Objective: To study the 3.0T multivoxel proton magnetic spectroscopy(1H-MRS) findings in brain glioma and to investigate the correlation between Cho/Cr ratio and expression of Ki-67. Methods: Fifty-seven patients of brain gliomas were studied, including 28 cases of low-grade group(grade Ⅰ~Ⅱ), 29 cases of high-grade group(grade Ⅲ~Ⅳ). All of them underwent 3.0T 1H-MRS examination before operation. The Cho/Cr ratios were detected. We analyzed the correlation between Cho/Cr ratio and pathological grade of gliomas. Ki-67 immunohistochemical staining and Ki-67 labeling index(Ki-67LI) were measured after operation. We also analyzed the correlation between Ki-67LI and the pathological grade, the Cho/Cr ratio of gliomas. Results: ①Significant differences were found in the ratios of Cho/Cr between low grade gliomas and high grade gliomas(P<0.001). The ratio of Cho/Cr was positively correlated with the tumor grade(r=0.616, P<0.001). The area under the curve(AUC) of Cho/Cr was 0.856. The threshold value of Cho/Cr ratio for differential diagnosis high grade and low grade brain gliomas was 2.44, the sensitivity was 79.3%, the specificity was 82.1%. ②Ki-67LI of low grade glioma was (3.41±2.35)%, Ki-67LI of high grade glioma was (19.78±11.45)%, the difference was statistically significant(Z=-0.617, P<0.001). The Ki-67LI was positively correlated with the tumor grade and the Cho/Cr ratio(r=0.804, P<0.001). Conclusion: The Cho/Cr ratios of gliomas are correlated with the expression of Ki-67. It may be a useful image index, which can evaluate the proliferation activity and malignancy degree of glioma, without invasion. And it may be helpful in the clinical treatment and prognosis assessment.
Key words
Glioma /
Ki-67 antigen /
Magnetic resonance imaging
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
References
[1]Ostrom QT, Gittleman H, Farah P, et al. CBTRUS statistical report: Primary brain and central nervous system tumors diagnosed in the United States in 2006-2010[J]. Neurooncology, 2013, 15(Suppl 2): ii1-56.
[2]梅莉,郑建刚,许建兴,等. 多体素1H磁共振波谱在胶质瘤诊断中的价值[J]. 南京医科大学学报,2009,29(8):1169-1171.
[3]Terzi A, Saglam EA, Barak A, et al. The significance of immunohistochemical expression of Ki-67, p53, p21, and p16 in meningiomas tissue arrays[J]. Pathol Res Pract, 2008, 204(5): 305-314.
[4]贺丹,杨丽,朱青峰,等. 1H-MRS在颅内胶质瘤分级中的应用价值[J]. 中国临床医学影像杂志,2011,22(2):77-82.
[5]姜亮,刘文,肖朝勇,等. 探讨联合应用MRS和DWI在脑胶质瘤分级中的诊断价值[J]. 临床放射学杂志,2015,34(4):514-519.
[6]Weybright P, Maly P, Gomez-Hassan D, et al. MR spectroscopy in the evaluation of recurrent contrast-enhancing lesions in the posterior fossa after tumor treatment[J]. Neuroradiology, 2004, 46(7): 541-549.
[7]项威,陈东,胡继良,等. 联合应用MRS及DWI对胶质瘤及侵袭性进行临床评估[J]. 中国微侵袭神经外科杂志,2014,19(6):241-244.
[8]楼晓剑,蒋定尧,倪丽欣,等. 脑星形细胞瘤3T MRI 3D多体素1H-MRS术前分级及病理对照研究[J]. 中国CT和MRI杂志,2015,13(11):16-20.
[9]Zeng Q, Liu H, Zhang K, et al. Noninvasive evaluation of cerebral glioma grade by using multivoxel 3D proton MR spectroscopy[J]. Magn Reson Imaging, 2011, 29(1): 25-31.
[10]Brodzki A, Lopuszyński W, Brodzki P, et al. Diagnostic and prognostic value of cellular proliferation assessment with Ki-67 protein in dogs suffering from benign and malignant perianal tumors[J]. Folia Biol(Krakow), 2014, 62(3): 235-241.
[11]Wykosky J, Fenton T, Furnari F, et al. Therapeutic targeting of epidermal growth factor receptor in human cancer: successes and limitations[J]. Chin J Cancer, 2011, 30(1): 5-12.
[12]Kayaselcuk F, Zorludemir S, Gumurduhu D, et al. PCNA and Ki-67 in central nervous system tumors: correlation with the histological type and grade[J]. Neurooncology, 2002, 57(2): 115-121.
[13]Yamashita Y, Kasugai I, Sato M, et al. CDC25A mRNA levels significantly correlate with Ki-67 expression in human glioma samples[J]. J Neurooncol, 2010, 100(1): 43-49.
[14]Qu DW, Xu HS, Han XJ, et al. Expression of Cyclin D1 and Ki-67 proteins in gliomas and its clinical significance[J]. Eur Rev Med Pharmacol Sci, 2014, 18(4): 516-519.
[15]Shimizu H, Kumabe T, Shirane R, et al. Correlation between choline level measured by proton MR spectroscopy and Ki-67 labeling index in gliomas[J]. AJNR, 2000, 21(4): 659-665.
[16]Tamiya T, Kinoshita K, Ono Y, et al. Proton magnetic resonance spectroscopy reflects cellular proliferative activity in astrocytomas[J]. Neuroradiology, 2000, 42(5): 333-338.