Evidence map›Paper›PMID 41087665›Full record

ArticleJournal of neurology2025

Beyond motor neurons: autonomic dysfunction and ECG findings in adults with 5q-spinal muscular atrophy.

Kaan Bacara, Stevan D Stojanovic, Camilla Wohnrade, Alma Osmanovic, Olivia Schreiber-Katz, Aiden Haghikia, Susanne Petri, Bogdan Bjelica

Abstract read
In one paragraph

Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Kaan BacaraDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, 30625, Hannover, Germany.
Stevan D StojanovicDepartment of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg-Strasse 1, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0002-6285-9721
Camilla WohnradeDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0003-3035-4638
Alma OsmanovicDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0002-6012-8423
Olivia Schreiber-KatzDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0001-5621-4487
Aiden HaghikiaDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0001-9629-3298
Susanne PetriDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, 30625, Hannover, Germany.ORCID http://orcid.org/0000-0002-9783-8584
Bogdan BjelicaDepartment of Neurology, Hannover Medical School, 1, Carl-Neuberg-Strasse, 30625, Hannover, Germany. bjelica.bogdan@mh-hannover.de.ORCID http://orcid.org/0000-0002-1783-703X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background5q-Spinal muscular atrophy (SMA) is a lower motor neuron disease. However, peripheral organ involvement might contribute to its complex clinical picture, especially in severe forms. This study evaluated frequency and characteristics of autonomic symptoms, prevalence of electrocardiographic (ECG) abnormalities, and the impact of autonomic dysfunction on quality of life (QoL) in adults with SMA.

methodsAutonomic function was assessed using the SCales for Outcomes in PArkinson's disease-Autonomic Dysfunction (SCOPA-AUT). 12-Lead ECG was recorded. The Hammersmith Functional Motor Scale Expanded (HFMSE), Revised Upper Limb Module (RULM), Fatigue Severity Scale (FSS), Beck Depression Inventory (BDI), and 36-Item Short Form Health Survey (SF-36) were collected to assess motor function, fatigue, depression, and QoL.

resultsForty-three SMA patients (23 males; mean age: 37.6 ± 14.1 years) and forty-three age- and sex-matched healthy controls were included. Compared to healthy controls, SMA patients scored worse on gastrointestinal domain (2.9 ± 2.9 vs. 1.1 ± 1.5, p < 0.001) and in total SCOPA-AUT score (9.8 ± 7.3 vs. 5.7 ± 4.4, p = 0.002). More severely affected patients reported a greater burden of autonomic symptoms compared to those with milder phenotypes. Burden of autonomic symptoms correlated with QoL (ρ = - 0.33, p = 0.028). The presence of major ECG abnormalities showed a negative correlation with SMA type (ρ = - 0.39, p = 0.027), age at the time of testing (ρ = - 0.45, p = 0.009), and ambulatory status (ρ = - 0.39, p = 0.027).

conclusionAdults with SMA demonstrate a substantial burden of autonomic symptoms, especially those with more severe disease. This burden significantly compromises patients' QoL. Further studies are needed to better understand autonomic dysfunction in this population.

Indexed as

Autonomic Nervous System DiseasesMuscular Atrophy, SpinalAdultAgedElectrocardiographyFemaleHumansMaleMiddle AgedQuality of LifeSeverity of Illness IndexYoung AdultAutonomic dysfunctionECGMultisystem disorderQuality of lifeSpinal muscular atrophy

Identifiers

PMID41087665
PMCPMC12521311

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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.