MRI ensemble model of plaque and perivascular adipose tissue as PET-equivalent for identifying carotid atherosclerotic inflammation.

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Fan Yu, Xiaoran Li, Yue Zhang, Yi Shan, Bixiao Cui, Liqun Jiao, Jie Lu
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引用次数: 0

Abstract

Background: Severe cerebrovascular events are associated with carotid atherosclerotic plaque progression and rupture that is mediated by inflammation. 18F-fluorodeoxyglucose ([18F]FDG) PET is important for assessing the inflammation of carotid atherosclerotic plaque, but it suffers from the limitations of radiation exposure. Additionally, inflammation of perivascular adipose tissue (PVAT) has been found to promote atherosclerosis progression through paracrine signaling mechanisms. The study aimed to develop an ensemble model based on carotid plaque and PVAT MRI radiomics for identifying highly inflammatory plaques (HIPs).

Results: 159 asymptomatic carotid atherosclerosis patients (137 males; 65 ± 8 years old) with 209 plaques (104 HIPs) were consecutively enrolled. 47.95% (70/146) of cases and 53.97% (34/63) were defined as HIPs in the training and testing datasets, respectively. There was more lipid core, more intraplaque hemorrhage, and less calcification in the HIPs compared to the non-highly inflammatory plaques (NHIPs) in the training dataset (p = 0.002, 0.019, and 0.013, respectively). Notably, the incidence of indistinct PVAT (IPVAT) in HIPs was higher than that in NHIPs, both in the training (81.43% vs. 46.05%; p < 0.001) and the testing (88.24% vs. 58.62%; p = 0.007) datasets. The correlations between plaque MRI characteristics and [18F]FDG uptake differed between the NHIPs and HIPs. However, IPVAT consistently correlated with SUVmax (r = 0.35, 0.30; p < 0.001, p = 0.002; for NHIPs and HIPs, respectively). The ensemble model that integrates the radiomics of carotid plaque and PVAT outperformed all models in predicting HIP (area under the curve [AUC] = 0.92/0.91, training/testing dataset). The follow-up further validated the PET for predicting plaque progression with the same accuracy as the ensemble model (AUC: 0.85 vs. 0.79).

Conclusions: The ensemble model integrating the radiomics of carotid plaque and perivascular adipose tissue provides an equivalent tool to PET in the visualization of the evaluation of carotid atherosclerosis inflammation and progression.

斑块和血管周围脂肪组织的MRI集合模型与pet等效,用于识别颈动脉粥样硬化性炎症。
背景:严重的脑血管事件与炎症介导的颈动脉粥样硬化斑块进展和破裂有关。18F-氟脱氧葡萄糖([18F]FDG) PET在评估颈动脉粥样硬化斑块炎症方面具有重要意义,但它受到辐射暴露的限制。此外,已经发现血管周围脂肪组织(PVAT)的炎症通过旁分泌信号机制促进动脉粥样硬化的进展。该研究旨在建立一个基于颈动脉斑块和PVAT MRI放射组学的整体模型,用于识别高度炎症斑块(HIPs)。结果:159例无症状颈动脉粥样硬化患者(男性137例;患者年龄65±8岁,斑块209个(髋部104个)。在训练和测试数据集中,分别有47.95%(70/146)和53.97%(34/63)的病例被定义为髋关节。与训练数据集中的非高度炎症斑块(NHIPs)相比,HIPs中有更多的脂质核心,更多的斑块内出血和更少的钙化(p分别= 0.002,0.019和0.013)。值得注意的是,在培训组中,HIPs患者的PVAT (IPVAT)发生率明显高于NHIPs患者(81.43% vs. 46.05%;[18] NHIPs和HIPs对FDG的摄取不同。但IPVAT与SUVmax的相关性一致(r = 0.35, 0.30;结论:整合颈动脉斑块和血管周围脂肪组织放射组学的集合模型在颈动脉粥样硬化炎症和进展的可视化评估中提供了与PET等效的工具。
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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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