Hu Tao, Freeze Joshua, Singh Prerna, Kim Justin, Song Yingnan, Wu Hao, Lee Juhwan, Al-Kindi Sadeer, Rajagopalan Sanjay, Wilson David L, Hoori Ammar
Department of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio, USA.
Center for Computational and Precision Health, DeBakey Heart and Vascular Center, Houston Methodist, Houston, Texas, USA.
JACC Adv. 2024 Aug 28;3(9):101188. doi: 10.1016/j.jacadv.2024.101188. eCollection 2024 Sep.
Recent studies have used basic epicardial adipose tissue (EAT) assessments (eg, volume and mean Hounsfield unit [HU]) to predict risk of atherosclerosis-related, major adverse cardiovascular events (MACEs).
The purpose of this study was to create novel, hand-crafted EAT features, "fat-omics," to capture the pathophysiology of EAT and improve MACE prediction.
We studied a cohort of 400 patients with low-dose cardiac computed tomography calcium score examinations. We purposefully used a MACE-enriched cohort (56% event rate) for feature engineering purposes. We divided the cohort into training/testing sets (80%/20%). We segmented EAT using a previously validated, deep-learning method with optional manual correction. We extracted 148 initial EAT features (eg, morphologic, spatial, and HU), dubbed fat-omics, and used Cox elastic-net for feature reduction and prediction of MACE. Bootstrap validation gave CIs.
Traditional EAT features gave marginal prediction (EAT-volume/EAT-mean-HU/BMI gave C-indices 0.53/0.55/0.57, respectively). Significant improvement was obtained with the 15-feature fat-omics model (C-index = 0.69, test set). High-risk features included the volume-of-voxels-having-elevated-HU-[-50,-30-HU] and HU-negative-skewness, both of which assess high HU values in EAT, a property implicated in fat inflammation. Other high-risk features include kurtosis-of-EAT-thickness, reflecting the heterogeneity of thicknesses, and EAT-volume-in-the-top-25%-of-the-heart, emphasizing adipose near the proximal coronary arteries. Kaplan-Meyer plots of Cox-identified, high- and low-risk patients were well separated with the median of the fat-omics risk, with the high-risk group having an HR 2.4 times that of the low-risk group ( < 0.001).
Preliminary findings indicate an opportunity to use finely tuned, explainable assessments on EAT for improved cardiovascular risk prediction.
近期研究已利用基本的心外膜脂肪组织(EAT)评估(如体积和平均豪斯菲尔德单位[HU])来预测动脉粥样硬化相关的主要不良心血管事件(MACE)的风险。
本研究的目的是创建新颖的、手工制作的EAT特征,即“脂肪组学”,以捕捉EAT的病理生理学特征并改善MACE预测。
我们研究了一组400例接受低剂量心脏计算机断层扫描钙评分检查的患者。出于特征工程的目的,我们特意使用了一个MACE富集队列(事件发生率为56%)。我们将该队列分为训练/测试集(80%/20%)。我们使用一种先前经过验证的深度学习方法并辅以可选的手动校正来分割EAT。我们提取了148个初始EAT特征(如形态学、空间和HU特征),将其称为脂肪组学,并使用Cox弹性网络进行特征约简和MACE预测。自助法验证给出了置信区间。
传统的EAT特征预测效果一般(EAT体积/EAT平均HU/BMI的C指数分别为0.53/0.55/0.57)。15特征的脂肪组学模型取得了显著改善(测试集的C指数 = 0.69)。高风险特征包括HU升高[-50, -30 HU]的体素体积和HU负偏度,这两者均评估EAT中的高HU值,这一特性与脂肪炎症有关。其他高风险特征包括EAT厚度的峰度,反映厚度的异质性,以及心脏前25%区域的EAT体积,强调近端冠状动脉附近的脂肪。Cox识别出的高风险和低风险患者的Kaplan - Meyer曲线通过脂肪组学风险中位数得到了很好的区分,高风险组的风险比是低风险组的2.4倍(<0.001)。
初步研究结果表明,有机会对EAT进行精细调整且可解释的评估,以改善心血管疾病风险预测。