Association of human myxovirus resistance protein A with severity of COVID-19

Abstract Background In this retrospective cohort study, we explored the correlation of blood human myxovirus resistance protein A (MxA) level with severity of disease in hospitalized COVID-19 patients. Methods All 304 patients admitted for COVID-19 in our hospital until 30th of April 2021 were inclu...

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Main Authors: Otto Lehtinen, Niklas Broman, Matti Waris, Tytti Vuorinen, Ville Peltola, Eliisa Löyttyniemi, Jarmo Oksi, Thijs Feuth
Format: Article
Language:English
Published: BMC 2022-09-01
Series:BMC Infectious Diseases
Subjects:
Online Access:https://doi.org/10.1186/s12879-022-07753-0
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author Otto Lehtinen
Niklas Broman
Matti Waris
Tytti Vuorinen
Ville Peltola
Eliisa Löyttyniemi
Jarmo Oksi
Thijs Feuth
author_facet Otto Lehtinen
Niklas Broman
Matti Waris
Tytti Vuorinen
Ville Peltola
Eliisa Löyttyniemi
Jarmo Oksi
Thijs Feuth
author_sort Otto Lehtinen
collection DOAJ
description Abstract Background In this retrospective cohort study, we explored the correlation of blood human myxovirus resistance protein A (MxA) level with severity of disease in hospitalized COVID-19 patients. Methods All 304 patients admitted for COVID-19 in our hospital until 30th of April 2021 were included in this study. MxA was measured from peripheral blood samples in 268 cases. Patients were divided into groups based on their level of MxA on admission. We studied baseline characteristics and severity of disease on admission based on clinical parameters and inflammatory biomarker levels in each group. Severity of disease during hospitalization was determined by the applied level of respiratory support, by the usage of corticosteroids and by the duration of hospitalization. Results Higher MxA levels on admission were associated with a shorter duration of symptoms before admission, and with more severe disease. Adjusted Odds Ratios for any respiratory support were 9.92 (95%CI 2.11–46.58; p = 0.004) in patients with MxA between 400 μg/L and 799 μg/L (p = 0.004) and 20.08 (95%CI 4.51–89.44; p < 0.001) in patients with MxA ≥ 800 μg/L in comparison with patients with initial MxA < 400 μg/L. The usage of corticosteroids was significantly higher in the high-MxA group (77%) in comparison with the intermediate-MxA group (62%, p = 0.013) and low-MxA group (47%, p < 0.001). Conclusions Higher initial levels of MxA were associated with more severe COVID-19. MxA may be a helpful additional biomarker to predict the severity of the disease.
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spelling doaj.art-e9544bcf51c244de9ee490877b53b9a12022-12-22T04:29:06ZengBMCBMC Infectious Diseases1471-23342022-09-012211710.1186/s12879-022-07753-0Association of human myxovirus resistance protein A with severity of COVID-19Otto Lehtinen0Niklas Broman1Matti Waris2Tytti Vuorinen3Ville Peltola4Eliisa Löyttyniemi5Jarmo Oksi6Thijs Feuth7Department of Pulmonary Diseases and Clinical Allergology, Turku University Hospital and University of TurkuDepartment of Infectious Diseases, Turku University Hospital and University of TurkuDepartment of Clinical Microbiology, Turku University Hospital and University of TurkuDepartment of Clinical Microbiology, Turku University Hospital and University of TurkuDepartment of Paediatrics and Adolescent Medicine, Turku University Hospital and University of TurkuDepartment of Biostatistics, University of TurkuDepartment of Infectious Diseases, Turku University Hospital and University of TurkuDepartment of Pulmonary Diseases and Clinical Allergology, Turku University Hospital and University of TurkuAbstract Background In this retrospective cohort study, we explored the correlation of blood human myxovirus resistance protein A (MxA) level with severity of disease in hospitalized COVID-19 patients. Methods All 304 patients admitted for COVID-19 in our hospital until 30th of April 2021 were included in this study. MxA was measured from peripheral blood samples in 268 cases. Patients were divided into groups based on their level of MxA on admission. We studied baseline characteristics and severity of disease on admission based on clinical parameters and inflammatory biomarker levels in each group. Severity of disease during hospitalization was determined by the applied level of respiratory support, by the usage of corticosteroids and by the duration of hospitalization. Results Higher MxA levels on admission were associated with a shorter duration of symptoms before admission, and with more severe disease. Adjusted Odds Ratios for any respiratory support were 9.92 (95%CI 2.11–46.58; p = 0.004) in patients with MxA between 400 μg/L and 799 μg/L (p = 0.004) and 20.08 (95%CI 4.51–89.44; p < 0.001) in patients with MxA ≥ 800 μg/L in comparison with patients with initial MxA < 400 μg/L. The usage of corticosteroids was significantly higher in the high-MxA group (77%) in comparison with the intermediate-MxA group (62%, p = 0.013) and low-MxA group (47%, p < 0.001). Conclusions Higher initial levels of MxA were associated with more severe COVID-19. MxA may be a helpful additional biomarker to predict the severity of the disease.https://doi.org/10.1186/s12879-022-07753-0COVID-19SARS-CoV-2Human myxovirus resistance protein AMxA
spellingShingle Otto Lehtinen
Niklas Broman
Matti Waris
Tytti Vuorinen
Ville Peltola
Eliisa Löyttyniemi
Jarmo Oksi
Thijs Feuth
Association of human myxovirus resistance protein A with severity of COVID-19
BMC Infectious Diseases
COVID-19
SARS-CoV-2
Human myxovirus resistance protein A
MxA
title Association of human myxovirus resistance protein A with severity of COVID-19
title_full Association of human myxovirus resistance protein A with severity of COVID-19
title_fullStr Association of human myxovirus resistance protein A with severity of COVID-19
title_full_unstemmed Association of human myxovirus resistance protein A with severity of COVID-19
title_short Association of human myxovirus resistance protein A with severity of COVID-19
title_sort association of human myxovirus resistance protein a with severity of covid 19
topic COVID-19
SARS-CoV-2
Human myxovirus resistance protein A
MxA
url https://doi.org/10.1186/s12879-022-07753-0
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