Literature DB >> 25148790

Relationship between ganglion cell layer thickness and estimated retinal ganglion cell counts in the glaucomatous macula.

Chunwei Zhang1, Andrew J Tatham2, Robert N Weinreb3, Linda M Zangwill3, Zhiyong Yang3, James Z Zhang3, Felipe A Medeiros4.   

Abstract

PURPOSE: To investigate the relationship between macular ganglion cell-inner plexiform layer (mGCIPL) thickness and estimated macular retinal ganglion cell (RGC) counts in glaucoma.
DESIGN: Observational cohort study. PARTICIPANTS: Cross-sectional study of 77 healthy, 154 glaucoma suspect, and 159 glaucomatous eyes from the Diagnostic Innovations in Glaucoma Study.
METHODS: All eyes underwent 24-2 standard automated perimetry (SAP) and optic nerve and macular imaging using high-definition optical coherence tomography (OCT). The total number of RGCs was estimated using a previously described model that uses SAP and OCT circumpapillary retinal nerve fiber layer (cpRNFL) measurements. The number of macular RGCs was estimated from the temporal cpRNFL and SAP test points within the central 10°. MAIN OUTCOME MEASURES: The correlation between mGCIPL thickness and estimates of macular RGC counts.
RESULTS: The average estimated macular RGC count in glaucomatous eyes was 306 010 ± 109 449 cells, which was significantly lower than the estimate of 520 678 ± 106 843 cells in healthy eyes (P < 0.001). Glaucomatous eyes had 41% fewer estimated macular RGCs than healthy eyes and suspects had 21% fewer estimated macular RGCs. There was strong correlation between estimated macular RGC counts and mGCIPL thickness (R(2) = 0.67; P < 0.001). Macular RGC counts performed better than average mGCIPL thickness in discriminating healthy and glaucomatous eyes with receiver operating characteristic curve areas of 0.873 and 0.775, respectively (P = 0.015).
CONCLUSIONS: The strong association between estimated macular RGC counts and mGCIPL thickness and the better diagnostic performance of the macular RGC counts compared with mGCIPL thickness provides further evidence that estimates of RGC number from cpRNFL thickness and SAP sensitivity can be used to assess neural losses in glaucoma.
Copyright © 2014 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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Year:  2014        PMID: 25148790      PMCID: PMC4252259          DOI: 10.1016/j.ophtha.2014.06.047

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  43 in total

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2.  Number of ganglion cells in glaucoma eyes compared with threshold visual field tests in the same persons.

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3.  Linking structure and function in glaucoma.

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5.  Estimating the rate of retinal ganglion cell loss in glaucoma.

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6.  Comparison of retinal nerve fiber layer and optic disc imaging for diagnosing glaucoma in patients suspected of having the disease.

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8.  Macular and peripapillary retinal nerve fiber layer measurements by spectral domain optical coherence tomography in normal-tension glaucoma.

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  32 in total

1.  Event-based analysis of visual field change can miss fast glaucoma progression detected by a combined structure and function index.

Authors:  Chunwei Zhang; Andrew J Tatham; Fábio B Daga; Alessandro A Jammal; Felipe A Medeiros
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Review 2.  Advances of optical coherence tomography in myopia and pathologic myopia.

Authors:  D S C Ng; C Y L Cheung; F O Luk; S Mohamed; M E Brelen; J C S Yam; C W Tsang; T Y Y Lai
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4.  Neuroprotective Effect of Lutein on NMDA-Induced Retinal Ganglion Cell Injury in Rat Retina.

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Review 5.  Optic nerve head and fibre layer imaging for diagnosing glaucoma.

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Review 6.  Macular imaging with optical coherence tomography in glaucoma.

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7.  Contrast-to-Noise Ratios for Assessing the Detection of Progression in the Various Stages of Glaucoma.

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8.  Spectral-Domain Optical Coherence Tomography for Glaucoma Diagnosis.

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9.  A Portable Platform for Evaluation of Visual Performance in Glaucoma Patients.

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Journal:  PLoS One       Date:  2015-10-07       Impact factor: 3.240

10.  Swept-source optical coherence tomography imaging of macular retinal and choroidal structures in healthy eyes.

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