Prediction Models of IDH and ATRX Gene Status in Diffuse Gliomas Based on Visually Accessible Rembrandt Images Features

ATRX公司 组内相关 接收机工作特性 医学 曲线下面积 预测建模 相关性 病理 曲线下面积 对比度(视觉) 试验预测值 预测值 胶质瘤 对比度增强 预测标记 肿瘤科 癌症研究 核医学 相关系数 内科学 基因
作者
Yànhuá Lǐ,Mingxiao Wang,Jun Zhang,Xinyue Zhang,Shuo Sun,Yahong Tan,Guoli Liu,Lin Ma
出处
期刊:American Journal of Neuroradiology [American Society of Neuroradiology]
卷期号:47 (4): 980-988 被引量:1
标识
DOI:10.3174/ajnr.a9049
摘要

BACKGROUND AND PURPOSE: Identifying isocitrate dehydrogenase (IDH) mutation and α-thalassemia/mental retardation syndrome X-linked (ATRX) mutation status is helpful for diagnosis and specific classification of diffuse gliomas, while currently, the detection of IDH and ATRX status mainly relies on invasive methods. In this study, we aimed to predict IDH and ATRX mutation status of diffuse gliomas utilizing clinically available MRI Visually Accessible Rembrandt Images (VASARI) features. MATERIALS AND METHODS: =72) for ATRX mutation prediction. Two radiologists independently analyzed the patients' MR images based on the VASARI feature set. Multivariable logistic regression analysis was employed to develop the prediction models. Receiver operating characteristic (ROC) curves, calibration plots, and decision curve analysis (DCA) were utilized to validate the models and nomograms were developed to visualize the models. RESULTS: For IDH prediction, 6 VASARI features combined with age and relative ADC values contributed to the model, with the area under the curve (AUC) of 0.96 (0.94-0.98) in training set and 0.92 (0.88-0.97) in validation set. For ATRX prediction, 3 VASARI features combined with age and minimum ADC values contributed to the model, with the AUC of 0.76 (0.68-0.83) in training set and 0.71 (0.58-0.83) in validation set. The DCA and calibration plots further confirmed the clinical utility of the 2 nomograms for IDH and ATRX prediction. CONCLUSIONS: The integration of MRI VASARI features and clinical data demonstrates strong predictive capability for IDH mutation status and moderate predictive capability for ATRX status in diffuse gliomas.
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