Cognitive and behavioral functioning in two neurogenetic disorders; how different are these aspects in Duchenne muscular dystrophy and Neurofibromatosis type 1?

Danique M J Hellebrekers*, Sandra A M van Abeelen, Coriene E Catsman, Sander M J van Kuijk, Annick M Laridon, Sylvia Klinkenberg, Jos G M Hendriksen, Johan S H Vles

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The presence of neurocognitive and behavioral problems are common features in various neurogenetic disorders. In Duchenne muscular dystrophy (DMD), these problems have been linked to mutations along the dystrophin gene affecting different brain dystrophin isoforms. However, comparable cognitive and behavioral problems have been found in Neurofibromatosis type 1 (NF1). This study aims to assess disorder specific differences in cognition and behavior between DMD and NF1. Retrospective data of 38 male patients with DMD were aged-matched with data of 38 male patients with NF1. Patients of both groups underwent neurocognitive assessment for regular clinical care. Intellectual abilities, sequential and simultaneous processing, verbal memory and sustained attention were evaluated. In addition, parents and teachers completed behavioral questionnaires. Males with DMD exhibited low intellectual abilities and sequential processing problems, but these outcomes not significantly differed from males with NF1. Simultaneous processing, verbal memory and sustained attention outcomes were equal for both groups. Outcomes of questionnaires displayed higher rates of aggressive behavior (13.2%) in DMD, whereas in NF1 higher rates of problems with thinking (15.8%), withdrawn (10.5%) and social behavior (10.5%) were noticed. In the neurogenetic disorders DMD and NF1, on average overlapping cognitive and behavioral problems are noticed, suggesting that these are not only caused by gene mutations resulting in a lack of one specific protein.

Original languageEnglish
Article numbere0275803
Number of pages23
JournalPLOS ONE
Volume17
Issue number10
DOIs
Publication statusPublished - 10 Oct 2022

Keywords

  • Aged
  • Cognition
  • Dystrophin/genetics
  • Humans
  • Male
  • Muscular Dystrophy, Duchenne/complications
  • Neurofibromatosis 1/complications
  • Protein Isoforms
  • Retrospective Studies

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