Huntington disease: somatic expansion, pathobiology and therapeutics (original) (raw)

Donaldson, Jasmine, Hensman Moss, Davina, Ciosi, Marc ORCID logoORCID: https://orcid.org/0000-0002-7663-4080, Usdin, Karen, Balmus, Gabriel, Monckton, Darren G. ORCID logoORCID: https://orcid.org/0000-0002-8298-8264 and Tabrizi, Sarah J.(2026) Huntington disease: somatic expansion, pathobiology and therapeutics.Nature Reviews Neurology, 22(1), pp. 5-21. (doi: 10.1038/s41582-025-01159-7) (PMID:41233526)

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Abstract

Expansion of simple DNA repeats causes over 45 human, predominantly neurodegenerative, inherited disorders. Huntington disease is a fatal, inherited, neurodegenerative disease caused by a CAG repeat expansion in the huntingtin gene (HTT), resulting in a toxic polyglutamine tract in the huntingtin protein. The disease leads to progressive motor, cognitive and psychiatric decline, primarily resulting from loss of medium spiny neurons in the striatum. Although Huntington disease has long been viewed as a consequence of age-dependent toxicity from mutant huntingtin, genome-wide association studies have identified genetic modifiers, mostly DNA repair genes, that significantly influence disease onset and progression. These findings point to somatic CAG repeat expansions in affected tissues as a key pathological mechanism. This emerging paradigm suggests that disease progression is not solely protein-driven but also shaped at the DNA level, a mechanism that is shared among other repeat expansion disorders. Therapeutically, this discovery opens new opportunities: interventions to limit somatic repeat expansion might be effective across multiple repeat expansion diseases and, when combined with disease-specific approaches, such as huntingtin lowering in Huntington disease, might offer more effective and longer-lasting clinical benefits than either strategy in isolation. This approach also poses challenges, determining the optimal point for therapeutic intervention and how best to establish phenotypic improvement in clinical trials when the target tissue is the brain.

Item Type: Articles
Status: Published
Refereed: Yes
Glasgow Author(s) Enlighten ID: Monckton, Professor Darren and Ciosi, Dr Marc
Authors: Donaldson, J., Hensman Moss, D., Ciosi, M., Usdin, K., Balmus, G., Monckton, D. G., and Tabrizi, S. J.
College/School: College of Medical Veterinary and Life Sciences > School of Molecular Biosciences
Journal Name: Nature Reviews Neurology
Publisher: Nature Research
ISSN: 1759-4758
ISSN (Online): 1759-4766
Published Online: 13 November 2025
Copyright Holders: Copyright © Springer Nature Limited 2025
First Published: First published in Nature Reviews Neurology 22(1):5-21
Publisher Policy: Reproduced in accordance with the publisher copyright policy

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Deposit and Record Details

ID Code: 376625
Depositing User: Dr Marc Ciosi
Datestamp: 16 Jan 2026 09:41
Last Modified: 17 Jan 2026 02:31
Date of acceptance: 3 October 2025
Date of first online publication: 13 November 2025
Date Deposited: 16 January 2026
Data Availability Statement: No