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Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration
BACKGROUND: Age-related macular degeneration (AMD) is a primary cause of blindness among the elderly in developed countries. The nature of AMD is complex and includes both environmental and hereditary factors. Oxidative stress is thought to be essential in AMD pathogenesis. Iron is suggested to be i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539623/ https://www.ncbi.nlm.nih.gov/pubmed/21804464 http://dx.doi.org/10.12659/MSM.881906 |
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author | Wysokinski, Daniel Synowiec, Ewelina Chmielewska, Marta Wozniak, Katarzyna Zaras, Małgorzata Sklodowska, Anna Blasiak, Janusz Szaflik, Jerzy Szaflik, Jacek Pawel |
author_facet | Wysokinski, Daniel Synowiec, Ewelina Chmielewska, Marta Wozniak, Katarzyna Zaras, Małgorzata Sklodowska, Anna Blasiak, Janusz Szaflik, Jerzy Szaflik, Jacek Pawel |
author_sort | Wysokinski, Daniel |
collection | PubMed |
description | BACKGROUND: Age-related macular degeneration (AMD) is a primary cause of blindness among the elderly in developed countries. The nature of AMD is complex and includes both environmental and hereditary factors. Oxidative stress is thought to be essential in AMD pathogenesis. Iron is suggested to be implicated in the pathogenesis of AMD through the catalysis of the production of reactive oxygen species, which can damage the retina. Heme oxygenase-2 is capable of degradation of heme producing free iron ions, thus, diversity in heme oxygenase-2 gene may contribute to AMD. In the present work we analyzed the association between the c.544G>A polymorphism of the heme oxygenase-2 gene (HMOX2) (rs1051308) and AMD. MATERIAL/METHODS: This study enrolled 276 AMD patients and 105 sex- and age-matched controls. Genotyping of the polymorphism was performed with restriction fragment length polymorphism polymerase chain reaction (RFLP-PCR) on DNA isolated from peripheral blood. RESULTS: We did not find any association between the genotypes of the c.544G>A polymorphism and the occurrence of AMD. This lack of association was independent of potential AMD risk factors: tobacco smoking, sex and age. Moreover, we did not find any association between AMD and smoking in our study population. CONCLUSIONS: The results suggest that the c.544G>A polymorphism of the heme oxygenase-2 gene is not associated with AMD in this Polish subpopulation. |
format | Online Article Text |
id | pubmed-3539623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-35396232013-04-24 Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration Wysokinski, Daniel Synowiec, Ewelina Chmielewska, Marta Wozniak, Katarzyna Zaras, Małgorzata Sklodowska, Anna Blasiak, Janusz Szaflik, Jerzy Szaflik, Jacek Pawel Med Sci Monit Clinical Research BACKGROUND: Age-related macular degeneration (AMD) is a primary cause of blindness among the elderly in developed countries. The nature of AMD is complex and includes both environmental and hereditary factors. Oxidative stress is thought to be essential in AMD pathogenesis. Iron is suggested to be implicated in the pathogenesis of AMD through the catalysis of the production of reactive oxygen species, which can damage the retina. Heme oxygenase-2 is capable of degradation of heme producing free iron ions, thus, diversity in heme oxygenase-2 gene may contribute to AMD. In the present work we analyzed the association between the c.544G>A polymorphism of the heme oxygenase-2 gene (HMOX2) (rs1051308) and AMD. MATERIAL/METHODS: This study enrolled 276 AMD patients and 105 sex- and age-matched controls. Genotyping of the polymorphism was performed with restriction fragment length polymorphism polymerase chain reaction (RFLP-PCR) on DNA isolated from peripheral blood. RESULTS: We did not find any association between the genotypes of the c.544G>A polymorphism and the occurrence of AMD. This lack of association was independent of potential AMD risk factors: tobacco smoking, sex and age. Moreover, we did not find any association between AMD and smoking in our study population. CONCLUSIONS: The results suggest that the c.544G>A polymorphism of the heme oxygenase-2 gene is not associated with AMD in this Polish subpopulation. International Scientific Literature, Inc. 2011-08-01 /pmc/articles/PMC3539623/ /pubmed/21804464 http://dx.doi.org/10.12659/MSM.881906 Text en © Med Sci Monit, 2011 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. |
spellingShingle | Clinical Research Wysokinski, Daniel Synowiec, Ewelina Chmielewska, Marta Wozniak, Katarzyna Zaras, Małgorzata Sklodowska, Anna Blasiak, Janusz Szaflik, Jerzy Szaflik, Jacek Pawel Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration |
title | Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration |
title_full | Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration |
title_fullStr | Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration |
title_full_unstemmed | Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration |
title_short | Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration |
title_sort | lack of association between the c.544g>a polymorphism of the heme oxygenase-2 gene and age-related macular degeneration |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3539623/ https://www.ncbi.nlm.nih.gov/pubmed/21804464 http://dx.doi.org/10.12659/MSM.881906 |
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