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Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus
PURPOSE: The purpose of this study was to compare ganglion cell complex and peripapillary retinal nerve fiber layer (RNFL) thickness between pregnant females with gestational diabetes mellitus (GDM) and healthy pregnant females. MATERIALS AND METHODS: This was a single-center, prospective, analytica...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843578/ https://www.ncbi.nlm.nih.gov/pubmed/36660129 http://dx.doi.org/10.4103/2211-5056.357848 |
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author | Parveen, Shadman Bhatnagar, Kavita Singh, Pratibha Meena, Seema Suman, Suwarna Shiromani, Sakshi |
author_facet | Parveen, Shadman Bhatnagar, Kavita Singh, Pratibha Meena, Seema Suman, Suwarna Shiromani, Sakshi |
author_sort | Parveen, Shadman |
collection | PubMed |
description | PURPOSE: The purpose of this study was to compare ganglion cell complex and peripapillary retinal nerve fiber layer (RNFL) thickness between pregnant females with gestational diabetes mellitus (GDM) and healthy pregnant females. MATERIALS AND METHODS: This was a single-center, prospective, analytical cross-sectional study including pregnant females with a gestational age of 24 weeks or more in the GDM and control groups. The GDM group included 162 pregnant females with GDM, and the control group included 162 healthy pregnant females. Peripapillary RNFL (pRNFL), macular RNFL (mRNFL), GCL+ (ganglion cell layer [GCL] + inner plexiform layer [IPL]), and GCL++ (mRNFL + GCL + IPL) thickness were analyzed using spectral-domain optical coherence tomography (OCT), and comparisons were made between the groups. RESULTS: Both the groups had similar mean age (P = 0.219), intraocular pressure (P = 0.186), central corneal thickness (P = 0.689), Schirmer test value (P = 0.931), and tear breakup time (P = 0.651). The mean pRNFL thickness of the GDM and control groups was 100.75 ± 8.36 μm and 106.77 ± 8.44 μm (P < 0.0001). pRNFL was significantly thinner in all four quadrants (P < 0.05) in the GDM compared to the control group. We observed that the mean mRNFL, GCL+, and GCL++ thickness were significantly reduced in GDM in comparison to the control group (P < 0.05). CONCLUSION: Our study showed that OCT plays an indispensable role in determining initial retinal changes caused by GDM before the development of diabetic retinopathy. |
format | Online Article Text |
id | pubmed-9843578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-98435782023-01-18 Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus Parveen, Shadman Bhatnagar, Kavita Singh, Pratibha Meena, Seema Suman, Suwarna Shiromani, Sakshi Taiwan J Ophthalmol Original Article PURPOSE: The purpose of this study was to compare ganglion cell complex and peripapillary retinal nerve fiber layer (RNFL) thickness between pregnant females with gestational diabetes mellitus (GDM) and healthy pregnant females. MATERIALS AND METHODS: This was a single-center, prospective, analytical cross-sectional study including pregnant females with a gestational age of 24 weeks or more in the GDM and control groups. The GDM group included 162 pregnant females with GDM, and the control group included 162 healthy pregnant females. Peripapillary RNFL (pRNFL), macular RNFL (mRNFL), GCL+ (ganglion cell layer [GCL] + inner plexiform layer [IPL]), and GCL++ (mRNFL + GCL + IPL) thickness were analyzed using spectral-domain optical coherence tomography (OCT), and comparisons were made between the groups. RESULTS: Both the groups had similar mean age (P = 0.219), intraocular pressure (P = 0.186), central corneal thickness (P = 0.689), Schirmer test value (P = 0.931), and tear breakup time (P = 0.651). The mean pRNFL thickness of the GDM and control groups was 100.75 ± 8.36 μm and 106.77 ± 8.44 μm (P < 0.0001). pRNFL was significantly thinner in all four quadrants (P < 0.05) in the GDM compared to the control group. We observed that the mean mRNFL, GCL+, and GCL++ thickness were significantly reduced in GDM in comparison to the control group (P < 0.05). CONCLUSION: Our study showed that OCT plays an indispensable role in determining initial retinal changes caused by GDM before the development of diabetic retinopathy. Wolters Kluwer - Medknow 2022-10-05 /pmc/articles/PMC9843578/ /pubmed/36660129 http://dx.doi.org/10.4103/2211-5056.357848 Text en Copyright: © 2022 Taiwan J Ophthalmol https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Parveen, Shadman Bhatnagar, Kavita Singh, Pratibha Meena, Seema Suman, Suwarna Shiromani, Sakshi Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus |
title | Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus |
title_full | Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus |
title_fullStr | Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus |
title_full_unstemmed | Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus |
title_short | Ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus |
title_sort | ganglion cell complex and retinal nerve fiber layer thickness in gestational diabetes mellitus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843578/ https://www.ncbi.nlm.nih.gov/pubmed/36660129 http://dx.doi.org/10.4103/2211-5056.357848 |
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