利用定量多参数磁共振成像的合成脑成像检测病理对比度增强

IF 2.3 4区 医学 Q3 CLINICAL NEUROLOGY Journal of Neuroimaging Pub Date : 2024-04-08 DOI:10.1111/jon.13201
Graziella Donatelli, Gianmichele Migaleddu, Matteo Cencini, Paolo Cecchi, Claudio D'Amelio, Luca Peretti, Guido Buonincontri, Michela Tosetti, Mauro Costagli, Mirco Cosottini
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引用次数: 0

摘要

背景和目的我们的目的是检验对比后定量瞬态成像(QTI)采集得到的合成 T1 加权成像是否能揭示颅内病变的病理对比增强。方法分析包括 141 名接受 3 Tesla-MRI 脑部检查并静脉注射对比剂的患者,对比后采集方案包括三维快速破坏梯度回波(FSPGR)序列和 QTI 采集。合成 T1 加权图像由 QTI 导出的弛豫时间和质子密度定量图生成。两位神经放射学专家对合成和常规对比后 T1 加权图像进行评估,以确定颅内病变是否存在病理对比度增强以及增强的模式。结果以常规成像为参考,合成 T1 加权成像在显示造影剂增强病变方面的敏感度为 93%。读者之间(传统成像和合成成像的 k = 1)和序列之间(两个读者的 k = 0.98)对是否存在造影剂增强几乎完全一致。在 91% 的病变中,合成 T1 加权成像显示出与常规成像相同的对比度增强模式。与 FSPGR 相比,QTI 的空间分辨率较低,造影剂用药后的采集延迟时间较长,因此其余病灶的增强模式可能存在差异。结论QTI衍生的对比后合成T1加权成像可捕捉到大多数颅内增强病变的病理性对比增强。为了支持我们的数据并探索未来在临床试验中的可能应用,还需要采用空间分辨率更高的定量成像技术进行进一步的比较研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Detection of pathological contrast enhancement with synthetic brain imaging from quantitative multiparametric MRI

Background and Purpose

We aimed to test whether synthetic T1-weighted imaging derived from a post-contrast Quantitative Transient-state Imaging (QTI) acquisition enabled revealing pathological contrast enhancement in intracranial lesions.

Methods

The analysis included 141 patients who underwent a 3 Tesla-MRI brain exam with intravenous contrast media administration, with the post-contrast acquisition protocol comprising a three-dimensional fast spoiled gradient echo (FSPGR) sequence and a QTI acquisition. Synthetic T1-weighted images were generated from QTI-derived quantitative maps of relaxation times and proton density. Two neuroradiologists assessed synthetic and conventional post-contrast T1-weighted images for the presence and pattern of pathological contrast enhancement in intracranial lesions. Enhancement volumes were quantitatively compared.

Results

Using conventional imaging as a reference, synthetic T1-weighted imaging was 93% sensitive in revealing the presence of contrast enhancing lesions. The agreement for the presence/absence of contrast enhancement was almost perfect both between readers (k = 1 for both conventional and synthetic imaging) and between sequences (k = 0.98 for both readers). In 91% of lesions, synthetic T1-weighted imaging showed the same pattern of contrast enhancement visible in conventional imaging. Differences in enhancement pattern in the remaining lesions can be due to the lower spatial resolution and the longer acquisition delay from contrast media administration of QTI compared to FSPGR. Overall, enhancement volumes appeared larger in synthetic imaging.

Conclusions

QTI-derived post-contrast synthetic T1-weighted imaging captures pathological contrast enhancement in most intracranial enhancing lesions. Further comparative studies employing quantitative imaging with higher spatial resolution is needed to support our data and explore possible future applications in clinical trials.

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来源期刊
Journal of Neuroimaging
Journal of Neuroimaging 医学-核医学
CiteScore
4.70
自引率
0.00%
发文量
117
审稿时长
6-12 weeks
期刊介绍: Start reading the Journal of Neuroimaging to learn the latest neurological imaging techniques. The peer-reviewed research is written in a practical clinical context, giving you the information you need on: MRI CT Carotid Ultrasound and TCD SPECT PET Endovascular Surgical Neuroradiology Functional MRI Xenon CT and other new and upcoming neuroscientific modalities.The Journal of Neuroimaging addresses the full spectrum of human nervous system disease, including stroke, neoplasia, degenerating and demyelinating disease, epilepsy, tumors, lesions, infectious disease, cerebral vascular arterial diseases, toxic-metabolic disease, psychoses, dementias, heredo-familial disease, and trauma.Offering original research, review articles, case reports, neuroimaging CPCs, and evaluations of instruments and technology relevant to the nervous system, the Journal of Neuroimaging focuses on useful clinical developments and applications, tested techniques and interpretations, patient care, diagnostics, and therapeutics. Start reading today!
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