Potential outcome measures and trial design issues for multiple system atrophy
Identifieur interne : 002C67 ( Main/Exploration ); précédent : 002C66; suivant : 002C68Potential outcome measures and trial design issues for multiple system atrophy
Auteurs : Susanne May [États-Unis] ; Sid Gilman [États-Unis] ; B. Brooke Sowell [États-Unis] ; Ronald G. Thomas [États-Unis] ; Matthew B. Stern [États-Unis] ; Amy Colcher [États-Unis] ; Caroline M. Tanner [États-Unis] ; Neng Huang [États-Unis] ; Peter Novak [États-Unis] ; Stephen G. Reich [États-Unis] ; Joseph Jankovic [États-Unis] ; William G. Ondo [États-Unis] ; Phillip A. Low [États-Unis] ; Paola Sandroni [États-Unis] ; Axel Lipp [États-Unis] ; Frederick J. Marshall [États-Unis] ; Frederick Wooten [États-Unis] ; Clifford W. Shults [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2007-12-15.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
- Aged, Antiparkinson Agents (therapeutic use), Cerebellar Diseases (physiopathology), Cerebellar Diseases (therapy), Clinical Trials as Topic, Disability Evaluation, Disease Progression, Female, Humans, Levodopa (therapeutic use), Male, Middle Aged, Multiple System Atrophy (epidemiology), Multiple System Atrophy (physiopathology), Multiple System Atrophy (therapy), Multiple system atrophy, Nervous system diseases, Parkinsonism, Prognosis, Research Design, Risk Factors, SF‐36, Sample Size, Socioeconomic Factors, Treatment Outcome, UMSARS, power, study design.
- MESH :
- chemical , therapeutic use : Antiparkinson Agents, Levodopa.
- epidemiology : Multiple System Atrophy.
- physiopathology : Cerebellar Diseases, Multiple System Atrophy.
- therapy : Cerebellar Diseases, Multiple System Atrophy.
- Aged, Clinical Trials as Topic, Disability Evaluation, Disease Progression, Female, Humans, Male, Middle Aged, Research Design, Risk Factors, Sample Size, Socioeconomic Factors, Treatment Outcome.
Abstract
Multiple system atrophy (MSA) is a neurodegenerative disorder exhibiting a combination of parkinsonism, cerebellar ataxia, and autonomic failure. A disease‐specific scale, the Unified Multiple System Atrophy Rating Scale (UMSARS), has been developed and validated to measure progression of MSA, but its use as an outcome measure for therapeutic trials has not been evaluated. On the basis of twelve months of follow‐up from an observational study of 67 patients with probable MSA, we evaluated three disease‐specific scores: Activities of Daily Living, Motor Examination, and a combined score from the UMSARS and two general health scores, the Physical Health and Mental Health scores of the SF‐36 health survey, for their use as outcome measures in a therapeutic trial. We discuss related design issues and provide sample size estimates. Scores based on the disease‐specific UMSARS seemed to be equal or superior to scores based on the SF‐36 health survey. They appeared to capture disease progression, were well correlated and required the smallest sample size. The UMSARS Motor Examination score exhibited the most favorable characteristics as an outcome measure for a therapeutic trial in MSA with 1 year of follow‐up. © 2007 Movement Disorder Society
Url:
DOI: 10.1002/mds.21734
Affiliations:
- États-Unis
- Californie, Maryland, Massachusetts, Michigan, Minnesota, Pennsylvanie, Texas, Virginie, État de New York
- Houston
- Baylor College of Medicine
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Le document en format XML
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<term>Cerebellar Diseases (physiopathology)</term>
<term>Cerebellar Diseases (therapy)</term>
<term>Clinical Trials as Topic</term>
<term>Disability Evaluation</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Humans</term>
<term>Levodopa (therapeutic use)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Multiple System Atrophy (epidemiology)</term>
<term>Multiple System Atrophy (physiopathology)</term>
<term>Multiple System Atrophy (therapy)</term>
<term>Multiple system atrophy</term>
<term>Nervous system diseases</term>
<term>Parkinsonism</term>
<term>Prognosis</term>
<term>Research Design</term>
<term>Risk Factors</term>
<term>SF‐36</term>
<term>Sample Size</term>
<term>Socioeconomic Factors</term>
<term>Treatment Outcome</term>
<term>UMSARS</term>
<term>power, study design</term>
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<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Multiple System Atrophy</term>
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<term>Multiple System Atrophy</term>
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<term>Multiple System Atrophy</term>
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<term>Clinical Trials as Topic</term>
<term>Disability Evaluation</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Research Design</term>
<term>Risk Factors</term>
<term>Sample Size</term>
<term>Socioeconomic Factors</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Atrophie multisystématisée</term>
<term>Parkinsonisme</term>
<term>Pathologie du système nerveux</term>
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<front><div type="abstract" xml:lang="en">Multiple system atrophy (MSA) is a neurodegenerative disorder exhibiting a combination of parkinsonism, cerebellar ataxia, and autonomic failure. A disease‐specific scale, the Unified Multiple System Atrophy Rating Scale (UMSARS), has been developed and validated to measure progression of MSA, but its use as an outcome measure for therapeutic trials has not been evaluated. On the basis of twelve months of follow‐up from an observational study of 67 patients with probable MSA, we evaluated three disease‐specific scores: Activities of Daily Living, Motor Examination, and a combined score from the UMSARS and two general health scores, the Physical Health and Mental Health scores of the SF‐36 health survey, for their use as outcome measures in a therapeutic trial. We discuss related design issues and provide sample size estimates. Scores based on the disease‐specific UMSARS seemed to be equal or superior to scores based on the SF‐36 health survey. They appeared to capture disease progression, were well correlated and required the smallest sample size. The UMSARS Motor Examination score exhibited the most favorable characteristics as an outcome measure for a therapeutic trial in MSA with 1 year of follow‐up. © 2007 Movement Disorder Society</div>
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<name sortKey="Ondo, William G" sort="Ondo, William G" uniqKey="Ondo W" first="William G." last="Ondo">William G. Ondo</name>
<name sortKey="Reich, Stephen G" sort="Reich, Stephen G" uniqKey="Reich S" first="Stephen G." last="Reich">Stephen G. Reich</name>
<name sortKey="Sandroni, Paola" sort="Sandroni, Paola" uniqKey="Sandroni P" first="Paola" last="Sandroni">Paola Sandroni</name>
<name sortKey="Shults, Clifford W" sort="Shults, Clifford W" uniqKey="Shults C" first="Clifford W." last="Shults">Clifford W. Shults</name>
<name sortKey="Shults, Clifford W" sort="Shults, Clifford W" uniqKey="Shults C" first="Clifford W." last="Shults">Clifford W. Shults</name>
<name sortKey="Sowell, B Brooke" sort="Sowell, B Brooke" uniqKey="Sowell B" first="B. Brooke" last="Sowell">B. Brooke Sowell</name>
<name sortKey="Stern, Matthew B" sort="Stern, Matthew B" uniqKey="Stern M" first="Matthew B." last="Stern">Matthew B. Stern</name>
<name sortKey="Tanner, Caroline M" sort="Tanner, Caroline M" uniqKey="Tanner C" first="Caroline M." last="Tanner">Caroline M. Tanner</name>
<name sortKey="Thomas, Ronald G" sort="Thomas, Ronald G" uniqKey="Thomas R" first="Ronald G." last="Thomas">Ronald G. Thomas</name>
<name sortKey="Thomas, Ronald G" sort="Thomas, Ronald G" uniqKey="Thomas R" first="Ronald G." last="Thomas">Ronald G. Thomas</name>
<name sortKey="Wooten, Frederick" sort="Wooten, Frederick" uniqKey="Wooten F" first="Frederick" last="Wooten">Frederick Wooten</name>
</country>
</tree>
</affiliations>
</record>
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