Evidence map›Paper›PMID 29867424›Full record

ArticleFrontiers in computational neuroscience2018

Classification of Alzheimer's Disease, Mild Cognitive Impairment, and Normal Controls With Subnetwork Selection and Graph Kernel Principal Component Analysis Based on Minimum Spanning Tree Brain Functional Network.

Xiaohong Cui, Jie Xiang, Hao Guo, Guimei Yin, Huijun Zhang, Fangpeng Lan, Junjie Chen

Abstract read
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Article in Frontiers in computational neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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15citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Novel methodology for detection and prediction of mild cognitive impairment using resting-state EEG.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Pathogenic Factors Identification of Brain Imaging and Gene in Late Mild Cognitive Impairment.Interdisciplinary sciences, computational life sciences · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Xiaohong CuiCollege of Information and Computer, Taiyuan University of Technology, Taiyuan, China.
Jie XiangCollege of Information and Computer, Taiyuan University of Technology, Taiyuan, China.
Hao GuoCollege of Information and Computer, Taiyuan University of Technology, Taiyuan, China.
Guimei YinCollege of Information and Computer, Taiyuan University of Technology, Taiyuan, China.
Huijun ZhangCollege of Information and Computer, Taiyuan University of Technology, Taiyuan, China.
Fangpeng LanCollege of Information and Computer, Taiyuan University of Technology, Taiyuan, China.
Junjie ChenCollege of Information and Computer, Taiyuan University of Technology, Taiyuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective and accurate diagnosis of Alzheimer's disease (AD), as well as its early stage (mild cognitive impairment, MCI), has attracted more and more attention recently. Researchers have constructed threshold brain function networks and extracted various features for the classification of brain diseases. However, in the construction of the brain function network, the selection of threshold is very important, and the unreasonable setting will seriously affect the final classification results. To address this issue, in this paper, we propose a minimum spanning tree (MST) classification framework to identify Alzheimer's disease (AD), MCI, and normal controls (NCs). The proposed method mainly uses the MST method, graph-based Substructure Pattern mining (gSpan), and graph kernel Principal Component Analysis (graph kernel PCA). Specifically, MST is used to construct the brain functional connectivity network; gSpan, to extract features; and subnetwork selection and graph kernel PCA, to select features. Finally, the support vector machine is used to perform classification. We evaluate our method on MST brain functional networks of 21 AD, 25 MCI, and 22 NC subjects. The experimental results show that our proposed method achieves classification accuracy of 98.3, 91.3, and 77.3%, for MCI vs. NC, AD vs. NC, and AD vs. MCI, respectively. The results show our proposed method can achieve significantly improved classification performance compared to other state-of-the-art methods.

Indexed as

Alzheimer's diseaseclassificationgraph kernel principal component analysisgSpanmild cognitive impairmentminimum spanning tree

Identifiers

PMID29867424
PMCPMC5954113

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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.