Combined near infrared photoacoustic imaging and ultrasound detects vulnerable atherosclerotic plaque.
Combined near infrared photoacoustic imaging and ultrasound detects vulnerable atherosclerotic plaque.
复制标题
结合近红外光声成像和超声检测易损动脉粥样硬化斑块。
DOI:
10.1016/j.biomaterials.2023.122314
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发表时间:
2023
期刊:
影响因子:
14
通讯作者:
H
中科院分区:
文献类型:
--
作者:
Schneider,MartinKarl;Wang,James;Kare,Aris;Adkar,ShaunakS;Salmi,Darren;Bell,CaitlinF;Alsaigh,Tom;Wagh,Dhananjay;Coller,John;Mayer,Aaron;Snyder,SarahJ;Borowsky,AlexanderD;Long,StevenR;Lansberg,MaartenG;Steinberg,GaryK;H
Atherosclerosis is an inflammatory process resulting in the deposition of cholesterol and cellular debris, narrowing of the vessel lumen and clot formation. Characterization of the morphology and vulnerability of the lesion is essential for effective clinical management. Here, near-infrared auto-photoacoustic (NIRAPA) imaging is shown to detect plaque components and, when combined with ultrasound imaging, to differentiate stable and vulnerable plaque. In anex vivostudy of photoacoustic imaging of excised plaque from 25 patients, 88.2% sensitivity and 71.4% specificity were achieved using a clinically-relevant protocol. In order to determine the origin of the NIRAPA signal, immunohistochemistry, spatial transcriptomics and spatial proteomics were co-registered with imaging and applied to adjacent plaque sections. The highest NIRAPA signal was spatially correlated with bilirubin and associated blood-based residue and with the cytoplasmic contents of inflammatory macrophages bearing CD74, HLA-DR, CD14 and CD163 markers. In summary, we establish the potential to apply the NIRAPA-ultrasound imaging combination to detect vulnerable carotid plaque and a methodology for fusing molecular imaging with spatial transcriptomic and proteomic methods.