Abstract

Summary

This thesis demonstrates that multifocal objective pupillographic perimetry (mfPOP) is a safe diagnostic tool for studying photosensitivity and cortical excitability in neurological disorders including epilepsy and migraine, even when protocols specifically target melanopsin-containing retinal ganglion cells. The findings have implications for understanding how light exposure can exacerbate neurological symptoms and inform safer lighting protocols for photosensitive populations.
Abstract

Key Findings

  • mfPOP testing was clinically and objectively safe for both migraine and epilepsy patients, with EEGs showing no epileptiform activity during testing.
  • Pupillary perimetry responses were increased post-ictally and inter-ictally in epilepsy patients, while decreased after migraine attacks and normal during inter-ictal periods in migraineurs.
  • Alpha rhythm entrainment to photic stimulation was more pronounced in epilepsy patients than in the general population, consistent with elevated cortical excitability.
  • Anti-epileptic medications in epilepsy patients and triptans in migraine patients both reversed the changes in mfPOP responses, suggesting medication dampens cortical excitability.
  • Disease-specific visual field defect patterns were observed, with response delays being more generalized across visual fields than sensitivity changes.
Categories

Categories

Eye Health & Vision: The study uses pupillary light response (mfPOP) to examine visual pathway changes in epilepsy and migraine, with specific attention to melanopsin-containing retinal ganglion cells and photosensitivity.
The Science of Light: The research investigates melanopsin-containing ipRGCs and their role in migraine photosensitivity, as well as alpha rhythm entrainment to photic stimulation as a measure of cortical excitability.
Authors

Author(s)

E Ali
Publication Date

Publication Year

2016
Citations

Number of Citations

1
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