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Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9

The association between pulmonary sequelae and markers of disease severity, as well as pro-fibrotic mediators, were studied in 108 patients 3 months after hospital admission for COVID-19. The COPD assessment test (CAT-score), spirometry, diffusion capacity of the lungs (DL(CO)), and chest-CT were pe...

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Autores principales: Lerum, Tøri Vigeland, Maltzahn, Niklas Nyboe, Aukrust, Pål, Trøseid, Marius, Henriksen, Katerina Nezvalova, Kåsine, Trine, Dyrhol-Riise, Anne-Ma, Stiksrud, Birgitte, Haugli, Mette, Blomberg, Bjørn, Kittang, Bård Reiakvam, Johannessen, Asgeir, Hannula, Raisa, Aballi, Saad, Kildal, Anders Benjamin, Eiken, Ragnhild, Dahl, Tuva Børresdatter, Lund-Johansen, Fridtjof, Müller, Fredrik, Rodriguez, Jezabel Rivero, Meltzer, Carin, Einvik, Gunnar, Ueland, Thor, Olsen, Inge Christoffer, Barratt-Due, Andreas, Aaløkken, Trond Mogens, Skjønsberg, Ole Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636497/
https://www.ncbi.nlm.nih.gov/pubmed/34853380
http://dx.doi.org/10.1038/s41598-021-02547-x
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author Lerum, Tøri Vigeland
Maltzahn, Niklas Nyboe
Aukrust, Pål
Trøseid, Marius
Henriksen, Katerina Nezvalova
Kåsine, Trine
Dyrhol-Riise, Anne-Ma
Stiksrud, Birgitte
Haugli, Mette
Blomberg, Bjørn
Kittang, Bård Reiakvam
Johannessen, Asgeir
Hannula, Raisa
Aballi, Saad
Kildal, Anders Benjamin
Eiken, Ragnhild
Dahl, Tuva Børresdatter
Lund-Johansen, Fridtjof
Müller, Fredrik
Rodriguez, Jezabel Rivero
Meltzer, Carin
Einvik, Gunnar
Ueland, Thor
Olsen, Inge Christoffer
Barratt-Due, Andreas
Aaløkken, Trond Mogens
Skjønsberg, Ole Henning
author_facet Lerum, Tøri Vigeland
Maltzahn, Niklas Nyboe
Aukrust, Pål
Trøseid, Marius
Henriksen, Katerina Nezvalova
Kåsine, Trine
Dyrhol-Riise, Anne-Ma
Stiksrud, Birgitte
Haugli, Mette
Blomberg, Bjørn
Kittang, Bård Reiakvam
Johannessen, Asgeir
Hannula, Raisa
Aballi, Saad
Kildal, Anders Benjamin
Eiken, Ragnhild
Dahl, Tuva Børresdatter
Lund-Johansen, Fridtjof
Müller, Fredrik
Rodriguez, Jezabel Rivero
Meltzer, Carin
Einvik, Gunnar
Ueland, Thor
Olsen, Inge Christoffer
Barratt-Due, Andreas
Aaløkken, Trond Mogens
Skjønsberg, Ole Henning
author_sort Lerum, Tøri Vigeland
collection PubMed
description The association between pulmonary sequelae and markers of disease severity, as well as pro-fibrotic mediators, were studied in 108 patients 3 months after hospital admission for COVID-19. The COPD assessment test (CAT-score), spirometry, diffusion capacity of the lungs (DL(CO)), and chest-CT were performed at 23 Norwegian hospitals included in the NOR-SOLIDARITY trial, an open-labelled, randomised clinical trial, investigating the efficacy of remdesivir and hydroxychloroquine (HCQ). Thirty-eight percent had a CAT-score ≥ 10. DL(CO) was below the lower limit of normal in 29.6%. Ground-glass opacities were present in 39.8% on chest-CT, parenchymal bands were found in 41.7%. At admission, low pO(2)/F(i)O(2) ratio, ICU treatment, high viral load, and low antibody levels, were predictors of a poorer pulmonary outcome after 3 months. High levels of matrix metalloproteinase (MMP)-9 during hospitalisation and at 3 months were associated with persistent CT-findings. Except for a negative effect of remdesivir on CAT-score, we found no effect of remdesivir or HCQ on long-term pulmonary outcomes. Three months after hospital admission for COVID-19, a high prevalence of respiratory symptoms, reduced DL(CO), and persistent CT-findings was observed. Low pO(2)/F(i)O(2) ratio, ICU-admission, high viral load, low antibody levels, and high levels of MMP-9 were associated with a worse pulmonary outcome.
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spelling pubmed-86364972021-12-03 Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9 Lerum, Tøri Vigeland Maltzahn, Niklas Nyboe Aukrust, Pål Trøseid, Marius Henriksen, Katerina Nezvalova Kåsine, Trine Dyrhol-Riise, Anne-Ma Stiksrud, Birgitte Haugli, Mette Blomberg, Bjørn Kittang, Bård Reiakvam Johannessen, Asgeir Hannula, Raisa Aballi, Saad Kildal, Anders Benjamin Eiken, Ragnhild Dahl, Tuva Børresdatter Lund-Johansen, Fridtjof Müller, Fredrik Rodriguez, Jezabel Rivero Meltzer, Carin Einvik, Gunnar Ueland, Thor Olsen, Inge Christoffer Barratt-Due, Andreas Aaløkken, Trond Mogens Skjønsberg, Ole Henning Sci Rep Article The association between pulmonary sequelae and markers of disease severity, as well as pro-fibrotic mediators, were studied in 108 patients 3 months after hospital admission for COVID-19. The COPD assessment test (CAT-score), spirometry, diffusion capacity of the lungs (DL(CO)), and chest-CT were performed at 23 Norwegian hospitals included in the NOR-SOLIDARITY trial, an open-labelled, randomised clinical trial, investigating the efficacy of remdesivir and hydroxychloroquine (HCQ). Thirty-eight percent had a CAT-score ≥ 10. DL(CO) was below the lower limit of normal in 29.6%. Ground-glass opacities were present in 39.8% on chest-CT, parenchymal bands were found in 41.7%. At admission, low pO(2)/F(i)O(2) ratio, ICU treatment, high viral load, and low antibody levels, were predictors of a poorer pulmonary outcome after 3 months. High levels of matrix metalloproteinase (MMP)-9 during hospitalisation and at 3 months were associated with persistent CT-findings. Except for a negative effect of remdesivir on CAT-score, we found no effect of remdesivir or HCQ on long-term pulmonary outcomes. Three months after hospital admission for COVID-19, a high prevalence of respiratory symptoms, reduced DL(CO), and persistent CT-findings was observed. Low pO(2)/F(i)O(2) ratio, ICU-admission, high viral load, low antibody levels, and high levels of MMP-9 were associated with a worse pulmonary outcome. Nature Publishing Group UK 2021-12-01 /pmc/articles/PMC8636497/ /pubmed/34853380 http://dx.doi.org/10.1038/s41598-021-02547-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lerum, Tøri Vigeland
Maltzahn, Niklas Nyboe
Aukrust, Pål
Trøseid, Marius
Henriksen, Katerina Nezvalova
Kåsine, Trine
Dyrhol-Riise, Anne-Ma
Stiksrud, Birgitte
Haugli, Mette
Blomberg, Bjørn
Kittang, Bård Reiakvam
Johannessen, Asgeir
Hannula, Raisa
Aballi, Saad
Kildal, Anders Benjamin
Eiken, Ragnhild
Dahl, Tuva Børresdatter
Lund-Johansen, Fridtjof
Müller, Fredrik
Rodriguez, Jezabel Rivero
Meltzer, Carin
Einvik, Gunnar
Ueland, Thor
Olsen, Inge Christoffer
Barratt-Due, Andreas
Aaløkken, Trond Mogens
Skjønsberg, Ole Henning
Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9
title Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9
title_full Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9
title_fullStr Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9
title_full_unstemmed Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9
title_short Persistent pulmonary pathology after COVID-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9
title_sort persistent pulmonary pathology after covid-19 is associated with high viral load, weak antibody response, and high levels of matrix metalloproteinase-9
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8636497/
https://www.ncbi.nlm.nih.gov/pubmed/34853380
http://dx.doi.org/10.1038/s41598-021-02547-x
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