Cited by 17Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsNeurological Disease Mechanisms and Treatments

Small vessel disease, but neither amyloid load nor metabolic deficit, is dependent on age at onset in Alzheimer’s disease.

Ortner, Marion, Kurz, Alexander, Alexopoulos, Panagiotis, Auer, Florian, Diehl-Schmid, Janine, Drzezga, Alexander, Förster, Stefan, Förstl, Hans +4 more·2015·Biological Psychiatry

Abstract

Background There is controversy concerning whether Alzheimer's disease (AD) with early onset is distinct from AD with late onset with regard to amyloid pathology and neuronal metabolic deficit. We hypothesized that compared with patients with early-onset AD, patients with late-onset AD have more comorbid small vessel disease (SVD) contributing to clinical severity, whereas there are no differences in amyloid pathology and neuronal metabolic deficit. Methods The study included two groups of patients with probable AD dementia with evidence of the AD pathophysiologic process: 24 patients with age at onset 70 years old. Amyloid deposition was assessed using carbon-11-labeled Pittsburgh compound B positron emission tomography, comorbid SVD was assessed using magnetic resonance imaging, and neuronal metabolic deficit was assessed using fluorodeoxyglucose positron emission tomography. Group differences of global and regional distribution of pathology were explored using region of interest and voxel-based analyses, respectively, carefully controlling for the influence of dementia severity, apolipoprotein E genotype, and in particular SVD. The pattern of cognitive impairment was determined using z scores of the subtests of the Consortium to Establish a Registry for Alzheimer's Disease Neuropsychological Assessment Battery. Results Patients with late-onset AD showed a significantly greater amount of SVD. No statistically significant differences in global or regional amyloid deposition…

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Crossref · 10.1016/j.biopsych.2014.01.019

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Authors
Ortner, M., Kurz, A., Alexopoulos, P., Auer, F., Diehl-Schmid, J., Drzezga, A., Förster, S., Förstl, H., Perneczky, R., Sorg, C., Yousefi, B. H., & Grimmer, T.
Affiliations
  • TUM Klinikum (DE)
  • University of Cologne (DE)
  • Technical University of Munich (DE)
Venue
Biological Psychiatry
Publisher
Elsevier BV
Published
2015-04
Volume
77
Issue
8
Pages
704-710
ISSN
0006-3223 (ISSN-L)
OpenAlex
W2002589018
Cited by
17
References
3
Citations by year
2023: 1 · 2022: 2 · 2021: 2 · 2020: 3 · 2019: 1 · 2018: 3 · 2017: 2 · 2016: 1 · 2015: 1 · 2014: 1
FWCI
1.27
Type
journal article
Language
en
Open access
closed
Locations
  • Biological Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
  • mediaTUM (Technical University of Munich) (submittedVersion)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Neurology › Neurological Disease Mechanisms and Treatments
Keywords
Alzheimer's disease, age of onset, early-onset Alzheimer's disease, late-onset Alzheimer's disease, cerebral small vessel disease, amyloid deposition, FDG-PET, amyloid PET, Pittsburgh compound B, cognitive impairment, dementia severity
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Amyloid, Aniline Compounds, Apolipoproteins E, Brain, Female, Humans, Male, Metabolic Diseases, Middle Aged, Radionuclide Imaging, Thiazoles, Vascular Diseases, Age of Onset, Fluorodeoxyglucose F18, Benzothiazoles

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