Blasi Francesco, Oliveira Bruno L, Rietz Tyson A, Rotile Nicholas J, Naha Pratap C, Cormode David P, Izquierdo-Garcia David, Catana Ciprian, Caravan Peter
From the Department of Radiology, Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Charlestown (F.B., B.L.O., T.A.R., N.J.R., D.I.-G., C.C., P.C.); Department of Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia (P.C.N., D.P.C.); and Institute for Innovation in Imaging, Massachusetts General Hospital, Boston (P.C.).
Arterioscler Thromb Vasc Biol. 2015 Oct;35(10):2114-21. doi: 10.1161/ATVBAHA.115.306055. Epub 2015 Aug 13.
Thrombosis is a leading cause of morbidity and mortality worldwide. Current diagnostic strategies rely on imaging modalities that are specific for distinct vascular territories, but a thrombus-specific whole-body imaging approach is still missing. Moreover, imaging techniques to assess thrombus composition are underdeveloped, although therapeutic strategies may benefit from such technology. Therefore, our goal was to test whether positron emission tomography (PET) with the fibrin-binding probe (64)Cu-FBP8 allows multisite thrombus detection and fibrin content estimation.
Thrombosis was induced in Sprague-Dawley rats (n=32) by ferric chloride application on both carotid artery and femoral vein. (64)Cu-FBP8-PET/CT imaging was performed 1, 3, or 7 days after thrombosis to detect thrombus location and to evaluate age-dependent changes in target uptake. Ex vivo biodistribution, autoradiography, and histopathology were performed to validate imaging results. Arterial and venous thrombi were localized on fused PET/CT images with high accuracy (97.6%; 95% confidence interval, 92-100). A single whole-body PET/MR imaging session was sufficient to reveal the location of both arterial and venous thrombi after (64)Cu-FBP8 administration. PET imaging showed that probe uptake was greater in younger clots than in older ones for both arterial and venous thrombosis (P<0.0001). Quantitative histopathology revealed an age-dependent reduction of thrombus fibrin content (P<0.001), consistent with PET results. Biodistribution and autoradiography further confirmed the imaging findings.
We demonstrated that (64)Cu-FBP8-PET is a feasible approach for whole-body thrombus detection and that molecular imaging of fibrin can provide, noninvasively, insight into clot composition.
血栓形成是全球发病和死亡的主要原因。目前的诊断策略依赖于针对不同血管区域的成像方式,但仍缺乏针对血栓的全身成像方法。此外,尽管治疗策略可能受益于此类技术,但评估血栓成分的成像技术仍不发达。因此,我们的目标是测试使用纤维蛋白结合探针(64)Cu-FBP8的正电子发射断层扫描(PET)是否能够进行多部位血栓检测和纤维蛋白含量估计。
通过在Sprague-Dawley大鼠(n = 32)的颈动脉和股静脉上应用氯化铁诱导血栓形成。在血栓形成后1、3或7天进行(64)Cu-FBP8-PET/CT成像,以检测血栓位置并评估目标摄取的年龄依赖性变化。进行体外生物分布、放射自显影和组织病理学检查以验证成像结果。动脉和静脉血栓在融合的PET/CT图像上定位准确(97.6%;95%置信区间,92 - 100)。单次全身PET/MR成像检查足以在给予(64)Cu-FBP8后揭示动脉和静脉血栓的位置。PET成像显示,对于动脉和静脉血栓形成,年轻血栓中的探针摄取均高于老年血栓(P < 0.0001)。定量组织病理学显示血栓纤维蛋白含量随年龄减少(P < 0.001),与PET结果一致。生物分布和放射自显影进一步证实了成像结果。
我们证明(64)Cu-FBP8-PET是一种可行的全身血栓检测方法,并且纤维蛋白的分子成像可以无创地提供对血栓成分的深入了解。