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Current Alzheimer Research

Editor-in-Chief

ISSN (Print): 1567-2050
ISSN (Online): 1875-5828

Research Article

Application of Diffusion Tensor Imaging Based on Automatic Fiber Quantification in Alzheimer's Disease

Author(s): Bo Yu, Zhongxiang Ding, Luoyu Wang, Qi Feng, Yifeng Fan, Xiufang Xu* and Zhengluan Liao*

Volume 19, Issue 6, 2022

Published on: 18 August, 2022

Page: [469 - 478] Pages: 10

DOI: 10.2174/1567205019666220718142130

Price: $65

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Abstract

Background: Neuroimaging suggests that white matter microstructure is severely affected in Alzheimer's disease (AD) progression. However, whether alterations in white matter microstructure are confined to specific regions and whether they can be used as potential biomarkers to distinguish normal control (NC) from AD are unknown.

Methods: In this cross-sectional study, 33 cases of AD and 25 cases of NC were recruited for automatic fiber quantification (AFQ). A total of 20 fiber bundles were equally divided into 100 segments for quantitative assessment of fractional anisotropy (FA), mean diffusivity (MD), volume and curvature. In order to further evaluate the diagnostic value, the maximum redundancy minimum (mRMR) and LASSO algorithms were used to select features, calculate the Radscore of each subject, establish logistic regression models, and draw ROC curves, respectively, to assess the predictive power of four different models.

Results: There was a significant increase in the MD values in AD patients compared with healthy subjects. The differences were mainly located in the left cingulum hippocampus (HCC), left uncinate fasciculus (UF) and superior longitudinal fasciculus (SLF). The point-wise level of 20 fiber bundles was used as a classification feature, and the MD index exhibited the best performance to distinguish NC from AD.

Conclusion: These findings contribute to the understanding of the pathogenesis of AD and suggest that abnormal white matter based on DTI-based AFQ analysis is helpful to explore the pathogenesis of AD.

Keywords: Alzheimer's disease, automatic fiber quantification, white matter microarchitecture, superior longitudinal fasciculus, Diffusion tensor imaging, normal controls.

[1]
Dubois B, Hampel H, Feldman HH, et al. Preclinical Alzheimer’s disease: Definition, natural history, and diagnostic criteria. Alzheimers Dement 2016; 12(3): 292-323.
[http://dx.doi.org/10.1016/j.jalz.2016.02.002] [PMID: 27012484]
[2]
Feigin VL, Nichols E, Alam T, et al. Global, regional, and national burden of neurological disorders, 1990-2016: A systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol 2019; 18(5): 459-80.
[http://dx.doi.org/10.1016/S1474-4422(18)30499-X] [PMID: 30879893]
[3]
Wang L, Feng Q, Wang M, et al. An effective brain imaging biomarker for AD and aMCI: ALFF in slow-5 frequency band. Curr Alzheimer Res 2021; 18(1): 45-55.
[http://dx.doi.org/10.2174/1567205018666210324130502] [PMID: 33761855]
[4]
Di Lazzaro V, Bella R, Benussi A, et al. Diagnostic contribution and therapeutic perspectives of transcranial magnetic stimulation in dementia. Clin Neurophysiol 2021; 132(10): 2568-607.
[http://dx.doi.org/10.1016/j.clinph.2021.05.035] [PMID: 34482205]
[5]
Han H, Qin Y, Ge X, et al. Risk assessment during longitudinal progression of cognition in older adults: A community-based bayesian networks model. Curr Alzheimer Res 2021; 18(3): 232-42.
[http://dx.doi.org/10.2174/1567205018666210608110329] [PMID: 34102974]
[6]
Amlien IK, Fjell AM. Diffusion tensor imaging of white matter degeneration in Alzheimer’s disease and mild cognitive impairment. Neuroscience 2014; 276: 206-15.
[http://dx.doi.org/10.1016/j.neuroscience.2014.02.017] [PMID: 24583036]
[7]
Yin RH, Tan L, Liu Y, et al. Multimodal voxel-based meta-analysis of white matter abnormalities in Alzheimer’s disease. J Alzheimers Dis 2015; 47(2): 495-507.
[http://dx.doi.org/10.3233/JAD-150139] [PMID: 26401571]
[8]
Ranzenberger LR, Snyder T. Diffusion tensor imaging. Treasure Island, (FL): StatPearls LLC 2021.
[9]
Perea RD, Rabin JS, Fujiyoshi MG, et al. Connectome-derived diffusion characteristics of the fornix in Alzheimer’s disease. Neuroimage Clin 2018; 19: 331-42.
[http://dx.doi.org/10.1016/j.nicl.2018.04.029] [PMID: 30013916]
[10]
Rajan S, Brettschneider J, Collingwood JF. Regional segmentation strategy for DTI analysis of human corpus callosum indicates motor function deficit in mild cognitive impairment. Neurosci Methods 2020; 345: 108870.
[http://dx.doi.org/10.1016/j.jneumeth.2020.108870] [PMID: 32687851]
[11]
Nir TM, Jahanshad N, Villalon-Reina JE, et al. Effectiveness of regional DTI measures in distinguishing Alzheimer’s disease, MCI, and normal aging. Neuroimage Clin 2013; 3: 180-95.
[http://dx.doi.org/10.1016/j.nicl.2013.07.006] [PMID: 24179862]
[12]
Struyfs H, Van Hecke W, Veraart J, et al. Diffusion kurtosis imaging: A possible MRI biomarker for AD diagnosis? J Alzheimers Dis 2015; 48(4): 937-48.
[http://dx.doi.org/10.3233/JAD-150253] [PMID: 26444762]
[13]
Smith CD, Chebrolu H, Andersen AH, et al. White matter diffusion alterations in normal women at risk of Alzheimer’s disease. Neurobiol Aging 2010; 31(7): 1122-31.
[http://dx.doi.org/10.1016/j.neurobiolaging.2008.08.006] [PMID: 18801597]
[14]
Bosch B, Arenaza-Urquijo EM, Rami L, et al. Multiple DTI index analysis in normal aging, amnestic MCI and AD. Relationship with neuropsychological performance. Neurobiol Aging 2012; 33(1): 61-74.
[http://dx.doi.org/10.1016/j.neurobiolaging.2010.02.004] [PMID: 20371138]
[15]
Smith SM, Jenkinson M, Johansen-Berg H, et al. Tract-based spatial statistics: Voxelwise analysis of multi-subject diffusion data. Neuroimage 2006; 31(4): 1487-505.
[http://dx.doi.org/10.1016/j.neuroimage.2006.02.024] [PMID: 16624579]
[16]
Bach M, Laun FB, Leemans A, et al. Methodological considerations on tract-based spatial statistics (TBSS). Neuroimage 2014; 100: 358-69.
[http://dx.doi.org/10.1016/j.neuroimage.2014.06.021] [PMID: 24945661]
[17]
Yeatman JD, Dougherty RF, Myall NJ, Wandell BA, Feldman HM. Tract profiles of white matter properties: Automating fiber-tract quantification. PLoS One 2012; 7(11): e49790.
[http://dx.doi.org/10.1371/journal.pone.0049790] [PMID: 23166771]
[18]
Dou X, Yao H, Feng F, et al. Characterizing white matter connectivity in Alzheimer’s disease and mild cognitive impairment: An automated fiber quantification analysis with two independent datasets. Cortex 2020; 129: 390-405.
[http://dx.doi.org/10.1016/j.cortex.2020.03.032] [PMID: 32574842]
[19]
Chen H, Sheng X, Qin R, et al. Aberrant white matter microstructure as a potential diagnostic marker in Alzheimer’s disease by automated fiber quantification. Front Neurosci 2020; 14: 570123.
[http://dx.doi.org/10.3389/fnins.2020.570123] [PMID: 33071742]
[20]
Baker LM, Cabeen RP, Cooley S, Laidlaw DH, Paul RH. Application of a novel quantitative tractography-based analysis of diffusion tensor imaging to examine fiber bundle length in human cerebral white matter. Technol Innov 2016; 18(1): 21-9.
[http://dx.doi.org/10.21300/18.1.2016.21] [PMID: 27721932]
[21]
Batchelor PG, Calamante F, Tournier JD, Atkinson D, Hill DL, Connelly A. Quantification of the shape of fiber tracts. Magn Reson Med 2006; 55(4): 894-903.
[http://dx.doi.org/10.1002/mrm.20858] [PMID: 16526017]
[22]
Dubois B, Feldman HH, Jacova C, et al. Research criteria for the diagnosis of Alzheimer’s disease: Revising the NINCDS-ADRDA criteria. Lancet Neurol 2007; 6(8): 734-46.
[http://dx.doi.org/10.1016/S1474-4422(07)70178-3] [PMID: 17616482]
[23]
Banfi C, Koschutnig K, Moll K, Schulte-Körne G, Fink A, Landerl K. White matter alterations and tract lateralization in children with dyslexia and isolated spelling deficits. Hum Brain Mapp 2019; 40(3): 765-76.
[http://dx.doi.org/10.1002/hbm.24410] [PMID: 30267634]
[24]
Acosta-Cabronero J, Alley S, Williams GB, Pengas G, Nestor PJ. Diffusion tensor metrics as biomarkers in Alzheimer’s disease. PLoS One 2012; 7(11): e49072.
[http://dx.doi.org/10.1371/journal.pone.0049072] [PMID: 23145075]
[25]
Bennett IJ, Madden DJ. Disconnected aging: Cerebral white matter integrity and age-related differences in cognition. Neuroscience 2014; 276: 187-205.
[http://dx.doi.org/10.1016/j.neuroscience.2013.11.026] [PMID: 24280637]
[26]
Shi F, Liu B, Zhou Y, Yu C, Jiang T. Hippocampal volume and asymmetry in mild cognitive impairment and Alzheimer’s disease: Meta-analyses of MRI studies. Hippocampus 2009; 19(11): 1055-64.
[http://dx.doi.org/10.1002/hipo.20573] [PMID: 19309039]
[27]
Tibshirani R. Regression shrinkage and selection via the lasso. J R Stat Soc Ser A Stat Soc 1996; 58(1): 267-88.
[28]
Rathore S, Habes M, Iftikhar MA, Shacklett A, Davatzikos C. A review on neuroimaging-based classification studies and associated feature extraction methods for Alzheimer’s disease and its prodromal stages. Neuroimage 2017; 155: 530-48.
[http://dx.doi.org/10.1016/j.neuroimage.2017.03.057] [PMID: 28414186]
[29]
Mesrob L, Sarazin M, Hahn-Barma V, et al. DTI and structural MRI classification in Alzheimer’s disease. Adv J Mol Imaging 2012; 2(2): 12-20.
[http://dx.doi.org/10.4236/ami.2012.22003]

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