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Brain Network Atlas Estimation using Centered Graph Shrinkage with Application to Developing and Aging Brains
Islem Rekik1, Gang Li1, Minjeong Kim1, Weili Lin1, and Dinggang Shen1,2

1Department of Radiology and BRIC, University of North Carolina, Chapel Hill, NC, United States, 2Department of Brain and Cognitive Engineering, Korea University, Seoul, Republic of Korea

Synopsis

Learning how to average brain networks (i.e., build a brain network atlas) constitutes a key step in creating a reliable ‘mean’ representation of a set of normal brains, which can be used to spot deviations from the normal network atlas (i.e., abnormal cases). However, this topic remains largely unexplored in neuroimaging field. In this work, we propose a network atlas estimation framework through a non-linear diffusion along the local neighbors of each node (network) in a graph. Our evaluation on both developing and aging datasets showed a better ‘centeredness’ of our atlas in comparison with the state-of-the-art network fusion method.

Purpose

A variety of methods have been developed to spatially normalize a population of brain images to estimate a ‘mean image’ (i.e., a population template or atlas), which were further refined to estimate a sharp atlas that is well-centered and more representative of each individual image [1]. However, methods for defining brain network atlases are still absent. Inspired from the network fusion method introduced in [2], we propose a new framework to estimate brain network (i.e., connectivity) atlas, through building a graph manifold of networks that progressively shrinks towards the ‘mean’ network.

Methods

Recently, Wang et al. introduced in [2] a robust method to non-linearly fuse a set of similarity matrices, where each matrix encodes a network. Basically, given $N$ networks, each network is iteratively updated through diffusing the global structure of the averaged remaining $(N-1)$ networks across its local structure. A key limitation of such an approach is that it averages all remaining networks without considering their proximity or relationship to the current network. To address this issue, we propose to explore the data distribution during the fusion process for network atlas estimation, through modeling their relationships using a graph [3]. This will better preserve the topology of the manifold, where the individual networks sit as they smoothly fuse toward a well-centered network. To do so, we propose the following steps described in Fig.1. (1) Use affinity propagation (AP) clustering method [4] to group similar nodes (i.e., networks) and define their representatives, so they can be fused in the same way. (2) Build a fully connected graph, where each node denotes an individual brain network. Specifically, on a local level, each identified AP cluster is defined as a sub-graph, where similar nodes are connected with a weighted edge; while on a higher level, the representatives of each cluster are connected within a global graph. (3) To ensure that the local fusion of each node with nearby nodes is smooth, we average the representatives of all sub-graphs to generate a center global network. Then, we move each node (i.e., locally update each network) by fusing it with its closest neighboring nodes (i.e., networks) through an iterative process as in [2] in the direction of the global center. (4) Since the representative nodes are moved, we subsequently update the global center. (5) Repeat steps (3-4) until the global center becomes stable. Eventually, as the original graph shrinks all nodes will locate at the vicinity of the global center, where their averaging is more reliable and meaningful to produce the sought ‘network atlas’.

Results

Fig. 2 shows the two different datasets used for evaluation:

Dataset 1 (developing infant brains): 40 infant brains at ages 0 and 6 months, where each cortical surface was parcellated into 35 regions [5]. By computing the pairwise absolute difference in cortical thickness between pairs of regions of interest, we generate a 35x35 morphological connectivity matrix.

Dataset 2 (aging brains): 40 normal and 40 MCI brains were parcellated into 90 regions using AAL template. Matrices of size 90x90 were estimated from resting-state fMRI.

Evaluation: To evaluate the centeredness of the estimated brain network atlas, we compute the mean squared distance between the estimated network atlas and each individual network in the population. Table 1 shows the mean squared distance computed using the proposed network atlas estimation method and the previous method in [2]. The smaller the evaluation distance the more centered is the atlas with respect to the data points on the manifold. We used t-test to evaluate the statistical significance of our method in comparison with [2]. Ours produced a more centered atlas than the previous method [2], with p <<0.001.


Discussion and conclusion

Building on the network fusion strategy introduced in [2], we proposed a graph shrinkage strategy that follows the local manifold structure of a set of brain networks to gradually fuse them through a diffusion process until reaching the final network atlas. As shown in Table 1, our method produces a more centered atlas within only a few iterations compared with [2], which requires more than (t* >20) iterations for the ‘centeredness’ error to decrease until convergence as demonstrated in [2]. Hence, our method is able to achieve better results within a smaller computational time. A potential clinical application of building network atlases is to learn the set of distinctive brain connections for each population of networks (e.g., normal) with respect to another population of networks (e.g., specific brain disorder).

Acknowledgements

This work was supported in part by National Institutes of Health grants (MH100217, MH108914 and MH107815).

References

[1] Wu G, Jia H, Wang Q, Shen D. Sharp Mean: Groupwise Registration Guided by Sharp Mean Image and Tree-based Registration. NeuroImage. 2011;56(4):1968-1981.

[2] Wang B, Mezlini AM, Demir F, Fiume M, Tu Z, Brudno M, Haibe-Kain B, Goldenberg A. Similarity network fusion for aggregating data types on a genomic scale. Nature Methods. 2014;11:333-337.

[3] Wu G, Peng X, Ying S, Wang Q, Yap PT, Shen D. eHUGS: Enhanced Hierarchical Unbiased Graph Shrinkage for Efficient Groupwise Registration. PloS one. 2016 Jan 22;11(1):e0146870.

[4] Frey BJ, Dueck D. Clustering by passing messages between data points. Science. 2007;315:972-976.

[5] Li G, Wang L, Shi F, Lin W, Shen D. Simultaneous and consistent labeling of longitudinal dynamic developing cortical surfaces in infants. Med Image Anal. 2014;18:1274-1289.

Figures

Figure 1. Illustration of the proposed network fusion strategy for ‘network atlas’ building using manifold-guided graph shrinkage.

Figure 2. Evaluation datasets: developing and aging populations of brain networks. (Left) Morphological brain networks estimation for each infant at 0 and 6 months of age using pairwise difference of mean cortical thickness between two regions of interest. (Right) Functional brain networks of patients with mild cognitive impairment and normal controls (elderly brains).

Table 1. Evaluation of the network atlas estimation method using the conventional similarity network fusion method introduced by Wang et al. in [2] and the proposed refinement based on dynamic graph shrinkage. Both methods were evaluated in a leave-one-out manner using mean squared distance between each individual and its corresponding atlas. Our proposed method, which is guided by the local manifold structure of the networks’ distribution, significantly outperforms the conventional method [2] (p-value << 0.001).

Proc. Intl. Soc. Mag. Reson. Med. 25 (2017)
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