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Lipidomic signature of stroke recurrence after transient ischemic attack
While TIA patients have transient symptoms, they should not be underestimated, as they could have an underlying pathology that may lead to a subsequent stroke: stroke recurrence (SR). Previously, it has been described the involvement of lipids in different vascular diseases. The aim of the current s...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444771/ https://www.ncbi.nlm.nih.gov/pubmed/37607967 http://dx.doi.org/10.1038/s41598-023-40838-7 |
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author | Purroy, F. Ois, A. Jove, M. Arque, G. Sol, J. Mauri-Capdevila, G. Rodriguez-Campello, A. Pamplona, R. Portero, M. Roquer, J. |
author_facet | Purroy, F. Ois, A. Jove, M. Arque, G. Sol, J. Mauri-Capdevila, G. Rodriguez-Campello, A. Pamplona, R. Portero, M. Roquer, J. |
author_sort | Purroy, F. |
collection | PubMed |
description | While TIA patients have transient symptoms, they should not be underestimated, as they could have an underlying pathology that may lead to a subsequent stroke: stroke recurrence (SR). Previously, it has been described the involvement of lipids in different vascular diseases. The aim of the current study was to perform a lipidomic analysis to identify differences in the lipidomic profile between patients with SR and patients without. Untargeted lipidomic analysis was performed in plasma samples of 460 consecutive TIA patients recruited < 24 h after the onset of symptoms. 37 (8%) patients suffered SR at 90 days. Lipidomic profiling disclosed 7 lipid species differentially expressed between groups: 5 triacylglycerides (TG), 1 diacylglyceride (DG), and 1 alkenyl-PE (plasmalogen) [specifically, TG(56:1), TG(63:0), TG(58:2), TG(50:5), TG(53:7, DG(38:5)) and PE(P-18:0/18:2)]. 6 of these 7 lipid species belonged to the glycerolipid family and a plasmalogen, pointing to bioenergetics pathways, as well as oxidative stress response. In this context, it was proposed the PE(P-18:0/18:2) as potential biomarker of SR condition. The observed changes in lipid patterns suggest pathophysiological mechanisms associated with lipid droplets metabolism and antioxidant protection that is translated to plasma level as consequence of a more intensive or high-risk ischemic condition related to SR. |
format | Online Article Text |
id | pubmed-10444771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104447712023-08-24 Lipidomic signature of stroke recurrence after transient ischemic attack Purroy, F. Ois, A. Jove, M. Arque, G. Sol, J. Mauri-Capdevila, G. Rodriguez-Campello, A. Pamplona, R. Portero, M. Roquer, J. Sci Rep Article While TIA patients have transient symptoms, they should not be underestimated, as they could have an underlying pathology that may lead to a subsequent stroke: stroke recurrence (SR). Previously, it has been described the involvement of lipids in different vascular diseases. The aim of the current study was to perform a lipidomic analysis to identify differences in the lipidomic profile between patients with SR and patients without. Untargeted lipidomic analysis was performed in plasma samples of 460 consecutive TIA patients recruited < 24 h after the onset of symptoms. 37 (8%) patients suffered SR at 90 days. Lipidomic profiling disclosed 7 lipid species differentially expressed between groups: 5 triacylglycerides (TG), 1 diacylglyceride (DG), and 1 alkenyl-PE (plasmalogen) [specifically, TG(56:1), TG(63:0), TG(58:2), TG(50:5), TG(53:7, DG(38:5)) and PE(P-18:0/18:2)]. 6 of these 7 lipid species belonged to the glycerolipid family and a plasmalogen, pointing to bioenergetics pathways, as well as oxidative stress response. In this context, it was proposed the PE(P-18:0/18:2) as potential biomarker of SR condition. The observed changes in lipid patterns suggest pathophysiological mechanisms associated with lipid droplets metabolism and antioxidant protection that is translated to plasma level as consequence of a more intensive or high-risk ischemic condition related to SR. Nature Publishing Group UK 2023-08-22 /pmc/articles/PMC10444771/ /pubmed/37607967 http://dx.doi.org/10.1038/s41598-023-40838-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Purroy, F. Ois, A. Jove, M. Arque, G. Sol, J. Mauri-Capdevila, G. Rodriguez-Campello, A. Pamplona, R. Portero, M. Roquer, J. Lipidomic signature of stroke recurrence after transient ischemic attack |
title | Lipidomic signature of stroke recurrence after transient ischemic attack |
title_full | Lipidomic signature of stroke recurrence after transient ischemic attack |
title_fullStr | Lipidomic signature of stroke recurrence after transient ischemic attack |
title_full_unstemmed | Lipidomic signature of stroke recurrence after transient ischemic attack |
title_short | Lipidomic signature of stroke recurrence after transient ischemic attack |
title_sort | lipidomic signature of stroke recurrence after transient ischemic attack |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10444771/ https://www.ncbi.nlm.nih.gov/pubmed/37607967 http://dx.doi.org/10.1038/s41598-023-40838-7 |
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