A. Bhandari et al., QUANTITATIVE-ANALYSIS OF THE LAMINA-CRIBROSA IN-VIVO USING A SCANNINGLASER OPTHALMOSCOPE, Current eye research, 16(1), 1997, pp. 1-8
Purpose. Structural changes in the lamina cribrosa have been implicate
d in the pathogenesis of glaucomatous optic nerve atrophy. The purpose
of this study was to develop a method for morphometric analysis of th
e lamina cribrosa pores in vivo, using a scanning laser ophthalmoscope
. Methods. A prototype Zeiss confocal laser scanning ophthalmoscope wa
s used to acquire images of the lamina cribrosa. The images were digit
ised and aligned to compensate for eye movements. Thirty-two consecuti
ve images were averaged to reduce noise. The images were processed to
adjust for luminance gradients prior to segmentation and analysis. Det
ails of the image processing are described. Results. The end result of
processing the images was a binary (black and white) image that can b
e used for automated computer assisted measurements. The pores of the
lamina cribrosa are well represented and retain their overall shape in
the binary image, as judged by superimposing the binary image on the
unprocessed image. We also established the repeatability, reproducibil
ity and intercession variability of this technique. Repeated images of
the internal lamina cribrosa of 10 patients were acquired, by two obs
ervers in two separate visits, and the images were processed before au
tomated computer measurements. The parameters evaluated were number of
pores, area covered by the pores and area covered by the visible lami
na cribrosa. The coefficient of variation for number of pores, pore ar
ea and lamina area was 6.9%, 2.1% and 4.3% for observer A and 5.5%, 2.
1% and 5.8% for observer B. Pearson product moment correlation coeffic
ient between the two observers was 0.94, 0.99 and 0.97 for the above p
arameters respectively. There was no significant difference between th
e measurements on visit 1 and 2 for both observers. Conclusions. The t
echnique described allows, for the first time, in vivo morphometry of
the internal lamine cribrosa surface. This method has good reproducibi
lity, suggesting future clinical applications.