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Assessment of neuron-specific enolase, S100B and malondialdehyde levels in serum and vitreous of patients with proliferative diabetic retinopathy

dc.contributor.authorAsadova, Vusala
dc.contributor.authorGül, Zülfiye
dc.contributor.buuauthorBüyükuysal, Rıfat Levent
dc.contributor.buuauthorYalçınbayır, Özgür
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentFarmakoloji Ana Bilim Dalı
dc.contributor.departmentGöz Hastalıkları Ana Bilim Dalı
dc.contributor.orcid0000-0002-7311-5277
dc.contributor.researcheridAAH-1657-2021
dc.contributor.researcheridAAH-6625-2021
dc.contributor.scopusid6602686612
dc.contributor.scopusid8702056700
dc.date.accessioned2023-10-26T05:28:02Z
dc.date.available2023-10-26T05:28:02Z
dc.date.issued2020-01
dc.description.abstractPurpose To assess the vitreous and serum levels of neuron-specific enolase (NSE), S100B and malondi-aldehyde (MDA) in proliferative diabetic retinopathy (PDR) cases and investigate the correlation between preoperative and postoperative anatomical and clinical features. Materials and methods The study group included patients who had pars plana vitrectomy (PPV) for PDR. The control group included non-diabetic individuals who underwent PPV surgery for vitreoretinal interface disorders. Samples of serum were taken from all participants preoperatively, while vitreous samples were taken during the PPV. Vitreous and serum levels of NSE, S100B and MDA were measured, and comparisons were made between the groups. Results The study group consisted of 56 eyes of 56 cases with PDR. The control group consisted of 20 eyes of 20 cases. The concentrations of vitreous NSE, S100B and MDA were significantly higher than the control group (p < 0.0001, p < 0.05, p < 0.001, respectively). Serum levels were statistically different for NSE and S100B (p < 0.05). Conclusion Our results clearly show that vitreous levels of S100B, NSE and MDA and serum concentrations of NSE and S100B increased significantly in patients with PDR. The findings may possibly indicate neurodegeneration and oxidative stress; therefore, these markers may have a diagnostic value in patients with PDR.
dc.identifier.citationAsadova, V. vd. (2020). "Assessment of neuron-specific enolase, S100B and malondialdehyde levels in serum and vitreous of patients with proliferative diabetic retinopathy". International Ophthalmology, 40(1), 227-234.
dc.identifier.doi10.1007/s10792-019-01175-9
dc.identifier.endpage234
dc.identifier.issn0165-5701
dc.identifier.issn1573-2630
dc.identifier.issue1
dc.identifier.pubmed31571092
dc.identifier.scopus2-s2.0-85073990981
dc.identifier.startpage227
dc.identifier.urihttps://doi.org/10.1007/s10792-019-01175-9
dc.identifier.urihttps://link.springer.com/article/10.1007/s10792-019-01175-9
dc.identifier.urihttp://hdl.handle.net/11452/34570
dc.identifier.volume40
dc.identifier.wos000519236900003
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherSpringer
dc.relation.collaborationSanayi
dc.relation.collaborationYurt içi
dc.relation.journalInternational Ophthalmology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectOphthalmology
dc.subjectDiabetic retinopathy
dc.subjectVitreous
dc.subjectMalondialdehyde
dc.subjectS100B
dc.subjectNeuron-specific enolase (NSE)
dc.subjectProtein-levels
dc.subjectProducts
dc.subjectStress
dc.subjectFluid
dc.subject.emtreeBiological marker
dc.subject.emtreeMalonaldehyde
dc.subject.emtreeNeuron specific enolase
dc.subject.emtreeProtein s100b
dc.subject.emtreeBiological marker
dc.subject.emtreeEnolase
dc.subject.emtreeMalonaldehyde
dc.subject.emtreeProtein s100b
dc.subject.emtreeS100b protein, human
dc.subject.emtreeAdult
dc.subject.emtreeAged
dc.subject.emtreeArticle
dc.subject.emtreeClinical assessment
dc.subject.emtreeClinical feature
dc.subject.emtreeControlled study
dc.subject.emtreeCorrelational study
dc.subject.emtreeFemale
dc.subject.emtreeFunctional status
dc.subject.emtreeHuman
dc.subject.emtreeMajor clinical study
dc.subject.emtreeMale
dc.subject.emtreePars plana vitrectomy
dc.subject.emtreePostoperative period
dc.subject.emtreePreoperative period
dc.subject.emtreePrognosis
dc.subject.emtreeProliferative diabetic retinopathy
dc.subject.emtreeProspective study
dc.subject.emtreeProtein blood level
dc.subject.emtreeVitreous body
dc.subject.emtreeAdolescent
dc.subject.emtreeBlood
dc.subject.emtreeDiabetic retinopathy
dc.subject.emtreeFollow up
dc.subject.emtreeMetabolism
dc.subject.emtreeMiddle aged
dc.subject.emtreeOptical coherence tomography
dc.subject.emtreeOxidative stress
dc.subject.emtreePathology
dc.subject.emtreeRetina
dc.subject.emtreeVery elderly
dc.subject.emtreeVitrectomy
dc.subject.emtreeVitreous body
dc.subject.emtreeYoung adult
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshBiomarkers
dc.subject.meshDiabetic retinopathy
dc.subject.meshFemale
dc.subject.meshFollow-up studies
dc.subject.meshHumans
dc.subject.meshMale
dc.subject.meshMalondialdehyde
dc.subject.meshMiddle aged
dc.subject.meshOxidative stress
dc.subject.meshPhosphopyruvate hydratase
dc.subject.meshPrognosis
dc.subject.meshProspective studies
dc.subject.meshRetina
dc.subject.meshS100 calcium binding protein beta subunit
dc.subject.meshTomography, optical coherence
dc.subject.meshVitrectomy
dc.subject.meshVitreous body
dc.subject.meshYoung adult
dc.subject.scopusUbiquitin thiolesterase; Phosphopyruvate hydratase; Biomarkers
dc.subject.wosOphthalmology
dc.titleAssessment of neuron-specific enolase, S100B and malondialdehyde levels in serum and vitreous of patients with proliferative diabetic retinopathy
dc.typeArticle
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/Farmakoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Göz Hastalıkları Ana Bilim Dalı
local.indexed.atScopus
local.indexed.atWOS

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