Abstract

The afferent visual system may be affected by neuro-degeneration in amyotrophic lateral sclerosis (ALS) based on observations of visual function impairment and retinal inclusions on histopathology in ALS patients. To test the hypothesis that visual acuity is impaired in ALS, we compared three measures of visual acuity in ALS patients (n = 25) attending a multidisciplinary ALS clinic and age matched control subjects (n = 25). Bilateral monocular and binocular visual acuities were assessed using high contrast (black letters on white background) and low contrast (2.5%, 1.25% grey letters on white background) visual acuity charts under controlled lighting conditions following refraction. Binocular summation was calculated as the difference between binocular and best monocular acuity scores. There were no associations between binocular or monocular high contrast visual acuity or low contrast visual acuity and amyotrophic lateral sclerosis diagnosis (generalized estimating equation models accounting for age). Binocular summation was similar in both amyotrophic lateral sclerosis and control subjects. There was a small magnitude association between increased duration of ALS symptoms and reduced 1.25% low contrast visual acuity. This study does not confirm prior observations of impaired visual acuity in patients with amyotrophic lateral sclerosis and does not support this particular measure of visual function for use in broad scale assessment of visual pathway involvement in ALS patients.

Highlights

  • Clinical and post-mortem observations of pathological effects spreading beyond the motor system in some people with amyotrophic lateral sclerosis (ALS) have led to a shift from the classical characterization of ALS as a disease exclusively of motor neurons to that of a multisystem disorder.[1]

  • ALSFRS-R and manual muscle testing (MMT) were obtained on a day different than vision testing

  • All subjects except one ALS patient had at least a high school education

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Summary

Introduction

Clinical and post-mortem observations of pathological effects spreading beyond the motor system in some people with amyotrophic lateral sclerosis (ALS) have led to a shift from the classical characterization of ALS as a disease exclusively of motor neurons to that of a multisystem disorder.[1] Though disorders of the efferent visual system were first reported in the literature.

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