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PMID: 19339712 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Effect of APOE genotype on amyloid plaque load and gray matter volume in Alzheimer disease.

Neurology ·Vol. 72 ·No. 17 ·2009-04-28 ·Pages 1487-94

Drzezga A, Grimmer T, Henriksen G, Mühlau M, Perneczky R, Miederer I, Praus C, Sorg C, Wohlschläger A, Riemenschneider M, Wester HJ, Foerstl H, Schwaiger M, Kurz A

Abstract

To examine the influence of the APOE genotype on levels of beta-amyloid (Abeta) plaque load and atrophy in patients with Alzheimer disease (AD) in vivo. Thirty-two patients with moderate AD were divided into carriers and noncarriers of the epsilon4 allele. These groups were matched for age, disease duration, education, and cognitive impairment. In all subjects, [11C]PIB-PET was performed for measurement of cerebral Abeta plaque deposition and cranial MRI for the assessment of gray matter volume by voxel-based morphometry (VBM) and for correction of partial volume effects (PVE) in the PET data. Voxel-based comparisons (SPM5) were performed between patient groups and healthy control populations and completed with multiple regression analyses between imaging data and epsilon4 allele frequency. Compared to controls, AD-typical patterns of [11C]PIB retention and atrophy were detected in both epsilon4-positive and epsilon4-negative patient groups. In direct comparison, significantly stronger and more extended [11C]PIB uptake was found in epsilon4-positive patients in bilateral temporoparietal and frontal cortex, surviving PVE correction. VBM analysis demonstrated comparable levels of atrophy in both patient groups. Regression analyses revealed a linear association between higher epsilon4 allele frequency and stronger temporoparietal Abeta plaque deposition, independently of other confounds. No major correlation between epsilon4 allele frequency and gray matter decrease was observed. These results indicate that the epsilon4-positive APOE genotype not only represents a risk factor for Alzheimer disease (AD), but also results in higher levels of Abeta plaque deposition in epsilon4-positive patients with AD compared to age-matched epsilon4-negative patients with similar levels of cognitive impairment and brain atrophy. The potential role of Abeta plaque imaging for patient inclusion and follow-up in anti-amyloid therapy trials is strengthened by these findings.

MeSH Terms
Aged Aged, 80 and over Alzheimer Disease/diagnostic imaging,genetics,pathology Amyloid beta-Peptides/metabolism Aniline Compounds Apolipoprotein E4/genetics Apolipoproteins E/genetics Benzothiazoles Brain/diagnostic imaging,metabolism,pathology Carbon Radioisotopes DNA Mutational Analysis Female Gene Frequency/genetics Genetic Predisposition to Disease/genetics Genetic Testing Genotype Humans Male Middle Aged Plaque, Amyloid/metabolism,pathology Polymorphism, Genetic/genetics Positron-Emission Tomography Risk Factors Thiazoles
Chemicals
2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazole Amyloid beta-Peptides Aniline Compounds Apolipoprotein E4 Apolipoproteins E Benzothiazoles Carbon Radioisotopes Thiazoles
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Drzezga A
Department of Nuclear Medicine, Klinikum Rechts der Isar, Technischen Universität München, Ismaninger Str. 22, D-81675 München/Munich, Germany. [email protected]
Grimmer T
Henriksen G
Mühlau M
Perneczky R
Miederer I
Praus C
Sorg C
Wohlschläger A
Riemenschneider M
Wester H J
Foerstl H
Schwaiger M
Kurz A
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
1526-632X
Published
2009-04-28
Epub
2009-00-01
Pages
1487-94
Language
English
Region
United States
NLM ID
0401060
Subset
IM
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