In:
The International Journal of Cardiovascular Imaging, Springer Science and Business Media LLC
Abstract:
Inflammation has been considered to promote atheroma instability. Coronary computed tomography angiography (CCTA) visualizes pericoronary adipose tissue (PCAT) attenuation, which reflects coronary artery inflammation. While PCAT attenuation has been reported to predict future coronary events, plaque phenotypes exhibiting high PCAT attenuation remains to be fully elucidated. The current study aims to characterize coronary atheroma with a greater vascular inflammation. We retrospectively analyzed culprit lesions in 69 CAD patients receiving PCI from the REASSURE-NIRS registry (NCT04864171). Culprit lesions were evaluated by both CCTA and near-infrared spectroscopy/intravascular ultrasound (NIRS/IVUS) imaging prior to PCI. PCAT attenuation at proximal RCA (PCAT RCA ) and NIRS/IVUS-derived plaque measures were compared in patients with PCAT RCA attenuation ≥ and 〈 -78.3 HU (median). Lesions with PCAT RCA attenuation ≥ -78.3 HU exhibited a greater frequency of maxLCBI 4mm ≥ 400 (66% vs. 26%, p 〈 0.01), plaque burden ≥ 70% (94% vs. 74%, p = 0.02) and spotty calcification (49% vs. 6%, p 〈 0.01). Whereas positive remodeling (63% vs. 41%, p = 0.07) did not differ between two groups. On multivariable analysis, maxLCBI 4mm ≥ 400 (OR = 4.07; 95%CI 1.12–14.74, p = 0.03), plaque burden ≥ 70% (OR = 7.87; 95%CI 1.01–61.26, p = 0.04), and spotty calcification (OR = 14.33; 95%CI 2.37–86.73, p 〈 0.01) independently predicted high PCAT RCA attenuation. Of note, while the presence of only one plaque feature did not necessarily elevate PCAT RCA attenuation (p = 0.22), lesions harboring two or more features were significantly associated with higher PCAT RCA attenuation. More vulnerable plaque phenotypes were observed in patients with high PCAT RCA attenuation. Our findings suggest PCAT RCA attenuation as the presence of profound disease substrate, which potentially benefits from anti-inflammatory agents.
Type of Medium:
Online Resource
ISSN:
1875-8312
DOI:
10.1007/s10554-023-02907-w
Language:
English
Publisher:
Springer Science and Business Media LLC
Publication Date:
2023
detail.hit.zdb_id:
2008950-8
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