Key result
Plasma exosomes from STEMI patients showed higher concentration, size, and expression of GPIIb and VE-cadherin than CCS patients, while GPIIb and PLP1 discriminated OHCA from uncomplicated STEMI.
Why the study?
New biomarkers for early, accurate characterization of STEMI are needed, but characterization of exosome protein cargo in relation to cardiovascular clinical manifestation is lacking.
Does plasma exosome profiling differentiate between STEMI patients with and without out-of-hospital cardiac arrest, and compared to chronic coronary syndrome?
Observational (n=67)
Does plasma exosome profiling differentiate between STEMI patients with and without out-of-hospital cardiac arrest, and compared to chronic coronary syndrome?
Plasma exosome profiling, specifically utilizing markers like GPIIb and PLP1, can differentiate STEMI patients with out-of-hospital cardiac arrest from uncomplicated STEMI and chronic coronary syndrome.
Exosome profiling may refine early risk stratification after STEMI; leaves open whether markers improve outcomes or warrant prospective validation.
The identification of new biomarkers allowing an early and more accurate characterization of patients with ST-segment elevation myocardial infarction (STEMI) is still needed, and exosomes represent an attractive diagnostic tool in this context. However, the characterization of their protein cargo in relation to cardiovascular clinical manifestation is still lacking. To this end, 35 STEMI patients (17 experiencing resuscitated out-of-hospital cardiac arrest (OHCA-STEMI) and 18 uncomplicated) and 32 patients with chronic coronary syndrome (CCS) were enrolled. Plasma exosomes were characterized by the nanoparticle tracking analysis and Western blotting. Exosomes from STEMI patients displayed a higher concentration and size and a greater expression of platelet (GPIIb) and vascular endothelial (VE-cadherin) markers, but a similar amount of cardiac troponin compared to CCS. In addition, a difference in exosome expression of acute-phase proteins (ceruloplasmin, transthyretin and fibronectin) between STEMI and CCS patients was found. GPIIb and brain-associated marker PLP1 accurately discriminated between OHCA and uncomplicated STEMI. In conclusion, the exosome profile of STEMI patients has peculiar features that differentiate it from that of CCS patients, reflecting the pathophysiological mechanisms involved in STEMI. Additionally, the exosome expression of brain- and platelet-specific markers might allow the identification of patients experiencing ischemic brain injury in STEMI.
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Zara et al. (2021) conducted an observational in ST-segment elevation myocardial infarction (STEMI) (n=67). ST-segment elevation myocardial infarction (STEMI) vs. Chronic coronary syndrome (CCS) was evaluated on Plasma exosome concentration, size, and protein expression. Plasma exosomes from STEMI patients showed higher concentration, size, and expression of GPIIb and VE-cadherin than CCS patients, while GPIIb and PLP1 discriminated OHCA from uncomplicated STEMI.
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