Faculty of Electrical Engineering, University of Ljubljana, Ljubljana, Slovenia.
Sci Rep. 2024 Aug 23;14(1):19609. doi: 10.1038/s41598-024-70453-z.
Growing intracranial aneurysms pose a high risk of rupture, making the detection and quantification of the growth crucial for timely treatment strategy adoption. In this paper we propose a computer-assisted approach based on the extraction of IA shapes from associated baseline and follow-up angiographic scans and non-rigid morphing of the two shapes. From the obtained shape deformations we computed four novel features, including differential volume (dV), surface area (dSA), aneurysm-size normalized median deformation path length (dMPL), and integral of cumulative deformation distances (dICDD). An experienced neuroradiologist manually extracted the IA shape models from the baseline and follow-up MRAs and, by utilizing size change and visual assessments, classified each aneurysm into stable with morphology changes, stable or growing. We investigated the classification performance and found that three of the novel and one cross-sectional feature exhibited significantly different mean values (p-value ; Tukey's HSD test) between the stable and growing IA groups, while the mean dICDD was significantly different between all the three groups. The cross-sectional features has sensitivity to growing IAs in range 0.05-0.86, while novel features had generally higher sensitivity in range 0.81-0.90, making them promising candidates as surrogate follow-up imaging-based biomarkers for IA growth detection. These findings may offer valuable information for clinical management of patients with IAs based on follow-up imaging.
不断增长的颅内动脉瘤有很高的破裂风险,因此对其进行检测和定量分析对于及时采取治疗策略至关重要。在本文中,我们提出了一种基于从相关基线和随访血管造影扫描中提取 IA 形状并对两个形状进行非刚性变形的计算机辅助方法。从获得的形状变形中,我们计算了四个新特征,包括差异体积(dV)、表面积(dSA)、动脉瘤大小归一化中位数变形路径长度(dMPL)和累积变形距离积分(dICDD)。一位有经验的神经放射科医生从基线和随访的 MRA 中手动提取 IA 形状模型,并利用大小变化和视觉评估,将每个动脉瘤分为形态变化稳定、稳定或生长。我们研究了分类性能,发现四个新特征中的三个和一个横截面特征在稳定和生长的 IA 组之间的平均值存在显著差异(p 值<0.05;Tukey 的 HSD 检验),而所有三组之间的平均 dICDD 差异显著。横截面特征对生长性 IAs 的灵敏度范围为 0.05-0.86,而新特征的灵敏度范围通常为 0.81-0.90,这使得它们成为有希望的替代基于随访成像的 IA 生长检测的生物标志物。这些发现可能为基于随访成像的 IA 患者的临床管理提供有价值的信息。