Culprit and Non-Culprit Plaque Characteristics With vs. Without a Healed Phenotype in Patients With Acute Myocardial Infarction Caused by Plaque Erosion ― A 3-Vessel OCT Study ―

罪魁祸首 医学 易损斑块 病变 心肌梗塞 心脏病学 内科学 病理
作者
Yan-Wei Yin,Chao Fang,Shuang Jiang,Jifei Wang,Yidan Wang,Junchen Guo,Fangmeng Lei,Sibo Sun,Xueying Pei,Ruyi Jia,Caiying Tang,Lulu Liu,Yini Wang,Yu Hou,Jihong Dai,Bo Yu
出处
期刊:Circulation journal [Japanese Circulation Society]
卷期号:86 (5): 846-854 被引量:5
标识
DOI:10.1253/circj.cj-21-0635
摘要

Plaque erosion can occur quietly without causing clinical symptoms, followed by a healing process resulting in healed plaque. This study aimed to assess culprit and non-culprit plaque characteristics of patients with acute myocardial infarction (AMI) caused by plaque erosion with vs. without healed phenotype at the culprit plaque using optical coherence tomography (OCT).Methods and Results: A total of 117 AMI patients caused by plaque erosion who underwent OCT imaging of 3 coronary arteries were included. Patients were divided into 2 groups based on presence or absence of a healed phenotype at the culprit site. Culprit and non-culprit plaque characteristics were compared between the 2 groups. A healed phenotype at the culprit lesion was identified in 47.9% of AMI patients caused by plaque erosion. Patients with a healed phenotype at the culprit site were more frequently with hyperlipidemia, and had a higher prevalence of macrophage infiltration, microchannels, cholesterol crystals, and calcification at the culprit lesion. Moreover, patients with a healed phenotype at the culprit site had more non-culprit plaques and more characteristics of plaque vulnerability at the non-culprit lesion. In addition, patients with a healed phenotype at the culprit site presented with more severe luminal stenosis at both the culprit and non-culprit lesion.A healed phenotype was identified in 47.9% of AMI patients caused by plaque erosion at the culprit site. A healed phenotype within eroded culprit plaque was associated with signs of pancoronary vulnerability and advanced atherosclerosis.
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