Demyelinating diseases, particularly multiple sclerosis (MS), present a unique therapeutic challenge in the management of inflammatory bowel disease (IBD). Although rare, the co-occurrence of IBD and demyelinating disorders is well-documented and may reflect shared immune, genetic, and environmental risk factors. As the therapeutic landscape of IBD expands to include biologics and small molecules that target immune pathways also implicated in MS, concerns around neurological safety have grown. In particular, anti-tumor necrosis factor agents have been consistently linked to new-onset or worsening demyelinating events, while other treatments such as sphingosine-1-phosphate receptor modulators and natalizumab are licensed for both IBD and MS, though real-world data in patients with coexisting disease remain limited. This review synthesizes current evidence regarding the neurological safety and efficacy of IBD therapies in the context of demyelinating disease. It proposes a practical framework for clinicians, addressing management strategies for patients with confirmed MS, those at increased risk, and individuals who develop neurological symptoms during treatment. In the absence of formal guidelines, multidisciplinary collaboration, early recognition of symptoms, and careful treatment selection are important to optimize both gastrointestinal and neurological outcomes.

Inflammatory bowel disease therapies and demyelinating diseases: a practical guide to therapeutic benefit and risk / Honap, S.; Debouverie, M.; Filippi, M.; Selchen, D.; Jairath, V.; Danese, S.; Peyrin-Biroulet, L.. - In: JOURNAL OF CROHN'S AND COLITIS. - ISSN 1873-9946. - 20:1(2026). [10.1093/ecco-jcc/jjaf215]

Inflammatory bowel disease therapies and demyelinating diseases: a practical guide to therapeutic benefit and risk

Filippi M.;Danese S.
Penultimo
;
2026-01-01

Abstract

Demyelinating diseases, particularly multiple sclerosis (MS), present a unique therapeutic challenge in the management of inflammatory bowel disease (IBD). Although rare, the co-occurrence of IBD and demyelinating disorders is well-documented and may reflect shared immune, genetic, and environmental risk factors. As the therapeutic landscape of IBD expands to include biologics and small molecules that target immune pathways also implicated in MS, concerns around neurological safety have grown. In particular, anti-tumor necrosis factor agents have been consistently linked to new-onset or worsening demyelinating events, while other treatments such as sphingosine-1-phosphate receptor modulators and natalizumab are licensed for both IBD and MS, though real-world data in patients with coexisting disease remain limited. This review synthesizes current evidence regarding the neurological safety and efficacy of IBD therapies in the context of demyelinating disease. It proposes a practical framework for clinicians, addressing management strategies for patients with confirmed MS, those at increased risk, and individuals who develop neurological symptoms during treatment. In the absence of formal guidelines, multidisciplinary collaboration, early recognition of symptoms, and careful treatment selection are important to optimize both gastrointestinal and neurological outcomes.
2026
29-nov-2025
Inglese
OXFORD UNIV PRESS
20
1
jjaf215
Pubblicato
Esperti anonimi
Internazionale
Goal 3: Good health and well-being
demyelinating disease
inflammatory bowel disease
monoclonal antibodies
multiple sclerosis
Inflammatory bowel disease therapies and demyelinating diseases: a practical guide to therapeutic benefit and risk / Honap, S.; Debouverie, M.; Filippi, M.; Selchen, D.; Jairath, V.; Danese, S.; Peyrin-Biroulet, L.. - In: JOURNAL OF CROHN'S AND COLITIS. - ISSN 1873-9946. - 20:1(2026). [10.1093/ecco-jcc/jjaf215]
none
7
info:eu-repo/semantics/article
262
Honap, S.; Debouverie, M.; Filippi, M.; Selchen, D.; Jairath, V.; Danese, S.; Peyrin-Biroulet, L.
1 Contributo su Rivista::1.1.1 Articolo in rivista - Review
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/195579
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