## Abstract Single‐photon emission computed tomography with ^123^I‐iodobenzamide, a dopamine D2 receptor antagonist, was employed to study dopamine D2 receptor densities in 17 patients with biochemically proved Wilson's disease and stable neurological status with therapy and in 5 age‐matched contro
Evidence of cortical metabolic dysfunction in early Huntington's disease by single-photon-emission computed tomography
✍ Scribed by Dr. Daniel S. Sax; Rachel Powsner; Anthony Kim; Shripad Tilak; Rita Bhatia; L. Adrienne Cupples; Richard H. Myers
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 628 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We compared perfusion of prefrontal, motor, and sensory cortices and basal ganglia in 29 Huntington's disease (HD) patients and nine controls. We found a significant reduction in perfusion in patients with HD of short (<6 years, n=10), medium (6–10 years, n=8), and long duration (>10 years, n=11) compared with controls. Among short‐duration patients, we observed decreases in cortical perfusion before evidence of atrophy on magnetic resonance imaging, suggesting that decreases in neuronal activity, as reflected by perfusion levels, precede gross structural changes. As expected, decreased perfusion was marked in basal ganglia. The extent of cortical perfusion correlated with clinical assessments of functional capabilities as well as with the duration of disease. Perfrontal perfusion correlated with cognitive measures, and motor cortical perfusion correlated with physical disability and activities of daily living scores. We found no significant clinical correlations with sensory cortical perfusion. Single‐photon‐emission computed tomography may be a sensitive method for assessing disease progression in clinical trials and pharmacologic intervention.
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## Abstract Both somatosensory evoked potentials (SEP) and striatal glucose consumption (rCMRGlc) measured by positron emission tomography (PET) have been reported to be abnormal early in the course of Huntington's disease (HD). To compare their diagnostic value, SEP and rCMRGlc were measured in a