Differences in retinal neovascular tissue and vitreous humour in patients with type 1 and type 2 diabetes

Aims:The aim of the study was to evaluate the histopathology of neovascular tufts and vitreous samples collected from patients with diabetes.Methods:Vitreous samples and neovascular tufts were collected from patients with type 1 (n = 13) and (n = 17) type 2 diabetes with proliferative retinopathy, a...

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Veröffentlicht in:British journal of ophthalmology 2009-08, Vol.93 (8), p.1109-1115
Hauptverfasser: Kinnunen, K, Puustjärvi, T, Teräsvirta, M, Nurmenniemi, P, Heikura, T, Laidinen, S, Paavonen, T, Uusitalo, H, Ylä-Herttuala, S
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Sprache:eng
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Zusammenfassung:Aims:The aim of the study was to evaluate the histopathology of neovascular tufts and vitreous samples collected from patients with diabetes.Methods:Vitreous samples and neovascular tufts were collected from patients with type 1 (n = 13) and (n = 17) type 2 diabetes with proliferative retinopathy, and from controls with a macular hole (n = 5). Neovessels were analysed using immunohistochemistry and vitreous samples with an enzyme-linked immunosorbent assay (ELISA). The main outcome measure was to examine differences in the levels of growth factors in patients with type 1 and type 2 diabetes with proliferative retinopathy.Results:Vascular endothelial growth factor (VEGF)-A was most strongly present in the samples from patients with type 1 diabetes. In type 2 diabetes, VEGF-D was more abundantly present than in type 1 diabetes. Angiopoietin (ANG)-2 was also abundantly present. Macrophages and nuclear factor kappa B (NFκB) were found, indicating the presence of an inflammatory process in the neovascular tissues.Conclusions:VEGF-A and ANG-2 are equally important in the neovascular process in both type 1 and type 2 diabetes. VEGF-D is abundantly present in type 2 diabetes. In order to achieve better control of diabetic retinopathy, it might be beneficial to develop treatments that prevent the actions of ANG-2 and VEGF-D.
ISSN:0007-1161
1468-2079
DOI:10.1136/bjo.2008.148841