Evidence map›Paper›PMID 42752999›Full record

SynthesisJournal of neurology2026

Prevalence of neuropsychiatric and seizure disorders in neurofibromatosis type 1: a systematic review and meta-analysis.

Elena Moreno-Charco, Carlos Pascual-Morena, Celia Álvarez-Bueno, Blanca Zuheros-Lara, Irene Martínez-García, Pilar Martínez-Sánchez, Miguel Contreras-Molina, Silvana Patiño-Cardona

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis 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.

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

8 authors.

Elena Moreno-CharcoAge-ABC Research Group, Health and Social Research Center, University of Castilla-La Mancha, 16071, Cuenca, Spain.ORCID http://orcid.org/0009-0009-5631-8337
Carlos Pascual-MorenaAge-ABC Research Group, Health and Social Research Center, University of Castilla-La Mancha, 16071, Cuenca, Spain. carlos.pascual@uclm.es.ORCID http://orcid.org/0000-0003-1154-8752
Celia Álvarez-BuenoAge-ABC Research Group, Health and Social Research Center, University of Castilla-La Mancha, 16071, Cuenca, Spain.ORCID http://orcid.org/0000-0002-6176-1618
Blanca Zuheros-LaraAge-ABC Research Group, Health and Social Research Center, University of Castilla-La Mancha, 16071, Cuenca, Spain.ORCID http://orcid.org/0009-0004-8496-628X
Irene Martínez-GarcíaFaculty of Nursing, University of Castilla-La Mancha, 02006, Albacete, Spain.ORCID http://orcid.org/0000-0001-7835-6953
Pilar Martínez-SánchezHealth and Social Research Center, University of Castilla-La Mancha, 16071, Cuenca, Spain.
Miguel Contreras-MolinaAge-ABC Research Group, Health and Social Research Center, University of Castilla-La Mancha, 16071, Cuenca, Spain.ORCID http://orcid.org/0000-0003-3042-5643
Silvana Patiño-CardonaAge-ABC Research Group, Health and Social Research Center, University of Castilla-La Mancha, 16071, Cuenca, Spain.ORCID http://orcid.org/0009-0001-3470-1724

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurofibromatosis type 1 (NF1) is associated with intellectual disability (ID), autism spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD), emotional and seizure disorders. However, published prevalence estimates vary widely. The aim of this meta-analysis was to estimate the prevalence of ID, ASD, ADHD, epileptic seizures and emotional disorders in NF1. A systematic search was conducted in MEDLINE, Scopus and Web of Science from inception to April 2026. Studies that estimated the proportion of patients with these disorders were included. Where possible, genotype was considered, i.e., NF1 general versus NF1 microdeletions. Random-effects meta-analyses with their 95% confidence intervals (CI) were performed. Fifty studies were included. The prevalence of ID was 8% (95% CI 6-11, n = 17) in NF1 and 41% (95% CI 29-52, n = 2) in NF1 microdeletion; the prevalence of ASD was 11% (95% CI 7-14, n = 17) in NF1; the prevalence of ADHD was 33% (95% CI 26-40, n = 29) in NF1 and 45% (95% CI 25-65, n = 2) in NF1 microdeletion; the prevalence of seizures was 11% (95% CI 8-14, n = 13); the prevalence of epilepsy was 9% (95% CI 6-11, n = 16); and the prevalence of depression and anxiety was 13% (95% CI 3-23, n = 11) and 12% (95% CI 5-20, n = 10). NF1 is associated with neuropsychiatric and seizure disorders, reinforcing existing recommendations for neuropsychiatric screening in this population. Further research incorporating molecular data is also required, particularly in the subgroup with NF1 microdeletions.

Indexed as

Attention Deficit Disorder with HyperactivityAutism Spectrum DisorderEpilepsyIntellectual DisabilityMental DisordersNeurofibromatosis 1SeizuresHumansPrevalenceChildrenNeurodevelopmental disordersNeurofibrominRAS/MAPKRASopathiesSeizures disorders

Identifiers

PMID42752999
PMCPMC13585979

What OpenQuestion holds

Textmetadata
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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.