Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy

To determine the differences in pupillary light reflex (PLR) between the acute and chronic phases of optic neuritis (ON) and nonarteritic anterior ischemic optic neuropathy (NAION). The study included 30 patients with ON and 22 patients with NAION whose PLR were measured by a dynamic pupillometer (P...

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Veröffentlicht in:PloS one 2017-10, Vol.12 (10), p.e0186741-e0186741
Hauptverfasser: Yoo, Yung Ju, Hwang, Jeong-Min, Yang, Hee Kyung
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description To determine the differences in pupillary light reflex (PLR) between the acute and chronic phases of optic neuritis (ON) and nonarteritic anterior ischemic optic neuropathy (NAION). The study included 30 patients with ON and 22 patients with NAION whose PLR were measured by a dynamic pupillometer (PLR-200; NeurOptics Inc., Irvine, USA). Age-matched controls included 58 healthy individuals with normal vision and optic nerve function. Pupil diameters, latency, constriction ratio, constriction velocity and dilation velocity were noted. The differences in PLR measurements were compared among the acute and chronic phases of ON and NAION, and in age-matched controls. Regression analysis determined factors associated with PLR measurements, including visual acuity, color vision defect, visual field defects and retinal nerve fiber layer thickness measurements on optical coherence tomography. Pupillary constriction velocity, constriction ratio and latency were all significantly decreased in the acute phase of ON and NAION. ON showed significantly delayed constriction latency compared to NAION (P = 0.047). Pupillary constriction velocity, constriction ratio and latency were recovered in the chronic phase of ON (P = 0.038, 0.018, and 0.045), however, these parameters were not recovered in NAION (P = 0.693, 0.173 and 0.994). Pupillary constriction velocity, constriction ratio, and latency were significantly decreased in the acute phase of ON and NAION compared to normal controls. ON showed delayed constriction latency compared to NAION. Decreased PLR were recovered in the chronic phase of ON, but not in NAION.
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Pupillary constriction velocity, constriction ratio and latency were recovered in the chronic phase of ON (P = 0.038, 0.018, and 0.045), however, these parameters were not recovered in NAION (P = 0.693, 0.173 and 0.994). Pupillary constriction velocity, constriction ratio, and latency were significantly decreased in the acute phase of ON and NAION compared to normal controls. ON showed delayed constriction latency compared to NAION. 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Pupillary constriction velocity, constriction ratio and latency were recovered in the chronic phase of ON (P = 0.038, 0.018, and 0.045), however, these parameters were not recovered in NAION (P = 0.693, 0.173 and 0.994). Pupillary constriction velocity, constriction ratio, and latency were significantly decreased in the acute phase of ON and NAION compared to normal controls. ON showed delayed constriction latency compared to NAION. Decreased PLR were recovered in the chronic phase of ON, but not in NAION.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>29049405</pmid><doi>10.1371/journal.pone.0186741</doi><tpages>e0186741</tpages><orcidid>https://orcid.org/0000-0003-0837-2864</orcidid><orcidid>https://orcid.org/0000-0002-1140-6036</orcidid><oa>free_for_read</oa></addata></record>
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subjects Acuity
Adult
Age
Biology and Life Sciences
Color vision
Comparative analysis
Constrictions
Defects
Development and progression
Edema
Female
Hospitals
Humans
Ischemia
Latency
Light
Male
Medicine and Health Sciences
Middle Aged
Multiple sclerosis
Nerve conduction
Neuritis
Neuropathy
Optic nerve
Optic neuritis
Optic Neuritis - physiopathology
Optic neuropathy
Optic Neuropathy, Ischemic - physiopathology
Optical Coherence Tomography
Patients
Pupil - physiology
Regression analysis
Retina
Retrospective Studies
Social Sciences
Thickness measurement
Velocity
Vision
Visual acuity
Visual field
Visual fields
Young Adult
title Differences in pupillary light reflex between optic neuritis and ischemic optic neuropathy
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