低级别胶质瘤放疗后MRI脑微出血和FLAIR高信号的空间分布

Justyna Kłos , Reina W. Kloet , Hiska L. van der Weide , Kelvin Ng Wei Siang , Peter F. Sinnige , Miranda C.A. Kramer , Rudi A.J.O. Dierckx , Ronald J.H. Borra , Anouk van der Hoorn
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引用次数: 0

摘要

背景和目的脑微出血(CMBs)和液体衰减反转恢复(FLAIR)在放射治疗(RT)后的脑MRI扫描中的高信号被认为是微血管损伤和相关认知变化的标志物。然而,使用现有评分系统的空间分布以及这些成像生物标志物的位置仍然不清楚,阻碍了临床解释。本研究旨在阐明这些标志物在低级别胶质瘤(LGG)患者中的分布和位置。材料和方法根据现有的微出血解剖评分量表(MARS),在回顾性1.5T磁化率加权MRI扫描中对脑胶质瘤进行空间分类,并对其位于海马、杏仁核、皮层、白质(WM),以及它们与FLAIR高信号的空间关系。对整个大脑、同侧大脑和对侧大脑(肿瘤体积)进行评分。结果共51次扫描,其中28次至少有一次CMB。大多数CMBs局限于肺叶区、深部和室周白质(DPWM),通常在WM中。在GM中仅发现少数CMBs。在RT完成后7年的扫描中,大多数CMBs未与FLAIR高信号共定位。结论CMBs和FLAIR高信号似乎是放射治疗诱导的微血管损伤的独立成像生物标志物,因为它们在LGG患者中没有共同定位,尤其是在RT完成后的早期。
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Spatial distribution of cerebral microbleeds and FLAIR hyperintensities on follow-up MRI after radiotherapy for lower grade glioma

Background and purpose

Cerebral microbleeds (CMBs) and fluid-attenuated-inversion recovery (FLAIR) hyperintensities on brain MRI scans after radiotherapy (RT) are considered markers for microvascular damage and related cognitive changes. However, the spatial distribution using existing scoring systems as well as colocation of these imaging biomarkers remain unclear, hampering clinical interpretation. This study aims to elucidate the distribution and colocation of these markers in patients with lower grade glioma (LGG).

Materials and methods

CMBs were spatially classified on retrospective 1.5 T susceptibility weighted MRI scans according to the existing Microbleed Anatomical Rating Scale (MARS) and were additionally scored for being located in hippocampus, amygdala, cortex, white matter (WM), grey matter (GM), WM/GM junction and for their spatial relation to FLAIR hyperintensities. Scoring was performed for whole, ipsilateral and contralateral cerebrum (with respect to tumour bulk).

Results

Fifty-one scans were included of which 28 had at least one CMB. The majority of CMBs were localized in the lobar area and in deep and periventricular white matter (DPWM) - generally in WM. Only few CMBs were found in GM. In scans obtained up to 7 years after RT completion the majority of CMBs were not colocalized with FLAIR hyperintensities.

Conclusion

CMBs and FLAIR hyperintensities appear to be separate imaging biomarkers for radiation therapy induced microvascular damage, as they are not colocalized in patients with LGG, especially not early on after completion of RT.

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