Olfactory Dysfunction in Patients With Relapsing-Remitting Multiple Sclerosis Treated With Disease-Modifying Therapies.


Journal

Ear, nose, & throat journal
ISSN: 1942-7522
Titre abrégé: Ear Nose Throat J
Pays: United States
ID NLM: 7701817

Informations de publication

Date de publication:
Dec 2022
Historique:
pubmed: 26 11 2020
medline: 16 11 2022
entrez: 25 11 2020
Statut: ppublish

Résumé

Olfactory dysfunction evaluated with time-consuming tests was more common in patients with multiple sclerosis (MS) than in controls and correlated with neurological deficit. The aim of the present study was to compare olfactory function between patients with relapsing-remitting MS (RRMS) and controls with short and simple screening tool-the Sniffin' Sticks Identification Test (SSIT)-and search for its association with clinical and radiological features of the disease. The study included 30 controls and 30 patients with RRMS treated with disease-modifying therapies-injectables (interferon β or glatiramer acetate, N = 18) and oral drugs (dimethyl fumarate or fingolimod, N = 12). Hyposmia was defined as a score of 6 points or fewer in the SSIT olfactory test. The data concerning number of previous relapses, disability in Expanded Disability Status Scale (EDSS), and recent brain magnetic resonance imaging (MRI) scan were collected. Moreover, thalamic volume and third ventricle width were recorded in every patient. Additionally, cognition and fatigue in patients were evaluated 24 months after olfactory assessment with the Symbol Digit Modalities Test (SDMT) and Fatigue Scale for Motor and Cognitive Functions (FSMC), respectively. Patients with RRMS had a higher risk of hyposmia than controls (66.7% vs 36.7%, OR = 1.82, 95% CI, 1.10-3.67, Olfactory dysfunction is nearly twice as common in RRMS as in controls and correlates with fatigue level in patients treated with dimethyl fumarate or fingolimod.

Sections du résumé

BACKGROUND UNASSIGNED
Olfactory dysfunction evaluated with time-consuming tests was more common in patients with multiple sclerosis (MS) than in controls and correlated with neurological deficit. The aim of the present study was to compare olfactory function between patients with relapsing-remitting MS (RRMS) and controls with short and simple screening tool-the Sniffin' Sticks Identification Test (SSIT)-and search for its association with clinical and radiological features of the disease.
METHODS UNASSIGNED
The study included 30 controls and 30 patients with RRMS treated with disease-modifying therapies-injectables (interferon β or glatiramer acetate, N = 18) and oral drugs (dimethyl fumarate or fingolimod, N = 12). Hyposmia was defined as a score of 6 points or fewer in the SSIT olfactory test. The data concerning number of previous relapses, disability in Expanded Disability Status Scale (EDSS), and recent brain magnetic resonance imaging (MRI) scan were collected. Moreover, thalamic volume and third ventricle width were recorded in every patient. Additionally, cognition and fatigue in patients were evaluated 24 months after olfactory assessment with the Symbol Digit Modalities Test (SDMT) and Fatigue Scale for Motor and Cognitive Functions (FSMC), respectively.
RESULTS UNASSIGNED
Patients with RRMS had a higher risk of hyposmia than controls (66.7% vs 36.7%, OR = 1.82, 95% CI, 1.10-3.67,
CONCLUSIONS UNASSIGNED
Olfactory dysfunction is nearly twice as common in RRMS as in controls and correlates with fatigue level in patients treated with dimethyl fumarate or fingolimod.

Identifiants

pubmed: 33236917
doi: 10.1177/0145561320973777
doi:

Substances chimiques

Dimethyl Fumarate FO2303MNI2
Fingolimod Hydrochloride G926EC510T

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

640-644

Auteurs

Marcin Wnuk (M)

Department of Neurology, Jagiellonian University Medical College, Krakow, Poland.
University Hospital in Krakow, Poland.

Leszek Drabik (L)

Department of Pharmacology, Jagiellonian University Medical College, Krakow, Poland.
John Paul II Hospital, Krakow, Poland.

Monika Marona (M)

Department of Neurology, Jagiellonian University Medical College, Krakow, Poland.
University Hospital in Krakow, Poland.

Joanna Szaleniec (J)

University Hospital in Krakow, Poland.
Department of Otorhinolaryngology, Jagiellonian University Medical College, Krakow, Poland.

Amira Bryll (A)

University Hospital in Krakow, Poland.
Department of Radiology, Jagiellonian University Medical College, Krakow, Poland.

Paulina Karcz (P)

Faculty of Health Sciences, Department of Electroradiology, Institute of Physiotherapy, Jagiellonian University Medical College, Krakow, Poland.

Justyna Kolasinska (J)

Jagiellonian University Medical College, Krakow, Poland.

Monika Kolasinska (M)

Jagiellonian University Medical College, Krakow, Poland.

Maciej Ziekiewicz (M)

Jagiellonian University Medical College, Krakow, Poland.

Jacek Skladzien (J)

University Hospital in Krakow, Poland.
Department of Otorhinolaryngology, Jagiellonian University Medical College, Krakow, Poland.

Tadeusz Popiela (T)

University Hospital in Krakow, Poland.
Department of Radiology, Jagiellonian University Medical College, Krakow, Poland.

Agnieszka Slowik (A)

Department of Neurology, Jagiellonian University Medical College, Krakow, Poland.
University Hospital in Krakow, Poland.

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Classifications MeSH