Optimizing timing for quantification of intracranial aneurysm enhancement: a multi-phase contrast-enhanced vessel wall MRI study.

IF 4.7 2区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Radiology Pub Date : 2024-12-01 Epub Date: 2024-06-10 DOI:10.1007/s00330-024-10827-z
Xiao Li, Jianjian Zhang, Jin Zhang, Lingling Wang, Jiaqi Tian, Hui Tang, Mahmud Mossa-Basha, Bing Zhao, Jieqing Wan, Jianrong Xu, Yan Zhou, Beibei Sun, Huilin Zhao, Chengcheng Zhu
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Abstract

Objectives: Aneurysm wall enhancement (AWE) on high-resolution contrast-enhanced vessel wall MRI (VWMRI) is an emerging biomarker for intracranial aneurysms (IAs) stability. Quantification methods of AWE in the literature, however, are variable. We aimed to determine the optimal post-contrast timing to quantify AWE in both saccular and fusiform IAs.

Materials and methods: Consecutive patients with unruptured IAs were prospectively recruited. VWMRI was acquired on 1 pre-contrast and 4 consecutive post-contrast phases (each phase was 9 min). Signal intensity values of cerebrospinal fluid (CSF) and aneurysm wall on pre- and 4 post-contrast phases were measured to determine the aneurysm wall enhancement index (WEI). AWE was also qualitatively analyzed on post-contrast images using previous grading criteria. The dynamic changes of AWE grade and WEI were analyzed for both saccular and fusiform IAs.

Results: Thirty-four patients with 42 IAs (27 saccular IAs and 15 fusiform IAs) were included. The changes in AWE grade occurred in 8 (30%) saccular IAs and 6 (40%) in fusiform IAs during the 4 post-contrast phases. The WEI of fusiform IAs decreased 22.0% over time after contrast enhancement (p = 0.009), while the WEI of saccular IAs kept constant during the 4 post-contrast phases (p > 0.05).

Conclusions: When performing quantitative analysis of AWE, acquiring post-contrast VWMRI immediately after contrast injection achieves the strongest AWE for fusiform IAs. While the AWE degree is stable for 36 min after contrast injection for saccular IAs.

Clinical relevance statement: The standardization of imaging protocols and analysis methods for AWE will be helpful for imaging surveillance and further treatment decisions of patients with unruptured IAs.

Key points: Imaging protocols and measurements of intracranial aneurysm wall enhancement are reported heterogeneously. Aneurysm wall enhancement for fusiform intracranial aneurysms (IAs) is strongest immediately post-contrast, and stable for 36 min for saccular IAs. Future multi-center studies should investigate aneurysm wall enhancement as an emerging marker of aneurysm growth and rupture.

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优化量化颅内动脉瘤增强的时机:一项多相对比增强血管壁磁共振成像研究。
目的:高分辨率造影剂增强血管壁磁共振成像(VWMRI)上的动脉瘤壁增强(AWE)是颅内动脉瘤(IAs)稳定性的新兴生物标志物。然而,文献中的 AWE 定量方法各不相同。我们的目的是确定在囊状和纺锤形动脉瘤中量化 AWE 的最佳对比后时间:我们前瞻性地招募了连续的未破裂IA患者。在 1 个对比前阶段和 4 个连续的对比后阶段(每个阶段 9 分钟)采集 VWMRI。测量对比前和对比后 4 个阶段的脑脊液(CSF)和动脉瘤壁的信号强度值,以确定动脉瘤壁增强指数(WEI)。此外,还使用以前的分级标准对对比后图像上的 AWE 进行定性分析。分析了囊状和纺锤形动脉瘤的 AWE 等级和 WEI 的动态变化:结果:共纳入34例患者,42例IA(27例囊状IA和15例纺锤形IA)。在对比后的 4 个阶段中,8 个(30%)囊状内膜和 6 个(40%)纺锤形内膜的 AWE 分级发生了变化。造影剂增强后,纺锤形内腔腺的WEI随着时间的推移下降了22.0%(p = 0.009),而囊状内腔腺的WEI在造影剂增强后的4个阶段保持不变(p > 0.05):在对AWE进行定量分析时,注射对比剂后立即采集对比剂后VWMRI对纺锤形IA的AWE最强。临床相关性声明:AWE成像方案和分析方法的标准化将有助于未破裂IAs患者的成像监测和进一步治疗决策:要点:颅内动脉瘤壁强化的成像方案和测量方法报道不一。纺锤形颅内动脉瘤(IAs)的动脉瘤壁强化在造影后立即最强,而囊状IAs的动脉瘤壁强化在36分钟内保持稳定。未来的多中心研究应将动脉瘤壁强化作为动脉瘤生长和破裂的新标记进行研究。
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来源期刊
European Radiology
European Radiology 医学-核医学
CiteScore
11.60
自引率
8.50%
发文量
874
审稿时长
2-4 weeks
期刊介绍: European Radiology (ER) continuously updates scientific knowledge in radiology by publication of strong original articles and state-of-the-art reviews written by leading radiologists. A well balanced combination of review articles, original papers, short communications from European radiological congresses and information on society matters makes ER an indispensable source for current information in this field. This is the Journal of the European Society of Radiology, and the official journal of a number of societies. From 2004-2008 supplements to European Radiology were published under its companion, European Radiology Supplements, ISSN 1613-3749.
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