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表观扩散系数直方图鉴别弥漫性较低级别脑胶质瘤分子亚型的价值
引用本文:刘丹,徐婧梅,廖鸿帆,文明.表观扩散系数直方图鉴别弥漫性较低级别脑胶质瘤分子亚型的价值[J].中国医学科学院学报,2020,42(4):444-451.
作者姓名:刘丹  徐婧梅  廖鸿帆  文明
作者单位:重庆医科大学附属第一医院放射科,重庆 400016
基金项目:国家自然科学基金(81171366)
摘    要:目的 研究基于肿瘤全域的表观扩散系数(ADC)信号灰度直方图鉴别弥漫性较低级别胶质瘤分子亚型的价值。方法 回顾经手术及病理证实为WHO Ⅱ、Ⅲ级胶质瘤,术前接受过头颅磁共振成像平扫、增强及扩散加权成像检查的55例患者的病理及影像学资料。先将其分为异柠檬酸脱氢酶(IDH)突变(IDH mut)组和IDH野生(IDH wt)组,再将IDH mut组分为IDH突变伴1p19q联合缺失(IDH mut1p19q del)组和IDH突变不伴1p19q联合缺失(IDH mut1p19q int)组。其中IDH wt组14例、IDH mut1p19q int组19例、IDH mut1p19q del组22例。记录不同分子亚型组的ADC直方图参数,包括平均值、最小值、 ADC5%、ADC10%、 ADC25%、 ADC50%、 ADC75%、 ADC90%、ADC95%、最大值、众数、峰度、偏度、标准差、不均一性、极差、熵值,并采用独立样本t检验(正态分布)或Mann-Whitney U检验(偏态分布)比较。采用受试者工作特征曲线(ROC)评价ADC直方图参数鉴别诊断WHO Ⅱ、Ⅲ级胶质瘤不同分子亚型的效能。结果 IDH mut组的 ADC75%(P=0.021)、 ADC90%(P=0.015)、ADC95%(P=0.014)、最大值(P=0.035)、标准差(P=0.001)、不均一性(P=0.001)和极差(P=0.009)均低于IDH wt组,而最小值(P=0.031)和峰度(P=0.020)则高于IDH wt组,差异有统计学意义。IDH mut1p19q del组的平均值(P=0.010)、ADC5%(P=0.016)、ADC10%(P=0.012)、 ADC25%(P=0.007)、 ADC50%(P=0.005)、ADC75%(P=0.015)及众数(P=0.002)均低于IDH mut1p19q int组。不均一性鉴别IDH wt组和IDH mut组的效能优于其他参数,ROC曲线下面积为0.811,以0.229为截断值鉴别二者的敏感度和特异度分别为85.7%和73.2%;众数鉴别IDH mut1p19q del组和IDH mut1p19q int组的效能高于其他参数,ROC曲线下面积为0.744,以1448.75×10 -6mm 2/s为截断值鉴别二者的灵敏度和特异度分别为57.9%和90.9%。结论 基于肿瘤全域感兴趣区的ADC信号强度直方图可以为弥漫性较低级别胶质瘤分子亚型的鉴别提供更多信息。

关 键 词:胶质瘤  分子病理分型  扩散加权成像  直方图  
收稿时间:2019-06-03

Apparent Diffusion Coefficient Histogram Analysis:Differentiation of Genetic Subtypes of Diffuse Lower-grade Gliomas
LIU Dan,XU Jingmei,LIAO Hongfan,WEN Ming.Apparent Diffusion Coefficient Histogram Analysis:Differentiation of Genetic Subtypes of Diffuse Lower-grade Gliomas[J].Acta Academiae Medicinae Sinicae,2020,42(4):444-451.
Authors:LIU Dan  XU Jingmei  LIAO Hongfan  WEN Ming
Institution:Department of Radiology,the First Affiliated Hospital of Chongqing Medical University,Chongqing 400016,China
Abstract:Objective To explore the utility of apparent diffusion coefficient(ADC)histogram analysis for differentiating genetic subtypes of diffuse lower-grade gliomas. Methods A total of 55 patients with WHO grade Ⅱ/Ⅲ diffuse lower-grade gliomas who underwent preoperative routine brain magnetic resonance imaging and diffusion weighted imaging in our center were retrospectively evaluated.Among whom there were 14 patients with isocitrate dehydrogenase(IDH)wild-type gliomas(IDH wt group),19 patients with IDH-mutant 1p19q intact gliomas(IDH mut1p19q int group),and 22 patients with IDH-mutant 1p19q co-deleted gliomas(IDH mut1p19q del group).The whole-lesion ADC values derived from histogram analysis(including ADCmean,ADCminimum,ADC5%,ADC10%,ADC25%,ADC50%,ADC75%,ADC90%,ADC95%,ADCmaximum,mode,range,skewness,kurtosis,standard deviation,inhomogeneity,and entrophy)were measured for each patient.All parameters between the different genetic subtypes were compared by using the Student’s t test or Mann-Whitney U test.Receiver operating curve(ROC)analysis was used to assess the diagnostic performance of ADC histogram in distinguishing the different genetic subtypes. Results Compared with IDH wt group,the ADC75%(P=0.021),ADC90%(P=0.015),ADC95%(P=0.014),ADCmaximum (P=0.035),range(P=0.009),standard deviation(P=0.001)and inhomogeneity(P=0.001)were significantly lower in IDH mut group;in contrast,the ADCminimum (P=0.031)and kurtosis(P=0.020)of IDH mut group were significantly higher than those in IDH wt group.The ADCmean(P=0.010),ADC5%(P=0.016),ADC10%(P=0.012),ADC25%(P=0.007),ADC50%(P=0.005),ADC75%(P=0.015),and mode(P=0.002)were significantly higher in IDH mut1p19q int group than in IDH mut1p19q del group.Inhomogeneity achieved the highest area under ROC(AUC)(0.811)in differentiating IDH mut gliomas and IDH wt gliomas,with a cutoff value of 0.229;the sensitivity and specificity were 85.7% and 73.2%.The mode achieved the highest AUC(0.744)in differentiating IDH mut1p19q int gliomas and IDH mut1p19q del gliomas,with a cutoff value was 1448.75×10 -6 mm 2/s;the sensitivity and specificity were 57.9% and 90.9%.Conclusion ADC histograms analysis may be helpful to differentiate genetic subtypes in lower-grade gliomas.
Keywords:gliomas  molecular pathology typing  diffusion weighted imaging  histogram  
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