Evidence map›Paper›PMID 37480400›Full record

ArticleJournal of neurology2023

Disability in cerebellar ataxia syndromes is linked to cortical degeneration.

Julian Conrad, Anna Huppert, Ria Maxine Ruehl, Max Wuehr, Roman Schniepp, Peter Zu Eulenburg

Open access · hybridAbstract read
In one paragraph

Article in Journal of neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.7field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
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

6 authors at 4 institutions in 1 country.

Julian Conrad *German Center for Vertigo and Balance Disorders and Department of Neurology, Munich University Hospital, LMU Munich, Marchioninistr. 15, 81377, Munich, Germany. Julian.conrad@med.uni-muenchen.de.ORCID http://orcid.org/0000-0001-7912-0571
Anna Huppert *German Center for Vertigo and Balance Disorders and Department of Neurology, Munich University Hospital, LMU Munich, Marchioninistr. 15, 81377, Munich, Germany.
Ria Maxine RuehlGerman Center for Vertigo and Balance Disorders and Department of Neurology, Munich University Hospital, LMU Munich, Marchioninistr. 15, 81377, Munich, Germany.
Max WuehrGerman Center for Vertigo and Balance Disorders (DSGZ), LMU Munich, Munich, Germany.
Roman Schniepp *German Center for Vertigo and Balance Disorders and Department of Neurology, Munich University Hospital, LMU Munich, Marchioninistr. 15, 81377, Munich, Germany.
Peter Zu Eulenburg *German Center for Vertigo and Balance Disorders (DSGZ), LMU Munich, Munich, Germany.
German Center for Lung Research · DELMU Klinikum · DELudwig-Maximilians-Universität München · DEUniversity of Mannheim · DE

Funding

Bundesministerium für Bildung, Wissenschaft, Forschung und Technologie BMBFBundesministerium für Bildung, Wissenschaft, Forschung und Technologie IFB 01EO1401Else Kröner-Fresenius-Stiftung 2018EKES09 80766157
6 · The paper itself

Abstract

objectiveWe aimed to relate clinical measures of disability in chronic cerebellar degeneration to structural whole-brain changes using voxel-based and surface-based morphometry (vbm and sbm). We were particularly interested in remote effects of cerebellar degeneration in the cerebral cortex.

methodsWe recruited 30 patients with cerebellar degeneration of different aetiologies (downbeat nystagmus syndrome, DBN n = 14, spinocerebellar ataxia, SCA n = 9, sporadic adult late-onset ataxia, SAOA n = 7). All patients were thoroughly characterised in the motor, cognitive, vestibular and ocular-motor domains. Vbm and sbm were used to evaluate structural differences between cerebellar degeneration patients and a group of healthy age- and gender-matched volunteers. Linear regression models were used to correlate functional measures of disease progression and postural stability with whole brain volumetry.

resultsPatients with SCA and SAOA showed widespread volume loss in the cerebellar hemispheres and less prominently in the vermis. Patients with DBN showed a distinct pattern of grey matter volume (GMV) loss that was restricted to the vestibular and ocular-motor representations in lobules IX, X and V-VII. Falls were associated with brainstem white matter volume. VBM and SBM linear regression models revealed associations between severity of ataxic symptoms, cognitive performance and preferred gait velocity. This included extra-cerebellar (sub-)cortical hubs of the motor and locomotion network (putamen, caudate, thalamus, primary motor cortex, prefrontal cortex) and multisensory areas involved in spatial navigation and cognition.

conclusionFunctional disability in multiple domains was associated with structural changes in the cerebral cortex.

Indexed as

Cerebellar AtaxiaCerebellar DiseasesAdultAtaxiaCerebellumHumansMagnetic Resonance ImagingSyndromeCerebellarDownbeat nystagmusSpinocerebellar ataxiaSurface-based morphometryVoxel-based morphometry

Identifiers

PMID37480400
PMCPMC10576698
OpenAlexW4385073947

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.