APOE is associated with age‐of‐onset, but not cognitive functioning, in late‐life depression
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.
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The APOE ε4 allele is associated with an earlier onset age of late-life depression.
“forwarding the onset age of late-life depression (LLD) [6]”
From APOE4 genotype exacerbates the depression-like behavior of mice during aging through ATP decline (2021) · cites this paper as [6]
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(1991) · American Journal of Psychiatry · doi:10.1176/ajp.148.1.102 · Cited by 647 · cited 1× · see citing works
“Cognitive functioning was assessed with the Mini-Mental Status Exam (MMSE; Folstein et al., 1975; Molloy et al., 1991) and the Dementia Rating Scale (DRS; Mattis, 1976; Mattis 1988).”
MethodA4POE*4-associated Alzheimer's disease risk is modified by α1–antichymotrypsin polymorphism
Kamboh, M. I., Sanghera, D. K., Ferrell, R. E., & DeKosky, S. T. (1995) · Nature Genetics · doi:10.1038/ng0895-486 · Cited by 336 · see citing works
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The Nature and Determinants of Neuropsychological Functioning in Late-LifeDepression
Butters, M. A., Whyte, E. M., Nebes, R. D., Begley, A. E., Dew, M. A., Mulsant, B. H., Zmuda, M. D., Bhalla, R., Meltzer, C. C., Pollock, B. G., et al. (2004) · Archives of General Psychiatry · doi:10.1001/archpsyc.61.6.587 · Cited by 622 · see citing works
Self-citationDepressive Symptoms and Cognitive Decline in Community‐Dwelling Older Adults
Köhler, S., van Boxtel, M. P. J., van Os, J., Thomas, A. J., O'Brien, J. T., Jolles, J., Verhey, F. R. J., & Allardyce, J. (2010) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.2010.02807.x · Cited by 152 · see citing works
Systematic review and meta-analysis of genetic studies of late-life depression
Tsang, R. S. M., Mather, K. A., Sachdev, P. S., & Reppermund, S. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.01.028 · Cited by 54 · see citing works
APOE4 genotype exacerbates the depression-like behavior of mice during aging through ATP decline
Fang, W., Xiao, N., Zeng, G., Bi, D., Dai, X., Mi, X., Ye, Q., Chen, X., & Zhang, J. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01631-0 · Cited by 42 · see citing works
- 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.
- ORCID
- 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
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