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. 2016 May;31(5):502-9.
doi: 10.1002/gps.4355. Epub 2015 Sep 7.

Apolipoprotein E and Clusterin can magnify effects of personality vulnerability on declarative memory performance in non-demented older adults

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Apolipoprotein E and Clusterin can magnify effects of personality vulnerability on declarative memory performance in non-demented older adults

Shraddha Sapkota et al. Int J Geriatr Psychiatry. 2016 May.

Abstract

Objectives: Recent research has linked psychological (personality) factors and specific genetic risk polymorphisms to performance on neurocognitive phenotypes. We examined whether episodic or semantic memory performance is associated with (a) three personality traits (i.e. neuroticism, extraversion, and openness to experience), (b) two neurodegenerative-related polymorphisms (i.e. Apolipoprotein E (APOE; rs7412; rs429358), Clusterin (CLU; rs11136000)), and (c) cross-domain risk interactions (magnification effects).

Methods: Linear growth models were examined to test independent associations between personality traits and declarative memory performance, and potential interaction effects with APOE and CLU genetic risk. Normal older adults (n = 282) with personality and genetic data from the Victoria Longitudinal Study were included at baseline and for up to 14 years of follow-up.

Results: First, we observed that higher openness to experience levels were associated with better episodic and semantic memory. Second, three significant gene × personality interactions were associated with poorer memory performance at baseline. These synergistic effects are: (a) APOE allelic risk (ε4+) carriers with lower openness to experience levels, (b) CLU (no risk: T/T) homozygotes with higher extraversion levels, and (c) CLU (no risk: T/T) homozygotes with lower neuroticism levels.

Conclusions: Specific neurodegenerative-related genetic polymorphisms (i.e. APOE and CLU) moderate and magnify the risk contributed by selected personality trait levels (i.e. openness to experience, extraversion) on declarative memory performance in non-demented aging. Future research could target interactions of other personality traits and genetic polymorphisms in different clinical populations to predict other neurocognitive deficits or transitions to cognitive impairment and dementia.

Keywords: Apolipoprotein E; Clusterin; Victoria Longitudinal Study; genetic risk; memory; personality traits.

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Conflict of interest statement

Conflict of Interest

All authors confirm that there is no actual or potential conflict of interest.

Figures

Figure 1
Figure 1
Personality by gene interaction effects for baseline declarative memory performance: (a) Adults with low openness to experience levels had poorer vocabulary performance and this effect was magnified for those with APOE allelic risk (ε4+). (b) CLU T/T homozygotes in the low neuroticism group had poorer word recall performance than CLU T/T homozygotes in the high neuroticism group. (c) CLU T/T homozygotes in the low neuroticism group had poorer vocabulary performance than CLU T/T homozygotes in the high neuroticism group. (d) CLU T/T homozygotes in low extraversion group had the best vocabulary performance, whereas those in the high extraversion group had the worst performance. (Note: High and low represent those above and below the mean personality trait score).

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