García Héctor A, Vera Demián A, Waks Serra María V, Baez Guido R, Iriarte Daniela I, Pomarico Juan A
CIFICEN (UNCPBA-CONICET-CICPBA), Pinto 399, B7000GHG Tandil, Argentina.
Biomed Opt Express. 2022 Mar 28;13(4):2516-2529. doi: 10.1364/BOE.449514. eCollection 2022 Apr 1.
Functional near infrared spectroscopy (fNIRS) is a valuable tool for assessing oxy- and deoxyhemoglobin concentration changes (Δ[HbO] and Δ[HbR], respectively) in the human brain. To this end, photon pathlengths in tissue are needed to convert from light attenuation to Δ[HbO] and Δ[HbR]. Current techniques describe the human head as a homogeneous medium, in which case these pathlengths are easily computed. However, the head is more appropriately described as a layered medium; hence, the partial pathlengths in each layer are required. The current way to do this is by means of Monte Carlo (MC) simulations, which are time-consuming and computationally expensive. In this work, we introduce an approach to theoretically calculate these partial pathlengths, which are computed several times faster than MC simulations. Comparison of our approach with MC simulations show very good agreement. Results also suggest that these analytical expressions give much more specific information about light absorption in each layer than in the homogeneous case.
功能近红外光谱技术(fNIRS)是评估人类大脑中氧合血红蛋白和脱氧血红蛋白浓度变化(分别为Δ[HbO]和Δ[HbR])的一种有价值的工具。为此,需要组织中的光子路径长度来将光衰减转换为Δ[HbO]和Δ[HbR]。当前技术将人类头部描述为均匀介质,在这种情况下,这些路径长度很容易计算。然而,将头部更恰当地描述为分层介质;因此,需要每层中的部分路径长度。目前实现这一点的方法是通过蒙特卡罗(MC)模拟,这既耗时又计算成本高昂。在这项工作中,我们引入了一种理论计算这些部分路径长度的方法,其计算速度比MC模拟快几倍。我们的方法与MC模拟的比较显示出非常好的一致性。结果还表明,这些解析表达式比均匀介质情况下能提供关于每层光吸收的更具体信息。