"Corresponding Ganglion Cell Atrophy in Patients With Postgeniculate Ho" by J. R. Mitchell, C. Oliveira et al.
 

Corresponding Ganglion Cell Atrophy in Patients With Postgeniculate Homonymous Visual Field Loss

Publication Date

2015

Journal Title

J Neuroophthalmol

Abstract

Background: The goal of our study was to look for the presence of homonymous ganglion cell layer–inner plexiform layer complex (GCL-IPL) thinning using spectral-domain optical coherence tomography (SD-OCT) in patients with a history of adult-onset injury to the postgeniculate pathways with rigorous radiological exclusion of geniculate and pregeniculate pathology. Methods: We performed a retrospective review of twenty-two patients (ages 24–75 y, 6 men, 16 women) with homonymous visual field (VF) defects secondary to postgeniculate injury examining the GCL-IPL with SD-OCT. An additional fifteen patients (ages 28–85 y, 5 men, 10 women) with no visual pathway pathology served as controls. Using segmentation analysis software applied to the macular scan, a normalized asymmetry score was calculated for each eye comparing GCL-IPL thickness ipsilateral vs contralateral to the patient's brain lesions. Results: We found that 15 of the twenty-two subjects had a relative thinning of the GCL-IPL ipsilateral to the postgeniculate lesion in both eyes (represented by a positive normalized asymmetry score in both eyes), whereas a similar pattern of right/left asymmetry was found in 4 controls (P = 0.0498). The magnitude of asymmetry was much greater in subjects compared with controls (P = 0.0004). There was no association between the degree of GCL-IPL thinning and the mean deviation on automated VF testing. A moderate correlation (R = 0.782, P = 0.004) between the magnitude of thinning and latency from onset of retrogeniculate injury was observed only after excluding patients beyond a cutoff point of 150 months. Conclusions: This data provides compelling new evidence of retrograde transsynaptic degeneration causing retinal ganglion cell loss after postgeniculate visual pathway injury.

Volume Number

35

Issue Number

4

Pages

353-359

Document Type

Article

Status

Faculty

Facility

School of Medicine

Primary Department

Ophthalmology

PMID

26035806

DOI

10.1097/wno.0000000000000268

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