Evidence map›Paper›PMID 31609508›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2019

How different aspects of motor dysfunction influence day-to-day function in huntington's disease.

Noelle E Carlozzi, Stephen G Schilling, Nicholas R Boileau, Kelvin L Chou, Joel S Perlmutter, Samuel Frank, Michael K McCormack, Julie C Stout, Jane S Paulsen, Jin-Shei Lai and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2019. 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
0.3field-weighted citation impact, top 46% 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, 6 citations in OpenAlex.

  1. Article
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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

11 authors at 7 institutions in 2 countries.

Noelle E CarlozziDepartment of Physical Medicine and Rehabilitation, University of Michigan, Ann Arbor, Michigan, USA.
Stephen G SchillingDepartment of Physical Medicine and Rehabilitation, University of Michigan, Ann Arbor, Michigan, USA.
Nicholas R BoileauDepartment of Physical Medicine and Rehabilitation, University of Michigan, Ann Arbor, Michigan, USA.
Kelvin L ChouDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-2597-7315
Joel S PerlmutterDepartment of Neurology, Radiology, Neuroscience, Physical Therapy and Occupational Therapy, Washington University in St. Louis, St. Louis, Missouri, USA.
Samuel FrankDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Michael K McCormackDepartment of Psychiatry, Rutgers-Robert Wood Johnson Medical School, Piscataway, New Jersey, USA.
Julie C StoutSchool of Psychological Sciences, Monash University, Clayton, Victoria, Australia.
Jane S PaulsenDepartment of Psychiatry, Neurology, and Psychological and Brain Sciences, The University of Iowa, Iowa City, Iowa, USA.
Jin-Shei LaiDepartment of Medical Social Sciences, Northwestern University, Chicago, Illinois, USA.
Praveen DayaluDepartment of Neurology, University of Michigan, Ann Arbor, Michigan, USA.
University of Michigan · USBeth Israel Deaconess Medical Center · USMonash University · AUNorthwestern University · USRutgers, The State University of New Jersey · USUniversity of Iowa · USWashington University in St. Louis · US

Funding

Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
NEUROBIOLOGICAL PREDICTORS OF HUNTINGTON'S DISEASER01NS040068 · NINDS · UNIVERSITY OF IOWA · PI PAULSEN, JANE S · 2001 to 2013
$48.5M
Validation of the HD-HRQOL (Huntington disease quality of life measure)R01NS077946 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CARLOZZI, NOELLE E. · 2012 to 2016
$3.2M
Preparing for preventive clinical trials in Huntington's diseaseU01NS105509 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI PAULSEN, JANE S · 2020 to 2025
$2.5M
Statistical disease modeling and clinimetrics to prepare for preventive trials in huntington diseaseU01NS103475 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI PAULSEN, JANE S · 2020 to 2022
$1.7M
NCATS NIH HHS UL1 TR000433NCATS NIH HHS UL1TR000433NINDS NIH HHS R01 NS040068NINDS NIH HHS R01NS040068NINDS NIH HHS R01 NS077946NINDS NIH HHS R01NS077946NINDS NIH HHS U01 NS103475NINDS NIH HHS U01 NS105509
6 · The paper itself

Abstract

purposeThis study examined the relationships between different aspects of motor dysfunction (chorea, dystonia, rigidity, incoordination, oculomotor dysfunction, dysarthria, and gait difficulties) and functional status in persons with Huntington's disease.

methodsA total of 527 persons with Huntington's disease completed the Unified Huntington's Disease Rating Scale motor, total functional capacity, and functional assessments.

resultsConfirmatory factor analysis indicated that a 4-factor model provided a better model fit than the existing 5-factor model. Exploratory factor analysis identified the following 4 factors from the motor scale: dystonia, chorea, rigidity, and a general motor factor. Regression indicated that dystonia (β = -0.47 and -0.79) and rigidity (β = -0.28 and -0.59) had strong associations with function, whereas chorea had modest correlations (β = -0.16 and -0.15).

conclusionsDystonia and rigidity have stronger relationships with functional status than chorea in persons with Huntington's disease. The findings underscore the need for further research regarding the effects of dystonia and rigidity on functioning. © 2019 International Parkinson and Movement Disorder Society.

Indexed as

AdultAgedChoreaDystoniaDystonic DisordersFactor Analysis, StatisticalFemaleHumansHuntington DiseaseMaleMiddle AgedMuscle RigidityPsychomotor PerformancechoreadystoniaHDQLIFEHealth-related quality of lifeHuntington's diseasemotor function

Identifiers

PMID31609508
PMCPMC7025393
OpenAlexW2981270811

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.