Evidence map›Paper›PMID 38855890›Full record

Observational studyAnnals of clinical and translational neurology2024

Modifiable factors associated with Huntington's disease progression in presymptomatic participants.

Andres Gil-Salcedo, Renaud Massart, Laurent Cleret de Langavant, Anne-Catherine Bachoud-Levi

Abstract readObservational Study
In one paragraph

Observational study in Annals of clinical and translational neurology, 2024. 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
–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.

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.

  1. Review
  2. Review
  3. Review
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

4 authors.

Andres Gil-SalcedoDépartement d'Études Cognitives, École Normale Supérieure, PSL University, Paris, 75005, France.ORCID 0000-0001-7838-8752
Renaud MassartDépartement d'Études Cognitives, École Normale Supérieure, PSL University, Paris, 75005, France.
Laurent Cleret de LangavantDépartement d'Études Cognitives, École Normale Supérieure, PSL University, Paris, 75005, France.ORCID 0000-0001-6551-4641
Anne-Catherine Bachoud-LeviDépartement d'Études Cognitives, École Normale Supérieure, PSL University, Paris, 75005, France.

Funding

Fondation pour la Recherche Médicale SPF202309017513Infrastructure NeurATRIS Investissement d'Avenir-ANR-11-INBS-0011
6 · The paper itself

Abstract

objectiveHuntington's disease (HD) is a neurodegenerative disorder characterized by progressive motor, cognitive, and psychiatric symptoms. Our aim here was to identify factors that can be modified to slow disease progression even before the first symptoms appear.

methodsWe included 2636 presymptomatic individuals (comparison with family controls) drawn from the prospective observational cohort Enroll-HD, with more than 35 CAG repeats and at least two assessments of disease progression measured with the composite Huntington's disease rating Scale (cUHDRS). The association between sociodemographic factors, health behaviors, health history, and cUHDRS trajectory was assessed with a mixed-effects random forest using partial dependence plots and Shapley additive explanation method.

resultsParticipants were followed by an average of 3.4 (SD = 1.97) years. We confirmed the negative impact of age and a high number of CAG repeats. We found that a high level of education, a body mass index (BMI) <23 kg/m

interpretationReducing modifiable risk factors for HD is one way to support the presymptomatic population. A high level of education, low-to-moderate alcohol consumption, no smoking, and BMI control are likely to slow disease progression in this population.

Indexed as

Disease ProgressionHuntington DiseaseProdromal SymptomsAdultAsymptomatic DiseasesBody Mass IndexFemaleHumansMaleMiddle AgedProspective Studies

Identifiers

PMID38855890
PMCPMC11251488

What OpenQuestion holds

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Registered trials

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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.