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Published on: October 12, 2017
Decreased serum fetuin-A levels are associated with coronary artery diseases
Oktay Bilgir1, Levent Kebapcilar, Ferda Bilgir
1Department of Internal Medicine, Izmir Bozyaka Training and Research Hospital, Izmir, Turkey.
Insights
Serum fetuin-A levels were lower in patients with stable angina and myocardial infarction, suggesting a role in coronary artery disease (CAD) pathophysiology. Soluble adhesion molecules were not significantly related to CAD.
Area of Science:
- Cardiology
- Biochemistry
- Immunology
Background:
- Acute coronary syndrome (ACS) involves complex pathophysiological processes.
- Biomarkers are crucial for understanding and diagnosing ACS.
- Fetuin-A and soluble cellular adhesion molecules are potential biomarkers.
Purpose of the Study:
- To investigate serum Fetuin-A levels.
- To analyze soluble intercellular adhesion molecule-1 (sICAM-1) and vascular cellular adhesion molecule-1 (sVCAM-1) levels.
- To correlate these levels with acute coronary syndrome (ACS).
Main Methods:
- Serum samples were collected from 127 patients presenting with chest pain.
- Patients were categorized into stable angina (SA), myocardial infarction (MI), and non-cardiac groups.
- Fetuin-A levels were logarithmically transformed for analysis.
Main Results:
- Log-Fetuin-A levels were higher in non-cardiac subjects than in MI and SA patients (p<0.05).
- SA patients had lower Fetuin-A levels than controls but higher than MI patients.
- sVCAM-1 and sICAM-1 levels did not differ between patients with coronary atherosclerosis and non-cardiac subjects.
Conclusions:
- Serum sVCAM-1 and sICAM-1 levels are not associated with coronary artery disease (CAD).
- Fetuin-A levels appear decreased in SA and MI patients.
- Reduced fetuin-A may contribute to the pathophysiology of CAD.
Background:
To analyze Fetuin-A levels and soluble cellular adhesion molecules in patients with acute coronary syndrome.
Methods And Results:
Serum Fetuin-A and intercellular adhesion molecule-1 (sICAM-1), vascular cellular adhesion molecule-1 (sVCAM-1) levels were examined in 127 patients who presented with chest pain. These patients were classified in three groups: stable angina (SA, n=51), myocardial infarction (MI, n=34) and non-cardiac group (n=42). Logarithmic transformations were made for Fetuin-A levels. Log-Fetuin-A levels were higher in non-cardiac subjects compared to MI and SA patients (p<0.05). Patients with SA showed lower levels than controls but higher levels as compared to MI patients. After controlling for age and gender, levels of sVCAM-1 and sICAM-1 in patients with coronary atherosclerosis were not different from those in non-cardiac subjects.
Conclusion:
Serum levels of soluble VCAM-1, ICAM-1 were not related to coronary artery disease (CAD), but fetuin-A levels seems to be decreased in SA and MI patients. Low fetuin-A may play a role in the pathophysiology of CAD.
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