Evidence map›Paper›PMID 25339740›Full record

Trial reportThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

Cognitive deterioration and functional compensation in ALS measured with fMRI using an inhibitory task.

Kelsey Witiuk, Juan Fernandez-Ruiz, Ryan McKee, Nadia Alahyane, Brian C Coe, Michel Melanson, Douglas P Munoz

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  4. Article
  5. Surface-based Analyses of Diffusional Kurtosis Imaging in Amyotrophic Lateral Sclerosis: Relationship with Onset Subtypes.Magnetic resonance in medical sciences : MRMS : an official journal of Japan Society of Magnetic Resonance in Medicine · 2025
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  15. Eye tracking metrics to screen and assess cognitive impairment in patients with neurological disorders.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2020
    Review
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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

7 authors at 2 institutions in 2 countries.

Kelsey WitiukCentre for Neuroscience Studies, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Juan Fernandez-RuizDepartamento de Fisiología, Facultad de Medicina, Universidad Nacional Autónoma de México, Distrito Federal 04510, México.ORCID http://orcid.org/0000-0002-4038-0904
Ryan McKeeDepartment of Medicine, Division of Neurology, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Nadia AlahyaneCentre for Neuroscience Studies, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Brian C CoeCentre for Neuroscience Studies, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Michel MelansonDepartment of Medicine, Division of Neurology, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Douglas P MunozCentre for Neuroscience Studies, Queen's University, Kingston, Ontario K7L 3N6, Canada, Department of Medicine, Division of Neurology, Queen's University, Kingston, Ontario K7L 3N6, Canada, Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Ontario K7L 3N6, Canada, and Department of Psychology, Queen's University, Kingston, Ontario K7L 3N6, Canada doug.munoz@queensu.ca.
Queen's University · CAUniversidad Nacional Autónoma de México · MX

Funding

Canadian Institutes of Health Research MOP-97741
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis (ALS) is characterized by degeneration of upper and lower motor neurons, resulting in progressive weakness and muscle atrophy. Recent studies suggest that nondemented ALS patients can show selective cognitive impairments, predominantly executive dysfunction, but little is known about the neural basis of these impairments. Oculomotor studies in ALS have described deficits in antisaccade execution, which requires the implementation of a task set that includes inhibition of automatic responses followed by generation of a voluntary action. It has been suggested that the dorsolateral prefrontal cortex (DLPFC) contributes in this process. Thus, we investigated whether deterioration of executive functions in ALS patients, such as the ability to implement flexible behavior during the antisaccade task, is related to DLPFC dysfunction. While undergoing an fMRI scan, 12 ALS patients and 12 age-matched controls performed an antisaccade task with concurrent eye tracking. We hypothesized that DLPFC deficits would appear during the antisaccade preparation stage, when the task set is being established. ALS patients made more antisaccade direction errors and showed significant reductions in DLPFC activation. In contrast, regions, such as supplementary eye fields and frontal eye fields, showed increased activation that was anticorrelated with the number of errors. The ALS group also showed reduced saccadic latencies that correlated with increased activation across the oculomotor saccade system. These findings suggest that ALS results in deficits in the inhibition of automatic responses that are related to impaired DLPFC activation. However, they also suggest that ALS patients undergo functional changes that partially compensate the neurological impairment.

Indexed as

Adaptation, PhysiologicalAdultAgedAmyotrophic Lateral SclerosisCognition DisordersFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNerve NetPhotic StimulationPsychomotor PerformanceReaction TimeSaccadesamyotrophic lateral sclerosisantisaccadecognitive controlfMRIprefrontal cortextask set

Identifiers

PMID25339740
PMCPMC6608393
OpenAlexW2139724215

What OpenQuestion holds

Textmetadata
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.