Back to Search
Start Over
Association of sex and APOE ε4 with brain tau deposition and atrophy in older adults with Alzheimer's disease.
- Source :
-
Theranostics [Theranostics] 2020 Aug 21; Vol. 10 (23), pp. 10563-10572. Date of Electronic Publication: 2020 Aug 21 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- The objective of this study was to assess the association of sex and the apolipoprotein E (APOE) ε4 allele with brain tau deposition and atrophy in older adults with Alzheimer's disease (AD) using quantitative <superscript>18</superscript> F-AV-1451 positron emission tomography (PET) and magnetic resonance imaging (MRI). Methods: Preprocessed <superscript>18</superscript> F-AV-1451 tau PET, raw T1-weighted structural MR images, demographic information, cerebrospinal fluid (CSF) total tau (t-tau) and phosphorylated tau (p-tau) measurements from 57 elderly individuals with AD were downloaded from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. An iteratively reblurred Van Cittert partial volume correction (PVC) method was applied to all preprocessed PET images. MRI images were used for PET spatial normalization and gray matter volume calculation. <superscript>18</superscript> F-AV-1451 PET standardized uptake value ratio (SUVR) was calculated relative to the cerebellum gray matter. The effect of sex and APOE ε4 status on SUVR and gray matter volume were assessed at both region of interest (ROI) and voxelwise levels. Results: Female APOE ε4 carriers (FACs) had significant higher <superscript>18</superscript> F-AV-1451 SUVRs in the lateral temporal, parietal, posterior cingulate, medial temporal, inferior temporal, entorhinal cortex, amygdala and parahippocampal gyrus regions, and exhibited smaller gray matter volumes in the posterior cingulate, medial temporal, inferior temporal and amygdala regions, as compared to the non-FACs (NFACs) comprised of female APOE ε4 non-carriers, male APOE ε4 carriers and male APOE ε4 non-carriers. Voxelwise analysis revealed forebrain and limbic clusters with greater <superscript>18</superscript> F-AV-1451 SUVRs and lower gray matter volume between FACs compared to the NFACs. Negative correlations between ROI <superscript>18</superscript> F-AV-1451 SUVRs and gray matter volumes were significant after adjusting for age and years of education. Conclusions: Among elderly individuals with AD, sex modified the effects of the APOE ε4 allele on region-specific tau deposition and gray matter volume. FACs had elevated brain region-specific tau PET SUVR and decreased gray matter volume in comparison to NFACs. The study provides a basis for the use of precision medicine in the diagnosis of AD and evaluation of therapeutics using <superscript>18</superscript> F-AV-1451 PET and structural MRI.<br />Competing Interests: Competing Interests: The authors have declared that no competing interest exists.<br /> (© The author(s).)
- Subjects :
- Aged
Aged, 80 and over
Alleles
Alzheimer Disease diagnosis
Alzheimer Disease drug therapy
Alzheimer Disease pathology
Atrophy diagnosis
Atrophy genetics
Atrophy pathology
Brain diagnostic imaging
Carbolines administration & dosage
Contrast Media administration & dosage
Female
Genetic Predisposition to Disease
Heterozygote
Humans
Magnetic Resonance Imaging
Male
Positron-Emission Tomography
Precision Medicine methods
Sex Factors
Alzheimer Disease genetics
Apolipoproteins E genetics
Brain pathology
tau Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1838-7640
- Volume :
- 10
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- Theranostics
- Publication Type :
- Academic Journal
- Accession number :
- 32929366
- Full Text :
- https://doi.org/10.7150/thno.48522