Chawla Sanjeev, Lee Seung-Cheol, Mohan Suyash, Wang Sumei, Nasrallah MacLean, Vossough Arastoo, Krejza Jaroslaw, Melhem Elias R, Nabavizadeh S Ali
1 Departments of Radiology, Perelman School of Medicine at the University of Pennsylvania, USA.
2 Department of Pathology and Laboratory Medicine, Perelman School of Medicine at the University of Pennsylvania, USA.
Neuroradiol J. 2019 Aug;32(4):250-258. doi: 10.1177/1971400919846509. Epub 2019 May 3.
Elevated levels of choline are generally emphasized as marker of increased cellularity and cell membrane turnover in gliomas. In this study, we investigated the incidence rate of lack of choline/creatine and choline/water elevation in a population of grade I-III gliomas. A cohort of 41 patients with histopathologically confirmed gliomas underwent multi-voxel proton magnetic resonance spectroscopy on a 3 T magnetic resonance system prior to treatment. Peak areas for choline and myoinositol were measured from all voxels that exhibited hyperintensity on fluid-attenuated inversion recovery images and were normalized to creatine and unsuppressed water from each voxel. The average metabolite/creatine and metabolite/water ratios from these voxels were then computed. Similarly, average metabolite ratios were computed from normal brain parenchyma. Gliomas were considered for lack of choline elevation when choline/creatine and choline/water ratios from neoplastic regions were less than those from normal brain parenchyma regions. Six of 41 (14.6%) grade I-III gliomas showed lack of elevation for choline/creatine and choline/water ratios compared to normal brain parenchyma. Four of these six gliomas also demonstrated elevated levels of myoinositol/creatine ratio. All other gliomas ( = 35) had elevated choline levels from neoplastic regions relative to normal parenchyma. The sensitivity of choline/creatine or choline/water in determining a grade I-III glioma was 85.4%. These findings suggest that a lack of choline/creatine or choline/water elevation may be seen in some gliomas and low choline levels should not prevent us from considering the possibility of a grade I-III glioma.
胆碱水平升高通常被视为胶质瘤细胞增多和细胞膜更新增加的标志物。在本研究中,我们调查了I-III级胶质瘤患者群体中胆碱/肌酸缺乏和胆碱/水升高的发生率。41例经组织病理学确诊的胶质瘤患者在治疗前于3T磁共振系统上接受了多体素质子磁共振波谱检查。从所有在液体衰减反转恢复图像上表现为高信号的体素中测量胆碱和肌醇的峰面积,并将其与每个体素的肌酸和未抑制水进行归一化。然后计算这些体素的平均代谢物/肌酸和代谢物/水比率。同样,从正常脑实质计算平均代谢物比率。当肿瘤区域的胆碱/肌酸和胆碱/水比率低于正常脑实质区域时,胶质瘤被认为存在胆碱升高不足。41例I-III级胶质瘤中有6例(14.6%)与正常脑实质相比,胆碱/肌酸和胆碱/水比率升高不足。这6例胶质瘤中有4例还表现出肌醇/肌酸比率升高。所有其他胶质瘤(n = 35)肿瘤区域的胆碱水平相对于正常实质均升高。胆碱/肌酸或胆碱/水在确定I-III级胶质瘤中的敏感性为85.4%。这些发现表明,在一些胶质瘤中可能会出现胆碱/肌酸或胆碱/水升高不足的情况,低胆碱水平不应妨碍我们考虑I-III级胶质瘤的可能性。