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Lipidomic Predictors of Coronary No-Reflow
The ‘no-reflow’ phenomenon (NRP) after primary percutaneous coronary intervention (PCI) is a serious complication among acute ST-segment elevation myocardial infarction (STEMI) patients. Herein, a comprehensive lipidomics approach was used to quantify over 300 distinct molecular species in circulati...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861202/ https://www.ncbi.nlm.nih.gov/pubmed/36677004 http://dx.doi.org/10.3390/metabo13010079 |
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author | Surendran, Arun Ismail, Umar Atefi, Negar Bagchi, Ashim K. Singal, Pawan K. Shah, Ashish Aliani, Michel Ravandi, Amir |
author_facet | Surendran, Arun Ismail, Umar Atefi, Negar Bagchi, Ashim K. Singal, Pawan K. Shah, Ashish Aliani, Michel Ravandi, Amir |
author_sort | Surendran, Arun |
collection | PubMed |
description | The ‘no-reflow’ phenomenon (NRP) after primary percutaneous coronary intervention (PCI) is a serious complication among acute ST-segment elevation myocardial infarction (STEMI) patients. Herein, a comprehensive lipidomics approach was used to quantify over 300 distinct molecular species in circulating plasma from 126 patients with STEMI before and after primary PCI. Our analysis showed that three lipid classes: phosphatidylcholine (PC), alkylphosphatidylcholine (PC(O)), and sphingomyelin (SM), were significantly elevated (p < 0.05) in no-reflow patients before primary PCI. The levels of individual fatty acids and total fatty acid levels were significantly lower (p < 0.05) in no-reflow subjects after PCI. The grouping of patients based on ECG ST-segment resolution (STR) also demonstrated the same trend, confirming the possible role of these differential lipids in the setting of no-reflow. Sphingomyelin species, SM 41:1 and SM 41:2, was invariably positively correlated with corrected TIMI frame count (CTFC) at pre-PCI and post-PCI. The plasma levels of SM 42:1 exhibited an inverse association (p < 0.05) consistently with tumor necrosis factor-alpha (TNF-α) at pre-PCI and post-PCI. In conclusion, we identified plasma lipid profiles that distinguish individuals at risk of no-reflow and provided novel insights into how dyslipidemia may contribute to NRP after primary PCI. |
format | Online Article Text |
id | pubmed-9861202 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98612022023-01-22 Lipidomic Predictors of Coronary No-Reflow Surendran, Arun Ismail, Umar Atefi, Negar Bagchi, Ashim K. Singal, Pawan K. Shah, Ashish Aliani, Michel Ravandi, Amir Metabolites Article The ‘no-reflow’ phenomenon (NRP) after primary percutaneous coronary intervention (PCI) is a serious complication among acute ST-segment elevation myocardial infarction (STEMI) patients. Herein, a comprehensive lipidomics approach was used to quantify over 300 distinct molecular species in circulating plasma from 126 patients with STEMI before and after primary PCI. Our analysis showed that three lipid classes: phosphatidylcholine (PC), alkylphosphatidylcholine (PC(O)), and sphingomyelin (SM), were significantly elevated (p < 0.05) in no-reflow patients before primary PCI. The levels of individual fatty acids and total fatty acid levels were significantly lower (p < 0.05) in no-reflow subjects after PCI. The grouping of patients based on ECG ST-segment resolution (STR) also demonstrated the same trend, confirming the possible role of these differential lipids in the setting of no-reflow. Sphingomyelin species, SM 41:1 and SM 41:2, was invariably positively correlated with corrected TIMI frame count (CTFC) at pre-PCI and post-PCI. The plasma levels of SM 42:1 exhibited an inverse association (p < 0.05) consistently with tumor necrosis factor-alpha (TNF-α) at pre-PCI and post-PCI. In conclusion, we identified plasma lipid profiles that distinguish individuals at risk of no-reflow and provided novel insights into how dyslipidemia may contribute to NRP after primary PCI. MDPI 2023-01-03 /pmc/articles/PMC9861202/ /pubmed/36677004 http://dx.doi.org/10.3390/metabo13010079 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Surendran, Arun Ismail, Umar Atefi, Negar Bagchi, Ashim K. Singal, Pawan K. Shah, Ashish Aliani, Michel Ravandi, Amir Lipidomic Predictors of Coronary No-Reflow |
title | Lipidomic Predictors of Coronary No-Reflow |
title_full | Lipidomic Predictors of Coronary No-Reflow |
title_fullStr | Lipidomic Predictors of Coronary No-Reflow |
title_full_unstemmed | Lipidomic Predictors of Coronary No-Reflow |
title_short | Lipidomic Predictors of Coronary No-Reflow |
title_sort | lipidomic predictors of coronary no-reflow |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861202/ https://www.ncbi.nlm.nih.gov/pubmed/36677004 http://dx.doi.org/10.3390/metabo13010079 |
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