A. Canton et al., Hepatocyte growth factor in vitreous and serum from patients with proliferative diabetic retinopathy, BR J OPHTH, 84(7), 2000, pp. 732-735
Background-Hepatocyte growth factor (HGF) is an endothelium specific growth
factor that has been implicated in angiogenesis, a crucial event for the d
evelopment of proliferative diabetic retinopathy (PDR). The aim of the stud
y is to determine the intravitreous concentrations of HGF in diabetic patie
nts with PDR, and to investigate whether its serum levels could contribute
to its intravitreous concentration.
Methods-17 diabetic patients and seven non-diabetic patients in whom a vitr
ectomy was performed were studied. Both groups were matched by serum levels
of HGF. Venous blood and vitreous samples were collected simultaneously at
the time of vitreoretinal surgery. Vitreous and serum HGF were determined
by ELISA.
Results-Intravitreous concentrations of HGF (median and range) were higher
in diabetic patients (17.04 ng/ml (9.98-80)) in comparison with non-diabeti
c patients (5.88 ng/ml (2.57-14.20); p=0.003). Intravitreous HGF concentrat
ions were strikingly higher than serum HGF concentrations both in diabetic
patients (17.04 ng/ml (9.98-80) v 0.66 ng/ml (0.26-1.26); p<0.001) and in t
he control group (5.88 ng/ml (2.57-14.20) v 0.68 ng/ml (0.49-0.96); p=0.003
). No correlation was found between serum and vitreous levels of HGF in bot
h groups (diabetic patients, r=-0.31; p=0.5 and control subjects r=-0.15; p
=0.5).
Conclusion-The high vitreous levels of HGF observed in diabetic patients wi
th PDR cannot be attributed to serum diffusion across the blood-retinal bar
rier. Therefore, intraocular synthesis appears to be the main contributing
factor for the high vitreous HGF concentrations in diabetic patients, a cyt
okine that seems to be directly involved in the pathogenesis of PDR.