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Published on: August 8, 2013
The serum pentraxin-3 is elevated in patients with cardiac syndrome X
Eyüp Büyükkaya1, Mehmet Fatih Karakaş, Mustafa Kurt
1Department of Cardiology, Mustafa Kemal University Tayfur Ata Sökmen Faculty of Medicine, Hatay, Turkey. dreyupbuyukkaya@hotmail.com
Insights
Pentraxin-3 (PTX-3), a novel inflammatory marker, is elevated in patients with Cardiac Syndrome X (CSX). This finding suggests PTX-3 may serve as a promising biomarker for assessing inflammation in CSX patients.
Area of Science:
- Cardiology
- Inflammation Research
- Biomarker Discovery
Background:
- Cardiac Syndrome X (CSX) is characterized by angina with normal coronary arteries and evidence of ischemia.
- High-sensitivity C-reactive protein (hs-CRP) is a known inflammatory marker associated with CSX.
- The role of pentraxin-3 (PTX-3) in CSX has not been previously investigated.
Purpose of the Study:
- To investigate the association between serum PTX-3 levels and Cardiac Syndrome X.
- To compare PTX-3 and hs-CRP levels in CSX patients versus coronary artery disease (CAD) and control groups.
Main Methods:
- A cohort of 122 patients with suspected coronary artery disease (CAD) was studied.
- Patients were categorized into CSX (normal angiography, n=41), CAD (lesions present, n=41), and control (no ischemia, n=40) groups.
- Serum levels of PTX-3 and hs-CRP were measured in all participants.
Main Results:
- PTX-3 levels were significantly higher in the CSX group compared to the control group (p<0.001).
- No significant differences in PTX-3 or hs-CRP were observed between CSX and CAD groups.
- The control group exhibited significantly lower hs-CRP levels than both CSX and CAD groups (p<0.05).
Conclusions:
- Elevated PTX-3 levels are observed in patients with CSX.
- PTX-3 may represent a novel inflammatory biomarker for assessing the inflammatory status in CSX.
- Further research is warranted to explore the clinical utility of PTX-3 in CSX.
Objectives:
Cardiac syndrome X (CSX) is a clinical entity that is defined as normal coronary arteries with angina pectoris and objective sins of ischemia. The correlation between CSX and inflammatory markers such as high-sensitivity C-reactive protein (hs-CRP) is well established, however an association with pentraxin-3 (PTX-3) has not been examined. The aim of this study was to investigate the association between PTX-3 and CSX.
Study Design:
A total of 122 patients (58 female, 64 male, mean age 49.6±5.8 years) with suspected of coronary artery disease (CAD) were included in the study. Those with evidence of ischemia (50 patients with positive treadmill tests, 32 patients with positive myocardial perfusion scintography) underwent coronary angiography (82 patients). Patients with a normal angiogram were considered the CSX group (n=41) and patients with coronary lesions were referred to as the CAD group (n=41). Patients without signs of ischemia served as the control group. Serum PTX-3 and hs-CRP levels were measured in all patients.
Results:
The CSX group had significantly increased PTX-3 levels relative to the control group (0.46±0.16 vs. 0.23±0.09 ng/ml, p<0.001). However there were no differences in levels of PTX-3 and hs-CRP between the CSX and the CAD groups (PTX-3: 0.46±0.16 vs. 0.51±0.13 ng/ml, p=0.21; hs-CRP: 1.04±0.45 vs. 1.16±0.64 mg/dl, p=0.62). The control group had significantly lower hs-CRP levels (0.73±0.51 mg/dl) when compared to the both CSX and CAD groups (p=0.03 and p=0.002, respectively). Serum PTX-3 levels were weakly correlated with hs-CRP levels (r=0.30, p=0.001).
Conclusion:
PTX-3, a novel inflammatory marker, is elevated in patients with CSX, similar to the well known inflammatory marker hs-CRP, and may be a promising biomarker reflecting inflammatory status in these patients.
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