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Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients
PURPOSE: To investigate the association between Apolipoprotein E (APOE), tumor suppressor protein p53 (p53), and cyclin-dependent kinase inhibitor 1A (p21) genes and primary open-angle glaucoma (POAG) in a cohort of Turkish subjects. METHODS: Seventy-five POAG patients (49 women, 26 men) and 119 hea...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Molecular Vision
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704913/ https://www.ncbi.nlm.nih.gov/pubmed/19578553 |
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author | Saglar, E. Yucel, D. Bozkurt, B. Ozgul, R.K. Irkec, M. Ogus, A. |
author_facet | Saglar, E. Yucel, D. Bozkurt, B. Ozgul, R.K. Irkec, M. Ogus, A. |
author_sort | Saglar, E. |
collection | PubMed |
description | PURPOSE: To investigate the association between Apolipoprotein E (APOE), tumor suppressor protein p53 (p53), and cyclin-dependent kinase inhibitor 1A (p21) genes and primary open-angle glaucoma (POAG) in a cohort of Turkish subjects. METHODS: Seventy-five POAG patients (49 women, 26 men) and 119 healthy subjects (67 women, 52 men) were genotyped with polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Allele and genotype frequencies between healthy subjects and glaucoma patients were compared by the χ(2) test, and intraocular pressure (IOP), cup/disc ratio (C/D) and visual field indices (MD and PSD) were compared among different APOE, p53, and p21 genotypes in POAG group. A p value <0.05 was considered as statistically significant. RESULTS: The mean ages were 63.8±9.5 and 61.8±10.2 years in POAG and control groups, respectively (p=0.18). There were no significant differences in the distribution of APOE, p53, and p21 genotypes between the healthy subjects and POAG patients (p=0.38, p=0.12, and p=0.2, respectively). There were no significant differences in maximum IOP, MD, and PSD values among different groups of p53 and p21 genotypes (p>0.05). POAG subjects with the ε2ε3 genotype had a worse PSD value (median=2.2) than those with the ε3ε4 genotype (median=1.77; p=0.01) and POAG subjects with the ε3ε3 genotype had worse MD and PSD values (median= -7.4 and 3.4, respectively) than those with the ε3ε4 genotype (median= -4.1 and 1.77, respectively; p=0.034 and 0.028, respectively). CONCLUSIONS: Our study found no link between polymorphisms in APOE, p53, and p21 genes and POAG in Turkish patients, although a larger sample is required to elucidate the role of these polymorphisms in the pathogenesis and course of glaucoma. |
format | Text |
id | pubmed-2704913 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Vision |
record_format | MEDLINE/PubMed |
spelling | pubmed-27049132009-07-02 Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients Saglar, E. Yucel, D. Bozkurt, B. Ozgul, R.K. Irkec, M. Ogus, A. Mol Vis Research Article PURPOSE: To investigate the association between Apolipoprotein E (APOE), tumor suppressor protein p53 (p53), and cyclin-dependent kinase inhibitor 1A (p21) genes and primary open-angle glaucoma (POAG) in a cohort of Turkish subjects. METHODS: Seventy-five POAG patients (49 women, 26 men) and 119 healthy subjects (67 women, 52 men) were genotyped with polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Allele and genotype frequencies between healthy subjects and glaucoma patients were compared by the χ(2) test, and intraocular pressure (IOP), cup/disc ratio (C/D) and visual field indices (MD and PSD) were compared among different APOE, p53, and p21 genotypes in POAG group. A p value <0.05 was considered as statistically significant. RESULTS: The mean ages were 63.8±9.5 and 61.8±10.2 years in POAG and control groups, respectively (p=0.18). There were no significant differences in the distribution of APOE, p53, and p21 genotypes between the healthy subjects and POAG patients (p=0.38, p=0.12, and p=0.2, respectively). There were no significant differences in maximum IOP, MD, and PSD values among different groups of p53 and p21 genotypes (p>0.05). POAG subjects with the ε2ε3 genotype had a worse PSD value (median=2.2) than those with the ε3ε4 genotype (median=1.77; p=0.01) and POAG subjects with the ε3ε3 genotype had worse MD and PSD values (median= -7.4 and 3.4, respectively) than those with the ε3ε4 genotype (median= -4.1 and 1.77, respectively; p=0.034 and 0.028, respectively). CONCLUSIONS: Our study found no link between polymorphisms in APOE, p53, and p21 genes and POAG in Turkish patients, although a larger sample is required to elucidate the role of these polymorphisms in the pathogenesis and course of glaucoma. Molecular Vision 2009-06-30 /pmc/articles/PMC2704913/ /pubmed/19578553 Text en http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of 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 Saglar, E. Yucel, D. Bozkurt, B. Ozgul, R.K. Irkec, M. Ogus, A. Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients |
title | Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients |
title_full | Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients |
title_fullStr | Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients |
title_full_unstemmed | Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients |
title_short | Association of polymorphisms in APOE, p53, and p21 with primary open-angle glaucoma in Turkish patients |
title_sort | association of polymorphisms in apoe, p53, and p21 with primary open-angle glaucoma in turkish patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2704913/ https://www.ncbi.nlm.nih.gov/pubmed/19578553 |
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