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Circulating Factors and Ultrasono-findings are Linked to Previous Atherosclerotic Burden and Recurrent Risk
Kyoung J Cho1, Jihye Kim2, Soung H Jeon2
1Department of Life Science, College of Science and Engineering, Kyonggi University, Suwon-si, South Korea.
Insights
Activated monocyte and platelet-monocyte aggregates are higher in individuals with a history of cerebrovascular disease (CVD). These factors, along with atherosclerotic severity, are crucial for managing CVD risk and outcomes.
Area of Science:
- Cardiovascular Research
- Neurology
- Hematology
Background:
- Platelet activation and platelet-leukocyte interactions are key in atherosclerosis and cerebrovascular disease (CVD) pathophysiology, including ischemic stroke.
- Atherosclerosis involves platelet-leukocyte interactions crucial for thrombus formation and cerebrovascular disease (CVD).
- This study examines circulating factors and platelet-leukocyte aggregates in aged individuals with and without a history of CVD.
Purpose of the Study:
- To investigate the relationship between circulating factors, ultrasonographic characteristics, and CVD risk.
- To evaluate changes in circulating factors and platelet-leukocyte aggregates in participants with and without a history of CVD.
- To determine if circulating factor changes and ultrasonographic characteristics correlate with CVD risk and long-term outcomes.
Main Methods:
- Two hundred fifteen participants were divided into groups with and without a history of CVD.
- Correlations between ultrasonography-based morphological characteristics and circulating factor-based functional changes were analyzed.
- Levels of p-selectin, activated monocytes, and platelet-monocyte aggregates were assessed.
Main Results:
- No significant difference in p-selectin levels was observed between groups.
- Activated monocyte and platelet-monocyte aggregate levels were elevated in participants with a history of CVD.
- Circulating factors and ultrasonographic characteristics correlated in the CVD group but not in the control group.
Conclusions:
- Circulating blood factor levels differ between participants with and without a history of CVD.
- Atherosclerotic severity appears to be influenced by CVD history and disease progression.
- Circulating factor levels, atherosclerotic severity, and CVD history are important for managing CVD progression and outcomes.
Background:
In the progression of atherosclerosis, platelet activation and the interaction of platelets with leukocytes play a crucial role in arterial thrombus formation and are associated with the pathophysiology of carotid and cerebrovascular disease (CVD), including ischemic stroke. With aged participants, we evaluated and followed up the change in circulating factor and platelet-leukocyte aggregate levels in participants with or without CVD history. This study investigated whether circulating factor changes and ultrasonographic characteristics link to CVD risk and other relating long-term outcomes.
Materials And Methods:
Two hundred fifteen participants who enrolled in the study were divided into two groups with CVD and without CVD history. We evaluated and analyzed the correlation between ultrasonography-based morphological characteristics and circulating factor-based functional changes in both groups.
Results:
There was no difference in p-selectin level between both groups. However, activated monocyte and platelet-monocyte aggregate levels were higher in patients with previous CVD than without previous CVD. Circulating factor and ultrasonographical characteristics were correlated in the group with CVD, whereas these factors were not correlated in the group without CVD.
Conclusion:
We found that circulating blood factor levels showed a different tendency in participants with and without CVD history. The results depict that atherosclerotic severity might depend on the history of CVD and progression of atherosclerosis. We suggest that the circulating factor levels, atherosclerotic severity, and history of CVD are considered in the observation of pathologic progression to manage the development of CVD risks and CVD relating outcomes.
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