低时间分辨率和高时间分辨率DCE-MRI纹理分析在区分乳腺病变和背景增强中的表现。

IF 1.6 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
American journal of translational research Pub Date : 2025-08-15 eCollection Date: 2025-01-01 DOI:10.62347/KKUZ9662
Yufeng Liu, Changliang Wang, Jianjun Wu, Fengchun Xiao, Chundan Wang
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引用次数: 0

摘要

目的:探讨基于纹理分析的动态对比增强MRI (DCE-MRI)对乳腺病变和背景增强(BE)的诊断潜力。方法:回顾性分析术前行高时间分辨率DCE-MRI(1+26期)的62例患者,其中恶性病变39例,良性病变23例。对照组78例患者术前行低颞部分辨率DCE-MRI(1+5期),其中恶性病变46例,良性病变32例。所有患者同时接受常规T1WI、T2WI MRI扫描和DCE-MRI检查。采用双室扩展Tofts模型获得定量参数,计算药代动力学参数:体积传递常数(Ktrans)、速率常数(Kep)、血管外细胞外体积分数(Ve)和血浆体积分数(Vp)。基于Ktrans贴图提取纹理特征。对病灶中心、周围周边区域和BE感兴趣的区域进行了划定。采用受试者工作特征(Receiver operating characteristic, ROC)分析评价Ktrans纹理特征模型的诊断性能。结果:高时间分辨率DCE-MRI与低时间分辨率DCE-MRI的药代动力学参数差异有统计学意义(P < 0.05)。恶性组高时间分辨率DCE-MRI病变区域平均Ktrans值与病理分级显著相关(r = 0.400, P = 0.012)。两个DCE-MRI组在病变、病灶周围和BE区的Ktrans、Kep、Ve、Vp和峰值时间(time to peak, TTP)的平均值有显著差异。在良恶性病变的鉴别上,ROC分析显示,高时间分辨率DCE-MRI在病灶中心BE区良恶性病变的鉴别上有轻微但显著的优势。结论:基于高时间分辨率DCE-MRI的纹理分析可能潜在地提高乳腺癌的诊断性能。具体而言,结合病灶、BE面积和Ktrans-mean参数有助于乳腺病变的诊断、背景增强和恶性肿瘤的病理分级。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Performance of low- and high-temporal-resolution DCE-MRI texture analysis in distinguishing breast lesions from background enhancement.

Objectives: To investigate the diagnostic potential of texture-based analysis of dynamic contrast-enhanced MRI (DCE-MRI) for breast lesions and background enhancement (BE).

Methods: This retrospective study analyzed 62 patients who underwent preoperative high-temporal resolution DCE-MRI (1+26 phases), including 39 malignant and 23 benign lesions. A control group of 78 patients received preoperative low-temporal resolution DCE-MRI (1+5 phases), comprising 46 malignant and 32 benign lesions. All patients also underwent conventional T1WI, T2WI MRI scans, and DCE-MRI. Quantitative parameters were obtained using a two-compartment Extended Tofts model, calculating pharmacokinetic parameters: volume transfer constant (Ktrans), rate constant (Kep), extravascular extracellular volume fraction (Ve), and fractional plasma volume (Vp). Texture features based on the Ktrans map were extracted. The region of interest for the lesion center, surrounding peripheral area, and BE was delineated. Receiver operating characteristic (ROC) analysis was used to evaluate the diagnostic performance of the Ktrans texture features model.

Results: Pharmacokinetic parameters significantly differed between high-temporal resolution and low-temporal resolution DCE-MRI (P < 0.05). In the malignant group, the average Ktrans of the lesion area from high-temporal resolution DCE-MRI was significantly correlated with pathological grading (r = 0.400, P = 0.012). There were significant differences in the mean values of Ktrans, Kep, Ve, Vp and time to peak (TTP) between the two DCE-MRI groups across the lesion, peri-lesional, and BE areas. In the differentiation between benign and malignant lesions, ROC analysis demonstrated that high-temporal resolution DCE-MRI provided slight but significant advantages in differentiating benign and malignant lesions in the lesion center, BE areas.

Conclusions: Texture analysis based on high-temporal resolution DCE-MRI may potentially improve breast cancer diagnostic performance. Specifically, combining the lesion, BE area, and Ktrans-mean parameters contributes to the diagnosis of breast lesions, background enhancement, and the pathological grading of malignant tumors.

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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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