Age-dependent microstructure alterations in 5xFAD mice by high-resolution diffusion tensor imaging

dc.contributor.authorMaharjan, Surendra
dc.contributor.authorTsai, Andy P.
dc.contributor.authorLin, Peter B.
dc.contributor.authorIngraham, Cynthia
dc.contributor.authorJewett, Megan R.
dc.contributor.authorLandreth, Gary E.
dc.contributor.authorOblak, Adrian L.
dc.contributor.authorWang, Nian
dc.contributor.departmentRadiology and Imaging Sciences, School of Medicine
dc.date.accessioned2024-05-30T12:59:52Z
dc.date.available2024-05-30T12:59:52Z
dc.date.issued2022-08-17
dc.description.abstractPurpose: To evaluate the age-dependent microstructure changes in 5xFAD mice using high-resolution diffusion tensor imaging (DTI). Methods: The 5xFAD mice at 4, 7.5, and 12 months and the wild-type controls at 4 months were scanned at 9.4T using a 3D echo-planar imaging (EPI) pulse sequence with the isotropic spatial resolution of 100 μm. The b-value was 3000 s/mm2 for all the diffusion MRI scans. The samples were also acquired with a gradient echo pulse sequence at 50 μm isotropic resolution. The microstructure changes were quantified with DTI metrics, including fractional anisotropy (FA) and mean diffusivity (MD). The conventional histology was performed to validate with MRI findings. Results: The FA values (p = 0.028) showed significant differences in the cortex between wild-type (WT) and 5xFAD mice at 4 months, while hippocampus, anterior commissure, corpus callosum, and fornix showed no significant differences for either FA and MD. FA values of 5xFAD mice gradually decreased in cortex (0.140 ± 0.007 at 4 months, 0.132 ± 0.008 at 7.5 months, 0.126 ± 0.013 at 12 months) and fornix (0.140 ± 0.007 at 4 months, 0.132 ± 0.008 at 7.5 months, 0.126 ± 0.013 at 12 months) with aging. Both FA (p = 0.029) and MD (p = 0.037) demonstrated significant differences in corpus callosum between 4 and 12 months age old. FA and MD were not significantly different in the hippocampus or anterior commissure. The age-dependent microstructure alterations were better captured by FA when compared to MD. Conclusion: FA showed higher sensitivity to monitor amyloid deposition in 5xFAD mice. DTI may be utilized as a sensitive biomarker to monitor beta-amyloid progression for preclinical studies.
dc.eprint.versionFinal published version
dc.identifier.citationMaharjan S, Tsai AP, Lin PB, et al. Age-dependent microstructure alterations in 5xFAD mice by high-resolution diffusion tensor imaging [published correction appears in Front Neurosci. 2022 Oct 13;16:1025457]. Front Neurosci. 2022;16:964654. Published 2022 Aug 17. doi:10.3389/fnins.2022.964654
dc.identifier.urihttps://hdl.handle.net/1805/41107
dc.language.isoen_US
dc.publisherFrontiers Media
dc.relation.isversionof10.3389/fnins.2022.964654
dc.relation.journalFrontiers in Neuroscience
dc.rightsAttribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourcePMC
dc.subjectAlzheimer’s disease
dc.subject5xFAD
dc.subjectMagnetic resonance imaging (MRI)
dc.subjectDiffusion tensor imaging (DTI)
dc.subjectDiffusion MRI (dMRI)
dc.titleAge-dependent microstructure alterations in 5xFAD mice by high-resolution diffusion tensor imaging
dc.typeArticle
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