Attention and Motor Learning in Adult Patients with Neurofibromatosis Type 1

Author:

Castricum Jesminne12ORCID,Tulen Joke H. M.12,Taal Walter12,Rietman André B.23,Elgersma Ype12

Affiliation:

1. Erasmus University Medical Center, Rotterdam, The Netherlands

2. The ENCORE Expertise Center for Neurodevelopmental Disorders, Erasmus MC, Rotterdam, the Netherlands

3. Erasmus University Medical Center Sophia Children’s Hospital, Rotterdam, The Netherlands

Abstract

Objective: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder that is associated with cognitive disabilities, including attention and motor learning problems. These disabilities have been extensively studied in children with NF1 but limited studies have been performed in adults. Method: Attention, motor learning and intellectual performance were studied with neuropsychological tasks in 32 adults with NF1 and 32 controls. Results: The NF1 and control group performed similarly on attention and motor learning tasks, although controls had shorter reaction times than adults with NF1 during the motor learning task ( t[60] = −2.20, p = .03). Measures of attention or motor learning were not significantly associated with reduced intellectual performance in NF1. Conclusion: In contrast to many studies in children with NF1, our findings did not provide evidence for presence of attention or motor learning problems in adults with NF1 in neuropsychological tasks. Our observations may be of clinical importance to determine treatment focus in adults with NF1.

Funder

Erasmus Medisch Centrum

Publisher

SAGE Publications

Subject

Clinical Psychology,Developmental and Educational Psychology

Reference54 articles.

1. Arffa S. (2007). The relationship of intelligence to executive function and non-executive function measures in a sample of average, above average, and gifted youth. Archives of Clinical Neuropsychology, 22(8), 969–978. https://doi.org/10.1016/j.acn.2007.08.001

2. Baudou E., Nemmi F., Biotteau M., Maziero S., Assaiante C., Cignetti F., Vaugoyeau M., Audic F., Peran P., Chaix Y. (2020). Are morphological and structural MRI characteristics related to specific cognitive impairments in neurofibromatosis type 1 (NF1) children? European Journal of Paediatric Neurology, 28, 89–100. https://doi.org/10.1016/j.ejpn.2020.07.003

3. Baudou E., Nemmi F., Biotteau M., Maziero S., Peran P., Chaix Y. (2019). Can the cognitive phenotype in neurofibromatosis type 1 (NF1) Be explained by neuroimaging? A review. Frontiers in Neurology, 10, 1373. https://doi.org/10.3389/fneur.2019.01373

4. Biotteau M., Déjean S., Lelong S., Iannuzzi S., Faure-Marie N., Castelnau P., Rivier F., Lauwers-Cancès V., Baudou E., Chaix Y. (2020). Sporadic and familial variants in NF1: An explanation of the wide variability in neurocognitive phenotype? Frontiers in Neurology, 11, 368. https://doi.org/10.3389/fneur.2020.00368

5. Biotteau M., Tournay E., Baudou E., Destarac S., Iannuzzi S., Faure-Marie N., Castelnau P., Schweitzer E., Rodriguez D., Kemlin I., Dorison N., Rivier F., Carneiro M., Preclaire E., Barbarot S., Lauwers-Cancès V., Chaix Y. (2021). Reading comprehension impairment in children with neurofibromatosis type 1 (NF1): The need of multimodal assessment of attention. Journal of Child Neurology, 883073820981270. https://doi.org/10.1177/0883073820981270

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