Purpose: The purpose of this study was to investigate choroidal perfus
ion in glaucoma, using histological and angiographic techniques. Metho
ds: We examined the choroidal vasculature in clinicopathological slide
s from 25 cases of primary open-angle glaucoma, five cases of optic at
rophy, and 18 normal eyes, We measured choroidal thickness at fixed di
stances from the disk margin with light microscopy. Using a quantitati
ve computer image analysis system, we established the depth of all ves
sels and the best fitting diameter and width-to-length ratio for each
vessel in three pairs of eyes. Separate statistical analyses were done
on the parapapillary area and the whole choroid. We compared standard
fluorescein angiographic measures to peak choroidal filling time in a
further 78 glaucoma and 84 normal eyes. Results: Choroids were signif
icantly (similar to 50 mu m) thinner in glaucoma than in normal or opt
ic atrophy irrespective of fundal position. Vessel frequency and mean
diameter, relative to normal, showed greatest decrease near the chorio
capillaris. Peak choroidal filling was the only fluorescein angiograph
ic measure that was significantly delayed in glaucoma irrespective of
age. Conclusions: Reduced choroidal thickness in primary open-angle gl
aucoma is primarily due to loss of the innermost choroidal vessels. Ov
erall size decreases without significant flattening. These changes are
not seen with optic atrophy alone and may be correlated with the dela
yed choroidal perfusion seen in fluorescein angiography.