Cumulant expansion framework for internal gradient distributions tensors

Leonardo A. Pedraza Pérez , Gonzalo A. Álvarez
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Abstract

Magnetic resonance imaging is a powerful, non invasive tool for medical diagnosis. The low sensitivity for detecting the nuclear spin signals, typically limits the image resolution to several tens of micrometers in preclinical systems and millimeters in clinical scanners. Other sources of information, derived from diffusion processes of intrinsic molecules such as water in the tissues, allow getting morphological information at micrometric and submicrometric scales as potential biomarkers of several pathologies. Here we consider extracting this morphological information by probing the distribution of internal magnetic field gradients induced by the heterogeneous magnetic susceptibility of the medium. We use a cumulant expansion to derive the dephasing on the spin signal induced by the molecules that explore these internal gradients while diffusing. Based on the cumulant expansion, we define internal gradient distributions tensors (IGDT) and propose modulating gradient spin echo sequences to probe them. These IGDT contain microstructural morphological information that characterize porous media and biological tissues. We evaluate the IGDT effects on the magnetization decay with typical conditions of brain tissue and show that their effects can be experimentally observed. Our results thus provide a framework for exploiting IGDT as quantitative diagnostic tools.

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内梯度分布张量的累积展开框架
磁共振成像是一种强大的、非侵入性的医学诊断工具。检测核自旋信号的低灵敏度通常限制了临床前系统的图像分辨率为几十微米,临床扫描仪的图像分辨率为毫米。其他信息来源,来自内部分子的扩散过程,如组织中的水,允许在微米和亚微米尺度上获得形态学信息,作为几种病理的潜在生物标志物。在这里,我们考虑通过探测由介质的非均质磁化率引起的内部磁场梯度分布来提取这些形态信息。我们使用累积展开来推导由分子在扩散时探索这些内部梯度所引起的自旋信号的消相。在累积展开的基础上,定义了内部梯度分布张量(IGDT),并提出了调制梯度自旋回波序列来探测它们。这些IGDT包含表征多孔介质和生物组织的微观结构形态学信息。我们在典型的脑组织条件下评估了IGDT对磁化衰减的影响,并表明它们的影响可以在实验中观察到。因此,我们的结果为利用IGDT作为定量诊断工具提供了一个框架。
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