Literature DB >> 12654953

Progression of gait, speech and swallowing deficits in progressive supranuclear palsy.

Christopher G Goetz1, Sue Leurgans, Anthony E Lang, Irene Litvan.   

Abstract

OBJECTIVE: To identify outcome measures for clinical trials in progressive supranuclear palsy (PSP), the authors determined the time to key motor impairments in a well-defined patient cohort.
METHODS: The records of consecutive patients with probable PSP, defined by National Institute of Neurological Disorders and Stroke-Society for Progressive Supranuclear Palsy workshop criteria on first visit to a tertiary care center, were selected for study if the patients were seen regularly at 3- to 6-month intervals, had at least 24 months of care at the Rush movement disorder center, and were originally seen in the movement disorder center before any of the following key motor impairments developed: unintelligible speech, no independent walking, inability to stand unassisted, wheelchair-bound, or recommendation for feeding tube placement. Using standardized criteria from the Unified Parkinson's Disease Rating Scale and Hoehn and Yahr stages taken at each clinic visit, the authors recorded the time that each patient reached the key motor impairments and death. Median months from first symptom onset and from first consultation at the movement disorder center to each motor impairment were derived from Kaplan-Meier curves.
RESULTS: Fifty subjects, mean age at study entry 64.2 years, were followed to death (n = 21, mean duration of surveillance 53.6 months) or in ongoing fashion (n = 29, mean duration of surveillance 46.2 months). Eighty-eight percent of the sample met at least one milestone. The median time from disease onset to the first key motor impairment was 48 months, 24 months after first consultation. The three gait items occurred temporally close, and the authors considered them thereafter as a single milestone, occurring at a median disease duration of 57 months, 34 months after first consultation. Unintelligible speech occurred at a median disease duration of 71 months, median 44 months after first consultation. As a composite end point, speech/gait accounted for 98% of the sample's first key motor impairment. Need for nasogastric tube was rarely the first milestone (8%).
CONCLUSIONS: Gait impairment and unintelligible speech are milestones that occur rapidly in PSP and can be monitored with standardized rating scales. The authors suggest that clinical trials use these indices to assess how interventions alter anticipated progression of clinical deterioration in PSP.

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Mesh:

Year:  2003        PMID: 12654953     DOI: 10.1212/01.wnl.0000052686.97625.27

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


  23 in total

1.  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

Review 2.  Scales to Assess Clinical Features of Progressive Supranuclear Palsy: MDS Task Force Report.

Authors:  Deborah A Hall; Maria João Forjaz; Lawrence I Golbe; Irene Litvan; Christine Ann M Payan; Christopher G Goetz; Albert F G Leentjens; Pablo Martinez-Martin; Anne Pavy-Le Traon; Cristina Sampaio; Bart Post; Glenn Stebbins; Daniel Weintraub; Anette Schrag
Journal:  Mov Disord Clin Pract       Date:  2015-05-22

3.  Improvement of balance after audio-biofeedback. A 6-week intervention study in patients with progressive supranuclear palsy.

Authors:  S Nicolai; A Mirelman; T Herman; A Zijlstra; M Mancini; C Becker; U Lindemann; D Berg; W Maetzler
Journal:  Z Gerontol Geriatr       Date:  2010-08       Impact factor: 1.281

4.  Current and future treatments in progressive supranuclear palsy.

Authors:  Irene van Balken; Irene Litvan
Journal:  Curr Treat Options Neurol       Date:  2006-05       Impact factor: 3.598

5.  Neuroimaging comparison of primary progressive apraxia of speech and progressive supranuclear palsy.

Authors:  J L Whitwell; J R Duffy; E A Strand; M M Machulda; M L Senjem; J L Gunter; K Kantarci; S D Eggers; C R Jack; K A Josephs
Journal:  Eur J Neurol       Date:  2012-10-18       Impact factor: 6.089

6.  Progressive supranuclear palsy: progression and survival.

Authors:  Julieta E Arena; Stephen D Weigand; Jennifer L Whitwell; Anhar Hassan; Scott D Eggers; Günter U Höglinger; Irene Litvan; Keith A Josephs
Journal:  J Neurol       Date:  2015-12-24       Impact factor: 4.849

Review 7.  Update on progressive supranuclear palsy.

Authors:  Irene Litvan
Journal:  Curr Neurol Neurosci Rep       Date:  2004-07       Impact factor: 5.081

8.  Dysphagia in Progressive Supranuclear Palsy.

Authors:  Heather M Clark; Julie A G Stierwalt; Nirubol Tosakulwong; Hugo Botha; Farwa Ali; Jennifer L Whitwell; Keith A Josephs
Journal:  Dysphagia       Date:  2019-11-01       Impact factor: 3.438

9.  Severity dependent distribution of impairments in PSP and CBS: Interactive visualizations.

Authors:  Claire Brittain; Andrew McCarthy; Michael C Irizarry; Dana McDermott; Kevin Biglan; Günter U Höglinger; Stefan Lorenzl; Teodoro Del Ser; Adam L Boxer
Journal:  Parkinsonism Relat Disord       Date:  2018-09-04       Impact factor: 4.891

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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