Evidence map›Paper›PMID 41201150›Full record

ArticleRevista de neurologia2025

[Epilepsy in Patients With Moyamoya Angiopathy].

Mario Bautista-Lacambra, Vanesa Garayoa-Irigoyen, Luisa-Fernanda Tique-Rojas, María Seral-Moral, Jesús Moles-Herbera, Amparo López-Lafuente, Rosario Barrena-Caballo, Carlos Tejero-Juste, Marta Palacín-Larroy, Herbert Tejada-Meza

Abstract readEnglish Abstract
In one paragraph

Article in Revista de neurologia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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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

10 authors.

Mario Bautista-LacambraServicio de Neurología, Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
Vanesa Garayoa-IrigoyenServicio de Neurología, Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
Luisa-Fernanda Tique-RojasServicio de Neurología, Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
María Seral-MoralServicio de Neurología, Hospital Universitario San Jorge, 22004 Huesca, España.
Jesús Moles-HerberaServicio de Neurocirugía, Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
Amparo López-LafuenteSección de Neuropediatría y Neurometabolismo, Servicio de Pediatría del Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
Rosario Barrena-CaballoUnidad de Neurorradiología Intervencionista del Servicio de Radiología del Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
Carlos Tejero-JusteServicio De Neurología, Hospital Clínico Universitario Lozano Blesa, 50009 Zaragoza, España.
Marta Palacín-LarroyServicio de Neurología, Hospital Universitario Miguel Servet, 50009 Zaragoza, España.
Herbert Tejada-MezaServicio de Neurología, Hospital Universitario Miguel Servet, 50009 Zaragoza, España.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMoyamoya angiopathy is a cerebrovascular disease characterized by progressive stenosis of the intracranial internal carotid arteries. There is limited literature addressing epilepsy in this condition, especially in Western countries. METHODOLOGY: This was a retrospective study conducted in the public hospitals of Aragón, analyzing data from all patients diagnosed with moyamoya angiopathy between 1981 and 2024. Epidemiological aspects of the disease were studied, as well as the presence of epilepsy and its management in this group of patients.

resultsA total of 26 patients were included, with an estimated prevalence in Aragón of 1.71 cases per 100,000 inhabitants. The mean age at diagnosis was 36.64 years, with an equal sex distribution. Half of the patients presented with moyamoya syndrome. Fifty percent of the patients experienced a seizure and 42.31% of the total met diagnostic criteria for epilepsy. Most seizures were focal (81.8%), with a predominance of frontal lobe semiology. Levetiracetam was the most commonly used treatment. Up to four of the twelve patients with epilepsy met diagnostic criteria for drug-resistant epilepsy.

conclusionsAlthough the prevalence of moyamoya in our series was lower than in Asian populations, the prevalence of epilepsy was significantly higher (50% of patients with seizures vs 0.9-18.9% in Asian series). In our cohort, epilepsy in moyamoya angiopathy was associated with the occurrence of syncope, cognitive impairment, affective disorders, and an earlier age at diagnosis. There are no other studies available addressing the percentage of drug-resistant epilepsy in these patients.

Indexed as

EpilepsyMoyamoya DiseaseAdolescentAdultAgedFemaleHumansMaleMiddle AgedPrevalenceRetrospective StudiesYoung Adultdrugresistant epilepsyepilepsymoyamoya angiopathymoyamoya diseasemoyamoya syndromeseizurestreatment

Identifiers

PMID41201150
PMCPMC12593773

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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.