Identification of Alzheimer’s Disease and Mild Cognitive Impairment Using Networks Constructed Based on Multiple Morphological Brain Features

Structural brain markers are important for characterizing the pathology of Alzheimer’s disease (AD) and mild cognitive impairment (MCI). Here, we constructed a multifeature-based network (MFN) for each individual using a sparse linear regression performed on six types of morphological features to pr...

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Published inBiological psychiatry : cognitive neuroscience and neuroimaging Vol. 3; no. 10; pp. 887 - 897
Main Authors Zheng, Weihao, Yao, Zhijun, Xie, Yuanwei, Fan, Jin, Hu, Bin
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.10.2018
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ISSN2451-9022
2451-9030
2451-9030
DOI10.1016/j.bpsc.2018.06.004

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Abstract Structural brain markers are important for characterizing the pathology of Alzheimer’s disease (AD) and mild cognitive impairment (MCI). Here, we constructed a multifeature-based network (MFN) for each individual using a sparse linear regression performed on six types of morphological features to promote the structure-based autodiagnosis. The categorization performance of the MFN was evaluated in 165 normal control subjects, 221 patients with MCI, and 142 patients with AD. We achieved 96.42% and 96.37% accuracy, respectively, in distinguishing the patients with AD and MCI from the normal control subjects, and reasonable discrimination of the two disease cohorts (70.52%) and prediction of the MCI to AD progression (65.61%). The performance was further improved by combining the properties of the MFN with the morphological features. Our results demonstrate the effectiveness of the MFN in combination with morphological features obtained from single imaging modality, serving as robust biomarkers in the diagnosis of AD and MCI.
AbstractList Structural brain markers are important for characterizing the pathology of Alzheimer's disease (AD) and mild cognitive impairment (MCI). Here, we constructed a multifeature-based network (MFN) for each individual using a sparse linear regression performed on six types of morphological features to promote the structure-based autodiagnosis. The categorization performance of the MFN was evaluated in 165 normal control subjects, 221 patients with MCI, and 142 patients with AD. We achieved 96.42% and 96.37% accuracy, respectively, in distinguishing the patients with AD and MCI from the normal control subjects, and reasonable discrimination of the two disease cohorts (70.52%) and prediction of the MCI to AD progression (65.61%). The performance was further improved by combining the properties of the MFN with the morphological features. Our results demonstrate the effectiveness of the MFN in combination with morphological features obtained from single imaging modality, serving as robust biomarkers in the diagnosis of AD and MCI.Structural brain markers are important for characterizing the pathology of Alzheimer's disease (AD) and mild cognitive impairment (MCI). Here, we constructed a multifeature-based network (MFN) for each individual using a sparse linear regression performed on six types of morphological features to promote the structure-based autodiagnosis. The categorization performance of the MFN was evaluated in 165 normal control subjects, 221 patients with MCI, and 142 patients with AD. We achieved 96.42% and 96.37% accuracy, respectively, in distinguishing the patients with AD and MCI from the normal control subjects, and reasonable discrimination of the two disease cohorts (70.52%) and prediction of the MCI to AD progression (65.61%). The performance was further improved by combining the properties of the MFN with the morphological features. Our results demonstrate the effectiveness of the MFN in combination with morphological features obtained from single imaging modality, serving as robust biomarkers in the diagnosis of AD and MCI.
Structural brain markers are important for characterizing the pathology of Alzheimer’s disease (AD) and mild cognitive impairment (MCI). Here, we constructed a multifeature-based network (MFN) for each individual using a sparse linear regression performed on six types of morphological features to promote the structure-based autodiagnosis. The categorization performance of the MFN was evaluated in 165 normal control subjects, 221 patients with MCI, and 142 patients with AD. We achieved 96.42% and 96.37% accuracy, respectively, in distinguishing the patients with AD and MCI from the normal control subjects, and reasonable discrimination of the two disease cohorts (70.52%) and prediction of the MCI to AD progression (65.61%). The performance was further improved by combining the properties of the MFN with the morphological features. Our results demonstrate the effectiveness of the MFN in combination with morphological features obtained from single imaging modality, serving as robust biomarkers in the diagnosis of AD and MCI.
Author Zheng, Weihao
Hu, Bin
Xie, Yuanwei
Fan, Jin
Yao, Zhijun
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Keywords MCI
AD
Alzheimer’s disease
MFN
Mild cognitive impairment
Structural brain markers
Sparse linear regression
Classification
Multifeature-based network
Language English
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Snippet Structural brain markers are important for characterizing the pathology of Alzheimer’s disease (AD) and mild cognitive impairment (MCI). Here, we constructed a...
Structural brain markers are important for characterizing the pathology of Alzheimer's disease (AD) and mild cognitive impairment (MCI). Here, we constructed a...
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StartPage 887
SubjectTerms Aged
Aged, 80 and over
Algorithms
Alzheimer Disease - diagnosis
Alzheimer Disease - pathology
Alzheimer’s disease
Biomarkers - analysis
Brain - pathology
Brain - physiopathology
Classification
Cognitive Dysfunction - diagnosis
Cognitive Dysfunction - pathology
Disease Progression
Female
Humans
Image Interpretation, Computer-Assisted - methods
Machine Learning
Male
MCI
MFN
Mild cognitive impairment
Multifeature-based network
Nerve Net - pathology
Sparse linear regression
Structural brain markers
Title Identification of Alzheimer’s Disease and Mild Cognitive Impairment Using Networks Constructed Based on Multiple Morphological Brain Features
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https://dx.doi.org/10.1016/j.bpsc.2018.06.004
https://www.ncbi.nlm.nih.gov/pubmed/30077576
https://www.proquest.com/docview/2084341963
Volume 3
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