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

Advances in Medicine Pub Date : 2016-01-01 Epub Date: 2016-08-29 DOI:10.1155/2016/3917916
Ruta Sakiene, Alvita Vilkeviciute, Loresa Kriauciuniene, Vilma Jurate Balciuniene, Dovile Buteikiene, Goda Miniauskiene, Rasa Liutkeviciene
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引用次数: 9

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.

CYP4F2 (rs2108622)基因多态性与年龄相关性黄斑变性的关系
背景。老年性黄斑变性是老年人失明的主要原因,老年性黄斑变性的病因和病理生理尚不完全清楚。目的。测定rs2108622基因型在早期和渗出性老年性黄斑变性患者中的频率。方法。该研究招募了190名早期年龄相关性黄斑变性患者,181名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210名受试者(对照组)。采用实时聚合酶链反应法对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组和对照组在C/C、C/T和T/T基因型分布上存在差异。CYP4F2 (1347C>T) T/T基因型在eAMD的男性中比女性更常见(10.2%比0.8%;P = 0.0052);此外,与健康对照女性相比,T/T基因型在eAMD女性中出现的频率较低(0.8%对6.2%;P = 0.027)。结论。Rs2108622基因多态性对早期AMD和eAMD的发展无显著影响。与女性相比,T/T基因型在eAMD男性患者中更常见,而在eAMD女性患者中较健康女性较少出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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