Abstract

Measurement of blood oxygen saturation (sO2) by optical imaging oximetry provides invaluable insight into local tissue functions and metabolism. Despite different embodiments and modalities, all label-free optical-imaging oximetry techniques utilize the same principle of sO2-dependent spectral contrast from haemoglobin. Traditional approaches for quantifying sO2 often rely on analytical models that are fitted by the spectral measurements. These approaches in practice suffer from uncertainties due to biological variability, tissue geometry, light scattering, systemic spectral bias, and variations in the experimental conditions. Here, we propose a new data-driven approach, termed deep spectral learning (DSL), to achieve oximetry that is highly robust to experimental variations and, more importantly, able to provide uncertainty quantification for each sO2 prediction. To demonstrate the robustness and generalizability of DSL, we analyse data from two visible light optical coherence tomography (vis-OCT) setups across two separate in vivo experiments on rat retinas. Predictions made by DSL are highly adaptive to experimental variabilities as well as the depth-dependent backscattering spectra. Two neural-network-based models are tested and compared with the traditional least-squares fitting (LSF) method. The DSL-predicted sO2 shows significantly lower mean-square errors than those of the LSF. For the first time, we have demonstrated en face maps of retinal oximetry along with a pixel-wise confidence assessment. Our DSL overcomes several limitations of traditional approaches and provides a more flexible, robust, and reliable deep learning approach for in vivo non-invasive label-free optical oximetry.

Highlights

  • Microvascular systems deliver oxygen to support cellular metabolism and maintain biological functions

  • Two deep spectral learning (DSL) models are investigated, including a 1D fully connected neural network (FNN) and a 1D convolutional neural network (CNN), the network architectures of which are shown in Fig. 2a, b, respectively

  • Our results show that both DSL models significantly outperform the least-squares fitting (LSF), in terms of both the estimation accuracy and the robustness to experimental variations

Read more

Summary

Introduction

Microvascular systems deliver oxygen to support cellular metabolism and maintain biological functions. The measurement of microvascular sO2 can help in assessing the local tissue oxygenation and provide invaluable insight into local tissue metabolism, inflammation, and oxygenrelated pathologies. Several non-invasive and label-free optical-imaging oximetry techniques have been developed to measure microvascular sO2 Despite their differences, the fundamental mechanism is the same, being based on the sO2-dependent spectral contrast from haemoglobin[6]. The spectral measurement is related to sO2 through a complex physical model incorporating tissue geometry, heterogeneous tissue scattering, light attenuation and propagation, and imaging optical instruments. This model is often simplified and analytically formulated under different approximations and assumptions. Examples include spatial frequency domain imaging[7,8] in the diffusive regime under the P3 approximation, multiwavelength imaging[9,10,11,12] and visible light optical coherence tomography (vis-OCT)[13,14,15] in the ballistic regime

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call