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
{"title":"CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration.","authors":"Ruta Sakiene,&nbsp;Alvita Vilkeviciute,&nbsp;Loresa Kriauciuniene,&nbsp;Vilma Jurate Balciuniene,&nbsp;Dovile Buteikiene,&nbsp;Goda Miniauskiene,&nbsp;Rasa Liutkeviciene","doi":"10.1155/2016/3917916","DOIUrl":null,"url":null,"abstract":"<p><p>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. </p>","PeriodicalId":53309,"journal":{"name":"Advances in Medicine","volume":" ","pages":"3917916"},"PeriodicalIF":0.0000,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2016/3917916","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advances in Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2016/3917916","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2016/8/29 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
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.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
5
审稿时长
22 weeks
期刊最新文献
Assessment of Knowledge and Attitude of General Practitioners Regarding Autism and Associated Factors at Gondar University Hospital, Gondar, Ethiopia. Influence of Staphylococcus aureus Infection on Partially Ischemic Excisional Skin Wounds. Impact of Obesity on Cardiac Volumes and Left Ventricular Diameter: A Cross-Sectional Study in an Iranian Heart Center. The Epidemiology of COVID-19 Vaccine-Induced Myocarditis Emerging Challenges in Staphylococcus aureus Bloodstream Infections: Insights from Coagulase Typing, Toxin Genes, and Antibiotic Resistance Patterns.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1