

Huntington’s Disease: Detecting the Silent Progression
Huntington’s disease (HD) is a genetic neurodegenerative disorder that progressively impairs movement, cognition, and behavior. However, a recent study led by researchers at University College London reveals that subtle brain changes begin as early as 20 years before clinical motor symptoms appear. These findings could revolutionize Huntington’s prevention strategies and early treatments for Huntington’s and other neurodegenerative diseases.
Key Study Findings
- Pre-Symptomatic Brain Changes:
Subtle neurodegeneration was detected in individuals with Huntington’s gene expansion years before symptom onset, particularly in the caudate and putamen brain regions. - Biomarker Insights:
Elevated neurofilament light chain (NfL) levels, indicating neuronal injury, and decreased proenkephalin (PENK) levels, marking neurodegenerative response, were observed. - Longitudinal Analysis:
Over five years, 57 participants with Huntington’s gene expansion showed no noticeable clinical decline in cognition or movement but exhibited progressive changes in brain scans and spinal fluid biomarkers. - Mechanistic Discovery:
Somatic CAG repeat expansions in the huntingtin gene were directly linked to early brain changes, offering evidence for their role in neurodegeneration.
Implications for Future Huntington’s Prevention Trials
This groundbreaking research emphasizes the significance of early intervention. The detection of subtle biomarkers decades before clinical symptoms highlights a potential therapeutic window.
- Validation of Therapeutic Targets:
Suppressing somatic CAG repeat expansion could delay or prevent neurodegenerative changes. - Broader Impact:
Insights into HD may inform approaches for conditions like Alzheimer’s, where early intervention could be transformative. - Hope for Prevention Trials:
With treatments targeting somatic CAG expansion under development, the study offers a solid foundation for future preventative clinical trials.
The Role of Somatic CAG Expansion in Huntington’s Prevention
CAG expansions in the huntingtin gene amplify over time, accelerating neuron damage. This process was found to be measurable through blood analysis, predicting brain volume reductions and validating it as a promising therapeutic target.
Future Directions
This study paves the way for preventive approaches:
- Earlier Diagnoses: Leveraging biomarkers like NfL and PENK for pre-symptomatic detection.
- Therapeutic Development: Supporting the ongoing development of drugs aimed at mitigating somatic CAG expansions.
- Broad Neurodegenerative Applications: Exploring similar early interventions for other conditions, including Alzheimer’s and Parkinson’s.
- Join Internation Brain Health Symposium 2025 for latest updates.
More Information: Somatic CAG repeat expansion in blood associates with biomarkers of neurodegeneration in Huntington’s disease decades before clinical motor diagnosis, Nature Medicine (2025). DOI: 10.1038/s41591-024-03424-6
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