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CYP4F2(rs2108622)基因多态性与年龄相关性黄斑变性的关联

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

作者信息

Sakiene Ruta, Vilkeviciute Alvita, Kriauciuniene Loresa, Balciuniene Vilma Jurate, Buteikiene Dovile, Miniauskiene Goda, Liutkeviciene Rasa

机构信息

Lithuanian University of Health Sciences, Medical Academy, Eiveniu 2, LT-50009 Kaunas, Lithuania.

Neuroscience Institute, Lithuanian University of Health Sciences, Medical Academy, Eiveniu 2, LT-50009 Kaunas, Lithuania.

出版信息

Adv Med. 2016;2016:3917916. doi: 10.1155/2016/3917916. Epub 2016 Aug 29.

Abstract

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.

摘要

背景。年龄相关性黄斑变性是老年人失明的主要原因,其病因和病理生理学尚未完全明确。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。该研究纳入了190例早期年龄相关性黄斑变性患者、181例渗出性年龄相关性黄斑变性(eAMD)患者以及从普通人群中随机抽取的210名受试者(对照组)。使用实时聚合酶链反应方法对rs2108622进行基因分型。结果。rs2108622基因多态性分析未发现早期AMD组、eAMD组和对照组之间C/C、C/T和T/T基因型分布存在任何差异。与女性相比,eAMD男性中CYP4F2(1347C>T)T/T基因型更为常见(10.2%对0.8%;p = 0.0052);与健康对照女性相比,eAMD女性中T/T基因型也较少见(0.8%对6.2%;p = 0.027)。结论。Rs2108622基因多态性对早期AMD和eAMD的发生没有显著影响。与女性相比,eAMD男性中T/T基因型更为常见,与健康女性相比,eAMD女性中T/T基因型较少见。

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