Executive function is inversely correlated with physical function: the cognitive profile of adult spinal muscular atrophy (SMA)

peer-reviewed
Erstveröffentlichung
2021-01-06Authors
Mix, Lucas John
Schreiber‑Katz, Olivia
Wurster, Claudia D.
Uzelac, Zeljko
Platen, Sophia
Wissenschaftlicher Artikel
Published in
Orphanet Journal of Rare Diseases ; 16 (2021). - Art.-Nr. 10. - eISSN 1750-1172
Link to original publication
https://dx.doi.org/10.1186/s13023-020-01661-9Institutions
UKU. Klinik für NeurologieRehabilitationskrankenhaus Ulm
External cooperations
Medizinische Hochschule HannoverDocument version
published version (publisher's PDF)Abstract
Background: Spinal muscular atrophy (SMA) issues from mutations in the survival of motor neuron (SMN) 1 gene. Loss
or reduction of the SMN protein results in progressive muscle weakness. Whether this protein deficiency also affects
cortical function remains unclear. While no data on adult patients exists so far, prior studies in children with SMA indicate
cognitive abilities equal or even superior to healthy controls. This may suggest a possible compensatory—neuropsychological
and interactional—process. The goal of this study was to assess the cognitive profile of adult patients
with SMA, with a special focus on social cognition as a potential candidate for enhanced cognitive function through
compensatory processes.
Methods: In a cross-sectional design, N = 31 adult SMA patients (types II and III) were assessed for language, verbal
fluency, memory, visuospatial abilities and executive function with the Edinburgh Cognitive and Behavioural ALS
Screen and for social cognition with the Reading the Mind in the Eyes Test. Physical function was evaluated using the
Hammersmith Functional Motor Scale Expanded. N = 19 neurologically healthy controls were matched with patients
for age, sex and years of education.
Results: In none of the abovementioned cognitive domains significant differences between SMA patients and
controls were found. Among patients, no differences between type II SMA and type III SMA were detected for any
domain. However, a trend towards better social cognition in patients with type II SMA, compared to those with type
III SMA was observed. Furthermore, a significant inverse correlation of physical function and executive function was
detected: lower motor function was associated with a better executive function.
Conclusions: This study shows cognitive abilities in adult SMA in the normal range for all assessed domains. Thus,
reduction of SMN protein has no obvious negative impact on cognitive function. Executive functions are identified
as the only cognitive domain correlated with disease severity. Therefore, executive functions may play a role in the
adaptation to physical restrictions in SMA, making them a promising target for future research.
Publication funding
Open-Access-Förderung durch die Medizinische Fakultät der Universität Ulm
Subject headings
[GND]: Spinale Muskelatrophie | Kognition[MeSH]: Muscular atrophy, Spinal | Cognition | Social cognition | Executive function
[Free subject headings]: Spinal muscular atrophy | SMA | Cognitive adaptation | Edinburgh cognitive and behavioural ALS screen (ECAS) | Reading the mind in the eyes test | Hammersmith functional motor scale expanded (HFMSE)
[DDC subject group]: DDC 610 / Medicine & health
Metadata
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Please use this identifier to cite or link to this item: http://dx.doi.org/10.18725/OPARU-38404
Mix, Lucas John et al. (2021): Executive function is inversely correlated with physical function: the cognitive profile of adult spinal muscular atrophy (SMA). Open Access Repositorium der Universität Ulm und Technischen Hochschule Ulm. http://dx.doi.org/10.18725/OPARU-38404
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