Longitudinal change in basal ganglia volume in patients with Huntington's disease
- 1 February 1997
- journal article
- Published by Wolters Kluwer Health in Neurology
- Vol. 48 (2) , 394-399
- https://doi.org/10.1212/wnl.48.2.394
Abstract
Article abstract-Cross-sectional MRI studies demonstrating an association between caudate atrophy and symptom severity and duration of symptoms in patients with Huntington9s disease (HD) have been assumed to reflect longitudinal changes in basal ganglia, but such neuropathologic progression has never been directly demonstrated. Subjects in the current study were 23 HD patients at various stages of the disorder who had two MRI images at least 10 months apart (mean interimage interval = 20.8 months). We measured volumes of caudate, putamen, and globus pallidus blind to the order of the images. For each structure, we calculated a change score by subtracting the volume obtained on the follow-up imaging from that obtained on the initial imaging. Results indicated significant decreases over time in caudate, putamen, and total basal ganglia volume. Age at onset and length of trinucleotide repeat correlated significantly with amount of volume change in caudate and total basal ganglia, even after controlling for length of interimage interval, duration of disease, and measures of symptom severity. Amount of change in basal ganglia structures was not significantly correlated with neurologic symptom severity at the time of the initial imaging or duration of symptoms. This is the first longitudinal MRI study to document progressive basal ganglia atrophy in HD, and suggests that quantitative neuroimaging with serial MRI may be useful in monitoring effectiveness of potential treatments. In addition, demonstration of greater rate of basal ganglia atrophy in patients with earlier symptom onset suggests that treatment effects may be more quickly observed in this subgroup of patients than in the general HD population. NEUROLOGY 1997;48: 394-399Keywords
This publication has 11 references indexed in Scilit:
- HUNTINGTON'S DISEASEMovement Disorders, 1996
- Message from the editorAnnals of Neurology, 1996
- Autosomal dominant cerebellar phenotypesNeurology, 1995
- Evidence of peripheral axonal neuropathy in primary restless legs syndromeMovement Disorders, 1995
- Neuropeptides in the sympathetic system: Presence, plasticity, modulation, and implicationsAnnals of Neurology, 1994
- cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the youngHuman Molecular Genetics, 1993
- Cortical auditory disorders: clinical and psychoacoustic features.Journal of Neurology, Neurosurgery & Psychiatry, 1987
- Decreased cerebral blood flow precedes multi‐infarct dementia, but follows senile dementia of Alzheimer typeNeurology, 1986
- Direct drainage of extracranial arteries into the superior sagittal sinus associated with dementiaZeitschrift für Neurologie, 1981
- Prevention of postischemic impairment of microvascular perfusionNeurology, 1977