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Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19
BACKGROUND: Retinal abnormalities are being increasingly reported in COVID-19, in addition to the well-known symptoms of this disease accounting for the neurological involvement. In this study, we aimed to investigate whether ganglion cell layer thickness (GCLT) was different in recovered COVID-19 p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040445/ https://www.ncbi.nlm.nih.gov/pubmed/35525105 http://dx.doi.org/10.1016/j.clineuro.2022.107263 |
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author | Taskiran-Sag, Aslihan Eroglu, Erdal Ozulken, Kemal Canlar, Sule Poyraz, Baris Mustafa Sekerlisoy, Manolya Berguzar Mumcuoglu, Tarkan |
author_facet | Taskiran-Sag, Aslihan Eroglu, Erdal Ozulken, Kemal Canlar, Sule Poyraz, Baris Mustafa Sekerlisoy, Manolya Berguzar Mumcuoglu, Tarkan |
author_sort | Taskiran-Sag, Aslihan |
collection | PubMed |
description | BACKGROUND: Retinal abnormalities are being increasingly reported in COVID-19, in addition to the well-known symptoms of this disease accounting for the neurological involvement. In this study, we aimed to investigate whether ganglion cell layer thickness (GCLT) was different in recovered COVID-19 patients compared to controls in the subacute stage and to determine whether it correlated with COVID-19-related neurological symptoms or pneumonia. METHODS: This study involved 40 patients who had recovered from COVID-19 and 40 age- and sex-matched healthy controls. All the participants underwent ophthalmological examination, spectral domain optical coherence tomography and neurological examination. The clinical and biochemical properties of the patients were noted and their correlations with GCLT were sought. RESULTS: The duration after COVID-19 infection was 113 ± 62 (mean ± SD) days. At this subacute stage, there was no significant difference between the GCLT measurements of the COVID-19 patients and the controls (14 ± 4.0 µm [median ± IQR] vs 16 ± 4.8 µm, respectively). When we analyzed the relationships with neurological symptoms in the patient group, we found that patients with cognitive symptoms had lower GCLT values compared to those without (13 ± 3 µm vs. 16 ± 4 µm, respectively; p = 0.002). Patients who suffered headache during the acute infection also had lower GCLT values compared to those without (14 ± 4 µm vs. 18 ± 5 µm, respectively; p = 0.015). The GCLT values did not differ significantly with respect to anosmia, ageusia, sleep disturbances, having had COVID-19 pneumonia, or smoking status. Age, duration after COVID-19, and blood levels of thyroid stimulating hormone, glucose, vitamin D and vitamin B12 were not in correlation with GCLT in our study. CONCLUSION: Our findings highlight an association between GCLT values and neurological symptoms such as cognitive disturbance (brain fog) and headache in patients who had recovered after non-severe COVID-19 infection. Neuroretinal involvement by SARS-CoV2 might be linked to central neurological symptoms. The patients with lower GCLT values may benefit from close monitoring for neurological problems. |
format | Online Article Text |
id | pubmed-9040445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90404452022-04-26 Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19 Taskiran-Sag, Aslihan Eroglu, Erdal Ozulken, Kemal Canlar, Sule Poyraz, Baris Mustafa Sekerlisoy, Manolya Berguzar Mumcuoglu, Tarkan Clin Neurol Neurosurg Full Length Article BACKGROUND: Retinal abnormalities are being increasingly reported in COVID-19, in addition to the well-known symptoms of this disease accounting for the neurological involvement. In this study, we aimed to investigate whether ganglion cell layer thickness (GCLT) was different in recovered COVID-19 patients compared to controls in the subacute stage and to determine whether it correlated with COVID-19-related neurological symptoms or pneumonia. METHODS: This study involved 40 patients who had recovered from COVID-19 and 40 age- and sex-matched healthy controls. All the participants underwent ophthalmological examination, spectral domain optical coherence tomography and neurological examination. The clinical and biochemical properties of the patients were noted and their correlations with GCLT were sought. RESULTS: The duration after COVID-19 infection was 113 ± 62 (mean ± SD) days. At this subacute stage, there was no significant difference between the GCLT measurements of the COVID-19 patients and the controls (14 ± 4.0 µm [median ± IQR] vs 16 ± 4.8 µm, respectively). When we analyzed the relationships with neurological symptoms in the patient group, we found that patients with cognitive symptoms had lower GCLT values compared to those without (13 ± 3 µm vs. 16 ± 4 µm, respectively; p = 0.002). Patients who suffered headache during the acute infection also had lower GCLT values compared to those without (14 ± 4 µm vs. 18 ± 5 µm, respectively; p = 0.015). The GCLT values did not differ significantly with respect to anosmia, ageusia, sleep disturbances, having had COVID-19 pneumonia, or smoking status. Age, duration after COVID-19, and blood levels of thyroid stimulating hormone, glucose, vitamin D and vitamin B12 were not in correlation with GCLT in our study. CONCLUSION: Our findings highlight an association between GCLT values and neurological symptoms such as cognitive disturbance (brain fog) and headache in patients who had recovered after non-severe COVID-19 infection. Neuroretinal involvement by SARS-CoV2 might be linked to central neurological symptoms. The patients with lower GCLT values may benefit from close monitoring for neurological problems. Elsevier B.V. 2022-06 2022-04-26 /pmc/articles/PMC9040445/ /pubmed/35525105 http://dx.doi.org/10.1016/j.clineuro.2022.107263 Text en © 2022 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Full Length Article Taskiran-Sag, Aslihan Eroglu, Erdal Ozulken, Kemal Canlar, Sule Poyraz, Baris Mustafa Sekerlisoy, Manolya Berguzar Mumcuoglu, Tarkan Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19 |
title | Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19 |
title_full | Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19 |
title_fullStr | Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19 |
title_full_unstemmed | Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19 |
title_short | Headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from COVID-19 |
title_sort | headache and cognitive disturbance correlate with ganglion cell layer thickness in patients who recovered from covid-19 |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040445/ https://www.ncbi.nlm.nih.gov/pubmed/35525105 http://dx.doi.org/10.1016/j.clineuro.2022.107263 |
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