Evidence map›Paper›PMID 40526577›Full record

ReviewDeutsches Arzteblatt international2025

Treatment Options for the Comorbidity of Multiple Sclerosis with Other Chronic Inflammatory Diseases.

Stefan Bittner, Martin A Kriegel, Britta Siegmund, Tania Kümpfel, Robert Sabat

Abstract readReview
In one paragraph

Review in Deutsches Arzteblatt international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Treatment approaches to patients with multiple sclerosis and coexisting psoriasis - A longitudinal multicenter observational cohort study.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Observational
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Stefan BittnerDepartment of Neurology, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany; Section of Rheumatology and Clinical Immunology, Medical Clinic D, University Hospital Münster, Münster, Germany and Department of Translational Rheumatology and Immunology, Institute of Musculoskeletal Medicine, Münster, Germany, and Department of Immunobiology, Yale School of Medicine, New Haven, Connecticut, USA; Medical Department, Division of Gastroenterology, Infectiology and Rheumatology, Charite - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Campus Benjamin Franklin, Berlin, Germany; Institute of Clinical Neuroimmunology, Ludwig-Maximilians-Universität München (LMU), Munich, Germany; Psoriasis Research and Treatment Center, Department of Dermatology, Venerology and Allergology and Institut für Medizinische Immunologie, Charite-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Berlin, Germany.
Martin A Kriegel
Britta Siegmund
Tania Kümpfel
Robert Sabat

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApproximately 280 000 people in Germany suffer from multiple sclerosis (MS), an autoimmune disease of the central nervous system. Of these, approximately 5% have a comorbid chronic inflammatory disease: the more common ones are psoriasis, rheumatoid arthritis (RA), and chronic inflammatory bowel diseases (IBDs, of which the main types are ulcerative colitis and Crohn's disease).

methodsThis narrative review is based on pertinent publications retrieved by a literature search in PubMed, as well as relevant guidelines. All statements in this article reflect a consensus among the authors, who represent different medical disciplines.

resultsAs the data from clinical trials to date are limited, judgments about the proposed treatments are a matter of expert opinion. In general, TNFα blockers should not be used in patients with MS, as they can worsen the disease. In patients with MS and psoriasis, dimethyl fumarate is a useful option for mild disease activity. In MS with comorbid RA, azathioprine and leflunomide/teriflunomide are suitable for mild disease activity. For more severe disease activity, anti-CD20 antibodies have been approved for both diseases and should be used. In MS with comorbid IBD, azathioprine is suitable for mild disease activity. Ozanimod has been approved for patients who have MS and comorbid ulcerative colitis with more severe disease activity, especially those who are JCnegative; it shares its mechanism of action (VLA-4 blockade) with natalizumab.

conclusionThe treatment of patients who have both MS and another chronic inflammatory disease should be interdisciplinary and personalized, and treatments must be planned with due attention to potential adverse effects. Further studies of treatment for this group of patients are needed.

Indexed as

Arthritis, RheumatoidImmunosuppressive AgentsInflammatory Bowel DiseasesMultiple SclerosisPsoriasisChronic DiseaseComorbidityEvidence-Based MedicineGermanyHumansTreatment OutcomeImmunosuppressive Agents

Identifiers

PMID40526577
PMCPMC12580836

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.