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Persistent (129)Xe MRI Pulmonary and CT Vascular Abnormalities in Symptomatic Individuals with Post-acute COVID-19 Syndrome
BACKGROUND: In patients with post-acute COVID-19 syndrome (PACS), abnormal gas-transfer and pulmonary vascular density have been reported, but such findings have not been related to each other or to symptoms and exercise limitation. The pathophysiologic drivers of PACS in patients previously infecte...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Radiological Society of North America
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272782/ https://www.ncbi.nlm.nih.gov/pubmed/35762891 http://dx.doi.org/10.1148/radiol.220492 |
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author | Matheson, Alexander M. McIntosh, Marrissa J. Kooner, Harkiran K. Lee, Justin Desaigoudar, Vedanth Bier, Elianna Driehuys, Bastiaan Svenningsen, Sarah Santyr, Giles E. Kirby, Miranda Albert, Mitchell S. Shepelytskyi, Yurii Grynko, Vira Ouriadov, Alexei Abdelrazek, Mohamed Dhaliwal, Inderdeep Nicholson, J. Michael Parraga, Grace |
author_facet | Matheson, Alexander M. McIntosh, Marrissa J. Kooner, Harkiran K. Lee, Justin Desaigoudar, Vedanth Bier, Elianna Driehuys, Bastiaan Svenningsen, Sarah Santyr, Giles E. Kirby, Miranda Albert, Mitchell S. Shepelytskyi, Yurii Grynko, Vira Ouriadov, Alexei Abdelrazek, Mohamed Dhaliwal, Inderdeep Nicholson, J. Michael Parraga, Grace |
author_sort | Matheson, Alexander M. |
collection | PubMed |
description | BACKGROUND: In patients with post-acute COVID-19 syndrome (PACS), abnormal gas-transfer and pulmonary vascular density have been reported, but such findings have not been related to each other or to symptoms and exercise limitation. The pathophysiologic drivers of PACS in patients previously infected with COVID-19 who were admitted to in-patient treatment in hospital (or ever-hospitalized patients) and never-hospitalized patients are not well understood. PURPOSE: To determine the relationship of persistent symptoms and exercise limitation with xenon 129 ((129)Xe) MRI and CT pulmonary vascular measurements in individuals with PACS. MATERIALS AND METHODS: In this prospective study, patients with PACS aged 18–80 years with a positive polymerase chain reaction COVID-19 test were recruited from a quaternary-care COVID-19 clinic between April and October 2021. Participants with PACS underwent spirometry, diffusing capacity of the lung for carbon monoxide (DLco), (129)Xe MRI, and chest CT. Healthy controls had no prior history of COVID-19 and underwent spirometry, DLco, and (129)Xe MRI. The (129)Xe MRI red blood cell (RBC) to alveolar-barrier signal ratio, RBC area under the receiver operating characteristic curve (AUC), CT volume of pulmonary vessels with cross-sectional area 5 mm(2) or smaller (BV5), and total blood volume were quantified. St George’s Respiratory Questionnaire, International Physical Activity Questionnaire, and modified Borg Dyspnea Scale measured quality of life, exercise limitation, and dyspnea. Differences between groups were compared with use of Welch t-tests or Welch analysis of variance. Relationships were evaluated with use of Pearson (r) and Spearman (ρ) correlations. RESULTS: Forty participants were evaluated, including six controls (mean age ± SD, 35 years ± 15, three women) and 34 participants with PACS (mean age, 53 years ± 13, 18 women), of whom 22 were never hospitalized. The (129)Xe MRI RBC:barrier ratio was lower in ever-hospitalized participants (P = .04) compared to controls. BV5 correlated with RBC AUC (ρ = .44, P = .03). The (129)Xe MRI RBC:barrier ratio was related to DLco (r = .57, P = .002) and forced expiratory volume in 1 second (ρ = .35, P = .03); RBC AUC was related to dyspnea (ρ = −.35, P = .04) and International Physical Activity Questionnaire score (ρ = .45, P = .02). CONCLUSION: Xenon 129 ((129)Xe) MRI measurements were lower in participants previously infected with COVID-19 who were admitted to in-patient treatment in hospital with post-acute COVID-19 syndrome, 34 weeks ± 25 after infection compared to controls. The (129)Xe MRI measures were associated with CT pulmonary vascular density, diffusing capacity of the lung for carbon monoxide, exercise capacity, and dyspnea. Clinical trial registration no.: NCT04584671 © RSNA, 2022 Online supplemental material is available for this article See also the editorial by Wild and Collier in this issue. |
format | Online Article Text |
id | pubmed-9272782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Radiological Society of North America |
record_format | MEDLINE/PubMed |
spelling | pubmed-92727822022-07-11 Persistent (129)Xe MRI Pulmonary and CT Vascular Abnormalities in Symptomatic Individuals with Post-acute COVID-19 Syndrome Matheson, Alexander M. McIntosh, Marrissa J. Kooner, Harkiran K. Lee, Justin Desaigoudar, Vedanth Bier, Elianna Driehuys, Bastiaan Svenningsen, Sarah Santyr, Giles E. Kirby, Miranda Albert, Mitchell S. Shepelytskyi, Yurii Grynko, Vira Ouriadov, Alexei Abdelrazek, Mohamed Dhaliwal, Inderdeep Nicholson, J. Michael Parraga, Grace Radiology Original Research BACKGROUND: In patients with post-acute COVID-19 syndrome (PACS), abnormal gas-transfer and pulmonary vascular density have been reported, but such findings have not been related to each other or to symptoms and exercise limitation. The pathophysiologic drivers of PACS in patients previously infected with COVID-19 who were admitted to in-patient treatment in hospital (or ever-hospitalized patients) and never-hospitalized patients are not well understood. PURPOSE: To determine the relationship of persistent symptoms and exercise limitation with xenon 129 ((129)Xe) MRI and CT pulmonary vascular measurements in individuals with PACS. MATERIALS AND METHODS: In this prospective study, patients with PACS aged 18–80 years with a positive polymerase chain reaction COVID-19 test were recruited from a quaternary-care COVID-19 clinic between April and October 2021. Participants with PACS underwent spirometry, diffusing capacity of the lung for carbon monoxide (DLco), (129)Xe MRI, and chest CT. Healthy controls had no prior history of COVID-19 and underwent spirometry, DLco, and (129)Xe MRI. The (129)Xe MRI red blood cell (RBC) to alveolar-barrier signal ratio, RBC area under the receiver operating characteristic curve (AUC), CT volume of pulmonary vessels with cross-sectional area 5 mm(2) or smaller (BV5), and total blood volume were quantified. St George’s Respiratory Questionnaire, International Physical Activity Questionnaire, and modified Borg Dyspnea Scale measured quality of life, exercise limitation, and dyspnea. Differences between groups were compared with use of Welch t-tests or Welch analysis of variance. Relationships were evaluated with use of Pearson (r) and Spearman (ρ) correlations. RESULTS: Forty participants were evaluated, including six controls (mean age ± SD, 35 years ± 15, three women) and 34 participants with PACS (mean age, 53 years ± 13, 18 women), of whom 22 were never hospitalized. The (129)Xe MRI RBC:barrier ratio was lower in ever-hospitalized participants (P = .04) compared to controls. BV5 correlated with RBC AUC (ρ = .44, P = .03). The (129)Xe MRI RBC:barrier ratio was related to DLco (r = .57, P = .002) and forced expiratory volume in 1 second (ρ = .35, P = .03); RBC AUC was related to dyspnea (ρ = −.35, P = .04) and International Physical Activity Questionnaire score (ρ = .45, P = .02). CONCLUSION: Xenon 129 ((129)Xe) MRI measurements were lower in participants previously infected with COVID-19 who were admitted to in-patient treatment in hospital with post-acute COVID-19 syndrome, 34 weeks ± 25 after infection compared to controls. The (129)Xe MRI measures were associated with CT pulmonary vascular density, diffusing capacity of the lung for carbon monoxide, exercise capacity, and dyspnea. Clinical trial registration no.: NCT04584671 © RSNA, 2022 Online supplemental material is available for this article See also the editorial by Wild and Collier in this issue. Radiological Society of North America 2022-06-28 /pmc/articles/PMC9272782/ /pubmed/35762891 http://dx.doi.org/10.1148/radiol.220492 Text en © 2022 by the Radiological Society of North America, Inc. This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections. |
spellingShingle | Original Research Matheson, Alexander M. McIntosh, Marrissa J. Kooner, Harkiran K. Lee, Justin Desaigoudar, Vedanth Bier, Elianna Driehuys, Bastiaan Svenningsen, Sarah Santyr, Giles E. Kirby, Miranda Albert, Mitchell S. Shepelytskyi, Yurii Grynko, Vira Ouriadov, Alexei Abdelrazek, Mohamed Dhaliwal, Inderdeep Nicholson, J. Michael Parraga, Grace Persistent (129)Xe MRI Pulmonary and CT Vascular Abnormalities in Symptomatic Individuals with Post-acute COVID-19 Syndrome |
title | Persistent (129)Xe MRI Pulmonary and CT Vascular
Abnormalities in Symptomatic Individuals with Post-acute COVID-19
Syndrome |
title_full | Persistent (129)Xe MRI Pulmonary and CT Vascular
Abnormalities in Symptomatic Individuals with Post-acute COVID-19
Syndrome |
title_fullStr | Persistent (129)Xe MRI Pulmonary and CT Vascular
Abnormalities in Symptomatic Individuals with Post-acute COVID-19
Syndrome |
title_full_unstemmed | Persistent (129)Xe MRI Pulmonary and CT Vascular
Abnormalities in Symptomatic Individuals with Post-acute COVID-19
Syndrome |
title_short | Persistent (129)Xe MRI Pulmonary and CT Vascular
Abnormalities in Symptomatic Individuals with Post-acute COVID-19
Syndrome |
title_sort | persistent (129)xe mri pulmonary and ct vascular
abnormalities in symptomatic individuals with post-acute covid-19
syndrome |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9272782/ https://www.ncbi.nlm.nih.gov/pubmed/35762891 http://dx.doi.org/10.1148/radiol.220492 |
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