ArticleMedical & biological engineering & computing2022
Estimating high-order brain functional networks by correlation-preserving embedding.
Article in Medical & biological engineering & computing, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Multi-band network fusion for Alzheimer's disease identification with functional MRI.Frontiers in psychiatry · 2022Article
- Adaptive noise depression for functional brain network estimation.Frontiers in psychiatry · 2022Article
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4 authors.
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Abstract
Brain functional network (FN) has emerged as a potential tool for identifying mental and neurological diseases. Traditional FN estimation methods such as Pearson's correlation (PC) and sparse representation (SR), despite their popularity, can only model low-order relationships between brain regions (i.e., nodes of FN), thus failing to capture more complex interaction in the brain. Recently, researchers proposed to estimate high-order FN (HoFN) and successfully used them in the early diagnosis of neurological diseases. In practice, however, such HoFN is constructed by directly considering the columns (or rows) of the adjacency matrix of low-order FN (LoFN) as node feature vectors that may contain some redundant or noisy information. In addition, it is not really reflected whether the original low-order relationship is maintained during the construction of the HoFN. To address these problems, we propose correlation-preserving embedding (COPE) to re-code the LoFN prior to constructing HoFN. Specifically, we first use SR to construct traditional LoFN. Then, we embed the LoFN via COPE to generate the new node representation for removing the potentially redundant/noisy information in original node feature vectors and simultaneously maintaining the low-order relationship between brain regions. Finally, the expected HoFN is estimated by SR based on the new node representation. To verify the effectiveness of the proposed scheme, we conduct experiments on 137 subjects from the public Alzheimer's Disease Neuroimaging Initiative (ADNI) database to identify subjects with mild cognitive impairment (MCI) from normal controls. Experimental results show that the proposed scheme can achieve better performance than the baseline method. Brain functional network (FN) has emerged as a potential tool for identifying mental and neurological diseases. Traditional FN estimation methods such as Pearson's correlation (PC) and sparse representation (SR), despite their popularity, can only model low-order relationships between brain regions (i.e., nodes of FN), thus failing to capture more complex interaction in the brain. Recently, researchers proposed to estimate high-order FN (HoFN) and successfully used them in the early diagnosis of neurological diseases. In practice, however, such HoFN is constructed by directly considering the columns (or rows) of the adjacency matrix of low-order FN (LoFN) as node feature vectors that may contain some redundant or noisy information. In addition, it is not really reflected whether the original low-order relationship is maintained during the construction of the HoFN. To address these problems, we propose correlation-preserving embedding (COPE) to re-code the LoFN prior to constructing HoFN. Specifically, we first use SR to construct traditional LoFN. Then, we embed the LoFN via COPE to generate the new node representation for removing the potentially redundant/noisy information in original node feature vectors and simultaneously maintaining the low-order relationship between brain regions. Finally, the expected HoFN is estimated by SR based on the new node representation. To verify the effectiveness of the proposed scheme, we conduct experiments on 137 subjects from the public Alzheimer's Disease Neuroimaging Initiative (ADNI) database to identify subjects with mild cognitive impairment (MCI) from normal controls. Experimental results show that the proposed scheme can achieve better performance than the baseline method.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.