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APOE is associated with age‐of‐onset, but not cognitive functioning, in late‐life depression
Author(s) -
Butters Meryl A.,
Sweet Robert A.,
Mulsant Benoit H.,
Ilyas Kamboh M.,
Pollock Bruce G.,
Begley Amy E.,
Reynolds, Charles F.,
DeKosky Steven T.
Publication year - 2003
Publication title -
international journal of geriatric psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 129
eISSN - 1099-1166
pISSN - 0885-6230
DOI - 10.1002/gps.1006
Subject(s) - late life depression , apolipoprotein e , dementia , depression (economics) , risk factor , allele , age of onset , psychology , medicine , allele frequency , cognitive decline , alzheimer's disease , disease , psychiatry , gerontology , cognition , genetics , biology , gene , economics , macroeconomics
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.