Evidence map›Paper›PMID 39985726›Full record

ArticleJournal of neurology2025

Specific contribution of cognitive and motor impairments with functional capacity and dependence in Huntington's disease.

Andres Gil-Salcedo, Marine Lunven, Charlotte Jacquemot, Renaud Massart, Anne-Catherine Bachoud-Levi

2 registry-linked trialsAbstract read
In one paragraph

Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this 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
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.

NCT01412125 unknown statusnot on this map

Study of Biomarkers That Predict the Evolution of Huntington's Disease

TypeobservationalSponsorAssistance Publique - Hôpitaux de ParisRan2003 to 2021Enrolled1,800ConditionsHuntington DiseaseArmsHuntington patient evaluation, Healthy subject evaluation
NCT03119246 naunknown statusnot on this map

Beta Testing of a New Assessment Protocol for Assessment of Complex Therapies in Huntington's Disease (HD)

TypeinterventionalSponsorAssistance Publique - Hôpitaux de ParisRan2016 to 2018Enrolled40ConditionsHuntington DiseaseArmsCAPIT-HD beta
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Visual cognition as a marker of longitudinal disease progression in Huntington's disease.International journal of clinical and health psychology : IJCHP
    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

5 authors.

Andres Gil-SalcedoDépartement d'Études Cognitives, École Normale Supérieure, PSL University, 75005, Paris, France. andres.gil-salcedo@inserm.fr.ORCID http://orcid.org/0000-0001-7838-8752
Marine LunvenDépartement d'Études Cognitives, École Normale Supérieure, PSL University, 75005, Paris, France.
Charlotte JacquemotDépartement d'Études Cognitives, École Normale Supérieure, PSL University, 75005, Paris, France.
Renaud MassartDépartement d'Études Cognitives, École Normale Supérieure, PSL University, 75005, Paris, France.
Anne-Catherine Bachoud-LeviDépartement d'Études Cognitives, École Normale Supérieure, PSL University, 75005, Paris, France.

Funding

Fondation pour la Recherche Médicale SPF202309017513Neuratris Avenir -ANR-11-INBS-0011
6 · The paper itself

Abstract

backgroundHuntington's disease (HD) leads to increasing dependence. Unlike psychiatric disorders, motor and cognitive deficits evolve progressively over time. Understanding their specific impact on daily activities is crucial for preserving autonomy. However, because cognitive tasks in HD rely on motor functions, and motor tasks demand cognitive processing, disentangling their specific impact remains a challenge.

objectiveTo identify the specific contribution of cognitive and motor impairments on global functional capacity, basic and instrumental activities of daily living (ADL/IADL), and work-related activities (WRA) in HD.

methods158 HD mutation carriers, enrolled in the BioHD (NCT01412125) and RepairHD (NCT03119246) studies, were evaluated with the Unified Huntington's Disease Rating Scale and the SelfCog. The SelfCog assesses motor processing separately from memory, language, executive functions and visuospatial processing. Linear regressions were fitted to assess how functional capacity declined with motor and cognition impairments. Odds of dependence in ADLs, IADLs and WRAs were estimated using logistic regressions.

resultsCognitive and motor performance were independently associated with functional capacities, though motor performance showed a stronger association than cognitive performance. Decline of all SelfCog cognitive domains contributed to functional decline, with stronger association with global and executive scores compared to language, visuospatial, and memory domains. Higher global and executive deficits were associated with an increased risk of dependence in ADLs, IADLs, and WRAs.

conclusionThe independent contributions of motor, followed by cognitive-mainly executive-functions to functional decline suggest targeted interventions to preserve autonomy and quality of life in HD.

Indexed as

Activities of Daily LivingCognitive DysfunctionHuntington DiseaseAdultExecutive FunctionFemaleHumansMaleMiddle AgedNeuropsychological TestsAutonomy lossCognitive and Motor impairmentDependencyFunctional capacityHuntinton's Disease

Identifiers

PMID39985726
PMCPMC11846732

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.