Cardiovascular Division, Hospital of the University of Pennsylvania and Cardiovascular Institute, University of Pennsylvania, Philadelphia, PA 19104, USA.
Arterioscler Thromb Vasc Biol. 2013 Feb;33(2):347-53. doi: 10.1161/ATVBAHA.112.300710. Epub 2013 Jan 3.
To prospectively evaluate whether the development of fibroatheromas exhibiting features of potential instability can be detected and predicted by serial invasive imaging.
Multivessel intravascular ultrasound and near infrared spectroscopy (NIRS) were performed in diabetic/hypercholesterolemic pigs 3, 6, and 9 months after induction. Animals were euthanized at 9 months and histological/immunohistochemical evaluation of the arteries was performed (n=304 arterial segments). Intravascular ultrasound demonstrated, over time, a progressive increase in plaque + media and necrotic core areas and positive vascular remodeling. By histology, NIRS+ lesions were significantly more likely to be a high-risk fibroatheroma (P=0.0001) containing larger plaque (P<0.0001) and necrotic core areas (P<0.0019) and thinner fibrous caps (P=0.04). NIRS + fibroatheromas possessed a greater concentration of inflammatory cells demonstrating protease activity (P=0.006), and proliferating (P=0.016), and apoptotic cells (P=0.04) within the fibrous cap. Eighty-eight percent of NIRS+ lesions at 3 and 6 months subsequently developed into a fibroatheroma at 9 months (P<0.01). By multivariate analysis NIRS positivity at 6 months predicted the subsequent presence of a fibroatheroma at 9 months (P=0.005; odds ratio, 2.71).
The future development of inflamed fibroatheromas with thinner fibrous caps, greater plaque, and necrotic core areas, and posessing characteristics of increased plaque instability were detected by intravascular ultrasound/NIRS imaging.
前瞻性评估连续的侵袭性成像是否能检测到并预测表现出潜在不稳定特征的纤维粥样瘤的形成。
在诱导后 3、6 和 9 个月,对糖尿病/高胆固醇血症猪进行多血管血管内超声和近红外光谱(NIRS)检查。动物在 9 个月时安乐死,并对动脉进行组织学/免疫组织化学评估(n=304 个动脉节段)。血管内超声显示,随着时间的推移,斑块+中膜和坏死核心区域逐渐增加,并出现阳性血管重构。通过组织学检查,NIRS+病变更有可能是高风险的纤维粥样瘤(P=0.0001),包含更大的斑块(P<0.0001)和坏死核心区域(P<0.0019)以及更薄的纤维帽(P=0.04)。NIRS+纤维粥样瘤内的炎症细胞具有更高的蛋白酶活性(P=0.006)、增殖(P=0.016)和凋亡(P=0.04)细胞浓度,位于纤维帽内。88%的 NIRS+病变在 3 个月和 6 个月后在 9 个月时发展为纤维粥样瘤(P<0.01)。通过多变量分析,6 个月时的 NIRS 阳性预测 9 个月时纤维粥样瘤的发生(P=0.005;优势比,2.71)。
血管内超声/NIRS 成像检测到具有更薄纤维帽、更大斑块和坏死核心区域以及具有斑块不稳定特征的炎症纤维粥样瘤的未来发展。