Knight et al., 2018. Olfactory Identification and Episodic Memory in Older Adults

Knight, J. E., Bennett, D. A., & Piccinin, A. M. (2018). Variability and Coupling of Olfactory Identification and Episodic Memory in Older Adults. The Journals of Gerontology: Series B. DOI: 10.1093/geronb/gby058. 

Year: 
2018
Status: 
complete
Presentation Citations: 

Knight, J. E., & Piccinin, A. M. (2018, April). Poster. Foreshadowing Alzheimer’s: Variability and Coupling of Olfaction and Cognition. In D. Burgoyne & R. Gooding (Eds.), Research Now: Contemporary Writing in the Disciplines. Broadview Press.

Knight, J. E., & Piccinin, A. M. (2017, July). Foreshadowing Alzheimer’s: Variability and Coupling of Olfaction and Cognition. Poster presented at 21st IAGG World Congress of Gerontology and Geriatrics (IAGG), San Francisco, USA.

Knight, J. E., & Piccinin, A. M. (2016, November). Olfaction as a Predictor of Alzheimer’s Disease Pathology in Old Age: A Growth Curve Analysis. Poster presented at Gerontological Society of America (GSA) Scientific Meeting, New Orleans, USA

Knight, J. E., & Piccinin, A. M. (2016, July). Olfaction as a Risk Factor for Dementia, Mortality and Stroke. Poster presented at Alzheimer’s International Conference (AAIC), Toronto, CA.

Abstract: 

Objectives: To determine whether assessment-to-assessment fluctuations in episodic memory (EM) reflect fluctuations in olfaction over time.

Methods: Within-person coupled variation in EM and the Brief Smell Identification Test (BSIT) was examined in 565 participants aged 58–106 with autopsy data from the Rush Memory and Aging Project. A growth model for up to 15 years of EM data, with BSIT as time-varying covariate, was estimated accounting for main effects of sex, education, ε4 allele, and Alzheimer’s disease (AD) pathology, BSIT and time-varying BSIT, as well as the interaction between AD pathology and time-varying BSIT.

Results: Individuals with higher BSIT scores (b = .01, standard error [SE] = .004, p = .009) had slower declines in EM. High AD pathology (b = −.06, SE = .02, p = .001) was associated with more rapid declines in EM. The association between time-specific fluctuations in EM and BSIT differed by level of AD pathology (b = .08, SE = .034, p = .028), with a higher EM–BSIT association at higher levels of pathology. Discussion: BSIT and EM fluctuate together over measurement occasions, particularly for individuals with AD pathology. Repeated intraindividual measurements provide information that could lead to early detection and inexpensive monitoring of accumulating AD pathology.