Cited by 58Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsGenetic Associations and Epidemiology

APOE is associated with age‐of‐onset, but not cognitive functioning, in late‐life depression

Butters, Meryl A., Sweet, Robert A., Mulsant, Benoit H., Ilyas Kamboh, M., Pollock, Bruce G., Begley, Amy E., Reynolds,, Charles F., DeKosky, Steven T.·2003·International Journal of Geriatric Psychiatry

Abstract

Objective: There is a recognized but poorly understood relationship between late‐life depression (LLD) and progressive dementia. Both cognitive impairment co‐occurring with LLD and a late age‐of‐onset of first lifetime depressive episode appear to be associated with subsequent progressive dementia. A history of major depression, especially when the first onset occurs in late‐life, has been identified as a risk factor for Alzheimer's disease (AD). The major genetic risk factor for sporadic AD is carrying one or more apolipoprotein E4 (APOE4) alleles. We hypothesized that the association between LLD and dementia risk would be mediated by APOE4, specifically that APOE4 allele frequency would be associated with cognitive impairment and later age‐of‐depression‐onset. We also predicted that APOE4 allele frequency would be increased among subjects with LLD. Methods: We compared the distribution of APOE2, APOE3, and APOE4 alleles in groups of LLD (n=160), AD (n=568) and elderly control (EC; n=156) subjects. Results: The allele distribution of the cognitively impaired LLD subgroup was not different from either the cognitively normal subgroup or the EC group but was different from the AD group. However, mean age‐of‐onset of depression in APOE4 carriers (51.4±20.7) was significantly lower than non‐carriers (58.8±16.8). The allele distribution in LLD overall was significantly different from the AD but not the EC group. Conclusions: The finding that neither LLD, accompanying cognitive impairment, nor late age‐of‐onset was associated with an increased APOE4 allele frequency suggests that LLD acts as a risk factor for developing AD as well as non‐AD dementia through mechanisms independent of APOE4. The unexpected finding that age‐of‐onset of LLD was significantly reduced in APOE4 carriers is similar to the association between APOE4 and age‐of‐onset in AD. Replication of the association of APOE4 with earlier age‐of‐depression‐onset is indicated. Copyright © 2003 John Wiley & Sons, Ltd.

Integrity signals

Registry

Crossref · 10.1002/gps.1006

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Butters, M. A., Sweet, R. A., Mulsant, B. H., Ilyas Kamboh, M., Pollock, B. G., Begley, A. E., Reynolds, & DeKosky, S. T.
Affiliations
  • University of Pittsburgh Medical Center (US)
  • Geriatric Research Education and Clinical Center (US)
  • University of Pittsburgh (US)
Corresponding author
Butters, Meryl A.
Venue
International Journal of Geriatric Psychiatry
Publisher
Wiley
Published
2003-12
Volume
18
Issue
12
Pages
1075-1081
ISSN
  • 0885-6230 (ISSN-L)
  • 1099-1166
OpenAlex
W2102916279
Cited by
58
References
2
Citations by year
2026: 2 · 2025: 2 · 2023: 2 · 2022: 1 · 2021: 3 · 2019: 4 · 2018: 3 · 2017: 4 · 2016: 4 · 2015: 3 · 2014: 2 · 2012: 2
FWCI
2.16
Type
journal article
Language
en
Open access
closed
Locations
  • International Journal of Geriatric Psychiatry (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institute on Aging (AG 05-133, P50AG005133, AG13672, R01AG013672)
  • National Institute of Mental Health (MH-01684, K01MH001613, MH-52247, R21MH066231, P30MH052247, K01MH001684, K24MH065416, MH-37869, MH66231, MH-43832, MH 65416, MH-01613, R01MH037869)
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 › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
Keywords
geriatric depression, APOE ε4, APOE alleles, age of onset of depression, cognitive impairment, Alzheimer's disease, dementia risk, genetic risk factors, major depressive disorder
MeSH terms
Aged, Alleles, Alzheimer Disease, Apolipoproteins E, Cognition Disorders, Depressive Disorder, Female, Gene Frequency, Humans, Male, Age of Onset

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review