Deep Ensemble Model for Quantitative Optical Property and Chromophore Concentration Images of Biological Tissues

IF 13.7
Bingbao Yan;Bowen Song;Chang Ge;Xinman Yin;Wenchao Jia;Gen Mu;Yanyu Zhao
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Abstract

The ability to quantify widefield tissue optical properties (OPs, i.e., absorption and scattering) has major implications on the characterization of various physiological and disease processes. However, conventional image processing methods for tissue optical properties are either limited to qualitative analysis, or have tradeoffs in speed and accuracy. The key to quantification of optical properties is the extraction of amplitude maps from reflectance images under sinusoidal illumination of different spatial frequencies. Conventional three-phase demodulation (TPD) method has been demonstrated for the mapping of OPs, but it requires as many as 14 measurement images for accurate OP extraction, which leads to limited throughput and hinders practical translation. Although single-phase demodulation (SPD) method has been proposed to map OPs with a single measurement image, it is typically subject to image artifacts and decreased measurement accuracy. To tackle those challenges, here we develop a deep ensemble model (DEM) that can map tissue optical properties with high accuracy in a single snapshot, increasing the measurement speed by $14\times $ compared to conventional TPD method. The proposed method was validated with measurements on an array of optical phantoms, ex vivo tissues, and in vivo tissues. The errors for OP extraction were $0.83~\pm ~5.0$ % for absorption and $0.40~\pm ~1.9$ % for reduced scattering, dramatically lower than that of the state-of-the-art SPD method ( $2.5~\pm ~15$ % for absorption and - $1.2~\pm ~11$ % for reduced scattering). It was further demonstrated that while trained with data from a single wavelength, the DEM can be directly applied to other wavelengths and effectively obtain optical property and chromophore concentration images of biological tissues. Together, these results highlight the potential of DEM to enable new capabilities for quantitative monitoring of tissue physiological and disease processes.
生物组织定量光学性质和发色团浓度图像的深系综模型
量化宽视场组织光学特性(OPs,即吸收和散射)的能力对各种生理和疾病过程的表征具有重大意义。然而,组织光学特性的传统图像处理方法要么局限于定性分析,要么在速度和准确性方面存在折衷。光学特性量化的关键是从不同空间频率正弦光照下的反射图像中提取振幅图。传统的三相解调(TPD)方法已被证明用于OP的映射,但它需要多达14个测量图像才能准确提取OP,这导致吞吐量有限,阻碍了实际翻译。虽然已经提出了单相解调(SPD)方法来用单个测量图像映射OPs,但它通常会受到图像伪影和测量精度降低的影响。为了解决这些挑战,我们开发了一种深度集成模型(DEM),可以在单次快照中高精度地绘制组织光学特性,与传统的TPD方法相比,测量速度提高了14倍。所提出的方法被光学幻影、离体组织和体内组织阵列的测量验证。OP提取的吸收误差为$0.83~\pm ~5.0$ %,减少散射误差为$0.40~\pm ~1.9$ %,显著低于最先进的SPD方法(吸收误差为$2.5~\pm ~15$ %,减少散射误差为- $1.2~\pm ~11$ %)。进一步证明,在单一波长数据训练的情况下,DEM可以直接应用于其他波长,有效地获得生物组织的光学性质和发色团浓度图像。总之,这些结果突出了DEM在组织生理和疾病过程定量监测方面的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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