Evidence map›Paper›PMID 34362104›Full record

ArticleJournal of clinical medicine2021

Cerebellar Dysfunction in Adults with Prader Willi Syndrome.

Laura Blanco-Hinojo, Laia Casamitjana, Jesus Pujol, Gerard Martínez-Vilavella, Susanna Esteba-Castillo, Olga Giménez-Palop, Valentín Freijo, Joan Deus, Assumpta Caixàs

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.7field-weighted citation impact, top 15% 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, 10 citations in OpenAlex.

  1. Analysis ofGenes · 2022
    Review
  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

9 authors at 5 institutions in 1 country.

Laura Blanco-HinojoMRI Research Unit, Department of Radiology, Hospital del Mar, 08003 Barcelona, Spain.
Laia CasamitjanaEndocrinology and Nutrition Department, Institut d'Investigació I Innovació Parc Taulí I3PT, Parc Taulí Hospital Universitari, 08208 Sabadell, Spain.
Jesus PujolMRI Research Unit, Department of Radiology, Hospital del Mar, 08003 Barcelona, Spain.
Gerard Martínez-VilavellaMRI Research Unit, Department of Radiology, Hospital del Mar, 08003 Barcelona, Spain.
Susanna Esteba-CastilloSpecialized Service in Mental Health and Intellectual Disability, Institut Assistència Sanitària (IAS), Parc Hospitalari Martí i Julià, 17190 Girona, Spain.
Olga Giménez-PalopEndocrinology and Nutrition Department, Institut d'Investigació I Innovació Parc Taulí I3PT, Parc Taulí Hospital Universitari, 08208 Sabadell, Spain.
Valentín FreijoPhysical Medicine and Rehabilitation Department, Parc Taulí Hospital Universitari, 08208 Sabadell, Spain.
Joan DeusMRI Research Unit, Department of Radiology, Hospital del Mar, 08003 Barcelona, Spain.
Assumpta CaixàsEndocrinology and Nutrition Department, Institut d'Investigació I Innovació Parc Taulí I3PT, Parc Taulí Hospital Universitari, 08208 Sabadell, Spain.ORCID 0000-0001-8472-9189
Universitat Autònoma de Barcelona · ESCentro de Investigación Biomédica en Red de Salud Mental · ESCorporació Sanitària Parc Taulí · ESHospital Del Mar · ESInstitut d'Investigació Biomèdica de Girona · ES

Funding

Fondo de Investigación Sanitaria del Instituto Carlos III and Fondo Europeo de Desarrollo Regional PI-18/00734
6 · The paper itself

Abstract

Severe hypotonia during infancy is a hallmark feature of Prader Willi syndrome (PWS). Despite its transient expression, moto development is delayed and deficiencies in motor coordination are present at older ages, with no clear pathophysiological mechanism yet identified. The diverse motor coordination symptoms present in adult PWS patients could be, in part, the result of a common alteration(s) in basic motor control systems. We aimed to examine the motor system in PWS using functional MRI (fMRI) during motor challenge. Twenty-three adults with PWS and 22 matched healthy subjects participated in the study. fMRI testing involved three hand motor tasks of different complexity. Additional behavioral measurements of motor function were obtained by evaluating hand grip strength, functional mobility, and balance. Whole brain activation maps were compared between groups and correlated with behavioral measurements. Performance of the motor tasks in PWS engaged the neural elements typically involved in motor processing. While our data showed no group differences in the simplest task, increasing task demands evoked significantly weaker activation in patients in the cerebellum. Significant interaction between group and correlation pattern with measures of motor function were also observed. Our study provides novel insights into the neural substrates of motor control in PWS by demonstrating reduced cerebellar activation during movement coordination.

Indexed as

cerebellumfMRImotor systemPrader Willi syndrome

Identifiers

PMID34362104
PMCPMC8347444
OpenAlexW3185044937

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.