Odor identification as a biomarker of preclinical AD in older adults at risk

Marie Elyse Lafaille-Magnan, Judes Poirier, Pierre Etienne, Jennifer Tremblay-Mercier, Joanne Frenette, Pedro Rosa-Neto, John C.S. Breitner

Research output: Contribution to journalArticlepeer-review

Abstract

Objective: To assess odor identification (OI) as an indicator of presymptomatic Alzheimer disease (AD) pathogenesis in cognitively normal aging individuals at increased risk of AD dementia. Methods: In 274 members of the PREVENT-AD cohort of healthy aging persons with a parental or multiple-sibling history of AD dementia, we assessed the cross-sectional association of OI with potential indicators of presymptomatic AD. Some 101 participants donated CSF, thus enabling assessment of AD pathology with the biomarkers total tau (t-tau), phospho-tau (P 181 -tau), and their ratios with β-amyloid (Aβ 1-42). Adjusted analyses considered age, cognition, APOE ϵ4 status, education, and sex as covariates. We measured OI using the University of Pennsylvania Smell Identification Test and cognitive performance using the Repeatable Battery for Assessment of Neuropsychological Status. Standard kits provided assays of the AD biomarkers. Analyses used robust-fit linear regression models. Results: Reduced OI was associated with lower cognitive score and older age, as well as increased ratios of CSF t-tau and P 181 -tau to Aβ 1-42 (all p < 0.02). However, the observed associations of OI with age and cognition were unapparent in adjusted models that restricted observations to CSF donors and included AD biomarkers. OI showed little association with CSF Aβ 1-42 alone except in APOE ϵ4 carriers having lowest-quartile Aβ 1-42 levels. Conclusions: These findings from healthy high-risk older individuals suggest that OI reflects degree of preclinical AD pathology, while its relationships with age and cognition result from the association of these latter variables with such pathology. Diminished OI may be a practical and affordable biomarker of AD pathology.

Original languageEnglish (US)
Pages (from-to)327-335
Number of pages9
JournalNeurology
Volume89
Issue number4
DOIs
StatePublished - Jul 25 2017

ASJC Scopus subject areas

  • Clinical Neurology

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