Evidence map›Paper›PMID 31985471›Full record

Trial reportJournal of Huntington's disease2020

Baseline Variables Associated with Functional Decline in 2CARE, A Randomized Clinical Trial in Huntington's Disease.

Andrew McGarry, Michael P McDermott, Karl Kieburtz, Jing Peng, Merit Cudkowicz, Huntington Study Group 2CARE Investigators and Coordinators

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of Huntington's disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 99% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Sertraline treatment prevents motor dysfunction in a Huntington's disease mouse model and functional decline in patients.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    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.

Andrew McGarryCooper University Healthcare at Rowan University, Camden, NJ, USA.
Michael P McDermottUniversity of Rochester, Rochester, NY, USA.
Karl KieburtzUniversity of Rochester, Rochester, NY, USA.
Jing PengThe Ohio State University, Columbus, OH, USA.
Merit CudkowiczHarvard Medical School, Boston, MA, USA.
Huntington Study Group 2CARE Investigators and Coordinators
Harvard University · USUniversity of Rochester · USRowan University · USThe Ohio State University · US

Funding

Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
NCATS NIH HHS UL1 TR001420
6 · The paper itself

Abstract

backgroundDespite the clearly recognized progressive functional decline of Huntington's disease (HD), detailed investigations of factors associated with the rate of functional progression are limited.

objectiveUnderstanding factors associated with functional decline through examination of existing HD clinical databases may improve efforts to mitigate it.

methodsWe analyzed data from 2CARE, a randomized clinical trial with up to 5 years of follow-up, to assess potential risk factors for more rapid functional decline in HD.

resultsVariables associated with faster functional decline included worse motor performance, worse cognitive test scores, female sex, lower weight and body mass index, and a higher CAG repeat length, especially in younger people.

conclusionWhile our data are limited to the structured environment and homogeneity of a clinical trial, attention to several of the identified risk factors may be useful towards managing functional decline over time. The observation that women progress faster than men, while potentially confounded by an association between sex and weight, deserves further study.

Indexed as

Disease ProgressionSeverity of Illness IndexAdultAge FactorsBody Mass IndexBody WeightCognitive DysfunctionFemaleFollow-Up StudiesHumansHuntington DiseaseMaleMiddle AgedMotor ActivityRisk FactorsSex Factorsclinical trialfunctional declineHuntington’s diseasetotal functional capacity

Identifiers

PMID31985471
PMCPMC8216232
OpenAlexW3002943976

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.