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"No association between disease modifying treatment and fatigue in multiple sclerosis".
Broch, Line; Flemmen, Heidi Øyen; Simonsen, Cecilia Smith; Berg-Hansen, Pål; Ormstad, Heidi; Brunborg, Cathrine; Celius, Elisabeth Gulowsen.
Afiliação
  • Broch L; Department of Neurology, Vestre Viken Hospital Trust, Drammen, Norway; Department of Neurology, Oslo University Hospital, Norway; Institute of Clinical Medicine, University of Oslo, Norway. Electronic address: line.broch@vestreviken.no.
  • Flemmen HØ; Department of Neurology, Telemark Hosptial Trust, Skien, Norway.
  • Simonsen CS; Department of Neurology, Vestre Viken Hospital Trust, Drammen, Norway.
  • Berg-Hansen P; Department of Neurology, Oslo University Hospital, Norway.
  • Ormstad H; University of South-Eastern Norway, Norway.
  • Brunborg C; Oslo Centre for Biostatistics and Epidemiology, Oslo University Hospital, Norway.
  • Celius EG; Department of Neurology, Oslo University Hospital, Norway; Institute of Clinical Medicine, University of Oslo, Norway.
Mult Scler Relat Disord ; 79: 104993, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37708819
ABSTRACT

BACKGROUND:

Fatigue affects 60-90% of people with multiple sclerosis (MS). It reduces quality of life and the ability to work. The cause of fatigue in MS remains unknown. Several disease-modifying treatments (DMTs) slow the disease process in relapsing MS by suppressing neuroinflammation. We aimed to investigate if treatment with a DMT is associated with lower rates of fatigue.

METHODS:

In this cross-sectional study of the MS population in three counties in Norway, we used the Fatigue Scale for Motor and Cognitive Functions (FSMC) and the Hospital Anxiety and Depression Scale (HADS) to assess patient-reported fatigue, anxiety and depression. Clinical data were retrieved from the electronic patient record system. We categorized DMTs as high-efficacy therapy or moderate-efficacy therapy. High-efficacy drugs included fingolimod, natalizumab, ocrelizumab, rituximab, alemtuzumab, daclizumab, and autologous hematopoietic stem cell transplantation. Moderate-efficacy drugs included interferons, glatiramer acetate, dimethyl fumarate, and teriflunomide. We included persons with relapsing MS only.

RESULTS:

Of 1142 patients, 80% had fatigue. Fifty-six percent of the patients were on DMTs (25% on moderate-efficacy treatment and 30% on high-efficacy treatment), 18% had discontinued treatment and 26% had never received any DMT. Sex, level of disability as measured by the Multiple Sclerosis Severity Score, anxiety and depression were independently associated with fatigue. Moderate-efficacy treatment was associated with less fatigue, but not after adjustment for other variables. There was no association between high-efficacy treatment and fatigue.

CONCLUSION:

We found no independent relationship between the use of disease-modifying treatment and fatigue in MS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Recidivante-Remitente / Esclerose Múltipla Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Mult Scler Relat Disord Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Recidivante-Remitente / Esclerose Múltipla Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Mult Scler Relat Disord Ano de publicação: 2023 Tipo de documento: Article