Investigation of light-induced lacrimation and pupillary responses in episodic migraine.

The purpose of this pilot study was to investigate the light-induced pupillary and lacrimation responses mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) in migraine. Ten participants with episodic migraine and normal tear production, as well as eleven visually normal control...

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Main Authors: Marija Zivcevska, Shaobo Lei, Alan Blakeman, Daune MacGregor, Herbert C Goltz, Agnes M F Wong
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0241490
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author Marija Zivcevska
Shaobo Lei
Alan Blakeman
Daune MacGregor
Herbert C Goltz
Agnes M F Wong
author_facet Marija Zivcevska
Shaobo Lei
Alan Blakeman
Daune MacGregor
Herbert C Goltz
Agnes M F Wong
author_sort Marija Zivcevska
collection DOAJ
description The purpose of this pilot study was to investigate the light-induced pupillary and lacrimation responses mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) in migraine. Ten participants with episodic migraine and normal tear production, as well as eleven visually normal controls participated in this study. Following an initial baseline trial (no light flash), participants received seven incremental and alternating red and blue light flashes. Pupillometry recording of the left eye and a 1-min anesthetized Schirmer's test of the right eye (using 0.5% proparacaine) were performed simultaneously. Intrinsic and extrinsic ipRGC photoactivities did not differ between migraine participants and controls across all intensities and wavelengths. Migraine participants, however, had significantly lower lacrimation than controls following the highest blue intensity. A positive correlation was found between melanopsin-driven post-illumination pupillary responses and lacrimation following blue stimulation in both groups. Our results show that participants with self-reported photophobia have normal ipRGC-driven responses, suggesting that photophobia and pupillary function may be mediated by distinct ipRGC circuits. The positive correlation between melanopsin-driven pupillary responses and light-induced lacrimation suggests the afferent arm of the light-induced lacrimation reflex is melanopsin-mediated and functions normally in migraine. Lastly, the reduced melanopsin-mediated lacrimation at the highest stimulus suggests the efferent arm of the lacrimation reflex is attenuated under certain conditions, which may be a harbinger of dry eye in migraine.
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spelling doaj.art-e3cbfb438bbe4127bd5582474e3615452022-12-21T22:40:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032020-01-011510e024149010.1371/journal.pone.0241490Investigation of light-induced lacrimation and pupillary responses in episodic migraine.Marija ZivcevskaShaobo LeiAlan BlakemanDaune MacGregorHerbert C GoltzAgnes M F WongThe purpose of this pilot study was to investigate the light-induced pupillary and lacrimation responses mediated by intrinsically photosensitive retinal ganglion cells (ipRGCs) in migraine. Ten participants with episodic migraine and normal tear production, as well as eleven visually normal controls participated in this study. Following an initial baseline trial (no light flash), participants received seven incremental and alternating red and blue light flashes. Pupillometry recording of the left eye and a 1-min anesthetized Schirmer's test of the right eye (using 0.5% proparacaine) were performed simultaneously. Intrinsic and extrinsic ipRGC photoactivities did not differ between migraine participants and controls across all intensities and wavelengths. Migraine participants, however, had significantly lower lacrimation than controls following the highest blue intensity. A positive correlation was found between melanopsin-driven post-illumination pupillary responses and lacrimation following blue stimulation in both groups. Our results show that participants with self-reported photophobia have normal ipRGC-driven responses, suggesting that photophobia and pupillary function may be mediated by distinct ipRGC circuits. The positive correlation between melanopsin-driven pupillary responses and light-induced lacrimation suggests the afferent arm of the light-induced lacrimation reflex is melanopsin-mediated and functions normally in migraine. Lastly, the reduced melanopsin-mediated lacrimation at the highest stimulus suggests the efferent arm of the lacrimation reflex is attenuated under certain conditions, which may be a harbinger of dry eye in migraine.https://doi.org/10.1371/journal.pone.0241490
spellingShingle Marija Zivcevska
Shaobo Lei
Alan Blakeman
Daune MacGregor
Herbert C Goltz
Agnes M F Wong
Investigation of light-induced lacrimation and pupillary responses in episodic migraine.
PLoS ONE
title Investigation of light-induced lacrimation and pupillary responses in episodic migraine.
title_full Investigation of light-induced lacrimation and pupillary responses in episodic migraine.
title_fullStr Investigation of light-induced lacrimation and pupillary responses in episodic migraine.
title_full_unstemmed Investigation of light-induced lacrimation and pupillary responses in episodic migraine.
title_short Investigation of light-induced lacrimation and pupillary responses in episodic migraine.
title_sort investigation of light induced lacrimation and pupillary responses in episodic migraine
url https://doi.org/10.1371/journal.pone.0241490
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