Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10294
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dc.contributor.authorOkur, Volkan.-
dc.contributor.authorÇetin, Ozan-
dc.contributor.authorÇetin, Ebru-
dc.contributor.authorTepeli, E.-
dc.contributor.authorBulgu, Y.-
dc.contributor.authorYildirim, C.-
dc.date.accessioned2019-08-16T13:15:24Z-
dc.date.available2019-08-16T13:15:24Z-
dc.date.issued2015-
dc.identifier.issn1442-6404-
dc.identifier.urihttps://hdl.handle.net/11499/10294-
dc.identifier.urihttps://doi.org/10.1111/ceo.12376-
dc.description.abstractBackground: 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.isoenen_US
dc.publisherBlackwell Publishingen_US
dc.relation.ispartofClinical and Experimental Ophthalmologyen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAMDen_US
dc.subjectCFHen_US
dc.subjectHIF1Aen_US
dc.subjectMYRIPen_US
dc.subjectSKIV2Len_US
dc.subjectageen_US
dc.subjectage related macular degenerationen_US
dc.subjectageden_US
dc.subjectalleleen_US
dc.subjectArticleen_US
dc.subjectblood analysisen_US
dc.subjectCFH geneen_US
dc.subjectcontrolled studyen_US
dc.subjectDNA isolationen_US
dc.subjectDNA sequenceen_US
dc.subjectfemaleen_US
dc.subjectgeneen_US
dc.subjectgene frequencyen_US
dc.subjectgenetic associationen_US
dc.subjectgenetic risken_US
dc.subjectgenotypeen_US
dc.subjectHIF1A geneen_US
dc.subjecthospital admissionen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectMYRIP geneen_US
dc.subjectprospective studyen_US
dc.subjectsingle nucleotide polymorphismen_US
dc.subjectSKIV2L geneen_US
dc.subjectgeneticsen_US
dc.subjectgeographic atrophyen_US
dc.subjectmetabolismen_US
dc.subjectmiddle ageden_US
dc.subjectpolymerase chain reactionen_US
dc.subjectwet macular degenerationen_US
dc.subjectcomplement factor Hen_US
dc.subjectcomplement factor H, humanen_US
dc.subjectDNA helicaseen_US
dc.subjectHIF1A protein, humanen_US
dc.subjecthypoxia inducible factor 1alphaen_US
dc.subjectMYRIP protein, humanen_US
dc.subjectSKIV2L protein, humanen_US
dc.subjectvasculotropin Aen_US
dc.subjectVEGFA protein, humanen_US
dc.subjectvesicular transport proteinen_US
dc.subjectAgeden_US
dc.subjectComplement Factor Hen_US
dc.subjectDNA Helicasesen_US
dc.subjectFemaleen_US
dc.subjectGene Frequencyen_US
dc.subjectGenotypeen_US
dc.subjectGeographic Atrophyen_US
dc.subjectHumansen_US
dc.subjectHypoxia-Inducible Factor 1, alpha Subuniten_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectPolymerase Chain Reactionen_US
dc.subjectPolymorphism, Single Nucleotideen_US
dc.subjectProspective Studiesen_US
dc.subjectSequence Analysis, DNAen_US
dc.subjectVascular Endothelial Growth Factor Aen_US
dc.subjectVesicular Transport Proteinsen_US
dc.subjectWet Macular Degenerationen_US
dc.titleHIF1A as a major vascular endothelial growth factor regulator: Do its polymorphisms have an association with age-related macular degeneration?en_US
dc.typeArticleen_US
dc.identifier.volume43en_US
dc.identifier.issue1en_US
dc.identifier.startpage47-
dc.identifier.startpage47en_US
dc.identifier.endpage53en_US
dc.authorid0000-0002-6100-7973-
dc.authorid0000-0002-2696-3425-
dc.identifier.doi10.1111/ceo.12376-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid24995509en_US
dc.identifier.scopus2-s2.0-84921517262en_US
dc.identifier.wosWOS:000348898800009en_US
dc.identifier.scopusqualityQ1-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.01. Surgical 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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