Contributions of the Melanopsin-Expressing Ganglion Cells, Cones, and Rods to the Pupillary Light Response in Obstructive Sleep Apnea.
Data
2019-07Autor
Duque–Chica, Gloria L.
Autor
Gracitelli, Carolina P. B.
Autor
Moura, Ana L. A.
Autor
Nagy, Balázs V.
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Vidal, Kallene S.
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Melo, Geraldine de
Autor
Paranhos Junior, Augusto
Autor
Cahali, Michel Burihan
Autor
Ventura, Dora F.
Tipo
Artigo
Metadata
Mostrar registro completoResumo
PURPOSE: To investigate the impact of obstructive sleep apnea (OSA) on the contribution of inner and outer retinal photoreceptors to the pupillary light response (PLR). METHODS: Ninety-three eyes from 27 patients with OSA and 25 healthy controls were tested. OSA severity was graded according to the apnea-hypopnea index. PLR was measured monocularly with an eye tracker in a Ganzfeld in response to 1-second blue (470 nm) and red (640 nm) flashes at −3, −2, −1, 0, 1, 2, and 2.4 log cd/m2. Peak pupil constriction amplitude, peak latency, and the postillumination pupil response were measured. The Cambridge Colour Test, standard automatic perimetry, spectral domain optical coherence tomography, polysomnography, and the Pittsburgh Sleep Quality Index were used. RESULTS: OSA patients have a significantly decreased peak pupil constriction amplitude for blue stimuli at −3, −2, −1, 1 log cd/m2 and at all red flash luminances (P < 0.050), revealing reduction of outer retina contributions to PLR. OSA patients showed reduced peak latency for blue (−2, 0, 2, 2.4 log cd/m2) and red stimuli (−2, 0 log cd/m2; P < 0.040). No significant difference was found in the melanopsin-mediated PLR. CONCLUSIONS: This study is the first to evaluate the inner and outer retinal contributions to PLR in OSA patients. The results showed that the outer retinal photoreceptor contributions to PLR were affected in moderate and severe OSA patients. In contrast, the inner retina contributions to PLR are preserved.
Título Abreviado
Invest Ophthalmol Vis Sci. 2019 Jul 1;60(8):3002-3012. doi: 10.1167/iovs.19-26944.
Palavras-chave
Obstructive Sleep Apnea Pupillary Light Responses Classical Photoreceptors Intrinsically Photosensitive Retinal Ganglion Cells Circadian Rhythm Retinal Nerve Fiber Layer Thickness Visual Field Defect
Coleções
- Artigo [10]