ABSTRACT
The lamina cribrosa is a primary site of damage in glaucoma. While mechanical distortion is hypothesized to cause reduction of axoplasmic flow, little is known about how the pores, which contains the retinal ganglion cell axons, traverse the lamina cribrosa. We investigated lamina cribrosa pore paths in vivo to quantify differences in tortuosity of pore paths between healthy and glaucomatous eyes. We imaged 16 healthy, 23 glaucoma suspect and 48 glaucomatous eyes from 70 subjects using a swept source optical coherence tomography system. The lamina cribrosa pores were automatically segmented using a previously described segmentation algorithm. Individual pore paths were automatically tracked through the depth of the lamina cribrosa using custom software. Pore path convergence to the optic nerve center and tortuosity was quantified for each eye. We found that lamina cribrosa pore pathways traverse the lamina cribrosa closer to the optic nerve center along the depth of the lamina cribrosa regardless of disease severity or diagnostic category. In addition, pores of glaucoma eyes take a more tortuous path through the lamina cribrosa compared to those of healthy eyes, suggesting a potential mechanism for reduction of axoplasmic flow in glaucoma.
Subject(s)
Glaucoma, Open-Angle/physiopathology , Nerve Fibers/pathology , Optic Nerve/physiopathology , Retinal Ganglion Cells/pathology , Aged , Axonal Transport/physiology , Axons/pathology , Female , Humans , Intraocular Pressure/physiology , Male , Middle Aged , Nerve Fibers/physiology , Ocular Hypertension/physiopathology , Optic Disk/diagnostic imaging , Optic Disk/physiopathology , Optic Nerve/diagnostic imaging , Tomography, Optical CoherenceABSTRACT
PURPOSE: We sought to visualize the aqueous outflow system in 3 dimensions (3D) in living human eyes, and to investigate the use of commercially available spectral-domain optical coherence tomographic (SD-OCT) systems for this purpose. DESIGN: Prospective, observational study. PARTICIPANTS: One randomly determined eye in each of 6 normal healthy subjects was included. TESTING: We performed 3D SD-OCT imaging of the aqueous humor outflow structures with 2 devices: The Cirrus HD-OCT and the Bioptigen SDOIS. MAIN OUTCOME MEASURES: We created 3D virtual castings of Schlemm's canal (SC) and more distal outflow structures from scan data from each device. RESULTS: Virtual casting of the SC provided visualization of more aqueous vessels branching from SC than could be located by interrogating the 2-dimensional (2D) image stack. Similarly, virtual casting of distal structures allowed visualization of large and small aqueous outflow channel networks that could not be appreciated with conventional 2D visualization. CONCLUSIONS: The outflow pathways from SC to the superficial vasculature can be identified and tracked in living human eyes using commercially available SD-OCT.
