Abstract

BackgroundDemographic, systemic and ocular factors may impact macular ganglion cell–inner plexiform layer (GCIPL) thickness measurements. This study aimed to investigate the influences of multiple potential determinants of macular GCIPL thickness in normal Chinese adults.MethodsThis was a retrospective study conducted on 225 normal eyes from 225 healthy Chinese adults. GCIPL thickness were obtained using Cirrus high-definition optical coherence tomography (OCT). The age, gender, laterality, spherical equivalent (SE) refractive error, intraocular pressure (IOP), axial length (AL), central cornea thickness (CCT), circumpapillary retinal nerve fibre layer (pRNFL) thickness and OCT signal strength were recorded and their respective effect on GCIPL thickness parameters were evaluated.ResultsThe mean (± SD) average, minimum, superotemporal, superior, superonasal, inferonasal, inferior, and inferotemporal GCIPL thickness was 84.56 ± 5.36, 81.32 ± 5.58, 83.08 ± 5.37, 85.70 ± 5.95, 87.15 ± 6.26, 85.07 ± 6.11, 82.46 ± 5.76, and 83.88 ± 5.59 μm, respectively. Determinants of thinner GCIPL thickness were older age (P = 0.001–0.117; effects enhanced if age over 40 years), thinner pRNFL (all P < 0.001), and weaker signal strength (all P < 0.001). No significant difference was found between males and females (P = 0.069–0.842), and between right eyes and the left eyes (P = 0.160–0.875) except that of superonasal GCIPL thickness (P < 0.001). There was no significant correlation between GCIPL thickness and SE, IOP, CCT, and AL (P = 0.135–0.968).ConclusionsIndividual determinants associated with thinner GCIPL thickness were older age (particularly over 40 years of age), thinner pRNFL, and weaker OCT signal strength. This is relevant in comprehensively understanding the normative data and differentiating normal aging from abnormalities.

Highlights

  • Demographic, systemic and ocular factors may impact macular ganglion cell–inner plexiform layer (GCIPL) thickness measurements

  • The thinning of macular ganglion cell layer (GCL) and peripapillary retinal nerve fiber layer has been well recognized as biomarkers of optic nerve damage, which can be quantitatively measured by optical coherence tomography (OCT) in a non-invasive, precise, and reproducible way

  • Variability of GCIPL thickness were assessed upon the following possible determinants: Gender The mean age of 96 males and 129 females was 45.9 ± 16.7 and 47.6 ± 16.8 years, respectively

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Summary

Introduction

Demographic, systemic and ocular factors may impact macular ganglion cell–inner plexiform layer (GCIPL) thickness measurements. The hallmark of glaucoma is progressive loss of retinal ganglion cells (RGCs) in the inner retina and their axons in the optic nerve head (ONH) [1]. The thinning of macular ganglion cell layer (GCL) and peripapillary retinal nerve fiber layer (pRNFL) has been well recognized as biomarkers of optic nerve damage, which can be quantitatively measured by optical coherence tomography (OCT) in a non-invasive, precise, and reproducible way. A number of studies have showed that the macular ganglion cell complex (GCC, the sum of RNFL, GCL, and inner plexiform layer) thickness or the macular ganglion cell–inner plexiform layer (GCIPL) thickness has similar glaucoma discriminating performance with that of pRNFL [6,7,8,9]. Combining GCC/GCIPL thickness, pRNFL thickness, ONH parameters, psychophysics examinations, and vasculature evaluations, though, can help to improve the overall glaucomatous diagnostic ability and accuracy [10]

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