Association between allergic inflammatory diseases and computerized tomography-derived coronary inflammation and atherosclerotic disease extent and phenotype: the ALLERGIC-CAD study
Author Block: C. Martini, F. L. Gurgoglione, E. Ridolo, A. A. Palumbo, G. Cicala, F. Nicoletta, C. Baldari, M. De Filippo, G. Niccoli; Parma/IT
Purpose: To evaluate whether patients with suspected chronic coronary syndromes (CCS) and allergic inflammatory diseases show differences in coronary CT angiography (CCTA)-derived atherosclerotic markers — including plaque extent, vulnerable phenotype, and pericoronary fat attenuation index (pFAI) — compared to non-allergic patients.
Methods or Background: Allergic inflammatory diseases are linked to higher risks of myocardial infarction and major adverse cardiovascular events. CCTA detects vulnerable plaques and inflammation markers, such as pFAI, enhancing risk stratification.
This study analyzed patients with suspected CCS undergoing clinically indicated CCTA at Parma University Hospital, stratified by allergic history. Plaque burden, vulnerable phenotype (≥2 high-risk features: positive remodeling, low-attenuation plaque, napkin-ring sign, spotty calcification), and pFAI were assessed at patient and lesion levels.
Results or Findings: A total of 289 patients (58 allergic, 20.1%) and 953 lesions were analyzed. CAD prevalence, extent, and severity were similar between groups. Allergic patients showed higher pFAI values (RCA: -65.72 vs -69.36, p=.012; LAD: -64.64 vs -68.81, p=.022; LCX: -61.36 vs -63.05, p=.024) and more vulnerable plaques (53 vs 186, p<.001), including more LAPs (51 vs 127, p<.001), spotty calcifications (31 vs 116, p=.015), and napkin-ring signs (27 vs 67, p<.001). Diabetes (OR 1.143, p<.001), allergy (OR 1.122, p=.003), and pFAI-RCA (OR 1.004, p=.014) predicted vulnerable plaque phenotype.
Conclusion: In suspected CCS, CAD prevalence and severity were similar regardless of allergy, but allergic patients showed greater pericoronary inflammation and more vulnerable plaques.
Limitations: - Single-center design
- Partial inclusion of allergic diseases
- Incomplete allergy characterization
- Lack of systemic inflammatory markers
- Exclusion of acute/prior CVD patients
- No clinical follow-up
Funding for this study: Nothing to declare
Has your study been approved by an ethics committee? Yes
Ethics committee - additional information: Protocol number of approval by the Ethics Committee of the University Hospital of Parma (AOUPR): 150/2023/OSS/AOUPR SIRER ID 5860