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A prospective study of C-reactive protein as a state marker in Cardiac Syndrome X
James Dollard1, Peter Kearney2, Gerard Clarke3
1Department of Cardiology, Cork University Hospital, Cork, Ireland; Alimentary Pharmabiotic Centre, University College Cork, Cork, Ireland.
Insights
C-reactive protein (CRP) levels are elevated in Cardiac Syndrome X (CSX) patients and vary with disease severity, indicating CRP is a state marker for this inflammatory condition.
Area of Science:
- Cardiology
- Inflammation Research
- Biomarker Analysis
Background:
- Cardiac Syndrome X (CSX) is characterized by angina pectoris with normal coronary arteries on angiography.
- CSX is associated with elevated inflammatory biomarkers, suggesting a role for inflammation in its pathogenesis.
- The nature of C-reactive protein (CRP) as a state or trait marker in CSX requires further investigation.
Purpose of the Study:
- To determine if C-reactive protein (CRP) levels correlate with disease severity in Cardiac Syndrome X (CSX).
- To ascertain whether CRP functions as a state or trait marker in CSX patients.
Main Methods:
- Studied 16 CSX patients with typical angina and normal coronary arteries, and 13 healthy controls (HC).
- Measured CRP levels and performed exercise stress tests (EST) at baseline and follow-up.
- Analyzed CRP levels in relation to EST results and symptom status.
Main Results:
- CSX patients exhibited significantly higher CRP levels than HC (1.5 vs 0.8 mg/L, p=0.02).
- CRP levels correlated with time to symptoms on EST at both visits (r=-0.690, p=0.013 and r=-0.899, p=0.015).
- CRP levels decreased in patients with improved symptoms/negative ESTs and increased in those with worsening symptoms.
Conclusions:
- Results suggest CSX is an inflammatory-mediated condition.
- CRP levels prospectively vary with functional measures of disease severity in CSX.
- CRP appears to be a state marker in Cardiac Syndrome X.
Abstract:
Cardiac Syndrome X (CSX), the presence of angina pectoris despite normal epicardial coronary arteries seen on invasive angiography, is known to be associated with an elevation of several inflammatory biomarkers, suggesting a possible role for inflammation in its pathogenesis. We sought to establish if C-reactive protein (CRP) levels varied with disease severity and so whether it is a state or trait marker. We studied 16 CSX patients with typical angina pectoris, normal coronary arteries and an electrically positive exercise stress test (EST) and 13 age- and sex-matched healthy controls (HC). CSX patients were followed up at a subsequent visit with repeated exercise stress testing and CRP measurement. We found that CRP levels were significantly higher in the CSX group compared to the HC (1.5 [0.8-4.5] v 0.8 [0.4-1.4] mg/L, p=0.02). This elevation in CRP persisted throughout the study length. CRP correlated with time to symptoms on EST at enrolment and at the second visit (r=-0.690, df=10, p=0.013 and r=-0.899, df=4, p=0.015, respectively). At the follow-up visit, 50% of CSX patients developed electrically and symptomatically negative ESTs. The mean CRP of this group was significantly lower than that of the CSX patients with ongoing symptoms and positive ESTs (1.2±0.2 v 2.8±0.6mg/L, p=0.018) and did not differ significantly from that of healthy controls. CRP levels also dropped in patients whose symptoms improved while they increased in patients who became more symptomatic (p=0.027). We conclude that the results of this small study support the concept of CSX being an inflammatory-mediated condition with CRP levels prospectively varying with functional measures of disease severity. This indicates that CRP is a state marker in CSX.
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