Evidence map›Paper›PMID 32886253›Full record

ArticleJournal of neurology2021

Does pallidal neuromodulation influence cognitive decline in Huntington's disease?

Emily Sanrey, Valérie Macioce, Victoria Gonzalez, Laura Cif, Fabienne Cyprien, Emilie Chan Seng, Philippe Coubes, Gaetan Poulen

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 1 country.

Emily SanreyUnité Pathologies Cérébrales Résistantes, Département de Neurochirurgie, Institut génomique Fonctionnelle, Hôpital Gui de Chauliac, INSERM, CNRS, Univ Montpellier, CHU Montpellier, 80 Avenue Augustin Fliche, 34 295, Montpellier Cedex 5, France. e-sanrey@chu-montpellier.fr.ORCID http://orcid.org/0000-0001-7942-5279
Valérie MacioceClinical Research and Epidemiology Unit, CHU Montpellier, Univ Montpellier, Montpellier, France.
Victoria GonzalezUnité Pathologies Cérébrales Résistantes, Département de Neurochirurgie, Institut génomique Fonctionnelle, Hôpital Gui de Chauliac, INSERM, CNRS, Univ Montpellier, CHU Montpellier, 80 Avenue Augustin Fliche, 34 295, Montpellier Cedex 5, France.
Laura CifUnité Pathologies Cérébrales Résistantes, Département de Neurochirurgie, Institut génomique Fonctionnelle, Hôpital Gui de Chauliac, INSERM, CNRS, Univ Montpellier, CHU Montpellier, 80 Avenue Augustin Fliche, 34 295, Montpellier Cedex 5, France.
Fabienne CyprienUnité Pathologies Cérébrales Résistantes, Département de Neurochirurgie, Institut génomique Fonctionnelle, Hôpital Gui de Chauliac, INSERM, CNRS, Univ Montpellier, CHU Montpellier, 80 Avenue Augustin Fliche, 34 295, Montpellier Cedex 5, France.
Emilie Chan SengUnité Pathologies Cérébrales Résistantes, Département de Neurochirurgie, Institut génomique Fonctionnelle, Hôpital Gui de Chauliac, INSERM, CNRS, Univ Montpellier, CHU Montpellier, 80 Avenue Augustin Fliche, 34 295, Montpellier Cedex 5, France.
Philippe CoubesUnité Pathologies Cérébrales Résistantes, Département de Neurochirurgie, Institut génomique Fonctionnelle, Hôpital Gui de Chauliac, INSERM, CNRS, Univ Montpellier, CHU Montpellier, 80 Avenue Augustin Fliche, 34 295, Montpellier Cedex 5, France.
Gaetan PoulenUnité Pathologies Cérébrales Résistantes, Département de Neurochirurgie, Institut génomique Fonctionnelle, Hôpital Gui de Chauliac, INSERM, CNRS, Univ Montpellier, CHU Montpellier, 80 Avenue Augustin Fliche, 34 295, Montpellier Cedex 5, France.
Centre National de la Recherche Scientifique · FRUniversité de Montpellier · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveHuntington's disease (HD) is an autosomal dominant neurodegenerative disorder associated with motor, psychiatric and cognitive deterioration over time. To date, Continuous Electrical Neuromodulation (CEN) of the globus pallidus internus (GPi) has been reported to improve chorea but little is known about cognitive progression in these patients. We propose to examine CEN impact on expected cognitive decline throughout long-term neuropsychological assessment of a cohort of HD patients.

method13 consecutive HD patients underwent GPi neuromodulation between January 2008 and February 2019. Over a 5-year follow-up period, they received systematic pre- and post-operative assessment according to the existing protocol in our unit. The main outcome measure was the total score obtained on the Mattis Dementia Rating Scale (MDRS) as an indicator of global cognitive function.

resultsChorea decreased in all patients postoperatively with a mean improvement of 56% despite disease progression over time, according to previous studies. Moreover we found that the global cognitive profile of HD patients treated with CEN was stable during the first 3 years of treatment.

conclusionWe report an unexpected positive influence of GPi continuous electrical neuromodulation on the progression of global cognitive functioning in operated HD patients. This is the most important group of patients treated with this method to our knowledge whatever the sample size remains small. This result provides promising evidence of GPi-CEN efficacy not only in reducing chorea, but also in delaying cognitive decline in HD patients operated at an early stage of the disease.

Indexed as

ChoreaCognitive DysfunctionDeep Brain StimulationHuntington DiseaseGlobus PallidusHumansCognitive declineContinuous electrical neuromodulationHuntington’s diseaseLongitudinal follow-up

Identifiers

PMID32886253
OpenAlexW3083036396

What OpenQuestion holds

Textmetadata
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.