Evidence map›Paper›PMID 42266578›Full record

ArticleFrontiers in neurology

Risk factors for disease generalization in acetylcholine receptor antibody-positive ocular myasthenia: a multicenter retrospective study.

Lorenzo Verriello, Roberto Sartor, Fabrizio Bellizzi, Chiara Dalla Torre, Maria Elena Pessa, Marco Belluzzo, Alessio Bratina, Magda Quagliotto, Chiara Rosa Mancinelli, Michele Rana and 7 more

Abstract read
In one paragraph

Article in Frontiers in neurology. 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
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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

17 authors.

Lorenzo VerrielloNeurology Unit, Department of Head-Neck and Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.
Roberto SartorSevere Acquired Brain Injury Unit, Department of Rehabilitation Medicine, Institute of Physical and Rehabilitation Medicine, University Hospital of Udine, Udine, Italy.
Fabrizio BellizziUniversity of Udine, Udine, Italy.
Chiara Dalla TorreNeurology Unit, Department of Head-Neck and Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.
Maria Elena PessaClinical Neurology Unit, Department of Head-Neck and Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.
Marco BelluzzoNeurology Unit, Department of Head-Neck and Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.
Alessio BratinaClinical Neurology Unit, Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.
Magda QuagliottoClinical Neurology Unit, Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.
Chiara Rosa MancinelliClinical Neurology Unit, Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.
Michele RanaNeurology Unit, Department of Medical, Gorizia-Monfalcone Hospital, Gorizia, Italy.
Fulvio PasquinNeurology Unit, Department of Medical, Gorizia-Monfalcone Hospital, Gorizia, Italy.
Martina FabrisDepartment of Medicine (DMED), Institute of Clinical Pathology, University of Udine, Udine, Italy.
Giada PaulettoNeurology Unit, Department of Head-Neck and Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.
Miriam IsolaDivision of Medical Statistic, Department of Medicine (DMED), University of Udine, Udine, Italy.
Maria De MartinoDivision of Medical Statistic, Department of Medicine (DMED), University of Udine, Udine, Italy.
Paolo ManganottiClinical Neurology Unit, Department of Medical, Surgical and Health Sciences, University of Trieste, Trieste, Italy.
Mariarosaria ValenteClinical Neurology Unit, Department of Head-Neck and Neurosciences, Santa Maria della Misericordia University Hospital, Udine, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: This study aimed to identify factors associated with secondary generalization in patients with ocular-onset myasthenia gravis (OoMG) who were positive for anti-acetylcholine receptor (AChR) antibodies. Early identification of patients at higher risk of progression to generalized myasthenia gravis (gMG) is clinically relevant to optimize therapeutic strategies and improve long-term outcomes. Methods: We conducted a multicenter retrospective cohort study including patients with anti-AChR-positive OoMG recruited from three Italian neurology centers. Demographic, clinical, electrophysiological, and serological data were collected. Univariable and multivariable Cox regression analyses were performed to identify factors associated with disease generalization. Results: Among 85 patients, 40 (47.1%) developed gMG during follow-up. In univariable Cox regression, higher anti-AChR antibody titers (HR 3.37, 95% CI 1.53-7.43; Conclusion: Higher anti-AChR antibody titers and abnormal facial repetitive nerve stimulation were associated with an increased risk of secondary generalization in seropositive OoMG. Although these factors did not independently predict generalization in multivariable analysis, their combined assessment may support early clinical risk stratification. Larger prospective studies are warranted to validate these findings and refine prognostic assessment.

Indexed as

anti-AChR antibodiesocular myasthenia gravispredictive factorsrepetitive nerve stimulationsecondary generalization

Identifiers

PMID42266578
PMCPMC13243071

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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.