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Plasma lipidome differences in patients with and without significant carotid plaque
Martin Malý1, Ondřej Kučerka2, Kamila Bechyňská3
1Department of Medicine, First Faculty of Medicine, Charles University in Prague and the Military University Hospital, Prague 16902, Czech Republic.
Plasma lipidomics can identify vulnerable atherosclerotic plaques. Distinct lipid profiles, particularly decreased lysophosphoethanolamines and triacylglycerols, help predict plaque instability and stroke risk.
Area of Science:
- Biochemistry
- Cardiovascular Medicine
- Analytical Chemistry
Background:
- Atherosclerosis in carotid arteries is a primary cause of ischemic stroke.
- Early detection of advanced atherosclerosis and plaque vulnerability is crucial for preventing adverse events.
- Plaque size alone does not accurately predict the risk of stroke.
Purpose of the Study:
- To investigate plasma lipidomics as a diagnostic tool for stratifying carotid plaque stability.
- To determine if lipid profiles can differentiate between stable and unstable plaques without invasive procedures.
Main Methods:
- Utilized liquid chromatography-high-resolution tandem mass spectrometry (LC-MS/MS) for plasma lipidomics.
- Characterized and compared lipid profiles in patients with stable versus vulnerable atherosclerotic plaques.
- Developed a statistical model for patient stratification based on lipid profiles.
Main Results:
- Significant differences in plasma lipid profiles were observed between patients with stable and unstable carotid plaques.
- Lysophosphoethanolamines, fatty acyl esters of hydroxy fatty acids, free fatty acids, plasmalogens, and triacylglycerols were key predictors of plaque vulnerability.
- Most predictive lipid compounds were decreased in plasma of patients with unstable plaques.
Conclusions:
- Plasma lipidomes differ between patients with stable and unstable carotid plaques.
- Specific lipid compounds show potential as biomarkers for identifying unstable plaques.
- LC-MS/MS-based lipidomics may offer a non-invasive method for clinical diagnosis of plaque vulnerability.
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