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Regional Comparison of Imaging Biomarkers in the Striatum between Early- and Late-onset Alzheimer’s Diseaseopen access

Authors
Kim, Ji EunLee, Dong-KyunHwang, Ji HyeKim, Chan-MiKim, YejiLee, Jae-HongLee, Jong MinRoh, Jee HoonAlzheimer's, Disease Neuroimaging Initiative (ADNI)
Issue Date
Dec-2022
Publisher
Korean Society for Neurodegenerative Disease
Keywords
Alzheimer?s disease; Striatum; Biomarkers; Amyloid PET; Early onset Alzheimer?s disease; Late onset Alzheimer?s disease
Citation
Experimental Neurobiology, v.31, no.6, pp.401 - 408
Indexed
SCIE
SCOPUS
KCI
Journal Title
Experimental Neurobiology
Volume
31
Number
6
Start Page
401
End Page
408
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/184949
DOI
10.5607/en22022
ISSN
1226-2560
Abstract
Striatal changes in the pathogenesis of Alzheimer’s disease (AD) is not fully understood yet. We compared structural and functional image differences in the striatum between patients with early onset AD (EOAD) and late onset AD (LOAD) to investigate whether EOAD harbors autosomal dominant AD like imaging findings. The clinical, neuropsychological and neuroimaging biomarkers of 77 probable AD patients and 107 elderly subjects with normal cognition (NC) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI)-2 dataset were analyzed. Enrolled each subject completed a 3-Tesla MRI, baseline 18F-FDG-PET, and baseline 18F-AV-45 (Florbetapir) amyloid PET studies. AD patients were divided into two groups based on the onset age of clinical symptoms (EOAD <65 yrs; LOAD ≥65 yrs). A standardized uptake value ratio of the striatum and subcortical structures was obtained from both amyloid and FDG-PET scans. Structural MR imaging analysis was conducted using a parametric boundary description protocol, SPHARM-PDM. Of the 77 AD patients, 18 were EOAD and 59 were LOAD. Except for age of symptom onset, there were no statistically significant differences between the groups in demographics and detailed neuropsychological test results. 18F-AV-45 amyloid PET showed marked β-amyloid accumulation in the bilateral caudate nucleus and left pallidum in the EOAD group. Intriguingly, the caudate nucleus and putamen showed maintained glucose metabolism in the EOAD group compared to the LOAD group. Our image findings in the striatum of EOAD patients suggest that sporadic EOAD may share some pathophysiological changes noted in autosomal dominant AD.
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