Quantification of spatially localized MRS by a novel deep learning approach without spectral fitting

Abstract

PurposeTo propose a novel end‐to‐end deep learning model to quantify absolute metabolite concentrations from in vivo J‐point resolved spectroscopy (JPRESS) without using spectral fitting.MethodsA novel encoder‐decoder‐style neural network was created, which was trained to predict metabolite concentrations and individual component signals concurrently from 3T JPRESS data in the time domain. The training data set contained 100 000 samples created by spin‐density simulations using experimentally used RF pulses. Concentrations, phase, frequencies, linewidths, and T2 relaxation times in the training data set were varied over a large range with uniform distributions. Random synthesized noise and extraneous signals were added to the data set. Two thousand validation samples were created similarly to the training data set but with mean concentrations close to in vivo values. An in vivo test was conducted with 20 samples acquired from the human brain.ResultsBoth validation and in vivo test results showed that the proposed model successfully predicted metabolite concentrations as well as individual metabolite signals without involving spectral fitting, while extraneous peaks or unregistered signals were filtered out. Compared with the short‐TE spectral fitting by LCModel, the proposed method had the advantage that the undesired correlations between the estimated concentrations and noise levels and between metabolites were eliminated or substantially reduced.ConclusionThe proposed method provides a working deep learning model that directly maps in vivo JPRESS data to metabolite concentrations. Because spectral fitting is not used, the trained model does not depend on the assumptions associated with parameter tuning when applied to in vivo data.