Key result
Extracellular vesicles contained the highest number of differentially-expressed proteins for 3-year major adverse cardiovascular events (n=21) compared to plasma (n=9) and carotid plaque (n=1).
Why the study?
A protein comparison of plasma extracellular vesicles to blood plasma and atherosclerotic plaque has not been performed to assess biomarker origin and association with atherosclerotic progression.
Do extracellular vesicle biomarkers predict MACE better than plasma or plaque biomarkers in carotid endarterectomy patients?
Cohort (n=88)
Yes
Do extracellular vesicle biomarkers predict MACE better than plasma or plaque biomarkers in carotid endarterectomy patients?
Extracellular vesicles appear to provide superior prognostic information regarding systemic atherosclerosis progression and MACE risk compared to standard plasma or plaque biomarkers.
Plasma EV protein profiling may aid atherosclerosis biomarker discovery; leaves open plaque-specific origins and clinical utility.
Extracellular vesicles (EV) are a novel biomarker source for diagnosis and prognosis of cardiovascular disease. A protein comparison of plasma EVs in relation to blood plasma and atherosclerotic plaque has not been performed but would provide insight into the origin and content of biomarker sources and their association with atherosclerotic progression. Using samples of 88 carotid endarterectomy patients in the Athero-Express, 92 proteins (Olink Cardiovascular III panel) were measured in citrate plasma, plasma derived LDL-EVs and atherosclerotic plaque. Proteins were correlated between sources and were related to pre-operative stroke and 3-year major adverse cardiovascular events (MACE). Plasma and EV proteins correlated moderately on average, but with substantial variability. Both showed little correlation with plaque, suggesting that these circulating biomarkers may not originate from the latter. Plaque (n = 17) contained most differentially-expressed proteins in patients with stroke, opposed to EVs (n = 6) and plasma (n = 5). In contrast, EVs contained most differentially-expressed proteins for MACE (n = 21) compared to plasma (n = 9) and plaque (n = 1). EVs appear to provide additional information about severity and progression of systemic atherosclerosis than can be obtained from plasma or atherosclerotic plaque.
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Verwer et al. (2023) conducted a cohort in Carotid artery stenosis / Atherosclerosis (n=88). Protein biomarker expression in extracellular vesicles, plasma, and carotid plaque vs. Patients without MACE or pre-operative stroke was evaluated on Differentially-expressed proteins for 3-year major adverse cardiovascular events (MACE). Extracellular vesicles contained the highest number of differentially-expressed proteins for 3-year major adverse cardiovascular events (n=21) compared to plasma (n=9) and carotid plaque (n=1).
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