Evidence map›Paper›PMID 35562536›Full record

ArticleExperimental brain research2022

Essential tremor impairs the ability to suppress involuntary action impulses.

Jessi M Kane, Jessica L McDonnell, Joseph S Neimat, Peter Hedera, Wery P M van den Wildenberg, Fenna T Phibbs, Elise B Bradley, Scott A Wylie, Nelleke C van Wouwe

Open access · bronzeAbstract read
In one paragraph

Article in Experimental brain research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Dopamine system involvement in impulse control.Experimental brain research · 2024
    Article
  2. 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 4 institutions in 2 countries.

Jessi M KaneDepartment of Neurosurgery, University of Louisville, Louisville, KY, USA.
Jessica L McDonnellDepartment of Neurosurgery, University of Louisville, Louisville, KY, USA.
Joseph S NeimatDepartment of Neurosurgery, University of Louisville, Louisville, KY, USA.
Peter HederaDepartment of Neurology, University of Louisville, Louisville, KY, USA.
Wery P M van den WildenbergDepartment of Psychology, University of Amsterdam, Amsterdam, The Netherlands.
Fenna T PhibbsDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA.
Elise B BradleyDepartment of Neurology, Vanderbilt University Medical Center, Nashville, TN, USA.
Scott A WylieDepartment of Neurosurgery, University of Louisville, Louisville, KY, USA.
Nelleke C van WouweDepartment of Neurosurgery, University of Louisville, Louisville, KY, USA. Nelleke.vanwouwe@uoflhealth.org.ORCID http://orcid.org/0000-0002-7839-0470
University of Louisville · USVanderbilt University Medical Center · USUniversity of Amsterdam · NLUniversity of Louisville Physicians · US

Funding

Vanderbilt Institute for Clinical and Translational Research (VICTR) -Identifying correlates of functional immunity in SARS-CoV-2 convalescent plasmaUL1TR002243 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Paul A. Harris, Wesley H Self · 2017 to 2026
$130.7M
Modulating Inhibitory Action Control Systems With Subthalamic Nucleus StimulationR01NS100996 · NINDS · UNIVERSITY OF LOUISVILLE · PI NEIMAT, JOSEPH S, VAN WOUWE, NELLEKE C. · 2018 to 2022
$1.7M
NCATS NIH HHS UL1 TR002243NINDS NIH HHS R01 NS100996
6 · The paper itself

Abstract

Essential tremor (ET) is a movement disorder characterized primarily by action tremor which affects the regulation of movements. Disruptions in cerebello-thalamocortical networks could interfere with cognitive control over actions in ET, for example, the ability to suppress a strong automatic impulse over a more appropriate action (conflict control). The current study investigated whether ET impacts conflict control proficiency. Forty-one ET patients and 29 age-matched healthy controls (HCs) performed a conflict control task (Simon task). Participants were instructed to give a left or right response to a spatially lateralized arrow (direction of the arrow). When the action signaled by the spatial location and direction of the arrow were non-corresponding (induced conflict), the inappropriate action impulse required suppression. Overall, ET patients responded slower and less accurately compared to HCs. ET patients were especially less accurate on non-corresponding conflict (Nc) versus corresponding (Cs) trials. A focused analysis on fast impulsive response rates (based on the accuracy rate at the fastest reaction times on Nc trials) showed that ET patients made more fast errors compared to HCs. Results suggest impaired conflict control in ET compared to HCs. The increased impulsive errors seen in the ET population may be a symptom of deficiencies in the cerebello-thalamocortical networks, or, be caused by indirect effects on the cortico-striatal pathways. Future studies into the functional networks impacted by ET (cortico-striatal and cerebello-thalamocortical pathways) could advance our understanding of inhibitory control in general and the cognitive deficits in ET.

Indexed as

Essential TremorCerebellumHumansImpulsive BehaviorReaction TimeCerebellumCognitive controlConflict controlEssential tremorMovement disorder

Identifiers

PMID35562536
PMCPMC11150918
OpenAlexW4280490546

What OpenQuestion holds

Textmetadata
LicenceTDM
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.