Evidence map›Paper›PMID 33407722›Full record

ArticleOrphanet journal of rare diseases2021

Executive function is inversely correlated with physical function: the cognitive profile of adult Spinal Muscular Atrophy (SMA).

Lucas Mix, Olivia Schreiber-Katz, Claudia D Wurster, Zeljko Uzelac, Sophia Platen, Christina Gipperich, Gresa Ranxha, Gary Wieselmann, Alma Osmanovic, Albert C Ludolph and 2 more

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

15 citing papers in PubMed, 22 citations in OpenAlex.

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  4. Exploring variability in cognitive functioning in patients with spinal muscular atrophy: a scoping review.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
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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

12 authors at 2 institutions in 1 country.

Lucas MixDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081, Ulm, Germany.ORCID 0000-0001-5707-7840
Olivia Schreiber-KatzDepartment of Neurology, Hannover Medical School, Hannover, Germany.
Claudia D WursterDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081, Ulm, Germany.
Zeljko UzelacDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081, Ulm, Germany.
Sophia PlatenDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081, Ulm, Germany.
Christina GipperichDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081, Ulm, Germany.
Gresa RanxhaDepartment of Neurology, Hannover Medical School, Hannover, Germany.
Gary WieselmannDepartment of Neurology, Hannover Medical School, Hannover, Germany.
Alma OsmanovicDepartment of Neurology, Hannover Medical School, Hannover, Germany.
Albert C LudolphDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081, Ulm, Germany. albert.ludolph@rku.de.
Susanne PetriDepartment of Neurology, Hannover Medical School, Hannover, Germany.
Dorothée LuléDepartment of Neurology, Ulm University, Oberer Eselsberg 45, 89081, Ulm, Germany.
Universität Ulm · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpinal 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.

methodsIn 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.

resultsIn 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.

conclusionsThis 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.

Indexed as

Muscular Atrophy, SpinalSpinal Muscular Atrophies of ChildhoodAdultChildCognitionCross-Sectional StudiesExecutive FunctionHumansCognitionCognitive adaptationEdinburgh cognitive and behavioural ALS screen (ECAS)Executive functionHammersmith functional motor scale expanded (HFMSE)Reading the mind in the eyes testSMASocial cognitionSpinal muscular atrophy

Identifiers

PMID33407722
PMCPMC7789267
OpenAlexW3119444798

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.