Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/10294
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Okur, Volkan | - |
dc.contributor.author | Çetin, Ozan | - |
dc.contributor.author | Çetin, Ebru | - |
dc.contributor.author | Tepeli, E. | - |
dc.contributor.author | Bulgu, Y. | - |
dc.contributor.author | Yildirim, C. | - |
dc.date.accessioned | 2019-08-16T13:15:24Z | - |
dc.date.available | 2019-08-16T13:15:24Z | - |
dc.date.issued | 2015 | - |
dc.identifier.issn | 1442-6404 | - |
dc.identifier.uri | https://hdl.handle.net/11499/10294 | - |
dc.identifier.uri | https://doi.org/10.1111/ceo.12376 | - |
dc.description.abstract | Background: To investigate the association between age-related macular degeneration (AMD) and the polymorphisms of HIF1A, a major vascular epithelial growth factor regulator under hypoxic conditions. The associations of AMD and polymorphisms of genes CFH, SKIV2L and MYRIP were also studied. Design: Prospective study. Participants: Eighty-seven AMD patients and 80 healthy subjects admitted to the Department of Ophthalmology at Pamukkale University Hospital, Denizli, Turkey, were included: 45 (52%) had wet type AMD, and 42 (48%) had dry type AMD. Methods: Polymorphisms rs1061170 (CFH), rs429608 (SKIV2L), rs2679798 (MYRIP) and both rs11549465 and rs11549467 (HIF1A) were investigated in DNA isolated from peripheral blood samples of the cases and controls by dye-termination DNA sequencing. Main Outcome Measures: Genotype distribution of rs1061170 (CFH), rs429608 (SKIV2L), rs2679798 (MYRIP) and both rs11549465 and rs11549467 (HIF1A) in AMD cases and healthy controls; association between genotypes and AMD subtypes. Results: Given the significant difference between the mean age of case and control groups (72.13±5.77 vs. 62.80±5.22, respectively) (P=.000), subsequent analyses were adjusted for age. We found that having at least one C allele for polymorphism rs1061170 increases AMD risk independent of age (OR=2.42, 95% confidence interval [CI], 1.22-4.81). The ancestral T allele for polymorphism rs1061170 has a protective effect for AMD (OR=0.53, 95% CI, 0.34-0.83). No statistically significant difference for distributions of other single nucleotide polymorphisms (SNPs) emerged between patients and healthy subjects. Conclusions: No associations appeared between HIF1A SNPs and AMD, which were studied here for the first time; however, polymorphism rs1061170 of the CFH gene is associated with AMD in our population. © 2014 Royal Australian and New Zealand College of Ophthalmologists. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Blackwell Publishing | en_US |
dc.relation.ispartof | Clinical and Experimental Ophthalmology | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | AMD | en_US |
dc.subject | CFH | en_US |
dc.subject | HIF1A | en_US |
dc.subject | MYRIP | en_US |
dc.subject | SKIV2L | en_US |
dc.subject | age | en_US |
dc.subject | age related macular degeneration | en_US |
dc.subject | aged | en_US |
dc.subject | allele | en_US |
dc.subject | Article | en_US |
dc.subject | blood analysis | en_US |
dc.subject | CFH gene | en_US |
dc.subject | controlled study | en_US |
dc.subject | DNA isolation | en_US |
dc.subject | DNA sequence | en_US |
dc.subject | female | en_US |
dc.subject | gene | en_US |
dc.subject | gene frequency | en_US |
dc.subject | genetic association | en_US |
dc.subject | genetic risk | en_US |
dc.subject | genotype | en_US |
dc.subject | HIF1A gene | en_US |
dc.subject | hospital admission | en_US |
dc.subject | human | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | MYRIP gene | en_US |
dc.subject | prospective study | en_US |
dc.subject | single nucleotide polymorphism | en_US |
dc.subject | SKIV2L gene | en_US |
dc.subject | genetics | en_US |
dc.subject | geographic atrophy | en_US |
dc.subject | metabolism | en_US |
dc.subject | middle aged | en_US |
dc.subject | polymerase chain reaction | en_US |
dc.subject | wet macular degeneration | en_US |
dc.subject | complement factor H | en_US |
dc.subject | complement factor H, human | en_US |
dc.subject | DNA helicase | en_US |
dc.subject | HIF1A protein, human | en_US |
dc.subject | hypoxia inducible factor 1alpha | en_US |
dc.subject | MYRIP protein, human | en_US |
dc.subject | SKIV2L protein, human | en_US |
dc.subject | vasculotropin A | en_US |
dc.subject | VEGFA protein, human | en_US |
dc.subject | vesicular transport protein | en_US |
dc.subject | Aged | en_US |
dc.subject | Complement Factor H | en_US |
dc.subject | DNA Helicases | en_US |
dc.subject | Female | en_US |
dc.subject | Gene Frequency | en_US |
dc.subject | Genotype | en_US |
dc.subject | Geographic Atrophy | en_US |
dc.subject | Humans | en_US |
dc.subject | Hypoxia-Inducible Factor 1, alpha Subunit | en_US |
dc.subject | Male | en_US |
dc.subject | Middle Aged | en_US |
dc.subject | Polymerase Chain Reaction | en_US |
dc.subject | Polymorphism, Single Nucleotide | en_US |
dc.subject | Prospective Studies | en_US |
dc.subject | Sequence Analysis, DNA | en_US |
dc.subject | Vascular Endothelial Growth Factor A | en_US |
dc.subject | Vesicular Transport Proteins | en_US |
dc.subject | Wet Macular Degeneration | en_US |
dc.title | HIF1A as a major vascular endothelial growth factor regulator: Do its polymorphisms have an association with age-related macular degeneration? | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 43 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.startpage | 47 | - |
dc.identifier.startpage | 47 | en_US |
dc.identifier.endpage | 53 | en_US |
dc.authorid | 0000-0002-6100-7973 | - |
dc.authorid | 0000-0002-2696-3425 | - |
dc.identifier.doi | 10.1111/ceo.12376 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 24995509 | en_US |
dc.identifier.scopus | 2-s2.0-84921517262 | en_US |
dc.identifier.wos | WOS:000348898800009 | en_US |
dc.identifier.scopusquality | Q1 | - |
dc.owner | Pamukkale University | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.cerifentitytype | Publications | - |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
item.openairetype | Article | - |
item.languageiso639-1 | en | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.01. Surgical Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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