Multiple sclerosis in the elderly: a retrospective cohort study.

Comorbidities Disease-modifying therapies Elderly Immunosenescence Late-onset multiple sclerosis Multiple sclerosis

Journal

Journal of neurology
ISSN: 1432-1459
Titre abrégé: J Neurol
Pays: Germany
ID NLM: 0423161

Informations de publication

Date de publication:
19 Oct 2023
Historique:
received: 07 07 2023
accepted: 30 09 2023
revised: 29 09 2023
medline: 19 10 2023
pubmed: 19 10 2023
entrez: 19 10 2023
Statut: aheadofprint

Résumé

There is a lack of knowledge of disease course, prognosis, comorbidities and potential treatments of elderly MS patients. To characterize the disease course including disability progression and relapses, to quantify the use of DMTs and to identify comorbidities and risk factors for progression in elderly multiple sclerosis (MS) patients. This is a retrospective study of 1200 Austrian MS patients older than 55 years as of May 1st, 2017 representing roughly one-third of all the MS patients of this age in Austria. Data were collected from 15 MS centers including demographics, first symptom at onset, number of relapses, evolvement of disability, medication, and comorbidities. Median observation time was 17.1 years with 957 (80%) relapsing and 243 (20%) progressive onsets. Average age at diagnosis was 45 years with a female predominance of 71%. Three-hundred and twenty-six (27%) patients were never treated with a DMT, while most treated patients received interferons (496; 41%) at some point. At last follow-up, 420 (35%) patients were still treated with a DMT. No difference was found between treated and never-treated patients in terms of clinical outcome; however, patients with worse disability progression had significantly more DMT switches. Pyramidal onset, number of comorbidities, dementia, epilepsy, and psychiatric conditions as well as a higher number of relapses were associated with worse outcome. The risk of reaching EDSS 6 rose with every additional comorbidity by 22%. In late and very-late-onset MS (LOMS, VLOMS) time to diagnosis took nearly twice the time compared to adult and early onset (AEOMS). The overall annualized relapse rate (ARR) decreased over time and patients with AEOMS had significantly higher ARR compared to LOMS and VLOMS. Four percent of MS patients had five medications or more fulfilling criteria of polypharmacy and 20% of psychiatric drugs were administered without a matching diagnosis. In this study, we identified number of comorbidities, pyramidal and cerebellar signs, and a higher number of relapses as unfavorable prognostic factors in elderly MS patients filling gaps of knowledge in patients usually underrepresented in clinical trials and may guide future therapeutic studies.

Sections du résumé

BACKGROUND BACKGROUND
There is a lack of knowledge of disease course, prognosis, comorbidities and potential treatments of elderly MS patients.
OBJECTIVE OBJECTIVE
To characterize the disease course including disability progression and relapses, to quantify the use of DMTs and to identify comorbidities and risk factors for progression in elderly multiple sclerosis (MS) patients.
METHODS METHODS
This is a retrospective study of 1200 Austrian MS patients older than 55 years as of May 1st, 2017 representing roughly one-third of all the MS patients of this age in Austria. Data were collected from 15 MS centers including demographics, first symptom at onset, number of relapses, evolvement of disability, medication, and comorbidities.
RESULTS RESULTS
Median observation time was 17.1 years with 957 (80%) relapsing and 243 (20%) progressive onsets. Average age at diagnosis was 45 years with a female predominance of 71%. Three-hundred and twenty-six (27%) patients were never treated with a DMT, while most treated patients received interferons (496; 41%) at some point. At last follow-up, 420 (35%) patients were still treated with a DMT. No difference was found between treated and never-treated patients in terms of clinical outcome; however, patients with worse disability progression had significantly more DMT switches. Pyramidal onset, number of comorbidities, dementia, epilepsy, and psychiatric conditions as well as a higher number of relapses were associated with worse outcome. The risk of reaching EDSS 6 rose with every additional comorbidity by 22%. In late and very-late-onset MS (LOMS, VLOMS) time to diagnosis took nearly twice the time compared to adult and early onset (AEOMS). The overall annualized relapse rate (ARR) decreased over time and patients with AEOMS had significantly higher ARR compared to LOMS and VLOMS. Four percent of MS patients had five medications or more fulfilling criteria of polypharmacy and 20% of psychiatric drugs were administered without a matching diagnosis.
CONCLUSIONS CONCLUSIONS
In this study, we identified number of comorbidities, pyramidal and cerebellar signs, and a higher number of relapses as unfavorable prognostic factors in elderly MS patients filling gaps of knowledge in patients usually underrepresented in clinical trials and may guide future therapeutic studies.

Identifiants

pubmed: 37855871
doi: 10.1007/s00415-023-12041-1
pii: 10.1007/s00415-023-12041-1
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

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Auteurs

Anne Zinganell (A)

Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

Georg Göbel (G)

Department of Medical Statistics, Informatics and Health Economics, Medical University Innsbruck, Innsbruck, Austria.

Klaus Berek (K)

Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

Barbara Hofer (B)

Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

Susanne Asenbaum-Nan (S)

Department of Neurology, Hospital of Mauer Amstetten, Mauer, Austria.

Matin Barang (M)

Department of Neurology, Hospital of St. Pölten, St. Pölten, Austria.

Klaus Böck (K)

Department of Neurology, Kepler Universitätsklinikum, Linz, Austria.

Christian Bsteh (C)

Neurologist, Salzburg, Austria.

Gabriel Bsteh (G)

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

Stephan Eger (S)

Department of Neurology, Kepler Universitätsklinikum, Linz, Austria.

Christian Eggers (C)

Department of Neurology, Kepler Universitätsklinikum, Linz, Austria.

Elisabeth Fertl (E)

Department of Neurology, Klinik Landstrasse, Vienna, Austria.

Damir Joldic (D)

Department of Neurology, Klinik Landstrasse, Vienna, Austria.

Michael Khalil (M)

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

Dieter Langenscheidt (D)

Department of Neurology, Hospital of Rankweil, Rankweil, Austria.

Martina Komposch (M)

Department of Neurology, Hospital of Klagenfurt, Klagenfurt, Austria.

Barbara Kornek (B)

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

Jörg Kraus (J)

Neurologist, Zell Am See, Austria.
Department of Laboratory Medicine, Paracelsus Medical University and Salzburger Landeskliniken, Salzburg, Austria.
Department of Neurology, Medical Faculty, Heinrich-Heine-University, Düsseldorf, Germany.

Reinhard Krendl (R)

Department of Neurology, Hospital of Villach, Villach, Austria.

Helmut Rauschka (H)

Department of Neurology, Klinik Donaustadt, Vienna, Austria.
Karl Landsteiner Institute for Neuroimmunological and Neurodegenerative Disorders, Department of Neurology, Klinik Donaustadt, Vienna, Austria.

Johann Sellner (J)

Department of Neurology, Landesklinikum Mistelbach, Mistelbach, Austria.

Michael Auer (M)

Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

Harald Hegen (H)

Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

Franziska Di Pauli (FD)

Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.

Florian Deisenhammer (F)

Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria. florian.deisenhammer@tirol-kliniken.at.

Classifications MeSH