Evidence map›Paper›PMID 42399797›Full record

ArticleThe journal of headache and pain2026

Predictive factors of response to anti-CGRP pathway drugs in people with multiple sclerosis.

Viviana Nociti, Simone Cesarano, Marina Romozzi, Rocco Totaro, Maria Albanese, Alfonsina Casalena, Pietro Annovazzi, Roberta Fantozzi, Carla Tortorella, Marco Vercellino and 18 more

Abstract readMulticenter Study
In one paragraph

Article in The journal of headache and pain, 2026. 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

28 authors.

Viviana Nociti *Centro di Ricerca per la Sclerosi Multipla 'Anna Paola Batocchi', Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy. viviana.nociti@policlinicogemelli.it.
Simone Cesarano *Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Marina RomozziNeurologia, Dipartimento di Neuroscienze, Organi di Senso e Torace, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy. marinaromozzi@gmail.com.
Rocco TotaroDepartment of Neurology, Multiple Sclerosis Center, San Salvatore Hospital, L'Aquila, Italy.
Maria AlbaneseUnit of Neurology, Department of Systems Medicine, Tor Vergata University, Rome, Italy.
Alfonsina CasalenaHeadache Center, UOC Neurologia and Stroke Unit, G. Mazzini Hospital, Teramo, Italy.
Pietro AnnovazziMultiple Sclerosis Center, Hospital of Gallarate - ASST della Valle Olona, Gallarate, Italy.
Roberta FantozziUnit of Neurology, IRCCS Neuromed, Pozzilli, Isernia, Italy.
Carla TortorellaMultiple Sclerosis Center, Neurology Unit S. Camillo-Forlanini Hospital, Rome, Italy.
Marco VercellinoDepartment of Neuroscience, City of Health and Science, University Hospital of Turin, Turin, Italy.
Luigi Francesco IannoneDepartment of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Giovanna De LucaCentre for Disability, Rehabilitation and Sports Medicine (CARES), Department of Neurosciences, Imaging and Clinical Sciences, University G. d'Annunzio, Chieti, Italy.
Valentina TomassiniCentre for Disability, Rehabilitation and Sports Medicine (CARES), Department of Neurosciences, Imaging and Clinical Sciences, University G. d'Annunzio, Chieti, Italy.
Massimiliano Di FilippoSection of Neurology, Department of Medicine and Surgery, University of Perugia, Perugia, Italy.
Lorena LoreficeMultiple Sclerosis Center, Binaghi Hospital, ASL Cagliari, Cagliari, Italy.
Giorgia Teresa ManiscalcoMultiple Sclerosis Center, Cardarelli Hospital, Naples, Italy.
Damiano PaolicelliDepartment of Translational Biomedicines and Neurosciences, University of Bari Aldo Moro, Bari, Italy.
Federica PinardiIRCCS Istituto delle scienze neurologiche di Bologna, UOSI Riabilitazione Sclerosi Multipla, Bologna, Italy.
Valentina Torri ClericiNeuroimmunology and Neuromuscular Diseases Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.
Girolama Alessandra MarfiaUnit of Neurology, Department of Systems Medicine, Tor Vergata University, Rome, Italy.
Diego CentonzeUnit of Neurology, Department of Systems Medicine, Tor Vergata University, Rome, Italy.
Claudio Marcello SolaroRehabilitation Department, Mons. L. Novarese, Moncrivello, Vercelli, Italy.
Claudio GasperiniMultiple Sclerosis Center, Neurology Unit S. Camillo-Forlanini Hospital, Rome, Italy.
Paolo CalabresiNeurologia, Dipartimento di Neuroscienze, Organi di Senso e Torace, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Massimiliano MirabellaCentro di Ricerca per la Sclerosi Multipla 'Anna Paola Batocchi', Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Catello VollonoNeurologia, Dipartimento di Neuroscienze, Organi di Senso e Torace, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Eleonora CoccoMultiple Sclerosis Center, Binaghi Hospital, ASL Cagliari, Cagliari, Italy.
Francesca PistoiaDepartment of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMigraine is common in people with multiple sclerosis (PwMS) and substantially contributes to disability and impaired quality of life. Although (CGRP)-targeting therapies have reshaped migraine prevention, evidence on their use in PwMS remains scarce, particularly in people receiving concomitant disease-modifying therapies (DMTs).

methodsWe retrospectively collected data from 17 Italian multiple sclerosis (MS) centers on adult PwMS with comorbid migraine treated with anti-CGRP monoclonal antibodies or gepants in addition to stable DMTs. Monthly headache days (MHDs) and total number of analgesics per month were compared between treatment initiation and last follow-up. MS activity was assessed through clinical relapses, Expanded Disability Status Scale (EDSS), and MRI findings. A ≥ 50% reduction in MHDs defined treatment response. Multivariate regression models were used to explore predictors of response to anti-CGRP therapies.

resultsFifty-four patients were included (46 women; mean age 42.3 years; 85% relapsing MS). Baseline MHDs averaged 19.87 ± 6.97 and declined to 11.40 ± 9.35 at follow-up (p < 0.001), with a parallel decrease in analgesic use (p < 0.001). Responder rate at the last follow-up was 53.7%. MS disease activity remained stable, with no significant changes in relapse rate, EDSS score, or MRI activity. Higher baseline headache burden was associated with greater reduction in MHDs (β=+0.685, p < 0.001), whereas longer MS duration predicted poorer response (OR1.43, 95%CI 1.06-1.92, p = 0.016). Mild adverse events occurred in four patients (7%), without treatment discontinuation.

conclusionAnti-CGRP pathway therapies provided meaningful migraine improvement in PwMS while maintaining MS stability. MS disease duration and baseline headache frequency may influence therapeutic response to anti-CGRP drugs in PwMS. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Antibodies, MonoclonalCalcitonin Gene-Related PeptideImmunologic FactorsMigraine DisordersMultiple SclerosisAdultAnalgesicsFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeAnalgesicsAntibodies, MonoclonalCalcitonin Gene-Related PeptideImmunologic FactorsCGRPDisease-modifying therapiesMigraineMultiple sclerosis

Identifiers

PMID42399797
PMCPMC13430695

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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.