颅内动脉瘤不稳定性的三维量化形态学预测:一项纵向研究。

Maarten J Kamphuis, Laura T van der Kamp, Ruben P A van Eijk, Kimberley M Timmins, Gabriel J E Rinkel, Jeroen Hendrikse, Mervyn D I Vergouwen, Irene C van der Schaaf
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引用次数: 0

摘要

背景与目的:目前颅内动脉瘤生长和破裂的预测模型的性能不理想,需要新的标志物来改善预测。有使用标准化形态参数的纵向研究的强烈需求。在这项纵向研究中,我们旨在确定标准化的三维(3D)量化形态学参数作为长期随访中动脉瘤生长或破裂的预测因素。材料和方法:我们使用了2008-2018年间诊断的连续囊状未破裂颅内动脉瘤患者的数据库。采用回顾性病例队列设计,我们从整个队列中随机抽取计算机生成的动脉瘤样本,以及随机样本外随访期间生长或破裂的动脉瘤。病例队列设计对于低发生率的结果是有效的,同时保持暴露与结果之间的时间关联。在基线CTA或MRA图像上标注动脉瘤,并量化3D形态参数。单变量和多变量Cox比例风险模型用于确定动脉瘤生长或破裂的三维形态学预测因子。应用逆抽样概率权来获得风险比的无偏估计。结果:我们纳入278例患者(中位年龄59岁[IQR50-66];209例女性),327个动脉瘤,其中239个在随访期间稳定(73%),68个动脉瘤生长后未破裂(21%),7个动脉瘤生长后破裂(2%),13个动脉瘤破裂后未生长(4%)。生长预测多变量模型(中位随访4.1年[IQR1.9-7.1])保留了2个参数:长轴(HR 1.16, 95%CI: 0.84-1.61)和形状指数(HR 1.53, 95%CI: 0.76-3.08), c统计量为0.56 (95%CI: 0.49-0.63)。预测破裂(中位随访时间为4.5年[IQR2.1-7.3])的多变量模型参数相同:长轴(HR 2.27, 95%CI: 1.36-3.80)和形状指数(HR 3.33, 95%CI: 0.95-11.62), c统计量为0.85 (95%CI: 0.77-0.94)。结论:我们确定了长轴和形状指数作为动脉瘤生长和破裂的候选3D量化形态学预测指标,但仅对于破裂,这些指标在我们的队列中具有良好的判别能力。这些参数需要外部验证,并应与现有的临床预测模型相结合。缩写:ELAPSS =早期蛛网膜下腔出血,动脉瘤位置,年龄,人群,动脉瘤大小,动脉瘤形状;成像生物标志物标准化倡议;分期:人群、高血压、年龄、动脉瘤大小、早期其他动脉瘤所致SAH、动脉瘤部位;UIA =未破裂颅内动脉瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Three-Dimensional Quantified Morphological Predictors of Intracranial Aneurysm Instability: A Longitudinal Study.

Background and purpose: The performance of current prediction models for intracranial aneurysm growth and rupture is suboptimal, and new markers are needed to improve prediction. There is a strong need for longitudinal studies that use standardized morphological parameters. In this longitudinal study, we aimed to identify standardized three-dimensional (3D) quantified morphological parameters as predictors of aneurysm growth or rupture during long-term follow-up.

Materials and methods: We used a database of consecutive patients with saccular unruptured intracranial aneurysms diagnosed between 2008-2018. Employing a retrospective case-cohort design, we included a computer-generated random sample of aneurysms from the full cohort and aneurysms with growth or rupture during follow-up outside the random sample. The case-cohort design is efficient for low-incidence outcomes while maintaining the temporal association between exposure and outcome. Aneurysms were annotated on baseline CTA or MRA images, and 3D morphological parameters were quantified. Univariable and multivariable Cox proportional hazards models were used to identify 3D morphological predictors of either aneurysm growth or aneurysm rupture. An inverse sampling probability weight was applied to obtain unbiased estimates of the hazard ratios.

Results: We included 278 patients (median age, 59 years [IQR50-66]; 209 women) with 327 aneurysms, of which 239 aneurysms were stable during follow-up (73%), 68 grew without subsequent rupture (21%), 7 grew with subsequent rupture (2%), and 13 ruptured without preceding growth (4%). In the multivariable model for growth prediction (median follow-up 4.1 years [IQR1.9-7.1]), 2 parameters were retained: major axis (HR 1.16, 95%CI: 0.84-1.61) and shape index (HR 1.53, 95%CI: 0.76-3.08), with a c-statistic of 0.56 (95%CI: 0.49-0.63). The same parameters were retained in the multivariable model for prediction of rupture (median follow-up 4.5 years [IQR2.1-7.3]): major axis (HR 2.27, 95%CI: 1.36-3.80) and shape index (HR 3.33, 95%CI: 0.95-11.62), with a c-statistic of 0.85 (95%CI: 0.77-0.94).

Conclusions: We identified major axis and shape index as candidate 3D quantified morphological predictors of both aneurysm growth and rupture, but only for rupture these had good discriminative power in our cohort. These parameters will need external validation and should be integrated with existing clinical prediction models.

Abbreviations: ELAPSS = Earlier subarachnoid hemorrhage, Location of the aneurysm, Age, Population, Size of the aneurysm, and Shape of the aneurysm; IBSI = imaging biomarker standardization initiative; PHASES = Population, Hypertension, Age, Size of aneurysm, Earlier SAH from another aneurysm, and Site of aneurysm; UIA = unruptured intracranial aneurysm.

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