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Abstract Details

Magnetic Resonance Imaging Measurement of Hippocampal Volume Using Voxel-Based Morphometry Analysis in Early Alzheimer's Disease
Aging, Dementia, and Behavioral Neurology
P2 - Poster Session 2 (8:00 AM-9:00 AM)
10-004

To investigate the relationship between hippocampal volume and biomarkers of amyloid-beta (Aβ) pathology in patients with the clinical diagnosis of mild Alzheimer's disease (AD) using voxel-based morphometry (VBM).

In the diagnosis of AD, the position of biomarkers from CSF and amyloid imaging with PET is increasing. However, it is often difficult to predict the presence of Aβ pathology with the clinical diagnosis and conventional imaging study. VBM provides an automated and unbiased assessment of brain atrophy. VBM supporting software, named BAAD (Brain Anatomical Analysis using Diffeomorphic deformation) displays z-scores and volumes of MNI anatomical ROIs.

In the present study, 19 mild AD patients with the results of Aβ biomarkers by CSF study and/or amyloid PET obtained were enrolled. The subjects were divided into two groups based on Aβ biomarkers. Nine patients were Aβ positive and ten patients were negative. BAAD was used to calculate the hippocampal volume and total intracranial volume (TIV). We corrected the hippocampal volume so that the TIV would be constant (1500 mL) to eliminate the influence of individual differences in the brain volume.

There were no significant differences in the age and MMSE scores between the two groups. The mean left hippocampal volume was smaller in Aβ positive group than in the negative group (p < 0.05). There were no significant differences in the right and total hippocampal volumes between the two groups. With receiver operating characteristic (ROC) analyses, the discrimination performance to predict the Aβ pathology provided an optimal cutoff of 3.10, a sensitivity of 89% and a specificity of 70% in the left hippocampal volume.
Although there was a significant difference between Aβ positive group and the negative group in the left hippocampal volume, it would probably be difficult to predict the presence of Aβ pathology with only hippocampal volume.
Authors/Disclosures
Nobutoshi Morimoto
PRESENTER
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file
No disclosure on file