Related Experiment Video
Updated: Jan 25, 2026

An Experimental Model of Diet-Induced Metabolic Syndrome in Rabbit: Methodological Considerations, Development, and Assessment
Published on: April 20, 2018
Circulating microparticle subpopulation in metabolic syndrome: relation to oxidative stress and coagulation markers
Asmaa M Zahran1, Sohair K Sayed2, Heba A Abd El Hafeez2
1Department of Clinical Pathology, South Egypt Cancer Institute, Assiut, Egypt.
Background:
Circulating microparticles (MPs) contribute to the pathogenesis of atherothrombotic disorders and are raised in cardiovascular diseases. Herein, we aimed to investigate the effect of moderate metabolic abnormalities in an early stage of metabolic syndrome (MetS) on the level of MP subpopulations and to study relationships between MP subpopulations and both oxidative stress and coagulation markers.
Methods:
Flow cytometry used to evaluate circulating MPs subpopulations in 40 patients with an early stage MetS and 30 healthy controls. ELISA was used to quantify plasminogen activator inhibitor type 1/tissue plasminogen activator (PAI-1/TPA) while plasma glutathione peroxidase (GPx) activity was measured spectrophotometrically.
Results:
Total MPs were significantly elevated in MetS (P<0.001). Glutathione peroxidase and PAI1/TPA activity was significantly increased in subjects with MetS (P<0.001). Waist circumference, diastolic blood pressure, and total cholesterol positively influenced levels of total MPs, platelet-derived microparticles, and endothelium-derived microparticles. Fasting blood glucose, cholesterol, triglycerides, and low-density lipoprotein positively influenced the coagulation factors (TPA, PAI1). However, high-density lipoprotein negatively influenced platelet-derived MPs and factors associated with fibrinolysis (TPA, PAI1).
Conclusion:
Elevated circulating MPs are associated with MetS abnormalities, oxidative stress and coagulation factors and may act as early predictor of metabolic syndrome with risk of cardiovascular disease.
Insights
Circulating microparticles (MPs) are elevated in metabolic syndrome (MetS), correlating with oxidative stress and coagulation markers. These findings suggest MPs may predict early MetS and cardiovascular disease risk.
Area of Science:
- Cardiovascular Research
- Metabolic Syndrome Studies
- Biomarker Discovery
Background:
- Circulating microparticles (MPs) are implicated in atherothrombotic disorders and elevated in cardiovascular diseases.
- Metabolic syndrome (MetS) is characterized by moderate metabolic abnormalities.
- Early detection of MetS and associated risks is crucial for cardiovascular health.
Purpose of the Study:
- To investigate the impact of early-stage MetS on circulating MP subpopulations.
- To examine the relationship between MP subpopulations and oxidative stress markers.
- To explore associations between MP subpopulations and coagulation factors.
Main Methods:
- Flow cytometry was employed to analyze circulating MP subpopulations in MetS patients and healthy controls.
- Enzyme-linked immunosorbent assay (ELISA) quantified plasminogen activator inhibitor type 1/tissue plasminogen activator (PAI-1/TPA).
- Plasma glutathione peroxidase (GPx) activity was measured spectrophotometrically.
Main Results:
- Total MPs were significantly higher in MetS patients (P<0.001).
- Glutathione peroxidase and PAI-1/TPA activity were significantly increased in MetS subjects (P<0.001).
- MetS parameters like waist circumference, blood pressure, and cholesterol levels correlated with MP levels and coagulation factors.
Conclusions:
- Elevated circulating MPs are linked to MetS, oxidative stress, and coagulation abnormalities.
- MP subpopulations may serve as early predictors for MetS.
- These findings highlight the potential of MPs in assessing cardiovascular disease risk in MetS patients.
Related Concept Videos
Coagulation
Coagulation
During the coagulation phase, clotting factors, or procoagulants, play a vital role in initiating and progressing the coagulation cascade. This cascade is a series of reactions...
Oxidation Numbers
What is Metabolism?
Responses to Heat and Cold Stress
Pyruvate Oxidation
First, the enzyme pyruvate dehydrogenase removes the carboxyl group from pyruvate and releases it as carbon dioxide. The stripped molecule is then oxidized and releases electrons, which are then picked up by NAD+...

