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Olfactory Dysfunction in Patients With Relapsing-Remitting Multiple Sclerosis Treated With Disease-Modifying
Marcin Wnuk1,2, Leszek Drabik3,4, Monika Marona1,2
1Department of Neurology, Jagiellonian University Medical College, Krakow, Poland.
Ear, Nose, & Throat Journal
|November 25, 2020
Summary
Olfactory dysfunction is nearly twice as common in relapsing-remitting multiple sclerosis (RRMS) patients compared to controls. This dysfunction was found to correlate with fatigue in patients taking oral disease-modifying therapies.
Area of Science:
- Neurology
- Neuroscience
- Olfactory Research
Background:
- Olfactory dysfunction is more prevalent in multiple sclerosis (MS) patients than controls.
- Previous olfactory assessments were time-consuming.
- Correlation between olfactory deficit and neurological impairment in MS was previously noted.
Purpose of the Study:
- To compare olfactory function in relapsing-remitting MS (RRMS) patients versus controls using a rapid screening tool.
- To investigate the association between olfactory function and clinical/radiological features in RRMS.
Main Methods:
- Utilized the Sniffin' Sticks Identification Test (SSIT) for olfactory screening in 30 RRMS patients and 30 controls.
- Collected data on relapses, Expanded Disability Status Scale (EDSS), brain MRI, thalamic volume, and third ventricle width.
- Assessed cognition (Symbol Digit Modalities Test - SDMT) and fatigue (Fatigue Scale for Motor and Cognitive Functions - FSMC) 24 months post-olfactory testing.
Main Results:
- RRMS patients exhibited a significantly higher risk of hyposmia (66.7%) compared to controls (36.7%).
- No significant correlation was found between olfactory scores and inflammatory or neurodegenerative MS markers.
- Olfactory dysfunction correlated with fatigue (FSMC cognitive subscale) in RRMS patients on oral medications.
Conclusions:
- Olfactory dysfunction is nearly twice as common in RRMS patients compared to healthy controls.
- Olfactory dysfunction is linked to fatigue in RRMS patients treated with oral therapies like dimethyl fumarate or fingolimod.
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