Literature DB >> 12654952

Clinical features and natural history of progressive supranuclear palsy: a clinical cohort study.

U Nath1, Y Ben-Shlomo, R G Thomson, A J Lees, D J Burn.   

Abstract

OBJECTIVE: To describe clinical features and identify prognostic predictors in progressive supranuclear palsy (PSP).
METHODS: Record-based diagnosis according to National Institute of Neurological Disorders and Stroke-Society for Progressive Supranuclear Palsy criteria was performed in 187 cases of PSP. Clinical information was abstracted from patient records. Sixty-two patients (33%) were examined by the investigators. Forty-nine of 62 patients (79%) underwent standardized clinical assessment. Predictors of survival were examined after a mean of 6.4 years.
RESULTS: The most common symptoms at disease onset related to mobility (69%). Of patients undergoing standardized clinical assessment, diplopia occurred in 61%, photophobia in 43%, and eyelid apraxia in 43%. Seventy-five cases (40%) died during follow-up. Older age at onset and classification as probable PSP were associated with poorer survival. Onset of falls (hazard ratio 3.28, 95% CI 1.17 to 9.13), speech problems (hazard ratio 4.74, 95% CI 1.10 to 20.4), or diplopia (hazard ratio 4.23, 95% CI 1.23 to 14.6) within 1 year and swallowing problems within 2 years (hazard ratio 3.91, 95% CI 1.39 to 11.0) were associated with a worse prognosis.
CONCLUSIONS: Mobility problems are the commonest early feature in PSP and visual symptoms are often functionally disabling. Early falls, speech and swallowing problems, diplopia, and early insertion of a percutaneous gastrostomy predict reduced survival.

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Year:  2003        PMID: 12654952     DOI: 10.1212/01.wnl.0000052991.70149.68

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  63 in total

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2.  Neuropathological findings of PSP in the elderly without clinical PSP: possible incidental PSP?

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3.  Instability of syllable repetition in progressive supranuclear palsy.

Authors:  Sabine Skodda; Wenke Grönheit; Uwe Schlegel
Journal:  J Neural Transm (Vienna)       Date:  2011-11-08       Impact factor: 3.575

4.  Predictors of falls and fractures in bradykinetic rigid syndromes: a retrospective study.

Authors:  D R Williams; H C Watt; A J Lees
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-04       Impact factor: 10.154

5.  The core body temperature rhythm is altered in progressive supranuclear palsy.

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6.  In vivo comparison of Richardson's syndrome and progressive supranuclear palsy-parkinsonism.

Authors:  Karin Srulijes; Grit Mallien; Sarah Bauer; Elisabeth Dietzel; Adriane Gröger; Georg Ebersbach; Daniela Berg; Walter Maetzler
Journal:  J Neural Transm (Vienna)       Date:  2011-01-05       Impact factor: 3.575

7.  Speech disorders reflect differing pathophysiology in Parkinson's disease, progressive supranuclear palsy and multiple system atrophy.

Authors:  Jan Rusz; Cecilia Bonnet; Jiří Klempíř; Tereza Tykalová; Eva Baborová; Michal Novotný; Aaron Rulseh; Evžen Růžička
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Review 8.  Cognitive impairment and dementia in basal ganglia disorders.

Authors:  Julie C Stout; Shannon A Johnson
Journal:  Curr Neurol Neurosci Rep       Date:  2005-09       Impact factor: 5.081

Review 9.  Parkinsonian syndromes.

Authors:  David R Williams; Irene Litvan
Journal:  Continuum (Minneap Minn)       Date:  2013-10

10.  Major depressive disorder preceding the onset of progressive supranuclear palsy.

Authors:  Won-Hyoung Kim; Young-Soo Lee; Seung-Ho Jung; Hye-Jin Choi; Myung-Ji Lee; Min-Hee Kang; Chul-Eung Kim; Jeong-Seop Lee; Jae-Nam Bae
Journal:  Psychiatry Investig       Date:  2009-06-30       Impact factor: 2.505

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