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Updated: Sep 27, 2026

Fractionation for Resolution of Soluble and Insoluble Huntingtin Species
Published on: February 27, 2018
Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course
Ferdinando Squitieri1, Cinzia Gellera, Milena Cannella
1Neurogenetics Unit, IRCCS INM Neuromed, Pozzilli (IS), Italy. neurogen@neuromed.it
Insights
Huntington disease homozygotes, while not experiencing earlier symptom onset, show a more severe disease course and faster progression compared to heterozygotes. This suggests distinct mechanisms influence Huntington disease onset versus progression.
Area of Science:
- Genetics
- Neurodegenerative Diseases
- Molecular Biology
Background:
- Huntington disease (HD) stems from a dominant CAG repeat expansion mutation in the huntingtin gene.
- This mutation is thought to cause a toxic gain of function in the mutant huntingtin protein.
- Patients with two mutant alleles (homozygotes) are rare, unlike in other poly(CAG) diseases where homozygosity exacerbates symptoms.
Purpose of the Study:
- To investigate clinical differences between Huntington disease homozygotes and heterozygotes.
- To compare disease features including age at onset, symptom presentation, severity, and progression.
Main Methods:
- A multicenter study involving eight Huntington disease homozygotes and 75 heterozygotes.
- DNA testing to identify homozygous subjects.
- Longitudinal clinical assessment of features and disease progression, with imaging and post-mortem data where available.
Main Results:
- Homozygotes for the Huntington disease mutation exhibited symptom onset within the expected range for their CAG repeat lengths.
- Homozygotes demonstrated a more severe clinical course with more rapid decline in motor, cognitive, and behavioral symptoms.
- Neurodegeneration extent in homozygotes correlated with clinical observations.
Conclusions:
- Homozygosity for the Huntington disease mutation does not alter the age of symptom onset but significantly impacts disease phenotype and progression rate.
- The findings suggest potentially different underlying mechanisms for age at onset versus disease progression in Huntington disease.
- Further validation in larger patient cohorts is warranted to confirm these observations.
Abstract:
Huntington disease is caused by a dominantly transmitted CAG repeat expansion mutation that is believed to confer a toxic gain of function on the mutant protein. Huntington disease patients with two mutant alleles are very rare. In other poly(CAG) diseases such as the dominant ataxias, inheritance of two mutant alleles causes a phenotype more severe than in heterozygotes. In this multicentre study, we sought differences in the disease features between eight homozygotes and 75 heterozygotes for the Huntington disease mutation. We identified subjects homozygous for the Huntington disease mutation by DNA testing and compared their clinical features (age at onset, symptom presentation, disease severity and disease progression) with those of a group of heterozygotes, who were assessed longitudinally. The age at onset of symptoms in the homozygote cases was within the range expected for heterozygotes with the same CAG repeat lengths, whereas homozygotes had a more severe clinical course. The observation of a more rapid decline in motor, cognitive and behavioural symptoms in homozygotes was consistent with the extent of neurodegeneration as available at imaging in three patients, and at the post-mortem neuropathological report in one case. Our analysis suggests that although homozygosity for the Huntington disease mutation does not lower the age at onset of symptoms, it affects the phenotype and the rate of disease progression. These data, once confirmed in a larger series of patients, point to the possibility that the mechanisms underlying age at onset and disease progression in Huntington disease may differ.
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