Hyposmia in progressive supranuclear palsy
β Scribed by Laura Silveira-Moriyama; Graham Hughes; Alistair Church; Hilary Ayling; David R. Williams; Aviva Petrie; Janice Holton; Tamas Revesz; Ann Kingsbury; Huw R. Morris; David J. Burn; Andrew J. Lees
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 239 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0885-3185
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Previous studies suggested that olfaction is normal in progressive supranuclear palsy (PSP). We applied the University of Pennsylvania Smell Identification Test (UPSIT) to 36 patients with PSP who scored more than 18 on the Mini Mental State Examination (MMSE), 140 patients with nondemented Parkinson's disease (PD) and 126 controls. Mean UPSIT scores in PSP were lower than in controls (P < 0.001) but higher than in PD (P < 0.001) after adjusting for age, gender, and smoking history. For patients with PSP, UPSIT scores correlated with MMSE (r = 0.44, P = 0.006) but not disease duration (P = 0.6), motor subscale of the Unified Parkinson's Disease Rating Scale (P = 0.2), or Frontal Assessment Battery (P = 0.5). The brains of six of the patients with PSP were examined postmortem and all revealed neurofibrillary tangles and tau accumulation in the rhinencephalon, although only three had hyposmia. Further prospective studies including patients with early PSP and PSPβP with postmortem confirmation might help clarify if smell tests could be useful when the differential diagnosis lies between PD and PSP. Β© 2010 Movement Disorder Society
π SIMILAR VOLUMES
We studied sleep patterns for three nights in 10 subjects with moderate to severe progressive supranuclear palsy and correlated the findings with disease severity using quantitative measures of motor, cognitive, abd eye movement impairment. All subjects had severe insomnia, spending 2 to 6 hours awa
## Abstract Patients with orthostatic tremor (OT) can be classified as having βprimary OT,β with or without postural arm tremor but no other abnormal neurological features, or βOT plus.β We describe a patient with OT, with postural tremor of the arms and restless legs syndrome (RLS), who developed
## Abstract Diagnostic accuracy has been addressed previously for Parkinson's disease in a brain bank collection, but accuracy of progressive supranuclear palsy (PSP) has not been addressed in a similar setting. Clinical and genetic features of pathologically confirmed cases of PSP were compared wi