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The role of the cytokines in the pathogenesis of pseudoexfoliation syndrome
Authors:Zuhal Yildirim,Filiz Yildirim,Nil Irem U&#  gun  Aylin Sepici-Din&#  el
Affiliation:1.Etimesgut Public Health Laboratory, Etimesgut 06770, Ankara, Turkey;2.Duatepe Government Hospital, Clinic of Internal Medicine, Polatli 06900, Ankara, Turkey;3.Ankara Numune Education and Research Hospital, Second Ophthalmology Clinic, Ankara 06100, Turkey;4.Gazi University, Faculty of Medicine, Department of Medical Biochemistry, Beşevler 06500, Ankara, Turkey
Abstract:

AIM

To examine the mechanism of the development of pseudoexfoliation (PSX) syndrome via both cytokine formation and endothelial vasorelaxing and growth factors that will provide us new therapeutic insights for the treatment.

METHODS

This is a cross sectional study included two groups; Group 1: control patients with nuclear cataract (n=20, aged 51-80 years). Group 2: PSX patients with nuclear cataract (n=18, aged 50-90 years). Patients with other ophthalmic problems and systemic diseases were excluded. Vascular endothelial growth factor (VEGF), interleukin-6 (IL-6) and interleukin-1β (IL-1β) and nitrotyrosine levels were determined through serum samples by Enzyme-linked immunosorbent assay (ELISA) method. Nitrite-nitrate levels were measured with photometric endpoint determination.

RESULTS

There were no significant differences between the groups in terms of age, VEGF, IL-1β, nitrite-nitrate and nitrotyrosine. The significant results were the mean IL-6 levels that were higher in PSX group 2 (37.68±29.52 pg/mL) compared to that in control group 1 (15.32±10.08 pg/mL) (P<0.001).

CONCLUSION

Several interacting and extending biochemical pathways may lead to the promotion of VEGF and IL-6 expressions. IL-6 which is the only altered marker in our study may indirectly cause an increase of vascular permeability and neovascularization. We suggest inflammation as a factor that can be involved in etiopathogenesis of PSX.
Keywords:pseudoexfoliation syndrome   inflammation   vascular endothelial growth factor   interleukin-6   interleukin-1β
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