Evidence map›Paper›PMID 41049089›Full record

ArticleMolecular therapy. Nucleic acids2025

Molecular and imaging biomarker responses to brain mutant HTT lowering in a mouse model of Huntington disease.

Nicholas S Caron, Jianjia Fan, Da Ma, Andrew Yung, Seunghyun Ko, Kirsten Bale, Christine Anderson, Piotr Kozlowski, Mahmoud A Pouladi, Cheryl L Wellington and 1 more

Abstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2025. 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
–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

0 citing papers in PubMed.

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

11 authors.

Nicholas S CaronCentre for Molecular Medicine and Therapeutics, Vancouver, BC V5Z 4H4, Canada.
Jianjia FanDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
Da MaSchool of Engineering Science, Simon Fraser University, Burnaby, BC V5A 1S6, Canada.
Andrew YungUBC MRI Research Centre, Department of Radiology, University of British Columbia, Vancouver, BC V6T 2B5, Canada.
Seunghyun KoCentre for Molecular Medicine and Therapeutics, Vancouver, BC V5Z 4H4, Canada.
Kirsten BaleUBC MRI Research Centre, Department of Radiology, University of British Columbia, Vancouver, BC V6T 2B5, Canada.
Christine AndersonCentre for Molecular Medicine and Therapeutics, Vancouver, BC V5Z 4H4, Canada.
Piotr KozlowskiUBC MRI Research Centre, Department of Radiology, University of British Columbia, Vancouver, BC V6T 2B5, Canada.
Mahmoud A PouladiCentre for Molecular Medicine and Therapeutics, Vancouver, BC V5Z 4H4, Canada.
Cheryl L WellingtonDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, BC V6T 1Z3, Canada.
Michael R HaydenCentre for Molecular Medicine and Therapeutics, Vancouver, BC V5Z 4H4, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Therapies targeting mutant huntingtin (mHTT) reduction in the brain hold promise as disease-modifying treatments for Huntington disease (HD), necessitating biomarkers that accurately reflect treatment response. We evaluated candidate molecular and imaging biomarkers after mHTT reduction in YAC128 HD mice, with equal numbers of males and females per group. At 6 months of age, YAC128 mice received unilateral intracerebroventricular injections of saline or mHTT-lowering antisense oligonucleotide (HTT ASO). Plasma neurofilament light chain (NEFL) and glial fibrillary acidic protein (GFAP) were measured longitudinally from 6 to 12 months. Structural MRI was performed at 6, 9, and 12 months. At study endpoint, we quantified mHTT target engagement in the brain and performed striatal RNA sequencing. Treatment with HTT ASO produced a sustained reduction of mHTT levels throughout the brain for up to 6 months, significantly slowed plasma NEFL increases, and moderately attenuated GFAP elevation. Although mHTT levels inversely correlated with gray and white matter volumes, treatment did not significantly stabilize regional brain atrophy, highlighting an association between mHTT load and neuroanatomical integrity. HTT ASO also partially reversed striatal transcriptome dysregulation and restored oligodendrocyte-specific gene expression. Plasma NEFL, but not brain imaging, emerges as a sensitive and dynamic response biomarker for mHTT-lowering therapies.

Indexed as

antisense oligonucleotideglial fibrillary acidic proteinhuntingtin loweringHuntington diseasemagnetic resonance imagingMT: Oligonucleotides: Therapies and Applicationsneurofilament light chainoligodendrocytesplasmaresponse biomarkerRNA sequencing

Identifiers

PMID41049089
PMCPMC12489819

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.