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Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience

PURPOSE: The systemic inflammatory response related to COVID-19 can be easily investigated in living patients. Unfortunately, not every biomarker is suitable for postmortem analysis since several factors may interfere. The aim of this study was to summarize key histopathological findings within each...

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Autores principales: Cut, Talida Georgiana, Ciocan, Veronica, Novacescu, Dorin, Voicu, Adrian, Marinescu, Adelina Raluca, Lazureanu, Voichita Elena, Muresan, Camelia Oana, Enache, Alexandra, Dumache, Raluca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805743/
https://www.ncbi.nlm.nih.gov/pubmed/36597439
http://dx.doi.org/10.2147/IJGM.S389300
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author Cut, Talida Georgiana
Ciocan, Veronica
Novacescu, Dorin
Voicu, Adrian
Marinescu, Adelina Raluca
Lazureanu, Voichita Elena
Muresan, Camelia Oana
Enache, Alexandra
Dumache, Raluca
author_facet Cut, Talida Georgiana
Ciocan, Veronica
Novacescu, Dorin
Voicu, Adrian
Marinescu, Adelina Raluca
Lazureanu, Voichita Elena
Muresan, Camelia Oana
Enache, Alexandra
Dumache, Raluca
author_sort Cut, Talida Georgiana
collection PubMed
description PURPOSE: The systemic inflammatory response related to COVID-19 can be easily investigated in living patients. Unfortunately, not every biomarker is suitable for postmortem analysis since several factors may interfere. The aim of this study was to summarize key histopathological findings within each organ system due to COVID-19 and to assess if serological inexpensive and widely available biomarkers such as CRP, IL-6, fibrinogen and d-Dimers, associated with adverse outcomes in COVID-19, can be implemented in a post-mortem assessment. PATIENTS AND METHODS: A total of 60 subjects divided in 2 groups were included. All subjects died outside a hospital setting and therefore did not receive specific or symptomatic therapies that could have modulated the inflammatory response. The first group included 45 subjects in which mandatory autopsy was performed in order to establish the cause of death and macroscopic examination of the lungs was highly suggestive of SARS-CoV-2 infection. As controls (Group 2), 20 subjects who died from polytrauma in high velocity car accidents and suicide were selected. Bronchial fluids collected during the autopsy procedure were used for the RT-PCR diagnosis of SARS-CoV-2 and serum samples were sent for analysis of IL-6, CRP, d-Dimers and fibrinogen. RESULTS: Compared with the control group, the subjects of the COVID-19 group were older (59±19.5 vs.38±19.15 years, p=0.0002) and had more underlying comorbidities such as hypertension (60% vs 35%, p=0.06) or were overweight (53.3% vs 30%, p=0.08). The levels of CRP, IL-6, fibrinogen and d-Dimers in postmortem plasma samples were significantly higher in COVID-19 subjects than in control group (p< 0.0001). Moreover, the level of IL-6 was significantly higher in overweight patients (r=0.52, P<0.001). In all COVID-19 subjects, the histological examination revealed features corresponding to the exudative and/or proliferative phases of diffuse alveolar damage. Large pulmonary emboli were observed in 7 cases. Gross cardiac enlargement with left ventricular hypertrophy was observed in 19 cases. The most frequent pathological finding of the central nervous system was acute/early-subacute infarction. CONCLUSION: Due to the complexity of the inflammatory response, we postulate that a combination of biomarkers, rather than a single laboratory parameter, might be more effective in obtaining a reliable postmortem COVID-19 diagnosis.
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spelling pubmed-98057432023-01-02 Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience Cut, Talida Georgiana Ciocan, Veronica Novacescu, Dorin Voicu, Adrian Marinescu, Adelina Raluca Lazureanu, Voichita Elena Muresan, Camelia Oana Enache, Alexandra Dumache, Raluca Int J Gen Med Original Research PURPOSE: The systemic inflammatory response related to COVID-19 can be easily investigated in living patients. Unfortunately, not every biomarker is suitable for postmortem analysis since several factors may interfere. The aim of this study was to summarize key histopathological findings within each organ system due to COVID-19 and to assess if serological inexpensive and widely available biomarkers such as CRP, IL-6, fibrinogen and d-Dimers, associated with adverse outcomes in COVID-19, can be implemented in a post-mortem assessment. PATIENTS AND METHODS: A total of 60 subjects divided in 2 groups were included. All subjects died outside a hospital setting and therefore did not receive specific or symptomatic therapies that could have modulated the inflammatory response. The first group included 45 subjects in which mandatory autopsy was performed in order to establish the cause of death and macroscopic examination of the lungs was highly suggestive of SARS-CoV-2 infection. As controls (Group 2), 20 subjects who died from polytrauma in high velocity car accidents and suicide were selected. Bronchial fluids collected during the autopsy procedure were used for the RT-PCR diagnosis of SARS-CoV-2 and serum samples were sent for analysis of IL-6, CRP, d-Dimers and fibrinogen. RESULTS: Compared with the control group, the subjects of the COVID-19 group were older (59±19.5 vs.38±19.15 years, p=0.0002) and had more underlying comorbidities such as hypertension (60% vs 35%, p=0.06) or were overweight (53.3% vs 30%, p=0.08). The levels of CRP, IL-6, fibrinogen and d-Dimers in postmortem plasma samples were significantly higher in COVID-19 subjects than in control group (p< 0.0001). Moreover, the level of IL-6 was significantly higher in overweight patients (r=0.52, P<0.001). In all COVID-19 subjects, the histological examination revealed features corresponding to the exudative and/or proliferative phases of diffuse alveolar damage. Large pulmonary emboli were observed in 7 cases. Gross cardiac enlargement with left ventricular hypertrophy was observed in 19 cases. The most frequent pathological finding of the central nervous system was acute/early-subacute infarction. CONCLUSION: Due to the complexity of the inflammatory response, we postulate that a combination of biomarkers, rather than a single laboratory parameter, might be more effective in obtaining a reliable postmortem COVID-19 diagnosis. Dove 2022-12-28 /pmc/articles/PMC9805743/ /pubmed/36597439 http://dx.doi.org/10.2147/IJGM.S389300 Text en © 2022 Cut et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Cut, Talida Georgiana
Ciocan, Veronica
Novacescu, Dorin
Voicu, Adrian
Marinescu, Adelina Raluca
Lazureanu, Voichita Elena
Muresan, Camelia Oana
Enache, Alexandra
Dumache, Raluca
Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience
title Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience
title_full Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience
title_fullStr Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience
title_full_unstemmed Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience
title_short Autopsy Findings and Inflammatory Markers in SARS-CoV-2: A Single-Center Experience
title_sort autopsy findings and inflammatory markers in sars-cov-2: a single-center experience
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805743/
https://www.ncbi.nlm.nih.gov/pubmed/36597439
http://dx.doi.org/10.2147/IJGM.S389300
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