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MS-based targeted profiling of oxylipins in COVID-19: A new insight into inflammation regulation
The key role of inflammation in COVID-19 induced many authors to study the cytokine storm, whereas the role of other inflammatory mediators such as oxylipins is still poorly understood. IMPRECOVID was a monocentric retrospective observational pilot study with COVID-19 related pneumonia patients (n =...
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Published in: | Free radical biology & medicine 2022-02, Vol.180, p.236-243 |
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creator | Biagini, Denise Franzini, Maria Oliveri, Paolo Lomonaco, Tommaso Ghimenti, Silvia Bonini, Andrea Vivaldi, Federico Macera, Lisa Balas, Laurence Durand, Thierry Oger, Camille Galano, Jean-Marie Maggi, Fabrizio Celi, Alessandro Paolicchi, Aldo Di Francesco, Fabio |
description | The key role of inflammation in COVID-19 induced many authors to study the cytokine storm, whereas the role of other inflammatory mediators such as oxylipins is still poorly understood.
IMPRECOVID was a monocentric retrospective observational pilot study with COVID-19 related pneumonia patients (n = 52) admitted to Pisa University Hospital between March and April 2020. Our MS-based analytical platform permitted the simultaneous determination of sixty plasma oxylipins in a single run at ppt levels for a comprehensive characterisation of the inflammatory cascade in COVID-19 patients. The datasets containing oxylipin and cytokine plasma levels were analysed by principal component analysis (PCA), computation of Fisher’s canonical variable, and a multivariate receiver operating characteristic (ROC) curve.
Differently from cytokines, the panel of oxylipins clearly differentiated samples collected in COVID-19 wards (n = 43) and Intensive Care Units (ICUs) (n = 27), as shown by the PCA and the multivariate ROC curve with a resulting AUC equal to 0.92. ICU patients showed lower (down to two orders of magnitude) plasma concentrations of anti-inflammatory and pro-resolving lipid mediators, suggesting an impaired inflammation response as part of a prolonged and unsolvable pro-inflammatory status. In conclusion, our targeted oxylipidomics platform helped shedding new light in this field. Targeting the lipid mediator class switching is extremely important for a timely picture of a patient’s ability to respond to the viral attack. A prediction model exploiting selected lipid mediators as biomarkers seems to have good chances to classify patients at risk of severe COVID-19.
•Sixty oxylipins were successfully quantified in plasma of COVID-19 patients by MEPS-UHPLC-MS/MS platform.•Lipid mediators help to classify patients at risk of severe COVID-19.•Severe COVID-19 is associated with a selective deficiency of pro-resolving mediators. |
doi_str_mv | 10.1016/j.freeradbiomed.2022.01.021 |
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IMPRECOVID was a monocentric retrospective observational pilot study with COVID-19 related pneumonia patients (n = 52) admitted to Pisa University Hospital between March and April 2020. Our MS-based analytical platform permitted the simultaneous determination of sixty plasma oxylipins in a single run at ppt levels for a comprehensive characterisation of the inflammatory cascade in COVID-19 patients. The datasets containing oxylipin and cytokine plasma levels were analysed by principal component analysis (PCA), computation of Fisher’s canonical variable, and a multivariate receiver operating characteristic (ROC) curve.
Differently from cytokines, the panel of oxylipins clearly differentiated samples collected in COVID-19 wards (n = 43) and Intensive Care Units (ICUs) (n = 27), as shown by the PCA and the multivariate ROC curve with a resulting AUC equal to 0.92. ICU patients showed lower (down to two orders of magnitude) plasma concentrations of anti-inflammatory and pro-resolving lipid mediators, suggesting an impaired inflammation response as part of a prolonged and unsolvable pro-inflammatory status. In conclusion, our targeted oxylipidomics platform helped shedding new light in this field. Targeting the lipid mediator class switching is extremely important for a timely picture of a patient’s ability to respond to the viral attack. A prediction model exploiting selected lipid mediators as biomarkers seems to have good chances to classify patients at risk of severe COVID-19.
•Sixty oxylipins were successfully quantified in plasma of COVID-19 patients by MEPS-UHPLC-MS/MS platform.•Lipid mediators help to classify patients at risk of severe COVID-19.•Severe COVID-19 is associated with a selective deficiency of pro-resolving mediators.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/j.freeradbiomed.2022.01.021</identifier><identifier>PMID: 35085774</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biochemistry, Molecular Biology ; COVID-19 ; Endocrinology and metabolism ; Human health and pathology ; Humans ; Inflamamtion ; Inflammation ; Inflammation regulation ; Life Sciences ; Lipid mediator class switching ; Oxylipins ; Retrospective Studies ; SARS-CoV-2 ; Severity predictors ; UHPLC-MS/MS</subject><ispartof>Free radical biology & medicine, 2022-02, Vol.180, p.236-243</ispartof><rights>2022 Elsevier Inc.</rights><rights>Copyright © 2022 Elsevier Inc. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2022 Elsevier Inc. All rights reserved. 2022 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4401-4799aca32740e24fff7aa2b5d2ae9efb208c0a2e59521c4b6a4e85a07950c50e3</citedby><cites>FETCH-LOGICAL-c4401-4799aca32740e24fff7aa2b5d2ae9efb208c0a2e59521c4b6a4e85a07950c50e3</cites><orcidid>0000-0002-1822-7399 ; 0000-0002-5177-5792 ; 0000-0001-6747-9712 ; 0000-0001-6086-7296 ; 0000-0001-6412-4967 ; 0000-0002-6687-3811</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35085774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03550506$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Biagini, Denise</creatorcontrib><creatorcontrib>Franzini, Maria</creatorcontrib><creatorcontrib>Oliveri, Paolo</creatorcontrib><creatorcontrib>Lomonaco, Tommaso</creatorcontrib><creatorcontrib>Ghimenti, Silvia</creatorcontrib><creatorcontrib>Bonini, Andrea</creatorcontrib><creatorcontrib>Vivaldi, Federico</creatorcontrib><creatorcontrib>Macera, Lisa</creatorcontrib><creatorcontrib>Balas, Laurence</creatorcontrib><creatorcontrib>Durand, Thierry</creatorcontrib><creatorcontrib>Oger, Camille</creatorcontrib><creatorcontrib>Galano, Jean-Marie</creatorcontrib><creatorcontrib>Maggi, Fabrizio</creatorcontrib><creatorcontrib>Celi, Alessandro</creatorcontrib><creatorcontrib>Paolicchi, Aldo</creatorcontrib><creatorcontrib>Di Francesco, Fabio</creatorcontrib><title>MS-based targeted profiling of oxylipins in COVID-19: A new insight into inflammation regulation</title><title>Free radical biology & medicine</title><addtitle>Free Radic Biol Med</addtitle><description>The key role of inflammation in COVID-19 induced many authors to study the cytokine storm, whereas the role of other inflammatory mediators such as oxylipins is still poorly understood.
IMPRECOVID was a monocentric retrospective observational pilot study with COVID-19 related pneumonia patients (n = 52) admitted to Pisa University Hospital between March and April 2020. Our MS-based analytical platform permitted the simultaneous determination of sixty plasma oxylipins in a single run at ppt levels for a comprehensive characterisation of the inflammatory cascade in COVID-19 patients. The datasets containing oxylipin and cytokine plasma levels were analysed by principal component analysis (PCA), computation of Fisher’s canonical variable, and a multivariate receiver operating characteristic (ROC) curve.
Differently from cytokines, the panel of oxylipins clearly differentiated samples collected in COVID-19 wards (n = 43) and Intensive Care Units (ICUs) (n = 27), as shown by the PCA and the multivariate ROC curve with a resulting AUC equal to 0.92. ICU patients showed lower (down to two orders of magnitude) plasma concentrations of anti-inflammatory and pro-resolving lipid mediators, suggesting an impaired inflammation response as part of a prolonged and unsolvable pro-inflammatory status. In conclusion, our targeted oxylipidomics platform helped shedding new light in this field. Targeting the lipid mediator class switching is extremely important for a timely picture of a patient’s ability to respond to the viral attack. A prediction model exploiting selected lipid mediators as biomarkers seems to have good chances to classify patients at risk of severe COVID-19.
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IMPRECOVID was a monocentric retrospective observational pilot study with COVID-19 related pneumonia patients (n = 52) admitted to Pisa University Hospital between March and April 2020. Our MS-based analytical platform permitted the simultaneous determination of sixty plasma oxylipins in a single run at ppt levels for a comprehensive characterisation of the inflammatory cascade in COVID-19 patients. The datasets containing oxylipin and cytokine plasma levels were analysed by principal component analysis (PCA), computation of Fisher’s canonical variable, and a multivariate receiver operating characteristic (ROC) curve.
Differently from cytokines, the panel of oxylipins clearly differentiated samples collected in COVID-19 wards (n = 43) and Intensive Care Units (ICUs) (n = 27), as shown by the PCA and the multivariate ROC curve with a resulting AUC equal to 0.92. ICU patients showed lower (down to two orders of magnitude) plasma concentrations of anti-inflammatory and pro-resolving lipid mediators, suggesting an impaired inflammation response as part of a prolonged and unsolvable pro-inflammatory status. In conclusion, our targeted oxylipidomics platform helped shedding new light in this field. Targeting the lipid mediator class switching is extremely important for a timely picture of a patient’s ability to respond to the viral attack. A prediction model exploiting selected lipid mediators as biomarkers seems to have good chances to classify patients at risk of severe COVID-19.
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subjects | Biochemistry, Molecular Biology COVID-19 Endocrinology and metabolism Human health and pathology Humans Inflamamtion Inflammation Inflammation regulation Life Sciences Lipid mediator class switching Oxylipins Retrospective Studies SARS-CoV-2 Severity predictors UHPLC-MS/MS |
title | MS-based targeted profiling of oxylipins in COVID-19: A new insight into inflammation regulation |
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