Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1782453130697375744 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5019857 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT sakieneruta cyp4f2rs2108622genepolymorphismassociationwithagerelatedmaculardegeneration AT vilkeviciutealvita cyp4f2rs2108622genepolymorphismassociationwithagerelatedmaculardegeneration AT kriauciunieneloresa cyp4f2rs2108622genepolymorphismassociationwithagerelatedmaculardegeneration AT balciunienevilmajurate cyp4f2rs2108622genepolymorphismassociationwithagerelatedmaculardegeneration AT buteikienedovile cyp4f2rs2108622genepolymorphismassociationwithagerelatedmaculardegeneration AT miniauskienegoda cyp4f2rs2108622genepolymorphismassociationwithagerelatedmaculardegeneration AT liutkevicienerasa cyp4f2rs2108622genepolymorphismassociationwithagerelatedmaculardegeneration |