Dynamic contrast enhanced (DCE) MRI estimation of vascular parameters using knowledge-based adaptive models.

Dynamic contrast enhanced (DCE) MRI estimation of vascular parameters using knowledge-based adaptive models.
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DOI:
10.1038/s41598-023-36483-9
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发表时间:
2023-06-14
期刊:
影响因子:
4.6
通讯作者:
--
中科院分区:
综合性期刊3区
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--
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我们介绍并验证了四个自适应模型(AM),以执行基于生理学的嵌套模型选择(NMS)估计等微血管参数,如前向体积传输常数,Ktranss,血浆体积分数,VP,血管外,细胞外空间,VE,直接从动态对比度增强(DCE)MRI原始信息,而不需要动脉输入功能(AIF)。在66只植入人U-251癌细胞的免疫受损RNU大鼠中,DCE-MRI研究使用组平均放射性AIF和扩展的基于Patlak的NMS范例估计药代动力学(PK)参数。从原始DCE-MRI信息中提取的190个特征用于构建和验证(嵌套交叉验证,NCV)4个AM,以估计基于模型的区域及其3个PK参数。一个基于NMS的先验知识被用来微调的AM,以提高其性能。与传统分析相比,AM产生了血管参数的稳定图和受AIF分散影响较小的嵌套模型区域。对于嵌套模型区域、vp、Ktranss和ve的预测,AM的性能(NCV测试队列的相关系数和校正R平方)分别为:0.914/0.834、0.825/0.720、0.938/0.880和0.890/0.792。本研究证明了AM的应用,其相对于常规方法加快并改善了基于DCE-MRI的肿瘤和正常组织的微血管特性的量化。
We introduce and validate four adaptive models (AMs) to perform a physiologically based Nested-Model-Selection (NMS) estimation of such microvascular parameters as forward volumetric transfer constant, Ktrans, plasma volume fraction, vp, and extravascular, extracellular space, ve, directly from Dynamic Contrast-Enhanced (DCE) MRI raw information without the need for an Arterial-Input Function (AIF). In sixty-six immune-compromised-RNU rats implanted with human U-251 cancer cells, DCE-MRI studies estimated pharmacokinetic (PK) parameters using a group-averaged radiological AIF and an extended Patlak-based NMS paradigm. One-hundred-ninety features extracted from raw DCE-MRI information were used to construct and validate (nested-cross-validation, NCV) four AMs for estimation of model-based regions and their three PK parameters. An NMS-based a priori knowledge was used to fine-tune the AMs to improve their performance. Compared to the conventional analysis, AMs produced stable maps of vascular parameters and nested-model regions less impacted by AIF-dispersion. The performance (Correlation coefficient and Adjusted R-squared for NCV test cohorts) of the AMs were: 0.914/0.834, 0.825/0.720, 0.938/0.880, and 0.890/0.792 for predictions of nested model regions, vp, Ktrans, and ve, respectively. This study demonstrates an application of AMs that quickens and improves DCE-MRI based quantification of microvasculature properties of tumors and normal tissues relative to conventional approaches.
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