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Article: Multimodal Voxel-Based Meta-Analysis of White Matter Abnormalities in Alzheimer's Disease.

TitleMultimodal Voxel-Based Meta-Analysis of White Matter Abnormalities in Alzheimer's Disease.
Authors
KeywordsAlzheimer's disease
diffusion tension imaging
fractional anisotropy
magnetic resonance imaging
voxel-based morphometry
white matter
Issue Date2015
Citation
Journal of Alzheimer's Disease, 2015, v. 47, p. 495-507 How to Cite?
AbstractAn increasing number of MRI investigations suggest that patients with Alzheimer's disease (AD) show not only gray matter decreases but also white matter (WM) abnormalities, including WM volume (WMV) deficits and integrity disruption of WM pathways. In this study, we applied multimodal voxel-wise meta-analytical methods to study WMV and fractional anisotropy in AD. Fourteen studies including 723 participants (340 with AD and 383 controls) were involved. The meta-analysis was performed using effect size signed differential mapping. Significant WMV reductions were observed in bilateral inferior temporal gyrus, splenium of corpus callosum, right parahippocampal gyrus, and hippocampus. Decreased fractional anisotropy was identified mainly in left posterior limb of internal capsule, left anterior corona radiata, left thalamus, and left caudate nucleus. Significant decreases of both WMV and fractional anisotropy were found in left caudate nucleus, left superior corona radiata, and right inferior temporal gyrus. Most findings showed to be highly replicable in the jackknife sensitivity analyses. In conclusion, AD patients show widespread WM abnormalities mainly in bilateral structures related to advanced mental and nervous activities.
Persistent Identifierhttp://hdl.handle.net/10722/227487
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYin, RH-
dc.contributor.authorTan, LAN-
dc.contributor.authorLiu, YONG-
dc.contributor.authorWang, WY-
dc.contributor.authorJiang, T-
dc.contributor.authorRadua, J-
dc.contributor.authorZhang, Y-
dc.contributor.authorGao, J-
dc.contributor.authorMigliaccio, R-
dc.contributor.authorYu, JT-
dc.date.accessioned2016-07-18T09:11:00Z-
dc.date.available2016-07-18T09:11:00Z-
dc.date.issued2015-
dc.identifier.citationJournal of Alzheimer's Disease, 2015, v. 47, p. 495-507-
dc.identifier.urihttp://hdl.handle.net/10722/227487-
dc.description.abstractAn increasing number of MRI investigations suggest that patients with Alzheimer's disease (AD) show not only gray matter decreases but also white matter (WM) abnormalities, including WM volume (WMV) deficits and integrity disruption of WM pathways. In this study, we applied multimodal voxel-wise meta-analytical methods to study WMV and fractional anisotropy in AD. Fourteen studies including 723 participants (340 with AD and 383 controls) were involved. The meta-analysis was performed using effect size signed differential mapping. Significant WMV reductions were observed in bilateral inferior temporal gyrus, splenium of corpus callosum, right parahippocampal gyrus, and hippocampus. Decreased fractional anisotropy was identified mainly in left posterior limb of internal capsule, left anterior corona radiata, left thalamus, and left caudate nucleus. Significant decreases of both WMV and fractional anisotropy were found in left caudate nucleus, left superior corona radiata, and right inferior temporal gyrus. Most findings showed to be highly replicable in the jackknife sensitivity analyses. In conclusion, AD patients show widespread WM abnormalities mainly in bilateral structures related to advanced mental and nervous activities.-
dc.languageeng-
dc.relation.ispartofJournal of Alzheimer's Disease-
dc.subjectAlzheimer's disease-
dc.subjectdiffusion tension imaging-
dc.subjectfractional anisotropy-
dc.subjectmagnetic resonance imaging-
dc.subjectvoxel-based morphometry-
dc.subjectwhite matter-
dc.titleMultimodal Voxel-Based Meta-Analysis of White Matter Abnormalities in Alzheimer's Disease.-
dc.typeArticle-
dc.identifier.emailGao, J: galeng@hku.hk-
dc.identifier.doi10.3233/JAD-150139-
dc.identifier.scopuseid_2-s2.0-84938677309-
dc.identifier.hkuros259574-
dc.identifier.volume47-
dc.identifier.spage495-
dc.identifier.epage507-
dc.identifier.isiWOS:000359191800020-

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