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Başlık: Assessment of neuron-specific enolase, S100B and malondialdehyde levels in serum and vitreous of patients with proliferative diabetic retinopathy
Yazarlar: Asadova, Vusala
Gül, Zülfiye
Bursa Uludağ Üniversitesi/Tıp Fakültesi/Farmakoloji Anabilim Dalı.
Bursa Uludağ Üniversitesi/Tıp Fakültesi/Göz Hastalıkları Anabilim Dalı.
0000-0002-7311-5277
Büyükuysal, Rıfat Levent
Yalçınbayır, Özgür
AAH-1657-2021
AAH-6625-2021
6602686612
8702056700
Anahtar kelimeler: Ophthalmology
Diabetic retinopathy
Vitreous
Malondialdehyde
S100B
Neuron-specific enolase (NSE)
Protein-levels
Products
Stress
Fluid
Yayın Tarihi: Oca-2020
Yayıncı: Springer
Atıf: Asadova, 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.
Özet: Purpose 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.
URI: https://doi.org/10.1007/s10792-019-01175-9
https://link.springer.com/article/10.1007/s10792-019-01175-9
http://hdl.handle.net/11452/34570
ISSN: 0165-5701
1573-2630
Koleksiyonlarda Görünür:Scopus
Web of Science

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