Evidence map›Paper›PMID 37626771›Full record

ReviewBiomedicines2023

Brain-Derived Neurotrophic Factor Dysregulation as an Essential Pathological Feature in Huntington's Disease: Mechanisms and Potential Therapeutics.

Andrew Speidell, Noman Bin Abid, Hiroko Yano

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Andrew SpeidellDepartment of Neurological Surgery, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.ORCID 0000-0002-0348-5301
Noman Bin AbidDepartment of Neurological Surgery, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.ORCID 0000-0001-6929-8878
Hiroko YanoDepartment of Neurological Surgery, Washington University School of Medicine in St. Louis, St. Louis, MO 63110, USA.ORCID 0000-0001-6548-0920
Washington University in St. Louis · US

Funding

Role of DNA methyltransferases in Huntington's diseaseR01NS111014 · NINDS · WASHINGTON UNIVERSITY · PI YANO, HIROKO · 2019 to 2023
$2.0M
NINDS NIH HHS R01 NS111014NINDS NIH HHS R01NS111014
6 · The paper itself

Abstract

Brain-derived neurotrophic factor (BDNF) is a major neurotrophin whose loss or interruption is well established to have numerous intersections with the pathogenesis of progressive neurological disorders. There is perhaps no greater example of disease pathogenesis resulting from the dysregulation of BDNF signaling than Huntington's disease (HD)-an inherited neurodegenerative disorder characterized by motor, psychiatric, and cognitive impairments associated with basal ganglia dysfunction and the ultimate death of striatal projection neurons. Investigation of the collection of mechanisms leading to BDNF loss in HD highlights this neurotrophin's importance to neuronal viability and calls attention to opportunities for therapeutic interventions. Using electronic database searches of existing and forthcoming research, we constructed a literature review with the overarching goal of exploring the diverse set of molecular events that trigger BDNF dysregulation within HD. We highlighted research that investigated these major mechanisms in preclinical models of HD and connected these studies to those evaluating similar endpoints in human HD subjects. We also included a special focus on the growing body of literature detailing key transcriptomic and epigenetic alterations that affect BDNF abundance in HD. Finally, we offer critical evaluation of proposed neurotrophin-directed therapies and assessed clinical trials seeking to correct BDNF expression in HD individuals.

Indexed as

axonal transportDNA methylationepigenetic processeshistoneshuntingtin proteinneurodegenerative diseasesneurotrophin receptorspolyglutaminetargeted molecular therapiesTrkB receptor

Identifiers

PMID37626771
PMCPMC10452871
OpenAlexW4385878752

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.