Huang Yuan, Teng Zhongzhao, Elkhawad Maysoon, Tarkin Jason M, Joshi Nikhil, Boyle Jonathan R, Buscombe John R, Fryer Timothy D, Zhang Yongxue, Park Ah Yeon, Wilkinson Ian B, Newby David E, Gillard Jonathan H, Rudd James H F
From the Department of Radiology (Y.H., Z.T., Y.Z., J.H.G.), EPSRC Centre for Mathematical and Statistical Analysis of Multimodal Clinical Imaging (Y.H.), Department of Engineering (Z.T.), Division of Cardiovascular Medicine (M.E., J.M.T., I.B.W., J.H.F.R.), Wolfson Brain Imaging Centre (T.D.F.), and Statistical Laboratory (A.Y.P.), University of Cambridge, United Kingdom; British Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, United Kingdom (N.J., D.E.N.); Department of Vascular Surgery (J.R. Boyle) and Department of Nuclear Medicine (J.R. Buscombe), Addenbrooke's Hospital, Cambridge, United Kingdom; and Department of Vascular Surgery, Changhai Hospital, Shanghai, China (Y.Z.).
Circ Cardiovasc Imaging. 2016 Nov;9(11):e004656. doi: 10.1161/CIRCIMAGING.116.004656.
Abdominal aortic aneurysm (AAA) wall inflammation and mechanical structural stress may influence AAA expansion and lead to rupture. We hypothesized a positive correlation between structural stress and fluorine-18-labeled 2-deoxy-2-fluoro-d-glucose (F-FDG) positron emission tomography-defined inflammation. We also explored the influence of computed tomography-derived aneurysm morphology and composition, including intraluminal thrombus, on both variables.
Twenty-one patients (19 males) with AAAs below surgical threshold (AAA size was 4.10±0.54 cm) underwent F-FDG positron emission tomography and contrast-enhanced computed tomography imaging. Structural stresses were calculated using finite element analysis. The relationship between maximum aneurysm F-FDG standardized uptake value within aortic wall and wall structural stress, patient clinical characteristics, aneurysm morphology, and compositions was explored using a hierarchical linear mixed-effects model. On univariate analysis, local aneurysm diameter, thrombus burden, extent of calcification, and structural stress were all associated with F-FDG uptake (P<0.05). AAA structural stress correlated with F-FDG maximum standardized uptake value (slope estimate, 0.552; P<0.0001). Multivariate linear mixed-effects analysis revealed an important interaction between structural stress and intraluminal thrombus in relation to maximum standardized uptake value (fixed effect coefficient, 1.68 [SE, 0.10]; P<0.0001). Compared with other factors, structural stress was the best predictor of inflammation (receiver-operating characteristic curve area under the curve =0.59), with higher accuracy seen in regions with high thrombus burden (area under the curve =0.80). Regions with both high thrombus burden and high structural stress had higher F-FDG maximum standardized uptake value compared with regions with high thrombus burdens but low stress (median [interquartile range], 1.93 [1.60-2.14] versus 1.14 [0.90-1.53]; P<0.0001).
Increased aortic wall inflammation, demonstrated by F-FDG positron emission tomography, was observed in AAA regions with thick intraluminal thrombus subjected to high mechanical stress, suggesting a potential mechanistic link underlying aneurysm inflammation.
腹主动脉瘤(AAA)壁炎症和机械结构应力可能影响AAA扩张并导致破裂。我们假设结构应力与氟-18标记的2-脱氧-2-氟-D-葡萄糖(F-FDG)正电子发射断层扫描定义的炎症之间存在正相关。我们还探讨了计算机断层扫描衍生的动脉瘤形态和组成,包括腔内血栓,对这两个变量的影响。
21例(19例男性)AAA直径低于手术阈值(AAA大小为4.10±0.54 cm)的患者接受了F-FDG正电子发射断层扫描和对比增强计算机断层扫描成像。使用有限元分析计算结构应力。使用分层线性混合效应模型探讨主动脉壁内最大动脉瘤F-FDG标准化摄取值与壁结构应力、患者临床特征、动脉瘤形态和组成之间的关系。单因素分析显示,局部动脉瘤直径、血栓负荷、钙化程度和结构应力均与F-FDG摄取相关(P<0.05)。AAA结构应力与F-FDG最大标准化摄取值相关(斜率估计值,0.552;P<0.0001)。多变量线性混合效应分析显示,结构应力与腔内血栓在最大标准化摄取值方面存在重要相互作用(固定效应系数,1.68 [标准误,0.10];P<0.0001)。与其他因素相比,结构应力是炎症的最佳预测指标(受试者操作特征曲线下面积=0.59),在血栓负荷高的区域准确性更高(曲线下面积=0.80)。与血栓负荷高但应力低的区域相比,血栓负荷高且结构应力高的区域F-FDG最大标准化摄取值更高(中位数[四分位间距],1.93 [1.60 - 2.14] 对1.14 [0.90 - 1.53];P<0.0001)。
在承受高机械应力的腔内血栓厚的AAA区域观察到F-FDG正电子发射断层扫描显示的主动脉壁炎症增加,提示动脉瘤炎症背后存在潜在的机制联系。