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Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue
Post-COVID-19 syndrome (PCS) is characterized by persisting sequelae after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). PCS can affect patients with all COVID-19 disease severities. As previous studies have revealed impaired blood flow as a provoking factor triggering...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9690863/ https://www.ncbi.nlm.nih.gov/pubmed/36430175 http://dx.doi.org/10.3390/ijms232213683 |
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author | Schlick, Sarah Lucio, Marianna Wallukat, Gerd Bartsch, Alexander Skornia, Adam Hoffmanns, Jakob Szewczykowski, Charlotte Schröder, Thora Raith, Franziska Rogge, Lennart Heltmann, Felix Moritz, Michael Beitlich, Lorenz Schottenhamml, Julia Herrmann, Martin Harrer, Thomas Ganslmayer, Marion Kruse, Friedrich E. Lämmer, Robert Mardin, Christian Hohberger, Bettina |
author_facet | Schlick, Sarah Lucio, Marianna Wallukat, Gerd Bartsch, Alexander Skornia, Adam Hoffmanns, Jakob Szewczykowski, Charlotte Schröder, Thora Raith, Franziska Rogge, Lennart Heltmann, Felix Moritz, Michael Beitlich, Lorenz Schottenhamml, Julia Herrmann, Martin Harrer, Thomas Ganslmayer, Marion Kruse, Friedrich E. Lämmer, Robert Mardin, Christian Hohberger, Bettina |
author_sort | Schlick, Sarah |
collection | PubMed |
description | Post-COVID-19 syndrome (PCS) is characterized by persisting sequelae after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). PCS can affect patients with all COVID-19 disease severities. As previous studies have revealed impaired blood flow as a provoking factor triggering PCS, it was the aim of the present study to investigate the potential association between self-reported chronic fatigue and retinal microcirculation in patients with PCS, potentially indicating an objective biomarker. A prospective study was performed, including 201 subjects: 173 patients with PCS and 28 controls. Retinal microcirculation was visualized by OCT angiography (OCT-A) and quantified using the Erlangen-Angio-Tool as macula and peripapillary vessel density (VD). Chronic fatigue (CF) was assessed according to the variables of Bell’s score, age and gender. VDs in the superficial vascular plexus (SVP), intermediate capillary plexus (ICP) and deep capillary plexus (DCP) were analyzed, considering the repetitions (12 times). Seropositivity for autoantibodies targeting G protein-coupled receptors (GPCR-AAbs) was determined by an established cardiomyocyte bioassay. Taking account of the repetitions, a mixed model was performed to detect possible differences in the least square means between the different groups included in the analysis. An age effect in relation to VD was observed between patients and controls (p < 0.0001). Gender analysis showed that women with PCS showed lower VD levels in the SVP compared to male patients (p = 0.0015). The PCS patients showed significantly lower VDs in the ICP as compared to the controls (p = 0.0001 (CI: 0.32; 1)). Moreover, considering PCS patients, the mixed model revealed a significant difference between those with chronic fatigue (CF) and those without CF with respect to VDs in the SVP (p = 0.0033 (CI: −4.5; −0.92)). The model included variables of age, gender and Bell’s score, representing a subjective marker for CF. Consequently, retinal microcirculation might serve as an objective biomarker in subjectively reported chronic fatigue in patients with PCS. |
format | Online Article Text |
id | pubmed-9690863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96908632022-11-25 Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue Schlick, Sarah Lucio, Marianna Wallukat, Gerd Bartsch, Alexander Skornia, Adam Hoffmanns, Jakob Szewczykowski, Charlotte Schröder, Thora Raith, Franziska Rogge, Lennart Heltmann, Felix Moritz, Michael Beitlich, Lorenz Schottenhamml, Julia Herrmann, Martin Harrer, Thomas Ganslmayer, Marion Kruse, Friedrich E. Lämmer, Robert Mardin, Christian Hohberger, Bettina Int J Mol Sci Article Post-COVID-19 syndrome (PCS) is characterized by persisting sequelae after infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). PCS can affect patients with all COVID-19 disease severities. As previous studies have revealed impaired blood flow as a provoking factor triggering PCS, it was the aim of the present study to investigate the potential association between self-reported chronic fatigue and retinal microcirculation in patients with PCS, potentially indicating an objective biomarker. A prospective study was performed, including 201 subjects: 173 patients with PCS and 28 controls. Retinal microcirculation was visualized by OCT angiography (OCT-A) and quantified using the Erlangen-Angio-Tool as macula and peripapillary vessel density (VD). Chronic fatigue (CF) was assessed according to the variables of Bell’s score, age and gender. VDs in the superficial vascular plexus (SVP), intermediate capillary plexus (ICP) and deep capillary plexus (DCP) were analyzed, considering the repetitions (12 times). Seropositivity for autoantibodies targeting G protein-coupled receptors (GPCR-AAbs) was determined by an established cardiomyocyte bioassay. Taking account of the repetitions, a mixed model was performed to detect possible differences in the least square means between the different groups included in the analysis. An age effect in relation to VD was observed between patients and controls (p < 0.0001). Gender analysis showed that women with PCS showed lower VD levels in the SVP compared to male patients (p = 0.0015). The PCS patients showed significantly lower VDs in the ICP as compared to the controls (p = 0.0001 (CI: 0.32; 1)). Moreover, considering PCS patients, the mixed model revealed a significant difference between those with chronic fatigue (CF) and those without CF with respect to VDs in the SVP (p = 0.0033 (CI: −4.5; −0.92)). The model included variables of age, gender and Bell’s score, representing a subjective marker for CF. Consequently, retinal microcirculation might serve as an objective biomarker in subjectively reported chronic fatigue in patients with PCS. MDPI 2022-11-08 /pmc/articles/PMC9690863/ /pubmed/36430175 http://dx.doi.org/10.3390/ijms232213683 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Schlick, Sarah Lucio, Marianna Wallukat, Gerd Bartsch, Alexander Skornia, Adam Hoffmanns, Jakob Szewczykowski, Charlotte Schröder, Thora Raith, Franziska Rogge, Lennart Heltmann, Felix Moritz, Michael Beitlich, Lorenz Schottenhamml, Julia Herrmann, Martin Harrer, Thomas Ganslmayer, Marion Kruse, Friedrich E. Lämmer, Robert Mardin, Christian Hohberger, Bettina Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue |
title | Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue |
title_full | Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue |
title_fullStr | Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue |
title_full_unstemmed | Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue |
title_short | Post-COVID-19 Syndrome: Retinal Microcirculation as a Potential Marker for Chronic Fatigue |
title_sort | post-covid-19 syndrome: retinal microcirculation as a potential marker for chronic fatigue |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9690863/ https://www.ncbi.nlm.nih.gov/pubmed/36430175 http://dx.doi.org/10.3390/ijms232213683 |
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