Aβ amyloid, cognition, and APOE genotype in healthy older adults. Issue 5 (16th November 2012)

• Record Type: Journal Article
• Authors: Lim, Yen Ying; Ellis, Kathryn A.; Ames, David; Darby, David; Harrington, Karra; Martins, Ralph N.; Masters, Colin L.; Rowe, Christopher; Savage, Greg; Szoeke, Cassandra; Villemagne, Victor L.; Maruff, Paul
• Is Part Of: Alzheimer's & dementia. Volume 9:Issue 5(2013)
• Page Start: 538
• Page End: 545
• Publication Date: 2012-11-16
• Subjects: Cerebral Aβ burden -- APOE ɛ4 -- Episodic memory -- Healthy older adults -- AIBL; Alzheimer's disease -- Periodicals; Alzheimer Disease -- Periodicals; Dementia -- Periodicals; Démence; Maladie d'Alzheimer; Périodique électronique (Descripteur de forme); Ressource Internet (Descripteur de forme); 616.83
• DOI: 10.1016/j.jalz.2012.07.004
• Languages: English
• ISSNs: 1552-5260

Abstract

Abstract: Background: Only one study has investigated the relationship between cerebral β‐amyloid (Aβ), apolipoprotein E ( APOE ) ɛ4 genotype, and cognition. Although significant relationships between cerebral Aβ and cognition were observed in ɛ4 carriers but not noncarriers, the magnitude of this relationship was not reported. Further, when demographic variables were controlled, the influence of APOE ɛ4 on the relationship between cerebral Aβ and cognition dissipated. Methods: In 144 healthy older adults who had undergone amyloid scanning and APOE ɛ4 genotyping in the Australian Imaging, Biomarkers, and Lifestyle (AIBL) Flagship Study of Ageing, correlations were conducted to determine the magnitude of relationship between cerebral Aβ and cognition in ɛ4 carriers and noncarriers. Fisher's Z was used to compare these correlations and Cohen's q determined the magnitude of difference between correlations. Results: Cerebral Aβ was significantly associated with tasks of visual and verbal episodic memory in APOE ɛ4 carriers. This association was not observed in ɛ4 noncarriers. The relationship between cerebral Aβ and episodic memory in ɛ4 carriers was significantly different from that in ɛ4 noncarriers, and the magnitude of this difference was small to moderate. Conclusions: In APOE ɛ4 carriers, there is a moderate negative relationship between cerebral Aβ and episodic memory. This suggests that increased cerebral Aβ may signify the onset of preclinical AD, especially in healthy older adults who are genetically at risk for AD.