Synopsis
Deep neural networks (DNN) recently have gained increasing interest in
neuroimaging research for different applications. However, it remains to be an
open question whether and how artificial neural networks can be used for
denoising neuroimaging data. In this study, we have designed a DNN network for
denoising task-based fMRI data. The result showed that DNN can efficiently
reduce physiological fluctuation and achieve more homogeneous fMRI activation
maps.
Introduction
Deep neural networks (DNN) recently have gained increasing interest in neuroimaging
research for different applications, such as automatic tissue/tumor segmentation,
group classification and age prediction [1]. However, it remains to be an open
question whether and how artificial neural networks can be used for denoising
neuroimaging data. The blood-oxygen-level dependent (BOLD) signal captured in
fMRI data is an indirect measure of neuronal activity and is contaminated by a
large proportion of non-neural fluctuations [2]. The non-neural fluctuation
introduced by these noise sources could considerably affect the result and
interpretation of any task-based fMRI experiments. In this study, we proposed a
DNN network to denoise task-based functional magnetic resonance imaging (fMRI)
data without explicitly modeling noise. Methods
Subjects: The structural and
functional MRI data used in this study were obtained from Human Connectome
Project (HCP) database (https://ida.loni.usc.edu/login.jsp). The working memory
task fMRI data were acquired from 88 healthy subjects (males, age 26-30 years
old). The minimally preprocessed fMRI data [2] with additional detrending step
were treated as raw fMRI data in our analysis. DNN architecture: The DNN network consists of four layers in
a sequential order, namely a 1-dimensional convolutional layer with V nodes, a long short-term memory (LSTM)
layer with L nodes, a
time-distributed fully-connected layer with K
nodes and a selection layer with a
single node, as shown in Fig.1. Each voxel is treated as a sample and each time
point is treated as a feature. The 1-dimensional convolutional layer, unlike a
fixed high-pass or low-pass filter, adaptively filters fMRI data. The LSTM
layer takes the information from previous time points to inform the current
time points, this property makes LSTM particularly useful for sequential data,
such as fMRI time series. The time-distributed fully-connected layer weights
the output of the LSTM layer and the selection
layer determines the output denoised fMRI time series. In the network, gray
matter (GM) voxels and non-GM (including white matter and ventricle) voxels are
treated as two input datasets but share exactly the same network. The
conventional cost function of DNN networks requires known true values or
classes, however, the true BOLD signal in fMRI data is not available. Instead,
a customized cost function is defined as the correlation difference between the
denoised GM and non-GM time series with task design matrix to optimize model
parameters. The correlation between time series and design matrix is calculated
by applying the general linear model. Analysis:
Multiple techniques were used to process fMRI data, including the proposed DNN
method, the ICA-based denoising technique FIX [3] with nuisance regression
included and 0.01-0.1 Hz temporal filtering (TF). GLM is applied to calculate the correlation
map between different denoised data and task design matrix for further
comparison.Results
With the hypothesis that the voxels having lower correlation with task design
matrix are less likely to be active in the task, the correlation difference
between 20% high-correlation voxels and 20% low-correlation voxels is calculated
to evaluate how well a method distinguishes active from inactive voxels. The
median values of correlation difference were 0.168, 0.137, 0.245, 0.344, and
0.374 for raw, FIX, FIX+TF, DNN, and FIX+DNN, respectively (see Fig.2a). The
subjects are expected to have similar brain correlation maps corresponding to
the working memory task. The Jaccard similarity coefficient indicates that the
similarity is considerably increased by DNN denoising and further improved with
additional FIX denoising. With the assistance of externally recorded respiratory
and cardiac signals, we have calculated the remaining physiological variance
after denoising. Physiological fluctuation accounts for the variance in the
denoised time series with median percentage as 7.7%, 4.8%, 3.6%, 4.4% and 4.0%
for raw, FIX, FIX+TF, DNN and FIX+DNN respectively. Compared to raw data, all
denoising techniques have significantly reduced physiological variance in the
time series with p<10-4. We have also
attempted to evaluate motion-related artifacts in the dataset, however,
motion-FC correlation barely has association with inter-node distance even in
the raw data (see Fig.2d) and thus no further steps are applied. In the
activation count maps [4] (Fig.3), DNN and FIX+DNN processed datasets have more
robust activation than the other three datasets in terms of cluster size and
magnitude. Discussion and Conclusion
In this study, a subject-level artificial neural network is designed to
denoise task-based fMRI data without assuming any explicit noise models. The result showed that DNN can efficiently
reduce physiological fluctuation and achieve more homogeneous fMRI activation
maps. To the best of our knowledge, this is the first study using a deep learning
algorithm for denoising task fMRI data.Acknowledgements
This research project was supported by the NIH (grant 1R01EB014284 and COBRE grant 5P20GM109025)
and a private grant from Peter and Angela Dal Pezzo. Data collection and
sharing for this project was provided by the Human Connectome Project (HCP;
Principal Investigators: Bruce Rosen, M.D., Ph.D., Arthur W. Toga, Ph.D., Van
J. Weeden, MD). References
[1]. Shen, D., Wu, G., Suk, H., 2017. Deep learning in
medical image analysis. Annual Review of Biomedical Engineering Vol.19:221-248.
[2]. Bianciardi, M., Fukunaga, M., van Gelderen, P.,
Horovitz, S.G., de Zwart, J.A., Shmueli, K., Duyn, J.H., 2009. Sources of
functional magnetic resonance imaging signal fluctuations in the human brain at
rest: a 7 T study. Magnetic resonance imaging 27, 1019-1029.
[3]. Glasser, M.F., Sotiropoulos, S.N., Wilson, J.A.,
Coalson, T.S., Fischl, B., Andersson, J.L., Xu, J., Jbabdi, S., Webster, M.,
Polimeni, J.R., 2013. The minimal preprocessing pipelines for the Human
Connectome Project. Neuroimage 80, 105-124.
[4]. Griffanti, L., Salimi-Khorshidi, G., Beckmann,
C.F., Auerbach, E.J., Douaud, G., Sexton, C.E., Zsoldos, E., Ebmeier, K.P.,
Filippini, N., Mackay, C.E., 2014. ICA-based artefact removal and accelerated
fMRI acquisition for improved resting state network imaging. Neuroimage 95,
232-247.
[5]. Barch, D.M., Burgess, G.C., Harms, M.P.,
Petersen, S.E., Schlaggar, B.L., Corbetta, M., Glasser, M.F., Curtiss, S.,
Dixit, S., Feldt, C., 2013. Function in the human connectome: task-fMRI and
individual differences in behavior. Neuroimage 80, 169-189.