4.2 Article

Age-related increase of monoamine oxidase B in amyloid-negative cognitively unimpaired elderly subjects

期刊

ANNALS OF NUCLEAR MEDICINE
卷 36, 期 8, 页码 777-784

出版社

SPRINGER
DOI: 10.1007/s12149-022-01760-6

关键词

Aging; Amyloid-negativity; F-18-THK5351; Positron emission tomography

资金

  1. AMED [20ae0101077h0003]
  2. National Center for Geriatrics and Gerontology [26-30, 27-4, 29-24, 30-3]

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This study investigated the age-related topographic change of F-18-THK5351 PET in amyloid-negative cognitively unimpaired elderly subjects. The results showed an age-dependent increase of F-18-THK5351 retention, particularly in the inferior temporal lobes, suggesting an increase in reactive astrocytes with aging.
Objective Monoamine oxidase B (MAO-B) is highly abundant in reactive astrocytes and upregulated in neuroinflammatory processes. However, the age-related change of MAO-B in amyloid-negative cognitively unimpaired elderly subjects has not yet been sufficiently evaluated on positron emission tomography (PET). F-18-THK5351 is a radiotracer with high affinity to MAO-B, which may potentially serve as an imaging biomarker for detecting neuroinflammation. The purpose of this study was to investigate the age-related topographic change of F-18-THK5351 PET in amyloid-negative cognitively unimpaired elderly subjects. Methods The age-related change of F-18-THK5351 retention was evaluated on the visual analysis, voxel and region of interest (ROI)-based analyses using Statistical Parametric Mapping and PETSurfer tool of FreeSurfer in 31 amyloid-negative cognitively unimpaired elderly subjects. Results On visual inspection, elderly groups showed the spread of F-18-THK5351 accumulation from the medial to inferolateral temporal and basal frontal lobes, and cingulate gyrus. Additionally, voxel- and ROI-based analysis demonstrated the correlation between F-18-THK5351 accumulation and participants' age, especially in the inferior temporal lobes. Conclusions This study demonstrated age-dependent increase of F-18-THK5351 retention in amyloid-negative cognitively unimpaired subjects, which suggests an increase in MAO-B positive reactive astrocytes with aging.

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