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Modifying Neuropsychiatric and Motor Trajectories in Huntington's Disease Through an Integrated Neurobehavioral
Shakaib Khan1, Luis Velez Figueroa1, Chindhuri Selvadurai2
1Department of Psychiatry, University of Connecticut Health Center, Farmington, CT, USA.
Neuropsychiatric Disease and Treatment
|June 24, 2026
Summary
A multidisciplinary clinic model improved symptom stability in Huntington's disease (HD) patients. This integrated care approach showed positive effects on motor and psychiatric symptoms, offering a meaningful deviation from the disease's typical progression.
Area of Science:
- Neuroscience
- Clinical Neurology
- Psychiatry
Background:
- Huntington's disease (HD) is a progressive neurodegenerative disorder with significant motor, cognitive, and psychiatric symptoms.
- Psychiatric symptoms often precede motor deficits and contribute substantially to patient disability.
- Current HD management focuses on symptom control and functional preservation due to a lack of disease-modifying treatments.
Purpose of the Study:
- To evaluate the impact of implementing a multidisciplinary clinic model on clinical outcomes in Huntington's disease patients.
- To compare longitudinal changes in motor, cognitive, and psychiatric symptoms before and after the introduction of integrated care.
Main Methods:
- A retrospective pre-post chart review of 56 Huntington's disease patients.
- Utilized paired-samples t-tests to analyze differences in outcomes.
- Assessed depressive symptoms (PHQ-9), anxiety symptoms (GAD-7), motor function (UHDRS), and cognitive function (MoCA).
Main Results:
- The multidisciplinary clinic model led to increased stability in depression and anxiety symptom trajectories.
- A higher percentage of patients responded to treatment post-clinic implementation (64-67%) compared to pre-clinic (33-43%).
- Significant decrease in motor symptom severity (d = -0.341) and stable cognitive performance were observed.
Conclusions:
- Multidisciplinary integrated care may positively influence motor and psychiatric symptom trajectories in Huntington's disease.
- A coordinated, team-based approach represents a clinically meaningful deviation from the expected progressive decline in HD.
- The study's findings are limited by its retrospective observational design and modest sample size.
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