Department of Neurosurgery, Sanbo Brain Hospital, Capital Medical University, Beijing, China.
Department of Neurosurgery, Yantaishan Hospital, Yantai, China.
Sci Rep. 2019 Nov 19;9(1):17080. doi: 10.1038/s41598-019-53629-w.
Susceptibility-weighted imaging (SWI) can be a useful tool to depict vascular structures in brain tumors as well as micro-bleedings, which represent tumor invasion to blood vessels and could also be representative of tumoral angiogenesis. In this study, we investigated the relationship between SWI features and glioma grades, and the expression of key molecular markers isocitrate dehydrogenase 1 (IDH1), O-6-methylguanine-DNA methyltransferase (MGMT), and 1p19q. The gliomas were graded according to the intratumoral susceptibility signals (ITSS). We used the Mann-Whitney test to analyze the relationship between ITSS grades and the pathological level and status of these markers. Additionally, the area under the curve (AUC) was used to determine the predictive value of glioma SWI characteristics for the molecular marker status. In these cases, the ITSS grades of low-grade gliomas (LGG) were significantly lower than those of high-grade gliomas (HGG). Similarly, the ITSS grades of gliomas with IDH1 mutations and MGMT methylation were significantly lower than those of gliomas with Wild-type IDH1 and unmethylated MGMT. However, ITSS grades showed no relationship with 1p19q deletion status, while they did show significant predictive ability for glioma grade, IDH1 mutation, and MGMT methylation. These findings indicate an association between some molecular markers and cerebral microbleeds in gliomas, providing a new avenue for non-invasive prediction of molecular genetics in gliomas and an important basis for preoperative personalized surgical treatment based on molecular pathology.
磁敏感加权成像(SWI)可以成为一种有用的工具,用于描绘脑肿瘤中的血管结构以及微出血,这些微出血代表肿瘤对血管的侵犯,也可能代表肿瘤血管生成。在这项研究中,我们研究了 SWI 特征与胶质瘤分级之间的关系,以及关键分子标志物异柠檬酸脱氢酶 1(IDH1)、O-6-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)和 1p19q 的表达。根据肿瘤内磁化率信号(ITSS)对胶质瘤进行分级。我们使用曼-惠特尼检验来分析 ITSS 分级与这些标志物的病理水平和状态之间的关系。此外,我们还使用曲线下面积(AUC)来确定胶质瘤 SWI 特征对分子标志物状态的预测价值。在这些病例中,低级别胶质瘤(LGG)的 ITSS 分级明显低于高级别胶质瘤(HGG)。同样,IDH1 突变和 MGMT 甲基化的胶质瘤的 ITSS 分级明显低于 IDH1 野生型和 MGMT 未甲基化的胶质瘤。然而,ITSS 分级与 1p19q 缺失状态无关,而与胶质瘤分级、IDH1 突变和 MGMT 甲基化具有显著的预测能力。这些发现表明一些分子标志物与脑肿瘤中的微出血之间存在关联,为胶质瘤的非侵入性预测分子遗传学提供了新途径,也为基于分子病理学的术前个体化手术治疗提供了重要依据。