2018
DOI: 10.1097/iae.0000000000001535
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Thickness of the Macula, Retinal Nerve Fiber Layer, and Ganglion Cell–inner Plexiform Layer in the Age-Related Macular Degeneration

Abstract: The automated measurement repeatability for GC-IPL thickness was significantly lower in patients with age-related macular degeneration with out of normal CMT range. The effect of changes in macular morphology should be considered when analyzing GC-IPL thicknesses in a variety of ocular diseases.

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Cited by 18 publications
(17 citation statements)
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“…The overall ICCs for the retinal disease group were lower than those for the normal group using both OCT devices, with the exception of macular thickness using SD-OCT. We found that the low and high CMT groups had ICCs that were lower than those in the normal CMT group using both OCT devices. This trend was consistent with that seen in previous studies comparing normal eyes with eyes affected by retinal disease using SD-OCT.[20, 21, 29] Lee et al reported that the ICCs for thickness measurements in groups with normal eyes, eyes with macular edema, and eyes with atrophy were 0.998, 0.985, and 0.903, respectively. Our data also showed high repeatability for macular thickness measurements (ICC > 0.8–0.9 on both OCT devices).…”
Section: Discussionsupporting
confidence: 91%
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“…The overall ICCs for the retinal disease group were lower than those for the normal group using both OCT devices, with the exception of macular thickness using SD-OCT. We found that the low and high CMT groups had ICCs that were lower than those in the normal CMT group using both OCT devices. This trend was consistent with that seen in previous studies comparing normal eyes with eyes affected by retinal disease using SD-OCT.[20, 21, 29] Lee et al reported that the ICCs for thickness measurements in groups with normal eyes, eyes with macular edema, and eyes with atrophy were 0.998, 0.985, and 0.903, respectively. Our data also showed high repeatability for macular thickness measurements (ICC > 0.8–0.9 on both OCT devices).…”
Section: Discussionsupporting
confidence: 91%
“…Shin et al also reported that repeatability of SD-OCT for GC-IPL measurements was low in eyes with AMD that were out of the normal CMT range. [29] In the present study, retinal diseases were classified by CMT rather than by specific disease because of the small sample sizes. Further studies are warranted to confirm the repeatability of SS-OCT for each specific retinal disease.…”
Section: Discussionmentioning
confidence: 99%
“…However, using multivariate analyses, the GC-IPL was not significant (p = 0.877). In eyes with macular edema, OCTA tends to measure a thinner GCIPL thickness than the actual thickness because of segmentation error [18,19]. Therefore, the impact of the actual GCIPL thickness on the repeatability of OCTA might have been diminished; additional studies are needed to prove this hypothesis.…”
Section: Plos Onementioning
confidence: 99%
“…AMD predominantly involves the outer retinal layers, where extracellular accumulation of lipoprotein in drusen is associated with photoreceptor loss and thinning of the outer nuclear layer. However, inner retinal layers, including the vascularized layers, such as the retinal nerve fibre, ganglion cell, inner plexiform, inner nuclear, and outer plexiform layers may also be involved following photoreceptor degeneration [2,3]. Recent classification of early AMD differentiates lipoprotein extracellular accumulations in drusen localized below the retinal pigment epithelium from subretinal drusenoid deposits (SDD) localized above the retinal pigment epithelium [4][5][6].…”
Section: Introductionmentioning
confidence: 99%
“…The pathogenesis of SDD, otherwise called reticular pseudodrusen, is not completely understood, however, numerous authors have found a reduction of choroidal thickness [5,6,11,12]. The ganglion cell-inner plexiform layer (GCL)-(IPL) has been reported to be thinner in AMD [2], but this layer has not been studied in eyes with SDD. The vascularized retinal layers correlate positively with choroidal thickness in normal eyes [13], owing to this correlation, the present study aimed to evaluate both the choroidal and macular GCL-IPL thicknesses in the presence of SDD in an attempt to further understand the pathogenetic mechanisms involved.…”
Section: Introductionmentioning
confidence: 99%