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Hypergraph representation of multimodal brain networks for patients with end-stage renal disease associated with mild cognitive impairment


  • Received: 16 August 2022 Revised: 27 October 2022 Accepted: 02 November 2022 Published: 08 November 2022
  • The structure and function of brain networks (BN) may be altered in patients with end-stage renal disease (ESRD). However, there are relatively few attentions on ESRD associated with mild cognitive impairment (ESRDaMCI). Most studies focus on the pairwise relationships between brain regions, without taking into account the complementary information of functional connectivity (FC) and structural connectivity (SC). To address the problem, a hypergraph representation method is proposed to construct a multimodal BN for ESRDaMCI. First, the activity of nodes is determined by connection features extracted from functional magnetic resonance imaging (fMRI) (i.e., FC), and the presence of edges is determined by physical connections of nerve fibers extracted from diffusion kurtosis imaging (DKI) (i.e., SC). Then, the connection features are generated through bilinear pooling and transformed into an optimization model. Next, a hypergraph is constructed according to the generated node representation and connection features, and the node degree and edge degree of the hypergraph are calculated to obtain the hypergraph manifold regularization (HMR) term. The HMR and L1 norm regularization terms are introduced into the optimization model to achieve the final hypergraph representation of multimodal BN (HRMBN). Experimental results show that the classification performance of HRMBN is significantly better than that of several state-of-the-art multimodal BN construction methods. Its best classification accuracy is 91.0891%, at least 4.3452% higher than that of other methods, verifying the effectiveness of our method. The HRMBN not only achieves better results in ESRDaMCI classification, but also identifies the discriminative brain regions of ESRDaMCI, which provides a reference for the auxiliary diagnosis of ESRD.

    Citation: Zhengtao Xi, Tongqiang Liu, Haifeng Shi, Zhuqing Jiao. Hypergraph representation of multimodal brain networks for patients with end-stage renal disease associated with mild cognitive impairment[J]. Mathematical Biosciences and Engineering, 2023, 20(2): 1882-1902. doi: 10.3934/mbe.2023086

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  • The structure and function of brain networks (BN) may be altered in patients with end-stage renal disease (ESRD). However, there are relatively few attentions on ESRD associated with mild cognitive impairment (ESRDaMCI). Most studies focus on the pairwise relationships between brain regions, without taking into account the complementary information of functional connectivity (FC) and structural connectivity (SC). To address the problem, a hypergraph representation method is proposed to construct a multimodal BN for ESRDaMCI. First, the activity of nodes is determined by connection features extracted from functional magnetic resonance imaging (fMRI) (i.e., FC), and the presence of edges is determined by physical connections of nerve fibers extracted from diffusion kurtosis imaging (DKI) (i.e., SC). Then, the connection features are generated through bilinear pooling and transformed into an optimization model. Next, a hypergraph is constructed according to the generated node representation and connection features, and the node degree and edge degree of the hypergraph are calculated to obtain the hypergraph manifold regularization (HMR) term. The HMR and L1 norm regularization terms are introduced into the optimization model to achieve the final hypergraph representation of multimodal BN (HRMBN). Experimental results show that the classification performance of HRMBN is significantly better than that of several state-of-the-art multimodal BN construction methods. Its best classification accuracy is 91.0891%, at least 4.3452% higher than that of other methods, verifying the effectiveness of our method. The HRMBN not only achieves better results in ESRDaMCI classification, but also identifies the discriminative brain regions of ESRDaMCI, which provides a reference for the auxiliary diagnosis of ESRD.



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