Characteristics of secondary progressive multiple sclerosis: Disease activity and provision of care in Germany - A registry-based/multicentric cohort study.


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:
Nov 2021
Historique:
received: 24 03 2021
revised: 02 09 2021
accepted: 23 09 2021
pubmed: 9 10 2021
medline: 17 12 2021
entrez: 8 10 2021
Statut: ppublish

Résumé

The tailored immunomodulatory treatment strategy for secondary progressive multiple sclerosis (SPMS) depends on disease activity. To assess the real-world situation in monitoring disease activity in SPMS patients and to identify associations of resulting subgroups with demographics, symptomatology, and therapy METHODS: This study included 4,263 SPMS patients from the German MS register (GMSR). For the classification into 'active' and 'inactive' according to relapse activity and MRI findings during the year prior to the latest clinical visit, we used the following definitions: active - gadolinium enhancing (Gd+)/new T2 lesions or ≥1 relapse, inactive - neither Gd+/new T2 lesions nor relapses. The active, inactive, and unclassifiable patients were compared in terms of clinical data, socio-demographics, symptomatology, healthcare, and DMT. Classification was possible for 1,513 (35.5%) SPMS patients, with 467 classified as active and 1,046 as inactive. For the classification, MRI data was available for 33.2% of the 4,263 patients. Higher MRI frequencies were observed for younger patients (OR 1.22 [1.12,1.33] per 10 years) with short disease duration (OR 1.19 [1.09, 1.30] per 10 years) (p < 0.001). MRI coverage was low, especially in elderly SPMS patients. Roughly one third of the SPMS patients presented markers of disease activity in the last year. Overall, the clinical differences (concerning symptomatology and care) between patients with active and inactive SPMS were small.

Sections du résumé

BACKGROUND BACKGROUND
The tailored immunomodulatory treatment strategy for secondary progressive multiple sclerosis (SPMS) depends on disease activity.
OBJECTIVE OBJECTIVE
To assess the real-world situation in monitoring disease activity in SPMS patients and to identify associations of resulting subgroups with demographics, symptomatology, and therapy METHODS: This study included 4,263 SPMS patients from the German MS register (GMSR). For the classification into 'active' and 'inactive' according to relapse activity and MRI findings during the year prior to the latest clinical visit, we used the following definitions: active - gadolinium enhancing (Gd+)/new T2 lesions or ≥1 relapse, inactive - neither Gd+/new T2 lesions nor relapses. The active, inactive, and unclassifiable patients were compared in terms of clinical data, socio-demographics, symptomatology, healthcare, and DMT.
RESULTS RESULTS
Classification was possible for 1,513 (35.5%) SPMS patients, with 467 classified as active and 1,046 as inactive. For the classification, MRI data was available for 33.2% of the 4,263 patients. Higher MRI frequencies were observed for younger patients (OR 1.22 [1.12,1.33] per 10 years) with short disease duration (OR 1.19 [1.09, 1.30] per 10 years) (p < 0.001).
CONCLUSION CONCLUSIONS
MRI coverage was low, especially in elderly SPMS patients. Roughly one third of the SPMS patients presented markers of disease activity in the last year. Overall, the clinical differences (concerning symptomatology and care) between patients with active and inactive SPMS were small.

Identifiants

pubmed: 34624644
pii: S2211-0348(21)00548-4
doi: 10.1016/j.msard.2021.103281
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

103281

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

Niklas Frahm (N)

MS Forschungs- und Projektentwicklungs- gGmbH (MS Research and Project Development gGmbH [MSFP]), Hannover, Germany. Electronic address: frahm@msregister.de.

David Ellenberger (D)

MS Forschungs- und Projektentwicklungs- gGmbH (MS Research and Project Development gGmbH [MSFP]), Hannover, Germany. Electronic address: ellenberger@msregister.de.

Firas Fneish (F)

MS Forschungs- und Projektentwicklungs- gGmbH (MS Research and Project Development gGmbH [MSFP]), Hannover, Germany. Electronic address: fneish@msregister.de.

Kleinschnitz Christoph (K)

Department of Neurology and Center of Translational and Behavioral Neurosciences (C-TNBS), University Hospital Essen, Essen, Germany. Electronic address: Christoph.Kleinschnitz@uk-essen.de.

Clemens Warnke (C)

Department of Neurology, Medical Faculty, University Hospital of Cologne, Cologne, Germany. Electronic address: clemens.warnke@uk-koeln.de.

Uwe K Zettl (UK)

Department of Neurology, Neuroimmunological Section, University of Rostock, Rostock, Germany. Electronic address: uwe.zettl@med.uni-rostock.de.

Friedemann Paul (F)

Experimental and Clinical Research Center and NeuroCure Clinical Research Center, Max Delbrueck Center for Molecular Medicine and Charité - Universitätsmedizin Berlin, Berlin, Germany. Electronic address: Friedemann.Paul@charite.de.

Benedict Rauser (B)

Novartis Pharma GmbH, Nürnberg, Germany. Electronic address: benedict.rauser@novartis.com.

Alexander Stahmann (A)

MS Forschungs- und Projektentwicklungs- gGmbH (MS Research and Project Development gGmbH [MSFP]), Hannover, Germany. Electronic address: stahmann@msregister.de.

Vroni Vogelmann (V)

Novartis Pharma GmbH, Nürnberg, Germany. Electronic address: vroni.vogelmann@novartis.com.

Peter Flachenecker (P)

Neurological Rehabilitation Center Quellenhof, Bad Wildbad, Germany. Electronic address: peter.flachenecker@sana.de.

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Classifications MeSH