Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Jun;105(6):751-760.
doi: 10.1136/bjophthalmol-2020-316417. Epub 2020 Jul 23.

Photophobia: shared pathophysiology underlying dry eye disease, migraine and traumatic brain injury leading to central neuroplasticity of the trigeminothalamic pathway

Affiliations
Free PMC article
Review

Photophobia: shared pathophysiology underlying dry eye disease, migraine and traumatic brain injury leading to central neuroplasticity of the trigeminothalamic pathway

Ryan J Diel et al. Br J Ophthalmol. 2021 Jun.
Free PMC article

Abstract

Background: Photophobia is a potentially debilitating symptom often found in dry eye disease (DE), migraine and traumatic brain injury (TBI).

Methods: We conducted a review of the literature via a PubMed search of English language articles with a focus on how photophobia may relate to a shared pathophysiology across DE, migraine and TBI.

Results: DE, migraine and TBI are common conditions in the general population, are often comorbid, and share photophobia as a symptom. Across the three conditions, neural dysregulation of peripheral and central nervous system components is implicated in photophobia in various animal models and in humans. Enhanced activity of the neuropeptide calcitonin gene-related peptide (CGRP) is closely linked to photophobia. Current therapies for photophobia include glasses which shield the eyes from specific wavelengths, botulinum toxin, and inhibition of CGRP and its receptor. Many individuals have persistent photophobia despite the use of these therapies, and thus, development of new therapies is needed.

Conclusions: The presence of photophobia in DE, migraine and TBI suggests shared trigeminothalamic pathophysiologic mechanisms, as explained by central neuroplasticity and hypersensitivity mediated by neuropeptide CGRP. Treatment strategies which target neural pathways (ie, oral neuromodulators, transcutaneous nerve stimulation) should be considered in patients with persistent photophobia, specifically in individuals with DE whose symptoms are not controlled with traditional therapies.

Keywords: Cornea; Ocular surface; Visual pathway.

Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Photophobia is a manifestation of dry eye, migraine and traumatic brain injury. Melanopsin-containing intrinsically photosensitive retinal ganglion cells (ipRGCs) transmit light-evoked signals (green pathway) to the olivary pretectal nucleus (OPN) and posterior thalamus. A parasympathetic-mediated vasodilatory response (gold pathway) is transmitted via the superior salivatory nucleus (SSN) and sphenopalatine ganglia (SPG) to ocular blood vessels. Nociceptive signals from ocular blood vessels, corneal surface and dural meninges are all transmitted via the ophthalmic branch (V1) of the trigeminal nerve (orange pathway) before converging at the trigeminal ganglia (TG), trigeminal nucleus caudalis (TNC) and posterior thalamus. Dry eye, migraine and traumatic brain injury all represent inputs which may act to sensitise the aforementioned underlying neuronal networks via calcitonin gene-related peptide (purple molecules). The TG, TNC and posterior thalamus are potential areas of neuroplasticity/sensitisation governing the sensations finally culminating as dryness, migraine pain, allodynia and photophobia (blue pathway). Direct activation of trigeminal afferents by an independent melanopsinmediated pathway originating from the iris and/or cornea is not shown. Light-sensing pathways mediating systemic hypothalamic-sympathetic and hypothalamic-parasympathetic pathways are also not shown. Illustration by Ryan J. Diel, MD.
Figure 2
Figure 2
The trigeminovascular system in migraine. The dysfunctions of several brainstem pathways have been implicated in the pathogenesis of migraine. Trigeminovascular input from meningeal vessels passes through the ophthalmic branch of the trigeminal nerve and trigeminal ganglion before synapsing at the trigeminal nucleus caudalis (TNC). These neurons decussate in the brainstem and synapse at the thalamus. Brain imaging studies have revealed nociceptive modulatory activity involving the magnus raphe nucleus (MRN), locus ceruleus (LC) and dorsal raphe nucleus (DRN). A reflex neural connection from the pons, originating at the superior salivatory nucleus (SSN), is responsible for cranial parasympathetic output to dural vessels, as mediated by the pterygopalatine, or sphenopalatine, ganglion; this trigemino-autonomic pathway may play a role in migraine. Genetic, environmental, dietary and metabolic factors in migraine are thought to ultimately incite pathologic activation of areas of the hypothalamus, limbic system and cortex. Illustration by Divy Mehra.

Similar articles

Cited by 7 articles

Publication types

MeSH terms