๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Lack of association between progressive supranuclear palsy and arterial hypertension: A clinicopathological study

โœ Scribed by Carlo Colosimo; Yasushi Osaki; Nicola Vanacore; Andrew J. Lees


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
62 KB
Volume
18
Category
Article
ISSN
0885-3185

No coin nor oath required. For personal study only.

โœฆ Synopsis


Abstract

It has been reported that up to 80% of patients clinically diagnosed as having progressive supranuclear palsy (PSP) may have arterial hypertension (HT). Because previous studies were performed on patients with presumed diagnosis of PSP, we tried to replicate these studies in a series of pathologically confirmed patients. Seventyโ€three patients with a neuropathological diagnosis of PSP autopsied at the Queen Square Brain Bank for Neurological Disorders in London were collected between 1989 and 1999. For the purpose of this study, patients were considered hypertensive if a blood pressure above 140/90 mm Hg was found in the clinical records. The prevalence of HT in PSP patients at the first and at the last visit during their neurological disease was compared with that found in a series of 21 normal controls who donated their brain to the same institution. Overall, 29 of 73 (39.7%) of the patients were recorded as having HT at the first visit during the disease course; this ratio increased to 42 of 73 (57.5%) at the last visit before death. When these figures were compared to the 21 normal controls (11 of 21 with HT, 52.4%), we were unable to find an increased prevalence of HT in PSP (odds ratio, 0.60; 95% confidence interval, 0.20โ€“1.76). Therefore, HT does not represent an important clinical feature of this neurodegenerative disorder, although cerebrovascular disease can masquerade clinically as PSP. ยฉ 2003 Movement Disorder Society


๐Ÿ“œ SIMILAR VOLUMES


Reply: Lack of association between progr
โœ Carlo Colosimo; Yasushi Osaki; Nicola Vanacore; Andrew J. Lees ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 45 KB

## Legends to the Video Segment 1. Patient 1. Part 1 shows the abnormal postures at rest and when talking. During activity, the abnormal postures may diminish or disappear for a moment. The patient delineates the area of hypesthesia, including the right side of the tongue. Part 2: with passive rep

Cerebellar involvement in progressive su
โœ Masato Kanazawa; Takayoshi Shimohata; Yasuko Toyoshima; Mari Tada; Akiyoshi Kaki ๐Ÿ“‚ Article ๐Ÿ“… 2009 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 203 KB

## Abstract The clinical heterogeneity of progressive supranuclear palsy (PSP), which is classified as classic Richardson's syndrome (RS) and PSPโ€Parkinsonism (PSPโ€P), has been previously discussed. We retrospectively analyzed 22 consecutive Japanese patients with pathologically proven PSP to inves

Long lasting pure freezing of gait prece
โœ Yaroslau Compta; Francesc Valldeoriola; Eduardo Tolosa; Marรญa Jesรบs Rey; Marรญa J ๐Ÿ“‚ Article ๐Ÿ“… 2007 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 129 KB

## Abstract Primary progressive freezing of gait (PPFG) is the term used to designate an uncommon condition featuring freezing of gait with frequent falls, without bradykinesia, rigidity or tremor, and unresponsive to levodopa. There are very few pathological reports of patients with PPFG in the li

Association between vestibuloocular refl
โœ Richard P. Di Fabio; Cris Zampieri; Paul Tuite; Jรผrgen Konczak ๐Ÿ“‚ Article ๐Ÿ“… 2006 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 174 KB

## Abstract With head movement, suppression of vestibular inputs during visual exploration is necessary not only for reorienting gaze, but also to direct attention to new visual targets. People with progressive supranuclear palsy (PSP) have difficulty suppressing the vestibuloocular reflex (VOR) an

In vivo demonstration of microstructural
โœ Susanne Knake; Marcus Belke; Katja Menzler; Ulrich Pilatus; Karla M. Eggert; Wol ๐Ÿ“‚ Article ๐Ÿ“… 2010 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 174 KB

## Abstract We investigated DTI changes, potentially indicating alterations of microstructure and brain tissue integrity in 13 patients with probable progressive supranuclear palsy (PSP, Richardson syndrome) at stage III or less and 10 ageโ€matched controls using a whole brain analysis of diffusion