Evidence map›Paper›PMID 42217027›Full record

ArticleJournal of neuromuscular diseases2026

Screening cognitive and academic problems in Duchenne Muscular Dystrophy: Validity and reliability of the Kempenhaeghe Learning Questionnaire.

Pien Mm Weerkamp, Ruben Miranda, Daniella Chieffo, Chloe Geagan, Erik H Niks, R Jeroen Vermeulen, Isabelle Desguerre, Volker Straub, Anna Wuergler Slipsager, Anna Kolesnik and 7 more

Abstract read
In one paragraph

Article in Journal of neuromuscular diseases, 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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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

17 authors.

Pien Mm WeerkampKempenhaeghe Centre for Neurological Learning Disabilities, Heeze, The Netherlands.ORCID 0000-0002-1703-486X
Ruben MirandaDepartment of Psychobiology and Methodology in Behavioural Sciences, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0002-5816-4417
Daniella ChieffoDepartment of Paediatric Neurology, Catholic University, Rome, Italy.
Chloe GeaganNewcastle University, Newcastle, UK.
Erik H NiksDepartment of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
R Jeroen VermeulenDepartment of Neurology, Maastricht University Medical Centre, Maastricht, The Netherlands.
Isabelle DesguerreImagine Institute des maladies genetiques Necker Enfant maladies foundation, Paris, France.
Volker StraubDepartment of Neurology, Danish Neuromuscular Centre, Rigshospitalet, Copenhagen, Denmark.
Anna Wuergler SlipsagerDepartment of Neurology, Danish Neuromuscular Centre, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0002-0014-1861
Anna KolesnikDubowitz Neuromuscular Centre, UCL Great Ormond Street, Institute of Child Health, London, UK.ORCID 0000-0002-1395-0377
Elizabeth VroomWorld Duchenne Organization, Veenendaal, The Netherlands.
David SkuseDubowitz Neuromuscular Centre, UCL Great Ormond Street, Institute of Child Health, London, UK.
Francesco MuntoniDubowitz Neuromuscular Centre, UCL Great Ormond Street, Institute of Child Health, London, UK.
Eugenio MercuriDepartment of Paediatric Neurology, Catholic University, Rome, Italy.
Sylvia KlinkenbergKempenhaeghe Centre for Neurological Learning Disabilities, Heeze, The Netherlands.
Jos Gm HendriksenKempenhaeghe Centre for Neurological Learning Disabilities, Heeze, The Netherlands.
BIND Consortium Clinical Working Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDuchenne Muscular Dystrophy (DMD) patients are at an increased risk for cognitive and academic difficulties. However, a comprehensive tool to measure DMD-specific learning and academic functioning has been lacking. To address this, we developed the Kempenhaeghe Learning Questionnaire (KLQ)Objective:This study aims to evaluate the reliability and validity of the KLQ in a large sample of individuals with DMD (

methodsThe KLQ is a 20-item proxy-report questionnaire based on existing instruments, designed to screen for problems in four cognitive and academic areas in DMD: Reading, Arithmetic, Memory/Attention, and Executive Functioning. Data analysis involved a principal component analysis to identify the KLQ's factor structure and a confirmatory factor analysis to verify this structure. Reliability and validity were assessed to determine the psychometric quality.

resultsFactor analyses revealed four distinct but correlated dimensions of cognitive functioning and academic challenges in DMD, confirming a robust four-factor model for the KLQ. The questionnaire demonstrated good psychometric quality.

conclusionsThe findings suggest that the KLQ is a useful and clinically informative, brief parent-report tool that can help clinicians identify DMD-specific key cognitive and academic challenges, with a specific focus on school-related areas such as reading, arithmetic, memory, attention, and executive functioning. While this targeted scope limits its use for assessing broader aspects of cognition, it can provide valuable insights in taking care decisions, including determining whether specialised (neuro)psychological assessment is warranted.

Indexed as

academicsbrain related comorbiditiesDuchenne muscular dystrophylearning difficultiesscreening

Identifiers

PMID42217027
PMCPMC13438745

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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.