Evidence map›Paper›PMID 41735672›Full record

ArticleJournal of neurology2026

Could galcanezumab modulate inflammatory cytokines? A single-centre exploratory study.

Giulia Ceccardi, Renata Rao, Francesca Schiano di Cola, Beatrice Fiducia, Chiara Tolassi, Virginia Quaresima, Irene Mattioli, Klaudia Eshja, Elena Cresta, Stefano Gipponi and 2 more

Abstract read
In one paragraph

Article in Journal of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

12 authors.

Giulia CeccardiNeurology Unit, Ospedale Maggiore di Cremona, ASST-Cremona, 26100, Cremona, Italy. giulia.ceccardi@outlook.it.ORCID http://orcid.org/0000-0003-1595-3894
Renata RaoDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.
Francesca Schiano di ColaDepartment of Clinical and Experimental Sciences, University of Brescia, 25123, Brescia, Italy.
Beatrice FiduciaDepartment of Clinical and Experimental Sciences, University of Brescia, 25123, Brescia, Italy.
Chiara TolassiDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.
Virginia QuaresimaDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.
Irene MattioliDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.ORCID https://orcid.org/0000-0002-8821-3523
Klaudia EshjaDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.
Elena CrestaDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.
Stefano GipponiNeurology Unit, Ospedale Maggiore di Cremona, ASST-Cremona, 26100, Cremona, Italy.
Andrea PilottoDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.ORCID https://orcid.org/0000-0003-2029-6606
Alessandro PadovaniDepartment of Continuity of Care and Frailty, Neurology Unit, ASST Spedali Civili Hospital, 25123, Brescia, Italy.ORCID https://orcid.org/0000-0002-0119-3639

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMigraine is a highly disabling neurological disorder. The pathophysiological mechanisms underlying this condition are complex and not yet fully elucidated. While calcitonin gene-related peptide (CGRP) plays a pivotal role in the genesis of migraine, not all patients respond to CGRP-targeted therapeutic interventions, suggesting the involvement of alternative mechanisms such as neuroinflammation. In this context, cytokines may act as modulators of inflammatory responses associated with migraine. The objective of this study is to evaluate cytokine profiles in patients with episodic and chronic migraine in comparison with healthy controls and to investigate the modulatory effect of galcanezumab treating episodic migraine patients.

methodsin this prospective pilot study, 17 patients with high-frequency episodic migraine (EM), 18 with chronic migraine (CM), and 17 healthy controls (HC) were enrolled. Plasma cytokine levels (IFN-γ, IL-1β, IL-10, IL-6, TNF-α) were measured using multiplex immunoassay during the interictal phase. Blood samples of the EM group eligible for treatment with galcanezumab were additionally collected at three time points: baseline (T0) and 5 and 27 days after administration of galcanezumab (T5, corresponding to the maximum serum concentration (Cmax), and T27, drug half-life, respectively).

resultsIn comparison with patients diagnosed with CM and HC, EM patients demonstrated elevated interictal levels of IFN-γ, IL-1β, IL-6 and IL-10 (p < 0.001). In perspective analyses, a significant decrease in cytokine levels was observed in the galcanezumab-treated group at Cmax (T5) for IFN-γ, IL-1β, IL-10, and TNF-α, but not for IL-6 (p = 0.640). DISCUSSION: This study highlights distinct cytokine profiles associated with chronic and episodic migraine. Treatment with galcanezumab was associated with a transient reduction in both pro- and anti-inflammatory cytokines during the first month of therapy. These findings support the hypothesis that CGRP could influence the inflammatory pathways in migraine pathophysiology.

Indexed as

Antibodies, Monoclonal, HumanizedCytokinesMigraine DisordersAdultFemaleHumansMaleMiddle AgedPilot ProjectsProspective StudiesAntibodies, Monoclonal, HumanizedCytokinesgalcanezumabAnti-CGRP monoclonal antibodiesCytokinesInflammationMigraine

Identifiers

PMID41735672
PMCPMC12932395

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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.