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Published on: May 17, 2024
Hypertension, Antihypertensive Use and the Delayed-Onset of Huntington's Disease
Jessica J Steventon1, Anne E Rosser2,3, Emma Hart4
1Cardiff University Brain Research Imaging Centre (CUBRIC), School of Physics and Astronomy, Maindy Road, Cardiff University, Cardiff, Wales, UK.
Insights
Hypertension in Huntington's disease is linked to worse symptoms, but medication may improve outcomes. This suggests potential benefits of blood pressure management in neurodegenerative conditions.
Area of Science:
- Neuroscience
- Cardiovascular Medicine
- Genetics
Background:
- Hypertension is a known risk factor for neurodegeneration and dementia.
- Autonomic and vascular issues are observed in Huntington's disease (HD), a monogenic neurodegenerative disorder.
Purpose of the Study:
- To investigate the association between hypertension and the severity and progression of Huntington's disease.
Main Methods:
- Utilized longitudinal data from a large international observational study of Huntington's disease (n=14,534).
- Employed propensity score matching to compare hypertensive and normotensive participants based on key demographic and genetic factors (age, sex, BMI, ethnicity, CAG length).
Main Results:
- Huntington's disease patients exhibited a lower prevalence of hypertension than controls.
- Hypertensive HD patients showed poorer cognitive function, higher depression scores, and faster motor progression compared to normotensive HD patients.
- Antihypertensive medication use in HD patients was associated with less severe motor, cognitive, and functional impairment, and a later age of clinical onset.
Conclusions:
- Hypertension and its treatment are novelly associated with altered disease course and onset in Huntington's disease.
- Findings suggest implications for hypertension management in HD patients.
- Further research into the potential symptomatic or disease-modifying effects of antihypertensives in neurodegenerative diseases is warranted.
Background:
Hypertension is a modifiable cardiovascular risk factor implicated in neurodegeneration and dementia risk. In Huntington's disease, a monogenic neurodegenerative disease, autonomic and vascular abnormalities have been reported. This study's objective was to examine the relationship between hypertension and disease severity and progression in Huntington's disease.
Methods:
Using longitudinal data from the largest worldwide observational study of Huntington's disease (n = 14,534), we assessed the relationship between hypertension, disease severity, and rate of clinical progression in Huntington's disease mutation carriers. Propensity score matching was used to statistically match normotensive and hypertensive participants for age, sex, body mass index, ethnicity, and CAG length.
Results:
Huntington's disease patients had a lower prevalence of hypertension compared with age-matched gene-negative controls. Huntington's disease patients with hypertension had worse cognitive function, a higher depression score, and more marked motor progression over time compared with Huntington's disease patients without hypertension. However, hypertensive patients taking antihypertensive medication had less motor, cognitive, and functional impairment than Huntington's disease patients with untreated hypertension and a later age of clinical onset compared with untreated hypertensive patients and normotensive individuals with Huntington's disease.
Conclusions:
We report the novel finding that hypertension and antihypertensive medication use are associated with altered disease severity, progression, and clinical onset in patients with Huntington's disease. These findings have implications for the management of hypertension in Huntington's disease and suggest that prospective studies of the symptomatic or disease-modifying potential of antihypertensives in neurodegenerative diseases are warranted. © 2020 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
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