Clinical studies have shown a relationship between diabetic retinopathy and vascular
endothelial growth factor (VEGF) levels in ocular fluid. Advanced glycation end products
(AGEs) have been implicated in diabetes complications, including diabetic retinopathy.
Nε-(carboxymethyl) lysine (CML) is a glycoxidation product that may be a marker of oxidative
stress. In this study, we used enzyme-linked immunosorbent assays to determine the
levels of VEGF, non-CML AGE and CML in the aqueous humor and serum of 82 Japanese
patients with type 2 diabetes and 60 non-diabetic subjects. VEGF, non-CML AGE, and
CML concentrations in aqueous humor and serum were then compared with the severity
of diabetic retinopathy. Immunohistochemical detection analysis of non-CML AGE and
CML was also performed using retinal tissues from patients with progressive diabetic
retinopathy. Aqueous levels of VEGF, non-CML AGE and CML increased along with the
progression of diabetic retinopathy compared to age-matched controls. After coagulation
therapy, the VEGF, non-CML AGE, and CML levels were significantly reduced. Immunostaining
showed diffuse co-localization of non-CML AGE and CML around microvessels and in the
glial cells of proliferative membranes from patients with progressive diabetic retinopathy.
These findings suggest that glycation and glycoxidation reactions (or oxidation, as
revealed by CML) may contribute to both the onset and progression of diabetic retinopathy.
Key words:
AGE - Glycation - Glycoxidation - Vascular Endothelial Growth Factor - Diabetic Retinopathy
- Nε-(carboxymethyl) Lysine
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K. Yanagisawa, M.D.
Department of Internal Medicine II
Hokkaido University School of Medicine,
N-15, W-7, Kita-ku
Sapporo 060-8638
Japan
Phone: Phone:+ 81 (11) 716-1161 (ext. 5915)
Fax: Fax:+ 81 (11) 706-7710
Email: E-mail:kyanagi@med.hokudai.ac.jp