Abstract | INTRODUCTION: METHODS: We used a data set on 2858 subjects (1098 AD, 260 vascular dementia [VaD], 145 mixed AD and VaD, 90 other dementia diagnoses, and 1265 controls) to examine the association of APOE polymorphisms with clinical dementia diagnoses, biomarker profiles, and longevity. RESULTS: The ε4 allele was associated with reduced longevity as ε4 versus ε3 homozygotes lived on average 2.6 years shorter (P = .006). In AD, ε4 carriers lived 1.0 years shorter than noncarriers (P = .028). The ε4 allele was more prevalent in AD, mixed AD and VaD, and VaD patients compared to controls, but not in other dementia disorders. DISCUSSION: The APOE ε4 allele is influential in AD but might also be of importance in VaD and in mixed AD and VaD, diseases in which concomitant AD pathology is common.
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Authors | Tobias Skillbäck, Ronald Lautner, Niklas Mattsson, Jonathan M Schott, Ingmar Skoog, Katarina Nägga, Lena Kilander, Anders Wimo, Bengt Winblad, Maria Eriksdotter, Kaj Blennow, Henrik Zetterberg |
Journal | Alzheimer's & dementia : the journal of the Alzheimer's Association
(Alzheimers Dement)
Vol. 14
Issue 7
Pg. 895-901
(07 2018)
ISSN: 1552-5279 [Electronic] United States |
PMID | 29548722
(Publication Type: Journal Article)
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Copyright | Copyright © 2018 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved. |
Chemical References |
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Topics |
- Aged
- Alleles
- Alzheimer Disease
(genetics)
- Apolipoproteins E
(genetics)
- Dementia, Vascular
(genetics)
- Female
- Gene Frequency
- Genotype
- Humans
- Longevity
(genetics)
- Male
- Middle Aged
- Risk Factors
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