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Updated: Aug 10, 2026

Quantification of Monocyte Transmigration and Foam Cell Formation from Individuals with Chronic Inflammatory Conditions
Published on: October 17, 2017
Circulating monocyte-platelet aggregates are an early marker of acute myocardial infarction
M I Furman1, M R Barnard, L A Krueger
1Center for Platelet Function Studies, Division of Cardiovascular Medicine, Worcester, Massachusetts 01655, USA. Mark.Furman@umassmed.edu
Objectives:
We investigated whether elevated levels of circulating monocyte-platelet aggregates (MPA) can be used to identify patients with acute myocardial infarction (AMI).
Background:
Commonly used blood markers of AMI reflect myocardial cell death, but do not reflect the earlier pathophysiologic processes of plaque rupture, platelet activation and resultant thrombus formation. Circulating MPA form after platelet activation.
Methods:
In a single center between October 1998 and November 1999, we measured circulating MPA in a blinded fashion by whole blood flow cytometry in 211 consecutive patients who presented to the emergency department (ED) with chest pain and were admitted to rule out AMI. Acute myocardial infarction was diagnosed by a CK-MB fraction greater than three times control.
Results:
Patients with AMI (n = 61), as compared with those without AMI (n = 150), had significantly higher numbers of circulating MPA (11.6 +/- 11.4 vs. 6.4 +/- 3.6, mean +/- SD, p < 0.0001). After controlling for age, the adjusted odds of developing AMI for patients in the 2nd, 3rd and 4th quartiles of MPA, in comparison with patients in the lowest quartile (odds ratio = 1.0), were 2.1 (95% confidence interval [CI]: 0.7, 6.8), 4.4 (95% CI: 1.5, 13.1) and 10.8 (95% CI: 3.6, 32.0), respectively. The number of circulating MPA in patients with AMI presenting within 4 h of symptom onset (14.4) was significantly greater than those presenting after 4 h (9.4) and after 8 h (7.0), (p < 0.001). Of the 61 patients with AMI, 35 (57%) had a normal creatine kinase isoenzyme ratio at the time of presentation to the ED, but had high levels of circulating MPA (13.3).
Conclusions:
Circulating MPA are an early marker of AMI.
Insights
Elevated monocyte-platelet aggregates (MPA) can identify acute myocardial infarction (AMI) early. This blood marker detects plaque rupture and thrombus formation before myocardial cell death.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Biomarker Discovery
Background:
- Current acute myocardial infarction (AMI) markers indicate myocardial cell death.
- Earlier pathophysiological events like plaque rupture and thrombus formation are not reflected by standard markers.
- Circulating monocyte-platelet aggregates (MPA) form subsequent to platelet activation.
Purpose of the Study:
- To investigate if elevated circulating monocyte-platelet aggregates (MPA) can serve as an early diagnostic marker for acute myocardial infarction (AMI).
Main Methods:
- Whole blood flow cytometry was used to measure circulating MPA in 211 patients presenting with chest pain.
- Patients were enrolled between October 1998 and November 1999.
- Acute myocardial infarction diagnosis was confirmed by elevated CK-MB fraction.
Main Results:
- Patients with AMI exhibited significantly higher circulating MPA levels compared to those without AMI (11.6 vs. 6.4, p < 0.0001).
- Higher quartiles of MPA were associated with increased odds of AMI, even after age adjustment.
- MPA levels were higher in AMI patients presenting within 4 hours of symptom onset.
- A significant proportion of AMI patients (57%) showed elevated MPA despite normal creatine kinase isoenzyme levels upon presentation.
Conclusions:
- Circulating monocyte-platelet aggregates (MPA) represent a promising early biomarker for acute myocardial infarction (AMI).
- MPA detection may aid in the early identification of AMI, potentially before traditional markers become elevated.
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