Olfactory threshold as a biomarker of long-term relapse activity in multiple sclerosis.

Biomarker Disease activity Multiple sclerosis Olfactory function Relapse

Journal

Multiple sclerosis and related disorders
ISSN: 2211-0356
Titre abrégé: Mult Scler Relat Disord
Pays: Netherlands
ID NLM: 101580247

Informations de publication

Date de publication:
11 Mar 2024
Historique:
received: 23 01 2024
revised: 25 02 2024
accepted: 07 03 2024
medline: 14 3 2024
pubmed: 14 3 2024
entrez: 13 3 2024
Statut: aheadofprint

Résumé

Olfactory threshold (OT) is a marker of short-term inflammatory activity in multiple sclerosis (MS). To investigate whether OT predicts long-term MS clinical disease course. This was a 6-year prospective longitudinal study on MS patients at the MS clinic Innsbruck. Clinical visits assessing the occurrence of relapses, Expanded Disability Status Scale (EDSS) scores, and disease-modifying treatment (DMT), were conducted biannually. OT testing was performed at baseline (BL), year 1 (Y1), year 2 (Y2) and year 6 (Y6), using the threshold subscore of the "Sniffin' Sticks" test. Cognitive function was assessed by the Symbol Digit Modalities Test. Of 139 MS patients, 92 were eligible for Y6 follow-up. 68% experienced relapses, 53% EDSS worsening, 29% progression independent of relapse activity (PIRA) and 41% cognitive deterioration. OT scores were lower at BL, Y1 and Y2 in patients requiring DMT escalation. In multivariable analysis, higher OT scores at BL, Y1, Y2 and Y6 were associated with lower risk of relapse (hazard ratio, HR: 0.65-0.92) and EDSS worsening (HR: 0.86-0.89), while no associations were found for PIRA and cognitive deterioration. OT is a potential surrogate marker for long-term inflammatory disease activity and DMT failure in MS.

Sections du résumé

BACKGROUND BACKGROUND
Olfactory threshold (OT) is a marker of short-term inflammatory activity in multiple sclerosis (MS).
OBJECTIVE OBJECTIVE
To investigate whether OT predicts long-term MS clinical disease course.
METHODS METHODS
This was a 6-year prospective longitudinal study on MS patients at the MS clinic Innsbruck. Clinical visits assessing the occurrence of relapses, Expanded Disability Status Scale (EDSS) scores, and disease-modifying treatment (DMT), were conducted biannually. OT testing was performed at baseline (BL), year 1 (Y1), year 2 (Y2) and year 6 (Y6), using the threshold subscore of the "Sniffin' Sticks" test. Cognitive function was assessed by the Symbol Digit Modalities Test.
RESULTS RESULTS
Of 139 MS patients, 92 were eligible for Y6 follow-up. 68% experienced relapses, 53% EDSS worsening, 29% progression independent of relapse activity (PIRA) and 41% cognitive deterioration. OT scores were lower at BL, Y1 and Y2 in patients requiring DMT escalation. In multivariable analysis, higher OT scores at BL, Y1, Y2 and Y6 were associated with lower risk of relapse (hazard ratio, HR: 0.65-0.92) and EDSS worsening (HR: 0.86-0.89), while no associations were found for PIRA and cognitive deterioration.
CONCLUSIONS CONCLUSIONS
OT is a potential surrogate marker for long-term inflammatory disease activity and DMT failure in MS.

Identifiants

pubmed: 38479044
pii: S2211-0348(24)00124-X
doi: 10.1016/j.msard.2024.105545
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105545

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Klaus Berek: has participated in meetings sponsored by and received travel funding or speaker honoraria from Roche, Teva, Merck, Biogen, Sanofi, Novartis. He is associate editor of Frontiers in Immunology / Section Multiple Sclerosis and Neuroimmunology. Harald Hegen: has participated in meetings sponsored by, received speaker honoraria or travel funding from Bayer, Biogen, Bristol Myers Squibb, Horizon, Janssen, Merck, Novartis, Sanofi-Genzyme, Siemens, Teva, and received honoraria for acting as consultant for Biogen, Bristol Myers Squibb, Novartis, Roche and Teva. He is associate editor of Frontiers in Neurology. Michael Auer: has participated in meetings sponsored by, received speaking honoraria or travel funding from Biogen, Merck, Novartis, Horizon Therapeutics and Sanofi Genzyme. Robert Barket: has participated in meetings sponsored by or received travel grants from, Novartis, Janssen-Cilag and Sanofi-Genzyme. Received honoraria from Janssen-Cilag and Biogen. Franziska Di Pauli: has participated in meetings sponsored by, received honoraria (lectures, advisory boards, consultations) or travel funding from Bayer, Biogen, BMS, Horizon, Merck, Novartis, Sanofi-Genzyme, Teva, and Roche. Jakob Hocher: has nothing to declare. Nik Krajnc: has participated in meetings sponsored by, received speaker honoraria or travel funding from Alexion, BMS/Celgene, Janssen-Cilag, Merck, Novartis, Roche and Sanofi-Genzyme and held a grant for a Multiple Sclerosis Clinical Training Fellowship Programme from the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS). Anne Zinganell: has participated in meetings sponsored by, received speaking honoraria or travel funding from Biogen, Merck, Sanofi-Genzyme, Novartis and Teva. Florian Deisenhammer: has participated in meetings sponsored by or received honoraria for acting as an advisor/speaker for Alexion, Almirall, Biogen, Celgene/BMS, Horizon, Merck, Novartis, Roche and Sanofi. His institution received scientific grants from Biogen, Novartis, and Sanofi. Thomas Berger: has participated in meetings sponsored by and received honoraria (lectures, advisory boards, consultations) from pharmaceutical companies marketing treatments for MS: Allergan, Bayer, Biogen, Bionorica, BMS, Eisai, GW/Jazz, Horizon, Janssen-Cilag, MedDay, Merck, Novartis, Octapharma, Roche, Sanofi-Genzyme, Teva, UPC. His institution has received financial support in the past 12 months by unrestricted research grants (Biogen, Bayer, BMS, Merck, Novartis, Roche, Sanofi Aventis, Teva and for participation in clinical trials in multiple sclerosis sponsored by Alexion, Bayer, Biogen, Merck, Novartis, Octapharma, Roche, Sanofi-Genzyme, Teva. Gabriel Bsteh: has participated in meetings sponsored by, received speaker honoraria or travel funding from Biogen, Celgene/BMS, Lilly, Merck, Novartis, Roche, Sanofi-Genzyme and Teva, and received honoraria for consulting Biogen, Celgene/BMS, Novartis, Roche, Sanofi-Genzyme and Teva. He has received unrestricted research grants from Celgene/BMS and Novartis.

Auteurs

Klaus Berek (K)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Harald Hegen (H)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Michael Auer (M)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Robert Barket (R)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Franziska Di Pauli (F)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Jakob Hocher (J)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Nik Krajnc (N)

Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, Vienna 1090, Austria; Comprehensive Center for Clinical Neurosciences and Mental Health, Medical University of Vienna, Vienna, Austria.

Anne Zinganell (A)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Florian Deisenhammer (F)

Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.

Thomas Berger (T)

Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, Vienna 1090, Austria; Comprehensive Center for Clinical Neurosciences and Mental Health, Medical University of Vienna, Vienna, Austria.

Gabriel Bsteh (G)

Department of Neurology, Medical University of Vienna, Waehringer Guertel 18-20, Vienna 1090, Austria; Comprehensive Center for Clinical Neurosciences and Mental Health, Medical University of Vienna, Vienna, Austria. Electronic address: gabriel.bsteh@meduniwien.ac.at.

Classifications MeSH