Evidence map›Paper›PMID 40387217›Full record

ArticleJournal of intellectual disability research : JIDR2025

Characterisation of Challenging Behaviours and Associated Genetic and Neurological Features in Cardiofaciocutaneous Syndrome.

Dante J Rogers, Rebekah L Hudock, Adele F Dimian, Josue Collazo-Lopez, Ryan Shanley, Elizabeth I Pierpont

Abstract read
In one paragraph

Article in Journal of intellectual disability research : JIDR, 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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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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Dante J RogersDepartment of Pediatrics, University of Minnesota Medical School, Minneapolis, USA.
Rebekah L HudockDepartment of Pediatrics, University of Minnesota Medical School, Minneapolis, USA.
Adele F DimianInstitute on Community Integration, University of Minnesota, Minneapolis, USA.
Josue Collazo-LopezPonce Health Sciences University School of Medicine, Ponce, Puerto Rico.
Ryan ShanleyClinical and Translational Science Institute, University of Minnesota, Minneapolis, USA.
Elizabeth I PierpontDepartment of Pediatrics, University of Minnesota Medical School, Minneapolis, USA.ORCID 0000-0001-7555-8613

Funding

University of Minnesota Clinical and Translational Science Institute (UMN CTSI)UM1TR004405 · NCATS · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar, Damien A Fair · 2023 to 2026
$30.8M
CFC InternationalNational Center for Advancing Translational Sciences of the National Institutes of Health Award UM1TR004405NCATS NIH HHS UM1 TR004405University of Minnesota Department of Pediatrics
6 · The paper itself

Abstract

backgroundChallenging behaviours such as self-injury and aggression are prevalent among individuals with intellectual disability (ID), significantly impacting quality of life. Cardiofaciocutaneous syndrome (CFCS), a rare multisystem genetic disorder caused by variants in the BRAF, MAP2K1, MAP2K2, or KRAS genes, commonly presents with ID and other neurobehavioural features. To inform effective clinical management, we aimed to characterise and quantify challenging and repetitive behaviours in CFCS, identify functions that may maintain the behaviours, and examine associations with genotype and neurological comorbidities.

methodsIn this cross-sectional cohort study, caregivers of 61 individuals with CFCS (mean age = 14.2 years; 61% female) completed an electronic survey to capture information regarding demographics, adaptive skills, and neurological history. Genotype was determined from molecular genetic testing results. The frequency, severity, topography, and function of challenging behaviours were assessed with behaviour questionnaires validated for children and adults with developmental disabilities. We evaluated trends using descriptive analyses and examined mean differences across age, genotype, and neurological variables.

resultsThe cohort consisted primarily of individuals with BRAF variants (62%), followed by MAP2K1 (28%) and MAP2K2 (10%) variants. Prevalence of challenging behaviour was high (77%), and self-injurious and aggressive behaviours were most frequent and severe among adolescents with CFCS relative to younger children or adults. Escape (seeking to avoid an unwanted situation or task) was the most endorsed behavioural function to maintain self-injurious and aggressive/destructive behaviours. BRAF gene variants were associated with the most frequent and variable challenging behaviours, followed by MAP2K1, and then MAP2K2. Challenging and repetitive behaviours were most prevalent among individuals with moderate adaptive functioning, clinically significant sleep disturbance, higher levels of pain interference, and more substantial sensory modulation differences. Individuals with epilepsy also exhibited more frequent repetitive and self-injurious behaviours.

conclusionCaregivers reported a high prevalence of challenging behaviours among individuals with CFCS, especially in late childhood and adolescence. Therapeutic approaches to address challenging behaviours are needed to optimally support individuals with CFCS and their caregivers.

Indexed as

Ectodermal DysplasiaFailure to ThriveHeart Defects, CongenitalIntellectual DisabilityProblem BehaviorSelf-Injurious BehaviorAdolescentAdultChildCohort StudiesComorbidityCross-Sectional StudiesFaciesFemaleHumansMaleBRAF protein, humanMAP2K1 protein, humanMAP Kinase Kinase 1MAP Kinase Kinase 2Proto-Oncogene Proteins B-rafcardiofaciocutanous syndromechallenging behaviourneurologicalpainRASopathiessensory

Identifiers

PMID40387217
PMCPMC12245549

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LicenceCC BY-NC-ND
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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.