## Abstract ## Methods: Using a validated questionnaire, we screened eye symptoms (burning sensation, grittiness, dry eye) in 333 first‐degree relatives of 140 probands with different forms of primary adult‐onset dystonia, 208 healthy subjects, and 293 patients with primary blepharospasm. ## Resu
Relative preservation of thalamic centromedian nucleus in parkinsonian patients with dystonia
✍ Scribed by Linda Truong; Daniel Brooks; Fabricio Amaral; Jasmine M. Henderson; Glenda M. Halliday
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 398 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
To determine whether variable thalamic degeneration in Parkinson's disease (PD) contributes to less drug responsive clinical features. Formalin‐fixed thalami from longitudinally followed patients with PD and early dystonia (N = 6), early falls (N = 5) or no dystonia or falls (N = 6) and age‐matched controls without neuropathology (N = 10) were serially sectioned, stained, and analyzed. Neurons in the centromedian parafascicular (CM‐Pf) nucleus were quantified using the optical disector method and analysis of variance with post hoc testing used to determine variability in neurodegeneration between groups. Patients with PD were confirmed to have significant neurodegeneration in the CM‐Pf complex, with no difference in the degree of neurodegeneration between patients with PD with early falls compared with patients with no history of falls or dystonia. In contrast, patients with PD with early dystonia had significantly less neurodegeneration of the CM but not the Pf than patients without this feature. Preservation of the CM in patients with PD with early dystonia would result in a relative increase in CM activity through the direct basal ganglia pathway and increased primary motor cortex activity. Overall this data provides evidence for pathway‐specific neurodegeneration as an underlying feature of the clinical variability observed in patients with PD. © 2009 Movement Disorder Society
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