Evidence map›Paper›PMID 41618146›Full record

SynthesisThe journal of headache and pain2026

Effectiveness and safety of anti-CGRP monoclonal antibodies in hemiplegic migraine: an individual patient quantitative analysis.

Marina Romozzi, Matteo Palermo, Daisuke Danno, Masahito Katsuki, Federico Tosto, Francesco Signorelli, Catello Vollono, Yasuhiko Matsumori, Paolo Calabresi, Raffaele Ornello and 1 more

Abstract readSystematic Review
In one paragraph

Synthesis 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. 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. Trial
  2. Hemiplegic migraine: genetics and pathophysiology.The Journal of clinical investigation · 2026
    Review
  3. Review
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

11 authors.

Marina Romozzi *Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Matteo Palermo *Department of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Daisuke DannoHeadache Center, Department of Neurology, Tominaga Hospital, Osaka, Japan.
Masahito KatsukiInsight Science Foundation Ireland Research Centre for Data Analytics, School of Human and Health Performance, Dublin City University, Dublin, Ireland. ktk1122nigt@gmail.com.ORCID http://orcid.org/0000-0002-0192-5430
Federico TostoDepartment of Neuroscience, "Giovanni Paolo II" Hospital, Catanzaro, Italy.
Francesco SignorelliDepartment of Neurosurgery, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Università Cattolica del Sacro Cuore, Rome, Italy.
Catello VollonoDepartment of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Yasuhiko MatsumoriSendai Headache and Neurology Clinic, Sendai, Japan.
Paolo CalabresiDepartment of Neuroscience, Università Cattolica del Sacro Cuore, Rome, Italy.
Raffaele Ornello *Department of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Luigi Francesco Iannone *Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHemiplegic migraine (HM) is a rare and disabling subtype of migraine with aura characterized by reversible motor weakness. Preventive treatment remains challenging, as patients with HM are systematically excluded from RCTs. Monoclonal antibodies targeting the calcitonin gene-related peptide pathway (anti-CGRP mAbs) have shown effectiveness in migraine with typical aura, but evidence in HM is limited.

methodsThis systematic review and quantitative synthesis followed PRISMA guidelines. PubMed, Scopus, and Web of Science were searched for studies reporting patients with HM treated with anti-CGRP mAbs. Individual patient data were extracted, and pooled analyses were conducted for changes in monthly headache days (MHDs), days with aura, and Migraine Disability Assessment (MIDAS) score from baseline to three months. Risk of bias was assessed using the GRADE approach.

resultsSix studies (four case series and two case reports), including 13 patients, met the inclusion criteria. MHDs decreased from 18 (IQR 15–25) at baseline to 9 (IQR 3–20) at three months; however, the numerical decrease was not statistically significant (p = 0.077). Median monthly days with aura decreased from 3 (IQR 2–8) to 0.6 (IQR 0–2.3; p = 0.018), and the MIDAS score decreased from 88 (IQR 66–154) to 28 (IQR 5–74; p = 0.018). Ten patients (83%) achieved > 50% reduction in MHDs and aura frequency, and nine (75%) > 50% MIDAS reduction. No adverse events were reported.

conclusionsAlthough the overall evidence certainty is very low, anti-CGRP mAbs appear to reduce aura burden and migraine-related disability in HM with good tolerability, supporting the need for prospective multicenter studies and registries to confirm their effectiveness and safety in this rare, highly disabling condition.

Indexed as

Antibodies, MonoclonalCalcitonin Gene-Related PeptideMigraine with AuraHumansTreatment OutcomeAntibodies, MonoclonalCalcitonin Gene-Related PeptideATP1A2CACN1AErenumabFamilial hemiplegic migraine (FHM)FremanezumabGalcanezumabSCN1A

Identifiers

PMID41618146
PMCPMC12930611

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Registered trials

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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.