Evidence map›Paper›PMID 34445070›Full record

ReviewInternational journal of molecular sciences2021

New Avenues for the Treatment of Huntington's Disease.

Amy Kim, Kathryn Lalonde, Aaron Truesdell, Priscilla Gomes Welter, Patricia S Brocardo, Tatiana R Rosenstock, Joana Gil-Mohapel

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed, 3 pooled it
12.7field-weighted citation impact, top 1% 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

107 citing papers in PubMed, 3 syntheses or guidelines pooled it, 182 citations in OpenAlex.

  1. Pooled it
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  17. Nursing in Huntington's Disease and Cell and Gene Therapy.Advances in experimental medicine and biology · 2026
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47 more citing papers are in PubMed but not listed here.

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

7 authors at 4 institutions in 3 countries.

Amy KimIsland Medical Program and Faculty of Medicine, University of British Columbia, Victoria, BC V8P 5C2, Canada.ORCID 0000-0003-1170-5551
Kathryn LalondeIsland Medical Program and Faculty of Medicine, University of British Columbia, Victoria, BC V8P 5C2, Canada.
Aaron TruesdellDivision of Medical Sciences, University of Victoria, Victoria, BC V8P 5C2, Canada.
Priscilla Gomes WelterNeuroscience Graduate Program, Federal University of Santa Catarina, Florianópolis 88040-900, Brazil.ORCID 0000-0002-0278-7746
Patricia S BrocardoNeuroscience Graduate Program, Federal University of Santa Catarina, Florianópolis 88040-900, Brazil.
Tatiana R RosenstockInstitute of Cancer and Genomic Science, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
Joana Gil-MohapelIsland Medical Program and Faculty of Medicine, University of British Columbia, Victoria, BC V8P 5C2, Canada.ORCID 0000-0003-4982-1662
University of British Columbia · CAUniversidade Federal de Santa Catarina · BRUniversidade de São Paulo · BRWestern University · CA

Funding

University of Victoria UVic-FAPESP SPRINT 1/2018 Grant
6 · The paper itself

Abstract

Huntington's disease (HD) is a neurodegenerative disorder caused by a CAG expansion in the HD gene. The disease is characterized by neurodegeneration, particularly in the striatum and cortex. The first symptoms usually appear in mid-life and include cognitive deficits and motor disturbances that progress over time. Despite being a genetic disorder with a known cause, several mechanisms are thought to contribute to neurodegeneration in HD, and numerous pre-clinical and clinical studies have been conducted and are currently underway to test the efficacy of therapeutic approaches targeting some of these mechanisms with varying degrees of success. Although current clinical trials may lead to the identification or refinement of treatments that are likely to improve the quality of life of those living with HD, major efforts continue to be invested at the pre-clinical level, with numerous studies testing novel approaches that show promise as disease-modifying strategies. This review offers a detailed overview of the currently approved treatment options for HD and the clinical trials for this neurodegenerative disorder that are underway and concludes by discussing potential disease-modifying treatments that have shown promise in pre-clinical studies, including increasing neurotropic support, modulating autophagy, epigenetic and genetic manipulations, and the use of nanocarriers and stem cells.

Indexed as

AnimalsAutophagyClinical Trials as TopicDisease ManagementDisease Models, AnimalHumansHuntington Diseaseautophagyclinical trialdisease-modifying treatmentepigeneticsgeneticsHuntington’s diseasepre-clinical studytransgenic mouse modeltrophic support

Identifiers

PMID34445070
PMCPMC8394361
OpenAlexW3187326368

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.