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

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 exudativ...

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Autores principales: Sakiene, Ruta, Vilkeviciute, Alvita, Kriauciuniene, Loresa, Balciuniene, Vilma Jurate, Buteikiene, Dovile, Miniauskiene, Goda, Liutkeviciene, Rasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019857/
https://www.ncbi.nlm.nih.gov/pubmed/27652291
http://dx.doi.org/10.1155/2016/3917916
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author Sakiene, Ruta
Vilkeviciute, Alvita
Kriauciuniene, Loresa
Balciuniene, Vilma Jurate
Buteikiene, Dovile
Miniauskiene, Goda
Liutkeviciene, Rasa
author_facet Sakiene, Ruta
Vilkeviciute, Alvita
Kriauciuniene, Loresa
Balciuniene, Vilma Jurate
Buteikiene, Dovile
Miniauskiene, Goda
Liutkeviciene, Rasa
author_sort Sakiene, Ruta
collection PubMed
description 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.
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spelling pubmed-50198572016-09-20 CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration Sakiene, Ruta Vilkeviciute, Alvita Kriauciuniene, Loresa Balciuniene, Vilma Jurate Buteikiene, Dovile Miniauskiene, Goda Liutkeviciene, Rasa Adv Med Research Article 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. Hindawi Publishing Corporation 2016 2016-08-29 /pmc/articles/PMC5019857/ /pubmed/27652291 http://dx.doi.org/10.1155/2016/3917916 Text en Copyright © 2016 Ruta Sakiene et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sakiene, Ruta
Vilkeviciute, Alvita
Kriauciuniene, Loresa
Balciuniene, Vilma Jurate
Buteikiene, Dovile
Miniauskiene, Goda
Liutkeviciene, Rasa
CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration
title CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration
title_full CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration
title_fullStr CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration
title_full_unstemmed CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration
title_short CYP4F2 (rs2108622) Gene Polymorphism Association with Age-Related Macular Degeneration
title_sort cyp4f2 (rs2108622) gene polymorphism association with age-related macular degeneration
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5019857/
https://www.ncbi.nlm.nih.gov/pubmed/27652291
http://dx.doi.org/10.1155/2016/3917916
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