Literature DB >> 25208547

Ganglion cell and inner plexiform layer thickness determined by spectral domain optical coherence tomography in patients with brain lesions.

Haein Moon1, Joo Young Yoon1, Hyun Taek Lim1, Kyung Rim Sung1.   

Abstract

PURPOSE: To evaluate the thickness of the macular ganglion cell and inner plexiform layer (GCIPL) using spectral domain optical coherence tomography (SD OCT) in patients with brain lesions.
METHODS: This case-control study included 58 healthy subjects and 98 patients with brain lesions confirmed by MRI. GCIPL and peripapillary retinal nerve fiber layer (pRNFL) thicknesses were determined using the Cirrus SD OCT. Area under the receiver operating characteristic curve (AUC) values of pRNFL and GCIPL thickness were used to discriminate patients with brain lesions from normal controls.
RESULTS: Average GCIPL thickness showed a good correlation with visual field mean deviation (r(2)=0.342, p<0.001). All GCIPL parameters, including average thickness (71.9±8.6 vs 85.1±4.8 μm, p<0.001), differed between the patient and control groups. The AUC of the average GCIPL thickness was significantly greater than that of average pRNFL thickness (0.941 vs 0.823, p<0.001).
CONCLUSIONS: Our results suggest that various kinds of brain lesions with different locations show considerable reduction in GCIPL thickness. Thickness of the GCIPL performed better than conventional pRNFL thickness for the diagnosis of retinal ganglion cell damage induced by brains lesions. The pattern of GCIPL loss may be of particular usefulness in recognising a potential intracranial lesion in cases suspected of having normal-tension glaucoma. GCIPL thickness determined by OCT can be an early and useful marker to estimate the status of the visual pathway in various brain lesions. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.

Entities:  

Keywords:  Glaucoma; Imaging; Visual pathway

Mesh:

Year:  2014        PMID: 25208547     DOI: 10.1136/bjophthalmol-2014-305361

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


  6 in total

1.  Retinal Ganglion Cell Atrophy in Homonymous Hemianopia due to Acquired Occipital Lesions Observed Using Cirrus High-Definition-OCT.

Authors:  Tsutomu Yamashita; Atsushi Miki; Katsutoshi Goto; Syunsuke Araki; Go Takizawa; Yoshiaki Ieki; Junichi Kiryu; Akio Tabuchi; Yasuyuki Iguchi; Kazumi Kimura; Yoshiki Yagita
Journal:  J Ophthalmol       Date:  2016-05-04       Impact factor: 1.909

2.  Analysis of Clinical Factors Associated with Retinal Morphological Changes in Patients with Primary Sjögren's Syndrome.

Authors:  Jee Myung Yang; Mi Sun Sung; Yong Sok Ji; Hwan Heo; Sang Woo Park
Journal:  PLoS One       Date:  2016-06-21       Impact factor: 3.240

3.  Reconciling visual field defects and retinal nerve fibre layer asymmetric patterns in retrograde degeneration: an extended case series.

Authors:  Barbara Zangerl; Andrew Whatham; Juno Kim; Agnes Choi; Nagi N Assaad; Michael P Hennessy; Michael Kalloniatis
Journal:  Clin Exp Optom       Date:  2016-10-11       Impact factor: 2.742

4.  Occipital tip injury with homonymous central scotoma: OCT-NFL and RGC correlation.

Authors:  Seth Newman-Wasser; Sruti S Akella; Jeffrey Schultz; Shira E Slasky; Cheng C Zhang
Journal:  Am J Ophthalmol Case Rep       Date:  2019-01-26

5.  Homonymous quadrantic macular ganglion cell complex loss as a sign of trans-synaptic degeneration from occipital lobe lesion.

Authors:  Kenzo Hokazono; Mário Luiz Ribeiro Monteiro
Journal:  Am J Ophthalmol Case Rep       Date:  2018-12-12

6.  The development of a reference database with the Topcon 3D OCT-1 Maestro.

Authors:  Michael Chaglasian; Murray Fingeret; Pinakin Gunvant Davey; Wei-Chieh Huang; Danny Leung; Edmund Ng; Charles A Reisman
Journal:  Clin Ophthalmol       Date:  2018-05-07
  6 in total

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