利用 7.0 T 的高分辨率 31P MR 光谱成像绘制胶质瘤的全脑细胞内 pH 图。

IF 5.6 Q1 ONCOLOGY Radiology. Imaging cancer Pub Date : 2024-01-01 DOI:10.1148/rycan.220127
Daniel Paech, Nina Weckesser, Vanessa L Franke, Johannes Breitling, Steffen Görke, Katerina Deike-Hofmann, Antje Wick, Moritz Scherer, Andreas Unterberg, Wolfgang Wick, Martin Bendszus, Peter Bachert, Mark E Ladd, Heinz-Peter Schlemmer, Andreas Korzowski
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引用次数: 0

摘要

与正常组织相比,恶性肿瘤通常表现出相反的 pH 梯度,细胞外 pH 值偏酸性,而细胞内 pH 值(pHi)偏碱性。在这项前瞻性研究中,采用 7.0 T 高分辨率磷 31 (31P) 光谱核磁共振成像技术对胶质瘤中的 pHi 值进行了量化,并将 pHi 变化与组织病理学发现联系起来。2018年9月至2019年11月期间,共纳入了12名经组织病理学证实的新诊断胶质瘤患者(平均年龄为58岁±18岁[SD];男性7名,女性5名)。31P光谱核磁共振成像扫描是使用双共振31P/1H相控阵头线圈和三维(3D)31P化学位移成像序列(5.7 mL体素体积)采集的,并在7.0-T全身系统上执行。对整个肿瘤体积(WTV)、坏死、钆增强和非增强 T2(NCE T2)高密度的肿瘤亚区以及正常显示的白质(NAWM)进行了三维容积分割,并比较了 pHi 值。Spearman 相关性用于评估 pHi 与增殖指数 Ki-67 之间的关系。在所有研究参与者中,WTV的平均pHi值(7.057 ± 0.024)高于NAWM(7.006 ± 0.012;P < .001)。在 8 名患有高级别胶质瘤的参与者中,与 NAWM(7.004 ± 0.014;所有 P <.01)相比,所有肿瘤亚分区(坏死,7.075 ± 0.033;钆增强,7.075 ± 0.024;NCE T2 高密度,7.043 ± 0.015)的 pHi 值均升高。WTV 的 pHi 值与 Ki-67 呈正相关(R2 = 0.74,r = 0.78,P = .001)。总之,7.0 T 的 31P 光谱核磁共振成像可高分辨率地量化胶质瘤的 pHi 值,pHi 值的改变与 Ki-67 增殖指数相关,有助于诊断和治疗监测。关键词31P MRSI pH值 胶质瘤 胶母细胞瘤 超高场磁共振成像 成像生物标志物 7特斯拉 本文有补充材料。© RSNA, 2023.
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Whole-Brain Intracellular pH Mapping of Gliomas Using High-Resolution 31P MR Spectroscopic Imaging at 7.0 T.

Malignant tumors commonly exhibit a reversed pH gradient compared with normal tissue, with a more acidic extracellular pH and an alkaline intracellular pH (pHi). In this prospective study, pHi values in gliomas were quantified using high-resolution phosphorous 31 (31P) spectroscopic MRI at 7.0 T and were used to correlate pHi alterations with histopathologic findings. A total of 12 participants (mean age, 58 years ± 18 [SD]; seven male, five female) with histopathologically proven, newly diagnosed glioma were included between September 2018 and November 2019. The 31P spectroscopic MRI scans were acquired using a double-resonant 31P/1H phased-array head coil together with a three-dimensional (3D) 31P chemical shift imaging sequence (5.7-mL voxel volume) performed with a 7.0-T whole-body system. The 3D volumetric segmentations were performed for the whole-tumor volumes (WTVs); tumor subcompartments of necrosis, gadolinium enhancement, and nonenhancing T2 (NCE T2) hyperintensity; and normal-appearing white matter (NAWM), and pHi values were compared. Spearman correlation was used to assess association between pHi and the proliferation index Ki-67. For all study participants, mean pHi values were higher in the WTV (7.057 ± 0.024) compared with NAWM (7.006 ± 0.012; P < .001). In eight participants with high-grade gliomas, pHi was increased in all tumor subcompartments (necrosis, 7.075 ± 0.033; gadolinium enhancement, 7.075 ± 0.024; NCE T2 hyperintensity, 7.043 ± 0.015) compared with NAWM (7.004 ± 0.014; all P < .01). The pHi values of WTV positively correlated with Ki-67 (R2 = 0.74, r = 0.78, P = .001). In conclusion, 31P spectroscopic MRI at 7.0 T enabled high-resolution quantification of pHi in gliomas, with pHi alteration associated with the Ki-67 proliferation index, and may aid in diagnosis and treatment monitoring. Keywords: 31P MRSI, pH, Glioma, Glioblastoma, Ultra-High-Field MRI, Imaging Biomarker, 7 Tesla Supplemental material is available for this article. © RSNA, 2023.

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