Olfactory dysfunction in cerebellar ataxia and multiple system atrophy

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

Abstract

Background:
Olfactory dysfunction has been reported in Parkinson’s (PD) and Alzheimer’s disease (AD).

Objective:
We studied olfactory function in eight patients with multiple system atrophy of cerebellar type (MSA-C), eleven patients with sporadic cerebellar ataxia of unknown etiology and thirteen controls matched for age and gender. Subjects received tests for n-butanol odor thresholds, odor identification, and odor discrimination.

Results:
Olfactory thresholds were abnormally high in 16% of the patients. Odor discrimination and odor identification were impaired in 44 % and 74% of the patients, respectively. There was no significant difference in olfactory function between patients with sporadic ataxia of unknown etiology and MSA-C patients.

Conclusions:
The present data suggest that olfactory dysfunction is common to various neurodegenerative disorders and not specifically restricted to PD or AD. Cerebellar dysfunction affected suprathreshold olfactory function more severely than odor thresholds. Thus cerebellar lesions may affect the processing of odor-related information to a higher degree than the transport of odorants to the receptor through sniffing.

Details

Original languageEnglish
Pages (from-to)1453-1455
Number of pages3
JournalJournal of neurology
Volume250
Publication statusPublished - Dec 2003
Peer-reviewedYes

External IDs

PubMed 14673578
Scopus 1642553299
ORCID /0000-0001-9713-0183/work/146645644

Keywords

Keywords

  • Multiple system atrophy, Olfactory dysfunction, Sporadic cerebellar ataxia

Library keywords