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October 25, 2022; 99 (17) Research Article

Olfactory Dysfunction and Incidence of Motoric Cognitive Risk Syndrome

A Prospective Clinical-Pathologic Study

Nigel L. Kravatz, Emmeline Ayers, View ORCID ProfileDavid A. Bennett, Joe Verghese
First published September 8, 2022, DOI: https://doi.org/10.1212/WNL.0000000000201030
Nigel L. Kravatz
From the Department of Neurology (N.L.K., E.A., J.V.), Albert Einstein College of Medicine, Bronx, NY; Rush Alzheimer's Disease Center (D.A.B.), Rush University Medical Center, Chicago, IL; and Department of Medicine (J.V.), Albert Einstein College of Medicine, Bronx, NY.
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Emmeline Ayers
From the Department of Neurology (N.L.K., E.A., J.V.), Albert Einstein College of Medicine, Bronx, NY; Rush Alzheimer's Disease Center (D.A.B.), Rush University Medical Center, Chicago, IL; and Department of Medicine (J.V.), Albert Einstein College of Medicine, Bronx, NY.
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David A. Bennett
From the Department of Neurology (N.L.K., E.A., J.V.), Albert Einstein College of Medicine, Bronx, NY; Rush Alzheimer's Disease Center (D.A.B.), Rush University Medical Center, Chicago, IL; and Department of Medicine (J.V.), Albert Einstein College of Medicine, Bronx, NY.
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  • ORCID record for David A. Bennett
Joe Verghese
From the Department of Neurology (N.L.K., E.A., J.V.), Albert Einstein College of Medicine, Bronx, NY; Rush Alzheimer's Disease Center (D.A.B.), Rush University Medical Center, Chicago, IL; and Department of Medicine (J.V.), Albert Einstein College of Medicine, Bronx, NY.
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Olfactory Dysfunction and Incidence of Motoric Cognitive Risk Syndrome
A Prospective Clinical-Pathologic Study
Nigel L. Kravatz, Emmeline Ayers, David A. Bennett, Joe Verghese
Neurology Oct 2022, 99 (17) e1886-e1896; DOI: 10.1212/WNL.0000000000201030

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Abstract

Background and Objectives To examine associations between olfactory dysfunction, Alzheimer disease (AD) pathology, and motoric cognitive risk syndrome (MCR), a predementia syndrome characterized by cognitive complaints and slow gait that is associated with risk for AD and other dementias.

Methods We conducted a retrospective analysis of a prospective cohort study to examine whether baseline olfactory function was associated with the risk of incident MCR in 1,119 adults aged 60 years and older (75.1% female). The association between performance on the Brief Smell Identification Test (BSIT) and incident MCR risk was computed using Cox models and reported as the hazard ratio (HR) with 95% CIs adjusted for demographic, comorbidity, and cognitive factors. Furthermore, we assessed the relationship between postmortem AD pathology and non-AD pathology and olfactory function at the time of MCR diagnosis using linear regression models adjusted for sex, education, age at death, and time from diagnosis to death.

Results There were 544 (48.6%) incident cases of MCR over a median follow-up of 3.94 years. Lower BSIT scores (poor olfaction) at baseline were associated with an increased risk of incident MCR (HR for a 1-point increase in BSIT score 0.92; 95% CI 0.88–0.96) in fully adjusted models. Those with hyposmia (scores of ≤8 on the BSIT) at baseline (26.6%) were at an increased risk of MCR (HR 1.44; 95% CI 1.19–1.74) compared with those with normal olfactory function. Higher levels of the composite measure of global AD pathology and presence of Lewy body pathology were associated with lower BSIT scores at the time of incident MCR diagnosis (n = 118). τ tangle density, a specific component of AD pathology, was inversely associated with olfactory function, and the correlation remained after controlling for mild cognitive impairment syndrome and the presence of Lewy body pathology.

Discussion The results provide evidence that olfactory dysfunction precedes MCR incidence and is related to Alzheimer pathology, providing a clinical approach to risk stratify and subtype MCR.

Glossary

AD=
Alzheimer disease;
BMI=
body mass index;
BSIT=
Brief Smell Identification Test;
HR=
hazard ratio;
MAP=
Memory and Aging Project;
MCI=
mild cognitive impairment;
MCR=
motoric cognitive risk syndrome;
PHF=
paired helical filament

Footnotes

  • Go to Neurology.org/N for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Submitted and externally peer reviewed. The handling editor was Rebecca Burch, MD.

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  • Received October 22, 2021.
  • Accepted in final form June 13, 2022.
  • © 2022 American Academy of Neurology
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