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Selective changes in human corneal sensation associated with herpes simplex virus keratitis

AuthorsGallar, Juana; Tervo, Timo M. T.; Neira-Zalentein, Waldir; Holopainen, Juha M.; Lamberg, Maria E.; Miñana, Fernando; Acosta, M. Carmen; Belmonte, Carlos
Issue Date2010
PublisherAssociation for Research in Vision and Ophthalmology
CitationInvestigative Ophthalmology and Visual Science 51(9): 4516- 4522 (2010)
AbstractPURPOSE. To determine corneal sensitivity to selective mechanical, chemical, and thermal (heat and cold) stimulation in patients with a history of herpes simplex virus (HSV) keratitis. METHODS. Corneal sensitivity to different modalities of stimulus was determined in both eyes of 16 patients with unilateral HSV keratitis diagnosed 1 to 12 months before the study. On slit lamp examination, 13 HSV-affected eyes showed corneal scarring or opacities, and three had no signs of previous keratitis. Corneal sensitivity was determined with the Belmonte gas esthesiometer. Mechanical, chemical, heat, and cold stimuli were applied on the central cornea. Eyes from 10 healthy subjects served as controls. RESULTS. In all control and contralateral eyes, selective mechanical, chemical, heat, and cold stimulation evoked sensations of subjective intensity proportional to the magnitude of the applied stimulus. In one HSV patient, the affected cornea was unresponsive to all types of stimuli, four lost only corneal sensitivity to mechanical stimulation, and three lost only sensitivity to heat. Mechanical (P < 0.005) and heat (P < 0.05) thresholds were raised in HSV eyes, whereas thresholds for CO 2 were not modified. Also, HSV subjects identified poorly the intensity of mechanical, chemical, and heat stimuli, whereas sensitivity to cold stimulation was unaffected. CONCLUSIONS. In eyes that had had HSV keratitis, corneal sensitivity to mechanical forces and heat was significantly impaired, suggesting that axonal damage and/or altered expression of membrane ion channels involved in transduction and membrane excitability affects primarily the mechano- and polymodal nociceptor terminals. Corneal cold-sensitive terminals remain largely unaffected.
Identifiersdoi: 10.1167/iovs.10-5225
issn: 0146-0404
e-issn: 1552-5783
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