Modeling the diffusion‐weighted imaging signal for breast lesions in the b = 200 to 3000 s/mm2 range: quality of fit and classification accuracy for different representations

峰度 阿卡克信息准则 接收机工作特性 核医学 医学 数学 曲线下面积 磁共振弥散成像 噪音(视频) 高斯分布 放射科 统计 磁共振成像 计算机科学 物理 人工智能 内科学 量子力学 图像(数学)
作者
Igor Vidić,Liv Egnell,Neil P. Jerome,Nathan S. White,Roshan Karunamuni,Rebecca Rakow‐Penner,Anders M. Dale,Tone F. Bathen,Pål Erik Goa
出处
期刊:Magnetic Resonance in Medicine [Wiley]
卷期号:84 (2): 1011-1023 被引量:17
标识
DOI:10.1002/mrm.28161
摘要

Purpose To evaluate different non‐Gaussian representations for the diffusion‐weighted imaging (DWI) signal in the b‐value range 200 to 3000 s/mm 2 in benign and malignant breast lesions. Methods Forty‐three patients diagnosed with benign (n = 18) or malignant (n = 25) tumors of the breast underwent DWI (b‐values 200, 600, 1200, 1800, 2400, and 3000 s/mm 2 ). Six different representations were fit to the average signal from regions of interest (ROIs) at different b‐value ranges. Quality of fit was assessed by the corrected Akaike information criterion (AICc), and the Friedman test was used for assessing representation ranks. The area under the curve (AUC) of receiver operating characteristic curves were used to evaluate the power of derived parameters to differentiate between malignant and benign lesions. The lesion ROI was divided in central and peripheral parts to assess potential effect of heterogeneity. Sensitivity to noise‐floor correction was also evaluated. Results The Padé exponent was ranked as the best based on AICc, whereas 3 models (kurtosis, fractional, and biexponential) achieved the highest AUC = 0.99 for lesion differentiation. The monoexponential model at b max = 600 s/mm 2 already provides AUC = 0.96, with considerably shorter acquisition time and simpler analysis. Significant differences between central and peripheral parts of lesions were found in malignant lesions. The mono‐ and biexponential models were most stable against varying degrees of noise‐floor correction. Conclusion Non‐Gaussian representations are required for fitting of the DWI curve at high b‐values in breast lesions. However, the added clinical value from the high b‐value data for differentiation of benign and malignant lesions is not clear.
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