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Problems meeting basic needs moderate the association between the APOE 4 allele and cognitive decline.

Authors :
Sachs-Ericsson N
Corsentino E
Collins N
Sawyer K
Blazer DG
Source :
Aging & Mental Health. Mar2010, Vol. 14 Issue 2, p138-144. 7p.
Publication Year :
2010

Abstract

Objectives: The ApolipoproteinE 4 (APOE 4) allele influences cognitive decline (CD) in some but not in all individuals. The purpose of this study was to investigate whether problems meeting basic needs (BN) (e.g., having enough money to meet needs, having enough money for emergencies, having adequate housing, and having enough heat) influences the relationship between the APOE 4 allele and CD. We predicted that problems meeting BN would have a greater influence on CD among those with the APOE 4 allele than those without the allele. Methods: Participants consisted of community-dwelling older adults from the Duke Established Populations for Epidemiologic Studies of the Elderly (EPESE). Data were drawn from Waves 1 and 2, which were 3 years apart. Cognitive functioning was assessed at both waves so that change in cognitive status was examined over time, and cognitive status was controlled at baseline. Genotyping, however, was not obtained until Wave 3. Results: The APOE 4 allele and problems meeting BN independently predicted CD. Importantly, the influence of BN on CD was greater for individuals with the APOE 4 allele compared to those without the allele. Other indicators of socioeconomic status (e.g., education, income) did not interact with the APOE 4 allele in predicting CD. Conclusions: There is a synergistic effect of perceived problems meeting BN and the APOE 4 allele on jointly influencing cognitive functioning. Although genetic risk factors are not easily modifiable, resource deprivation may be more amenable to interventions, which may reduce risk for CD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13607863
Volume :
14
Issue :
2
Database :
Academic Search Index
Journal :
Aging & Mental Health
Publication Type :
Academic Journal
Accession number :
105155668
Full Text :
https://doi.org/10.1080/13607860903421060