OP3 Improved cardiac risk stratification in individuals with high risk plaque features using the perivascular fat attenuation index on CCTA

C. Kotanidis, E. Oikonomou, M. Marwan, Laura Kluener, K. Thomas, A. Alashi, A. Antonopoulos, C. Shirodaria, S. Neubauer, K. Channon, S. Achenbach, M. Desai, C. Antoniades
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Abstract

Introduction High-risk plaque (HRP) features on coronary computed tomography angiography (CCTA) are indicators of increased cardiac risk. Coronary inflammation induces spatial changes in perivascular adipose tissue (PVAT) composition, which can be quantified with the perivascular Fat Attenuation Index (FAI). We hypothesized that perivascular FAI mapping can further stratify the cardiac risk associated with HRP on CCTA. Methods Individuals from the CRISP-CT (Cardiovascular RISk Prediction using Computed Tomography) study were included (n=3,912, mean age 55.7±13.7 years, 41.1% females). Perivascular FAI mapping was performed around the proximal right coronary artery and was calculated based on the weighted average attenuation of PVAT using the CaRi-HEART algorithm, as previously described. HRP features were defined as the presence of either positive remodelling, low-attenuation plaque, spotty calcification or napkin-ring sign. The association with future incidence of major adverse cardiac events (cardiac mortality or non-fatal myocardial infarction) was assessed using Cox regression models (adjusted for age, sex, epicardial fat volume and coronary artery disease [≥50% stenosis]). Results The prevalence of HRP and high FAI (≥-70.1 Hounsfield Units, as previously validated) was 23.6% (n=923) and 24.3% (n=952), respectively. Over a median follow-up of 5.6 years (25th-75th percentile: 4.0–7.0 years) 91 MACE were recorded. Patients with both HRP features and high FAI (FAI+/HRP+) had a 6.3-fold higher adjusted risk of MACE compared to those with neither of these risk features (HRP-/FAI-). Furthermore, patients without HRP features but with high FAI (HRP-/FAI+) had a 4.9-fold higher adjusted risk of MACE compared to the reference (HRP-/FAI-) group. Conclusion FAI is a stronger predictor of cardiac mortality than high-risk plaques, and there is additive predictive value between plaque morphology and coronary inflammatory burden. There is need for tools to provide comprehensive risk assessment based on CCTA, by extracting, weighting and interpreting all available information from these scans.
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使用CCTA血管周围脂肪衰减指数改善具有高危斑块特征个体的心脏风险分层
冠状动脉ct血管造影(CCTA)显示的高危斑块(HRP)特征是心脏风险增加的指标。冠状动脉炎症引起血管周围脂肪组织(PVAT)组成的空间变化,这可以用血管周围脂肪衰减指数(FAI)来量化。我们假设血管周围FAI制图可以在CCTA上进一步分层HRP相关的心脏风险。方法纳入来自CRISP-CT(使用计算机断层扫描进行心血管风险预测)研究的个体(n=3,912,平均年龄55.7±13.7岁,女性41.1%)。如前所述,在右冠状动脉近端周围进行血管周围FAI制图,并使用CaRi-HEART算法根据PVAT加权平均衰减计算。HRP特征定义为存在阳性重构、低衰减斑块、点状钙化或餐巾环征。使用Cox回归模型(调整年龄、性别、心外膜脂肪量和冠状动脉疾病[狭窄≥50%])评估与未来主要不良心脏事件(心脏死亡或非致死性心肌梗死)发生率的关联。结果HRP和高FAI(≥-70.1 Hounsfield单位,先前验证)的患病率分别为23.6% (n=923)和24.3% (n=952)。中位随访5.6年(25 -75百分位:4.0-7.0年),记录了91例MACE。具有HRP特征和高FAI (FAI+/HRP+)的患者发生MACE的调整风险比没有这两种风险特征(HRP-/FAI-)的患者高6.3倍。此外,没有HRP特征但具有高FAI (HRP-/FAI+)的患者与参考(HRP-/FAI-)组相比,MACE调整风险高4.9倍。结论FAI比高危斑块更能预测心脏死亡,且斑块形态与冠状动脉炎症负担之间存在叠加预测价值。需要有工具来提供基于CCTA的综合风险评估,通过提取、加权和解释来自这些扫描的所有可用信息。
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