2015
DOI: 10.1093/pm/pnv070
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Burning Eye Syndrome: Do Neuropathic Pain Mechanisms Underlie Chronic Dry Eye?

Abstract: Dry eye is becoming a major health concern due to its increasing incidence, significant morbidity, and economic burden. Recent evidence suggests that a subset of dry eye may be better represented as a chronic neuropathic pain disorder due to its features of dysesthesia, spontaneous pain, allodynia, and hyperalgesia. Future therapies targeted at the underlying neuroplasticity may yield improved efficacy for patients with this subset of dry eye, which we term "burning eye syndrome."

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Cited by 41 publications
(60 citation statements)
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“…Acute axonal injury during corneal nerve damage facilitates the release of inflammatory mediators, including prostaglandins, cytokines such as interleukin-1 and tumor necrosis factor-α, and neuropeptides such as substance P, which can reduce the threshold potentials of ion channels of corneal nerve endings 56. Subsequent release of nerve growth factor leads to upregulation and expression of genes, resulting in hypersensitivity of corneal nociceptors to stimuli 2,56. In addition, chronic severe or repeated axonal injury promotes the transition of the function of corneal nociceptors from signal transmission to nerve regeneration 2.…”
Section: Association With Neurological Problemsmentioning
confidence: 99%
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“…Acute axonal injury during corneal nerve damage facilitates the release of inflammatory mediators, including prostaglandins, cytokines such as interleukin-1 and tumor necrosis factor-α, and neuropeptides such as substance P, which can reduce the threshold potentials of ion channels of corneal nerve endings 56. Subsequent release of nerve growth factor leads to upregulation and expression of genes, resulting in hypersensitivity of corneal nociceptors to stimuli 2,56. In addition, chronic severe or repeated axonal injury promotes the transition of the function of corneal nociceptors from signal transmission to nerve regeneration 2.…”
Section: Association With Neurological Problemsmentioning
confidence: 99%
“…Subsequent release of nerve growth factor leads to upregulation and expression of genes, resulting in hypersensitivity of corneal nociceptors to stimuli 2,56. In addition, chronic severe or repeated axonal injury promotes the transition of the function of corneal nociceptors from signal transmission to nerve regeneration 2. With regeneration, the injured nerve can develop microneuromas, endobulbs and nerve sprouts, which can be sources of spontaneous pain 2,56.…”
Section: Association With Neurological Problemsmentioning
confidence: 99%
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