Publication:
Investigation of tnf-alpha gene (g308a) and gstp1 gene (ile105val) polymorphisms in Turkish patients with retinopathy of prematurity

dc.contributor.authorKarkucak, Mutlu
dc.contributor.buuauthorTüre, Mehmet
dc.contributor.buuauthorYıldız, Meral
dc.contributor.buuauthorÖZMEN, AHMET TUNCER
dc.contributor.buuauthorYILDIZ, MERAL
dc.contributor.buuauthorGülten, Emine Tuna
dc.contributor.buuauthorSığırlı, Deniz
dc.contributor.buuauthorSIĞIRLI, DENİZ
dc.contributor.buuauthorÖzmen, Ahmet Tuncer
dc.contributor.buuauthorYakut, Tahsin
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentGenetik Ana Bilim Dalı
dc.contributor.researcheridAAH-1885-2021
dc.contributor.researcheridAAA-7472-2021
dc.date.accessioned2024-08-13T06:15:40Z
dc.date.available2024-08-13T06:15:40Z
dc.date.issued2015-01-01
dc.description.abstractBackground/aim: Retinopathy of prematurity (ROP) is one of the most frequent causes of blindness in newborn babies. Currently, its etiology is not fully understood. In this study we aimed to investigate the correlation between a patient group with ROP and a control group in terms of the tumor necrosis factor- alpha (TNF-alpha) (G308A) gene and glutathione-S-transferase P1 (GSTP1) (Ile105Val) gene polymorphism.Materials and methods: Sixty-two patients diagnosed with ROP and 58 control subjects were included in this study. For TNF-alpha (G308A) gene and GSTP1 (Ile105Val) gene polymorphisms, the polymerase chain reaction- restriction fragment length polymorphism method was used. In statistical analysis the significance level was determined as P < 0.05.Results: When the patient and control groups were compared in terms of TNF-alpha (G308A) gene and GSTP1 (Ile105Val) gene polymorphisms, no statistically significant difference was found (P > 0.05).Conclusion: In our study, no correlation was identified between TNF-alpha (G308A) gene and GSTP1 (Ile105Val) gene polymorphisms and susceptibility for development of ROP. Further studies are required with more cases of ROP patients and other gene polymorphisms that could be related.
dc.identifier.doi10.3906/sag-1307-94
dc.identifier.endpage169
dc.identifier.issn1300-0144
dc.identifier.issue1
dc.identifier.startpage164
dc.identifier.urihttps://doi.org/10.3906/sag-1307-94
dc.identifier.urihttps://hdl.handle.net/11452/43952
dc.identifier.volume45
dc.identifier.wos000347840000026
dc.indexed.wosWOS.SCI
dc.language.isoen
dc.publisherTubitak Scientific & Technological Research Council Turkey
dc.relation.journalTurkish Journal Of Medical Sciences
dc.subjectTumor-necrosis-factor
dc.subjectNorrie-disease gene
dc.subjectEndothelial growth-factor
dc.subjectBirth-weight infants
dc.subjectPromoter region
dc.subjectDiabetic-retinopathy
dc.subjectMissense mutations
dc.subjectAssociation
dc.subjectSusceptibility
dc.subjectPopulation
dc.subjectTnf-alpha
dc.subjectGstp1
dc.subjectGene polymorphism
dc.subjectRetinopathy of prematurity
dc.subjectScience & technology
dc.subjectLife sciences & biomedicine
dc.subjectMedicine, general & internal
dc.subjectGeneral & internal medicine
dc.titleInvestigation of tnf-alpha gene (g308a) and gstp1 gene (ile105val) polymorphisms in Turkish patients with retinopathy of prematurity
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Genetik Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Oftalmoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Biyoistatistik Ana Bilim Dalı
relation.isAuthorOfPublication25dafd98-92ca-4a4a-87f7-0e3da9257beb
relation.isAuthorOfPublicationf8b7b771-12ea-4f9a-889d-25079d8c862d
relation.isAuthorOfPublicationa4a355f6-b241-4347-b214-60f5cd2c2bd6
relation.isAuthorOfPublication.latestForDiscovery25dafd98-92ca-4a4a-87f7-0e3da9257beb

Files

Collections