Evidence map›Paper›PMID 41021051›Full record

ReviewRheumatology international2025

Biological therapy in a patient with coexistence of multiple sclerosis and ankylosing spondylitis: a case based review.

Iva Žagar, Marita Babić, Kristina Kovač Durmiš, Nadica Laktašić Žerjavić, Porin Perić

Abstract readCase ReportsReview
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In one paragraph

Review in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Iva ŽagarClinic for Rheumatic Diseases and Rehabilitation, University Hospital Centre Zagreb, Kišpatićeva 12, Zagreb, 10000, Croatia.ORCID 0000-0003-2168-7078
Marita BabićClinic for Rheumatic Diseases and Rehabilitation, University Hospital Centre Zagreb, Kišpatićeva 12, Zagreb, 10000, Croatia.ORCID 0009-0001-0317-006X
Kristina Kovač DurmišClinic for Rheumatic Diseases and Rehabilitation, University Hospital Centre Zagreb, Kišpatićeva 12, Zagreb, 10000, Croatia.ORCID 0000-0001-8716-4654
Nadica Laktašić ŽerjavićClinic for Rheumatic Diseases and Rehabilitation, University Hospital Centre Zagreb, Kišpatićeva 12, Zagreb, 10000, Croatia.ORCID 0000-0003-1279-3928
Porin PerićClinic for Rheumatic Diseases and Rehabilitation, University Hospital Centre Zagreb, Kišpatićeva 12, Zagreb, 10000, Croatia. porin.peric@gmail.com.ORCID 0000-0001-7416-1868

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) and ankylosing spondylitis (AS) rarely coexist. Due to possibly progressive course of disease, both AS and MS may require biological treatment. Tumor necrosis alpha (TNF-alpha) inhibitors are a group of biologics approved for treatment of AS (e.g. adalimumab, certolizumab pegol, golimumab, infliximab, etanercept), and they are usually first choice of treatment when starting biological therapy. Another group of biologic agents approved for the treatment of AS are interleukin-17 (IL-17) inhibitors, such as secukinumab and ixekizumab. It is well established that TNF-alpha inhibitors increase the risk of demyelination, and are therefore contraindicated in patients with MS. Since the patient presented in this review was diagnosed with MS few years prior to the onset of AS symptoms, selecting an appropriate biologic therapy posed a clinical challenge due to the contraindication of TNF-alpha inhibitors in individuals with MS. After consulting with the treating neurologist, we initiated treatment of AS using the IL-17 inhibitor secukinumab. This decision was supported by evidence suggesting a significant role of IL-17 in the pathogenesis of MS, potentially offering a safer alternative to TNF-alpha inhibitors in this context. The selected therapy proved to be effective, leading to a notable reduction in overall pain and morning stiffness. Clinical improvement was measured by a decrease in the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI), which dropped from 5.3 prior to treatment to 2.95 after six months of therapy.

Indexed as

Biological ProductsMultiple SclerosisSpondylitis, AnkylosingAdultAntibodies, Monoclonal, HumanizedFemaleHumansInterleukin-17MaleTreatment OutcomeAntibodies, Monoclonal, HumanizedBiological ProductsInterleukin-17secukinumab

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.