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Impact of myocardial reperfusion on human plasma lipidome

The primary aim of the study is to investigate the temporal changes in plasma lipidome before and after reperfusion in patients with ST-segment elevation myocardial infarction (STEMI) and their association with myocardial injury. We found that 56% of the identified lipid species were significantly a...

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Autores principales: Surendran, Arun, Atefi, Negar, Ismail, Umar, Shah, Ashish, Ravandi, Amir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850755/
https://www.ncbi.nlm.nih.gov/pubmed/35198888
http://dx.doi.org/10.1016/j.isci.2022.103828
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author Surendran, Arun
Atefi, Negar
Ismail, Umar
Shah, Ashish
Ravandi, Amir
author_facet Surendran, Arun
Atefi, Negar
Ismail, Umar
Shah, Ashish
Ravandi, Amir
author_sort Surendran, Arun
collection PubMed
description The primary aim of the study is to investigate the temporal changes in plasma lipidome before and after reperfusion in patients with ST-segment elevation myocardial infarction (STEMI) and their association with myocardial injury. We found that 56% of the identified lipid species were significantly altered (corrected p< 0.05) in the first 24 h following reperfusion in patients with STEMI. Three lipid species, namely, acylcarnitine 18:2, TG 51:0, and LPC 17:1 were associated with a change in troponin concentration (delta troponin) and in-hospital cardiovascular events. Of these, acylcarnitine 18:2, and LPC 17:1 and their respective whole class levels, were significantly higher (p < 0.05) in the STEMI population than the age/sex-matched control subjects. Overall, our analyses showed a large shift in plasma lipidome in patients that undergo myocardial reperfusion. The differences found for acylcarnitines and LPC species and their association with both cardiac markers and cardiac outcomes need further validation.
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spelling pubmed-88507552022-02-22 Impact of myocardial reperfusion on human plasma lipidome Surendran, Arun Atefi, Negar Ismail, Umar Shah, Ashish Ravandi, Amir iScience Article The primary aim of the study is to investigate the temporal changes in plasma lipidome before and after reperfusion in patients with ST-segment elevation myocardial infarction (STEMI) and their association with myocardial injury. We found that 56% of the identified lipid species were significantly altered (corrected p< 0.05) in the first 24 h following reperfusion in patients with STEMI. Three lipid species, namely, acylcarnitine 18:2, TG 51:0, and LPC 17:1 were associated with a change in troponin concentration (delta troponin) and in-hospital cardiovascular events. Of these, acylcarnitine 18:2, and LPC 17:1 and their respective whole class levels, were significantly higher (p < 0.05) in the STEMI population than the age/sex-matched control subjects. Overall, our analyses showed a large shift in plasma lipidome in patients that undergo myocardial reperfusion. The differences found for acylcarnitines and LPC species and their association with both cardiac markers and cardiac outcomes need further validation. Elsevier 2022-01-29 /pmc/articles/PMC8850755/ /pubmed/35198888 http://dx.doi.org/10.1016/j.isci.2022.103828 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Surendran, Arun
Atefi, Negar
Ismail, Umar
Shah, Ashish
Ravandi, Amir
Impact of myocardial reperfusion on human plasma lipidome
title Impact of myocardial reperfusion on human plasma lipidome
title_full Impact of myocardial reperfusion on human plasma lipidome
title_fullStr Impact of myocardial reperfusion on human plasma lipidome
title_full_unstemmed Impact of myocardial reperfusion on human plasma lipidome
title_short Impact of myocardial reperfusion on human plasma lipidome
title_sort impact of myocardial reperfusion on human plasma lipidome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850755/
https://www.ncbi.nlm.nih.gov/pubmed/35198888
http://dx.doi.org/10.1016/j.isci.2022.103828
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