Coronary artery disease reporting and data system (CAD-RADS), vascular inflammation and plaque vulnerability

医学 冠状动脉疾病 罪魁祸首 内科学 心脏病学 计算机辅助设计 冠状动脉 放射科 动脉 心肌梗塞 工程制图 工程类
作者
Daisuke Kinoshita,Keishi Suzuki,Haruhito Yuki,Takayuki Niida,Daichi Fujimoto,Yoshiyasu Minami,Damini Dey,Hang Lee,Iris McNulty,Junya Ako,Brian Ghoshhajra,Maros Ferencik,Tsunekazu Kakuta,Ik‐Kyung Jang
出处
期刊:Journal of Cardiovascular Computed Tomography [Elsevier]
卷期号:17 (6): 445-452 被引量:7
标识
DOI:10.1016/j.jcct.2023.09.008
摘要

Coronary artery disease reporting and data system (CAD-RADS) predicts future cardiovascular events in patients with coronary artery disease (CAD). However, information on vascular inflammation and vulnerability remains scarce.Patients who underwent coronary computed tomography angiography (CTA) and optical coherence tomography (OCT) prior to coronary intervention were enrolled. All three coronary arteries were evaluated for CAD-RADS score and pericoronary adipose tissue (PCAT) attenuation, while the culprit vessel was analyzed for plaque vulnerability by OCT.A total of 385 patients with 915 lesions were divided into two groups based on CAD-RADS score: 103 (26.8%) were categorized as CAD-RADS 4b/5 and 282 (73.2%) as CAD-RADS ≤4a. Patients with CAD-RADS 4b/5 had a higher level of PCAT attenuation (mean of 3 coronary arteries) than those with CAD-RADS ≤4a (-68.4 ​± ​6.7 HU vs. -70.1 ​± ​6.5, P ​= ​0.022). The prevalence of macrophage was higher, and lipid index was greater in patients with CAD-RADS 4b/5 than CAD-RADS ≤4a (94.2% vs. 83.0%, P ​= ​0.004, 1845 vs. 1477; P ​= ​0.003). These associations were significant in the culprit vessels of patients with chronic coronary syndrome but not in those with acute coronary syndromes.Higher CAD-RADS score was associated with higher levels of vascular inflammation and plaque vulnerability.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
孔乙己发布了新的文献求助10
刚刚
自觉紫安发布了新的文献求助10
1秒前
Ava应助灵巧的白昼采纳,获得10
1秒前
sun发布了新的文献求助20
1秒前
LFZ发布了新的文献求助10
1秒前
1秒前
路会飞发布了新的文献求助10
1秒前
RXL完成签到,获得积分10
1秒前
西蜀小吏发布了新的文献求助10
2秒前
water完成签到,获得积分10
2秒前
复杂海豚完成签到 ,获得积分10
2秒前
科目三应助12345采纳,获得10
3秒前
王小橘完成签到,获得积分10
3秒前
3秒前
3秒前
草中有粑粑完成签到,获得积分10
3秒前
因子完成签到,获得积分10
4秒前
乔科立发布了新的文献求助30
4秒前
4秒前
Murmansk完成签到,获得积分10
4秒前
pi完成签到 ,获得积分10
5秒前
歪歪比比完成签到,获得积分10
5秒前
2以李发布了新的文献求助10
5秒前
懒羊羊发布了新的文献求助10
5秒前
田様应助wer采纳,获得10
5秒前
温暖凡灵完成签到,获得积分10
5秒前
xxx完成签到,获得积分10
5秒前
害羞菲鹰发布了新的文献求助10
6秒前
科研通AI6应助魔幻的稚晴采纳,获得10
6秒前
无奈醉柳完成签到,获得积分10
6秒前
ding应助33采纳,获得10
7秒前
8秒前
8秒前
8秒前
Dawn完成签到,获得积分10
9秒前
9秒前
harden发布了新的文献求助20
9秒前
9秒前
linliqing完成签到,获得积分10
9秒前
尧九完成签到,获得积分10
10秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Binary Alloy Phase Diagrams, 2nd Edition 8000
Encyclopedia of Reproduction Third Edition 3000
Comprehensive Methanol Science Production, Applications, and Emerging Technologies 2000
From Victimization to Aggression 1000
Translanguaging in Action in English-Medium Classrooms: A Resource Book for Teachers 700
Exosomes Pipeline Insight, 2025 500
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 计算机科学 有机化学 物理 生物化学 纳米技术 复合材料 内科学 化学工程 人工智能 催化作用 遗传学 数学 基因 量子力学 物理化学
热门帖子
关注 科研通微信公众号,转发送积分 5651984
求助须知:如何正确求助?哪些是违规求助? 4786417
关于积分的说明 15057609
捐赠科研通 4810610
什么是DOI,文献DOI怎么找? 2573282
邀请新用户注册赠送积分活动 1529204
关于科研通互助平台的介绍 1488110