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IFI27 transcription is an early predictor for COVID-19 outcomes; a multi-cohort observational study
Maryam Shojaei; Amir Shamshirian; James Monkman; Laura Grice; Minh Tran; Chin Wee Tan; Gustavo Rodrigues Rossi; Timothy R Mcculloch; Marek Nalos; Keng Y Chew; Yanshan Zhu; Yao Xia; Timothy J Wells; Alexandra C Senegaglia; Carmen LK Rebelatto; Claudio L Franck; Anna FR dos Santos; Lucia Noronha; Sepideh Motamen; Reza Valadan; Omolbanin Amjadi; Rajan Gogna; Esha Madan; Reza Alizadeh-Navaei; Liliana Lamperti; Felipe Zuniga; Estefania Nova-Lamperti; Gonzalo Labarca; Ben Knippenberg; Velma Herwanto; Ya Wang; Amy Phu; Tracy Chew; Timothy Kwan; Karen Kim; Sally Teoh; Tiana M Pelaia; Win S Kuan; Yvette Jee; Jon Iredell; Ken O'Byrne; John F Fraser; Melissa J Davis; Gabrielle T Belz; Majid E Warkiani; Carlos Salomon Gallo; Fernando SF Guimaraes; Quan Nguyen; Anthony Mclean; Arutha Kulasinghe; Kirsty R Short; Benjamin Tang.
Afiliación
  • Maryam Shojaei; Centre for Immunology and Allergy Research, Westmead Institute for Medical Research, Sydney, NSW, Australia
  • Amir Shamshirian; Mazandaran University of Medical Sciences
  • James Monkman; Queensland University of Technology
  • Laura Grice; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia
  • Minh Tran; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia
  • Chin Wee Tan; The Walter and Eliza Hall Institute of Medical Research, Parkville, Melbourne, Victoria 3052, Australia
  • Gustavo Rodrigues Rossi; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia
  • Timothy R Mcculloch; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia
  • Marek Nalos; Department of Intensive Care Medicine, Nepean Hospital, NSW, Australia
  • Keng Y Chew; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
  • Yanshan Zhu; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, Australia
  • Yao Xia; School of Science, Edith Cowan University; School of Biomedical Science, University of Western Australia, Perth, Australia
  • Timothy J Wells; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia
  • Alexandra C Senegaglia; Complexo Hospital de Clinicas, Universidade Federal do Parana, Curitiba, PR, Brazil
  • Carmen LK Rebelatto; Core for Cell Technology, School of Medicine, Pontificia Universidade Catolica do Parana, Curitiba, PR, Brazil
  • Claudio L Franck; Complexo Hospital de Clinicas, Universidade Federal do Parana, Curitiba, PR, Brazil
  • Anna FR dos Santos; Complexo Hospital de Clinicas, Universidade Federal do Parana, Curitiba, PR, Brazil
  • Lucia Noronha; Pontificia Universidade Catolica do Parana
  • Sepideh Motamen; Department of Medical Biotechnology, Faculty of Medical Sciences, Tarbiat Modares University, Iran
  • Reza Valadan; Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
  • Omolbanin Amjadi; Gastrointestinal Cancer Research Centre, Non-Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran
  • Rajan Gogna; Biotech Research and Innovation Centre (BRIC), University of Copenhagen, Ole Maaloes Vej 5, 2200 Copenhagen N, Denmark
  • Esha Madan; Champalimaud Center for the Unknown, 1400-038 Lisbon, Portugal
  • Reza Alizadeh-Navaei; Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran
  • Liliana Lamperti; Department of Clinical Biochemistry and Immunology, Faculty of Pharmacy, University of Concepcion, Concepcion, Chile.
  • Felipe Zuniga; Department of Clinical Biochemistry and Immunology, Faculty of Pharmacy, University of Concepcion, Concepcion, Chile.
  • Estefania Nova-Lamperti; Molecular and Translational Immunology Laboratory, Department of Clinical Biochemistry and Immunology, Faculty of Pharmacy, Universidad de Concepcion, Concepcio
  • Gonzalo Labarca; Department of Clinical Biochemistry and Immunology, Faculty of Pharmacy, University of Concepcion, Concepcion, Chile.
  • Ben Knippenberg; Infectious Diseases Department, Royal Darwin Hospital, Northern Territories, Australia
  • Velma Herwanto; Faculty of Medicine, Universitas Tarumanagara, Jakarta, Indonesia
  • Ya Wang; Department of Intensive Care Medicine, Nepean Hospital, NSW, Australia
  • Amy Phu; Department of Intensive Care Medicine, Nepean Hospital, NSW, Australia
  • Tracy Chew; Sydney Informatics Hub, Core Research Facilities, University of Sydney, NSW, Australia
  • Timothy Kwan; Department of Intensive Care Medicine, Nepean Hospital, NSW, Australia
  • Karen Kim; Centre for Immunology and Allergy Research, Westmead Institute for Medical Research, Sydney, NSW, Australia
  • Sally Teoh; Department of Intensive Care Medicine, Nepean Hospital, NSW, Australia
  • Tiana M Pelaia; Department of Intensive Care Medicine, Nepean Hospital, NSW, Australia
  • Win S Kuan; Emergency Medicine Department, National University Hospital, National University Health System, Singapore
  • Yvette Jee; Emergency Medicine Department, National University Hospital, National University Health System, Singapore
  • Jon Iredell; Centre for Infectious Diseases and Microbiology, Westmead Institute for Medical Research, Sydney, NSW, Australia
  • Ken O'Byrne; Queensland University of Technology
  • John F Fraser; Critical Care Research Group, The University of Queensland, Brisbane, Australia.
  • Melissa J Davis; The Walter and Eliza Hall Institute of Medical Research, Parkville, Melbourne, Victoria 3052, Australia
  • Gabrielle T Belz; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia
  • Majid E Warkiani; Australia Centre for Health Technologies (CHT) & Institute for Biomedical Materials & Devices (IBMD), School of Biomedical Engineering, University of Technology
  • Carlos Salomon Gallo; Exosome Biology Laboratory, Centre for Clinical Diagnostics, University of Queensland Centre for Clinical Research, Royal Brisbane and Women's Hospital, The Uni
  • Fernando SF Guimaraes; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, QLD, Australia
  • Quan Nguyen; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.
  • Anthony Mclean; Department of Intensive Care Medicine, Nepean Hospital, NSW, Australia
  • Arutha Kulasinghe; Queensland University
  • Kirsty R Short; University of Queensland
  • Benjamin Tang; Centre for Immunology and Allergy Research, Westmead Institute for Medical Research, Sydney, NSW, Australia
Preprint en En | PREPRINT-MEDRXIV | ID: ppmedrxiv-21265555
ABSTRACT
BackgroundRobust biomarkers that predict disease outcomes amongst COVID-19 patients are necessary for both patient triage and resource prioritisation. Numerous candidate biomarkers have been proposed for COVID-19. However, at present, there is no consensus on the best diagnostic approach to predict outcomes in infected patients. Moreover, it is not clear whether such tools would apply to other potentially pandemic pathogens and therefore of use as stockpile for future pandemic preparedness. MethodsWe conducted a multi-cohort observational study to investigate the biology and the prognostic role of interferon alpha-inducible protein 27 (IFI27) in COVID-19 patients. FindingsWe show that IFI27 is expressed in the respiratory tract of COVID-19 patients and elevated IFI27 expression is associated with the presence of a high viral load. We further demonstrate that systemic host response, as measured by blood IFI27 expression, is associated with COVID-19 severity. For clinical outcome prediction (e.g. respiratory failure), IFI27 expression displays a high positive (0.83) and negative (0.95) predictive value, outperforming all other known predictors of COVID-19 severity. Furthermore, IFI27 is upregulated in the blood of infected patients in response to other respiratory viruses. For example, in the pandemic H1N1/09 swine influenza virus infection, IFI27-like genes were highly upregulated in the blood samples of severely infected patients. InterpretationThese data suggest that prognostic biomarkers targeting the family of IFI27 genes could potentially supplement conventional diagnostic tools in future virus pandemics, independent of whether such pandemics are caused by a coronavirus, an influenza virus or another as yet-to-be discovered respiratory virus. Research in contextO_ST_ABSEvidence before this studyC_ST_ABSWe searched the scientific literature using PubMed to identify studies that used the IFI27 biomarker to predict outcomes in COVID-19 patients. We used the search terms "IFI27", "COVID-19, "gene expression" and "outcome prediction". We did not identify any study that investigated the role of IFI27 biomarker in outcome prediction. Although ten studies were identified using the general terms of "gene expression" and "COVID-19", IFI27 was only mentioned in passing as one of the identified genes. All these studies addressed the broader question of the host response to COVID-19; none focused solely on using IFI27 to improve the risk stratification of infected patients in a pandemic. Added value of this studyHere, we present the findings of a multi-cohort study of the IFI27 biomarker in COVID-19 patients. Our findings show that the host response, as reflected by blood IFI27 gene expression, accurately predicts COVID-19 disease progression (positive and negative predictive values; 0.83 and 0.95, respectively), outperforming age, comorbidity, C-reactive protein and all other known risk factors. The strong association of IFI27 with disease severity occurs not only in SARS-CoV-2 infection, but also in other respiratory viruses with pandemic potential, such as the influenza virus. These findings suggest that host response biomarkers, such as IFI27, could help identify high-risk COVID-19 patients - those who are more likely to develop infection complications - and therefore may help improve patient triage in a pandemic. Implications of all the available evidenceThis is the first systemic study of the clinical role of IFI27 in the current COVID-19 pandemic and its possible future application in other respiratory virus pandemics. The findings not only could help improve the current management of COVID-19 patients but may also improve future pandemic preparedness.
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Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Observational_studies / Prognostic_studies / Review Idioma: En Año: 2021 Tipo del documento: Preprint
Texto completo: 1 Colección: 09-preprints Base de datos: PREPRINT-MEDRXIV Tipo de estudio: Cohort_studies / Observational_studies / Prognostic_studies / Review Idioma: En Año: 2021 Tipo del documento: Preprint