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Linking Systemic Inflammation to Coronary Lesion Complexity: A Combined FFR and OCT Study
Nicoleta-Monica Popa-Fotea1,2, Miruna-Mihaela Micheu2, Lucian Calmac1,2
1Department of Cardiology, University of Medicine and Pharmacy Carol Davila, 8, Eroii Sanitari, 050474 Bucharest, Romania.
Insights
Higher levels of inflammatory biomarkers interleukin-1 receptor antagonist (IL-1ra), resistin, and C-reactive protein (CRP) are linked to more complex coronary artery disease in acute coronary syndrome (ACS) patients. This suggests inflammatory markers can help assess ACS risk and vulnerability.
Area of Science:
- Cardiovascular Medicine
- Biomarkers
- Atherosclerosis Research
Background:
- Residual inflammation post-acute coronary syndrome (ACS) drives atherosclerosis progression and plaque instability.
- Key inflammatory biomarkers like interleukin-1 receptor antagonist (IL-1ra), resistin, and C-reactive protein (CRP) may indicate coronary lesion complexity and vulnerability.
Purpose of the Study:
- To assess the association between IL-1ra, resistin, and CRP levels with coronary disease extent, functional significance of non-culprit lesions (FFR), and plaque vulnerability (OCT-defined TCFA) in ACS patients.
Main Methods:
- Prospective study of 93 ACS patients undergoing invasive coronary assessment.
- Measured inflammatory biomarkers at admission and 6 months.
- Stratified patients into tertiles by biomarker levels.
- Assessed coronary disease extent (SYNTAX score), lesion significance (FFR), and plaque morphology (OCT-defined TCFA).
- Utilized multivariate logistic regression analysis.
Main Results:
- Higher tertiles of IL-1ra, resistin, and CRP correlated with increased SYNTAX scores, reduced FFR (<0.80), and higher prevalence of thin-cap fibroatheroma (TCFA).
- Specifically, 68% in the highest tertile had FFR < 0.80, and 62% had TCFA compared to 20% in lower tertiles.
- IL-1ra, resistin, and CRP independently predicted high-risk coronary profiles in multivariate models.
Conclusions:
- IL-1ra, resistin, and CRP are independently associated with coronary lesion complexity, functional significance, and vulnerability in ACS patients.
- Inflammatory biomarker profiling offers a complementary approach to anatomical and physiological assessments for ACS risk stratification.
Abstract:
Residual inflammatory risk after acute coronary syndromes (ACSs) remains a critical contributor to atherosclerosis progression and plaque destabilization. Inflammatory biomarkers such as interleukin-1 receptor antagonist (IL-1ra), resistin, and C-reactive protein (CRP) may provide additional insights into coronary lesion complexity and vulnerability. The main aim of the study was to evaluate the association of interleukin-1 receptor antagonist (IL-1ra), resistin, and C-reactive protein (CRP) with coronary disease extent; functional significance of non-culprit lesions, assessed by fractional flow reserve (FFR); and plaque vulnerability, assessed by optical coherence tomography (OCT) in patients with acute coronary syndrome (ACS). This prospective study enrolled 93 ACS patients undergoing invasive coronary assessment for an ACS. Inflammatory biomarkers were measured at admission and 6 months post-event. Patients were stratified post hoc into tertiles by biomarker distribution. SYNTAX score, FFR, and OCT-defined thin-cap fibroatheroma (TCFA) were used to characterize lesion burden and morphology. Multivariate logistic regression was performed adjusting for conventional cardiovascular risk factors and ACS type. Higher tertiles of IL-1ra, resistin, and CRP were significantly associated with increased SYNTAX score (p < 0.05), FFR < 0.80 (68% in the highest tertile), and presence of TCFA (62% vs. 20%, p < 0.01). All biomarkers correlated with coronary disease severity. In multivariate logistic models, IL-1ra (OR 1.23 per 100 pg/mL, p = 0.03), resistin (OR 2.35 per 1 ng/mL, p = 0.001), and CRP (OR 1.11 per 0.001 ng/mL, p = 0.006) independently predicted high-risk coronary profiles. IL-1ra, resistin, and CRP are independently associated with lesion complexity, functional significance, and vulnerability in ACS. Inflammatory biomarker profiling may provide complementary anatomical and physiological assessment in future ACS risk stratification strategies.
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