C/C, C/T, and T/T genotypes between the early AMD group, the eAMD group, and the control group. The CYP4F2 (1347C>T) T/T genotype was more frequent in males with eAMD compared to females (10.2% versus 0.8%; p = 0.0052); also T/T genotype was less frequently present in eAMD females compared to healthy control females (0.8% versus 6.2%; p = 0.027). Conclusion. Rs2108622 gene polymorphism had no predominant effect on the development of early AMD and eAMD. The T/T genotype was more frequent in males with eAMD compared to females and less frequently present in eAMD females compared to healthy females.
机译:背景。与年龄有关的黄斑变性是老年患者失明的主要原因,因为与年龄有关的黄斑变性的病因和病理生理学尚不十分清楚。目的。确定早期和渗出性年龄相关性黄斑变性患者中rs2108622基因型的频率。方法。该研究招募了190名与早期年龄相关的黄斑变性的患者,181例与渗出性年龄相关的黄斑变性(eAMD)的患者,并从普通人群(对照组)中随机抽取了210名受试者作为样本。 rs2108622的基因分型使用实时聚合酶链反应方法进行。结果。 rs2108622基因多态性的分析未发现早期AMD组,eAMD组和对照组之间C / C,C / T和T / T基因型的分布存在任何差异。 CYP4F2(1347C> T)T / T基因型在eAMD男性中比女性更频繁(10.2%对0.8%; p = 0.0052)。与健康对照女性相比,eAMD女性中T / T基因型的出现频率也较低(0.8%比6.2%; p = 0.027)。结论。 Rs2108622基因多态性对早期AMD和eAMD的发展没有主要影响。与女性相比,具有eAMD的男性中T / T基因型更为常见,而与健康女性相比,在eAMD女性中T / T基因型的出现频率较低。

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