Evidence map›Paper›PMID 33374658›Full record

ArticleBrain sciences2020

Cognitive Performance of Patients with Adult 5q-Spinal Muscular Atrophy and with Amyotrophic Lateral Sclerosis.

Alma Osmanovic, Gary Wieselmann, Lucas Mix, Hannah Alexandra Siegler, Mareike Kumpe, Gresa Ranxha, Claudia D Wurster, Alexander Steinke, Albert C Ludolph, Bruno Kopp and 3 more

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. 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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  9. Cognitive reserve protects ALS-typical cognitive domains: A longitudinal study.Annals of clinical and translational neurology · 2022
    Article
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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

13 authors at 2 institutions in 1 country.

Alma OsmanovicDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.
Gary WieselmannDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.
Lucas MixDepartment of Neurology, Neuropsychology, University of Ulm, 89081 Ulm, Germany.
Hannah Alexandra SieglerDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.
Mareike KumpeDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.
Gresa RanxhaDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.
Claudia D WursterDepartment of Neurology, University of Ulm, 89081 Ulm, Germany.
Alexander SteinkeDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0002-9892-9189
Albert C LudolphDepartment of Neurology, Neuropsychology, University of Ulm, 89081 Ulm, Germany.
Bruno KoppDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0001-8358-1303
Dorothée LuléDepartment of Neurology, Neuropsychology, University of Ulm, 89081 Ulm, Germany.
Susanne PetriDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.
Olivia Schreiber-KatzDepartment of Neurology, Hannover Medical School, 30625 Hannover, Germany.ORCID 0000-0001-5621-4487
Medizinische Hochschule Hannover · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motor neuron diseases, such as spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS), share several clinical similarities while differing substantially in etiology, disease onset and progression. Cognitive dysfunction, a clinically relevant non-motor feature in a substantial proportion of ALS patients, has been less frequently investigated in SMA. In this prospective multicenter cross-sectional study, cognitive function was assessed by the Edinburgh Cognitive (and Behavioural) ALS Screen (ECAS) and a German vocabulary test (Wortschatztest, WST) in 34 adult patients with SMA types 2-4 and in 34 patients with ALS. Demographic and clinical parameters were assessed to identify factors that potentially influence cognitive function. While SMA and ALS patients were comparable in the vocabulary test, on average, SMA patients performed better than ALS patients in the cognitive domains of memory, language and executive function. Better cognitive abilities in SMA patients seemed to be related to the early onset, rather than the extent or the duration, of their physical handicap. Future studies should focus on disease-specific cognitive functions in SMA.

Indexed as

amyotrophic lateral sclerosis (ALS)cognitive functionEdinburgh Cognitive and Behavioural ALS Screen (ECAS)German vocabulary test (Wortschatztest, WST)motor neuron diseasespinal muscular atrophy (SMA)

Identifiers

PMID33374658
PMCPMC7822456
OpenAlexW3116841091

What OpenQuestion holds

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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.