Endothelial cell loss in irradiated optic nerves.
Levin L A, Gragoudas E S, Lessell S
AI Summary
Optic nerve radiation damage correlates with fewer endothelial cells, suggesting vascular injury underlies radiation optic neuropathy, highlighting the importance of radiation dose.
Abstract
Objective
Radiation optic neuropathy usually occurs months to years after exposure of the anterior visual pathways to ionizing radiation. It is characterized by high signal on gadolinium-enhanced T1-weighted magnetic resonance imaging. Radiation-induced endothelial cell damage resulting in blood-nerve barrier breakdown is hypothesized to produce this pattern, but histologic evidence of this in the optic nerve is lacking. We attempted to evaluate the effect of radiation on endothelial cells in the optic nerve.
Design
Case-controlled histologic study.
Methods
We studied the optic nerves of 16 enucleated eyes from patients with uveal melanoma treated with proton beam irradiation, 6 from normal eyes and 5 from eyes with unirradiated uveal melanomas. Binding of Ulex europaeus agglutinin I (UEA-I) lectin was used to identify endothelial cells in single paraffin sections. Transverse and longitudinal sections of vessels were counted in masked fashion.
Results
There were 49.4+/-6.9 transversely sectioned endothelial cells per millimeter of nerve in 6 optic nerves exposed to 0 to 1000 cGyE ("low-dose") compared with 17.3+/-5.3 in 10 nerves exposed to 5500 to 7000 cGyE ("high-dose") (P = 0.002). Longitudinally sectioned vessels stained with UEA-I were separately identified, with 11.5+/-2.1 in the low-dose group and 5.6+/-1.6 in the high-dose group (P = 0.044). The thickness and staining of the endothelial cell layer appeared greater in the high-dose group. Endothelial cell counts did not correlate with age, gender, acuity, or interval after irradiation.
Conclusions
Increased radiation dosage to the optic nerve correlates with smaller numbers of endothelial cells.
MeSH Terms
Shields Classification
Related Articles5
Rapid Amplification of Cerebrospinal Fluid Pressure as a Possible Mechanism for Optic Nerve Sheath Bleeding in Infants With Nonaccidental Head Injury.
Basic ScienceTemporal Alterations of Sphingolipids in Optic Nerves After Indirect Traumatic Optic Neuropathy.
Basic ScienceRGC and Vision Loss From Traumatic Optic Neuropathy Induced by Repetitive Closed Head Trauma Is Dependent on Timing and Force of Impact.
Basic ScienceCaspase-2 Mediates Site-Specific Retinal Ganglion Cell Death After Blunt Ocular Injury.
Basic ScienceA Controlled Impact of Optic Nerve as a New Model of Traumatic Optic Neuropathy in Mouse.
Basic ScienceIs this article assigned to the wrong chapter(s)? Let us know.