Natural history of Huntington disease.
Identifieur interne : 000044 ( PubMed/Checkpoint ); précédent : 000043; suivant : 000045Natural history of Huntington disease.
Auteurs : E Dorsey [États-Unis] ; Christopher. Beck [États-Unis] ; Kristin Darwin [États-Unis] ; Paige Nichols [États-Unis] ; Alicia. Brocht [États-Unis] ; Kevin. Biglan [États-Unis] ; Ira Shoulson [États-Unis]Source :
- JAMA neurology ; 2013.
Descripteurs français
- Wicri :
- geographic : Australie, Canada, États-Unis.
English descriptors
- KwdEn :
- Adult, Aged, Australia, Canada, Cognition Disorders (etiology), Cohort Studies, Disability Evaluation, Disease Progression, Female, Humans, Huntington Disease (complications), Male, Mental Disorders (etiology), Middle Aged, Movement Disorders (etiology), Nerve Tissue Proteins (genetics), Retrospective Studies, Severity of Illness Index, Trinucleotide Repeats (genetics), United States.
- MESH :
- chemical , genetics : Nerve Tissue Proteins.
- geographic : Australia, Canada, United States.
- complications : Huntington Disease.
- etiology : Cognition Disorders, Mental Disorders, Movement Disorders.
- genetics : Trinucleotide Repeats.
- Adult, Aged, Cohort Studies, Disability Evaluation, Disease Progression, Female, Humans, Male, Middle Aged, Retrospective Studies, Severity of Illness Index.
Abstract
Understanding the natural history of Huntington disease will inform patients and clinicians on the disease course and researchers on the design of clinical trials.
DOI: 10.1001/jamaneurol.2013.4408
PubMed: 24126537
Affiliations:
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pubmed:24126537Le document en format XML
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<term>Cohort Studies</term>
<term>Disability Evaluation</term>
<term>Disease Progression</term>
<term>Female</term>
<term>Humans</term>
<term>Huntington Disease (complications)</term>
<term>Male</term>
<term>Mental Disorders (etiology)</term>
<term>Middle Aged</term>
<term>Movement Disorders (etiology)</term>
<term>Nerve Tissue Proteins (genetics)</term>
<term>Retrospective Studies</term>
<term>Severity of Illness Index</term>
<term>Trinucleotide Repeats (genetics)</term>
<term>United States</term>
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<term>Canada</term>
<term>United States</term>
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<term>Mental Disorders</term>
<term>Movement Disorders</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Trinucleotide Repeats</term>
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<term>Aged</term>
<term>Cohort Studies</term>
<term>Disability Evaluation</term>
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<term>Middle Aged</term>
<term>Retrospective Studies</term>
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<front><div type="abstract" xml:lang="en">Understanding the natural history of Huntington disease will inform patients and clinicians on the disease course and researchers on the design of clinical trials.</div>
</front>
</TEI>
<pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">24126537</PMID>
<DateCreated><Year>2014</Year>
<Month>02</Month>
<Day>07</Day>
</DateCreated>
<DateCompleted><Year>2014</Year>
<Month>02</Month>
<Day>20</Day>
</DateCompleted>
<DateRevised><Year>2014</Year>
<Month>08</Month>
<Day>20</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">2168-6157</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>70</Volume>
<Issue>12</Issue>
<PubDate><Year>2013</Year>
<Month>Dec</Month>
</PubDate>
</JournalIssue>
<Title>JAMA neurology</Title>
<ISOAbbreviation>JAMA Neurol</ISOAbbreviation>
</Journal>
<ArticleTitle>Natural history of Huntington disease.</ArticleTitle>
<Pagination><MedlinePgn>1520-30</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1001/jamaneurol.2013.4408</ELocationID>
<Abstract><AbstractText Label="IMPORTANCE" NlmCategory="OBJECTIVE">Understanding the natural history of Huntington disease will inform patients and clinicians on the disease course and researchers on the design of clinical trials.</AbstractText>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">To determine the longitudinal change in clinical features among individuals with Huntington disease compared with controls.</AbstractText>
<AbstractText Label="DESIGN, SETTING, AND PARTICIPANTS" NlmCategory="METHODS">Prospective, longitudinal cohort study at 44 research sites in Australia (n = 2), Canada (n =4), and the United States (n = 38). Three hundred thirty-four individuals with clinically manifest Huntington disease who had at least 3 years of annually accrued longitudinal data and 142 controls consisting of caregivers and spouses who had no genetic risk of Huntington disease.</AbstractText>
<AbstractText Label="MAIN OUTCOMES AND MEASURES" NlmCategory="METHODS">Change in movement, cognition, behavior, and function as measured by the Unified Huntington's Disease Rating Scale, the Mini-Mental State Examination, and vital signs.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Total motor score worsened by 3.0 points (95% CI, 2.5-3.4) per year and chorea worsened by 0.3 point per year (95% CI, 0.1-0.5). Cognition declined by 0.7 point (95% CI, 0.6-0.8) per year on the Mini-Mental State Examination. Behavior, as measured by the product of frequency and severity score on the Unified Huntington's Disease Rating Scale, worsened by 0.6 point per year (95% CI, 0.0-1.2). Total functional capacity declined by 0.6 point per year (95% CI, 0.5-0.7). Compared with controls, baseline body mass index was lower in those with Huntington disease (25.8 vs 28.8; P < .001), and average pulse was higher (74.2 vs 69.6 beats/min; P < .001).</AbstractText>
<AbstractText Label="CONCLUSIONS AND RELEVANCE" NlmCategory="CONCLUSIONS">Over 3 years, the cardinal features of Huntington disease all declined in a monotonic manner. These data quantify the natural history of the disease and may inform the design of trials aimed at reducing its burden.</AbstractText>
<AbstractText Label="TRIAL REGISTRATION" NlmCategory="BACKGROUND">clinicaltrials.gov Identifier: NCT00313495.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Dorsey</LastName>
<ForeName>E Ray</ForeName>
<Initials>ER</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, Johns Hopkins Medicine, Baltimore, Maryland6now with the University of Rochester Medical Center, Rochester, New York.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Beck</LastName>
<ForeName>Christopher A</ForeName>
<Initials>CA</Initials>
<AffiliationInfo><Affiliation>Department of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, New York.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Darwin</LastName>
<ForeName>Kristin</ForeName>
<Initials>K</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, Johns Hopkins Medicine, Baltimore, Maryland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Nichols</LastName>
<ForeName>Paige</ForeName>
<Initials>P</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, Johns Hopkins Medicine, Baltimore, Maryland.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Brocht</LastName>
<ForeName>Alicia F D</ForeName>
<Initials>AF</Initials>
<AffiliationInfo><Affiliation>Center for Human Experimental Therapeutics, University of Rochester Medical Center, Rochester, New York.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Biglan</LastName>
<ForeName>Kevin M</ForeName>
<Initials>KM</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, University of Rochester Medical Center, Rochester, New York.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Shoulson</LastName>
<ForeName>Ira</ForeName>
<Initials>I</Initials>
<AffiliationInfo><Affiliation>Department of Neurology, Georgetown University Medical Center, Washington, DC.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><CollectiveName>Huntington Study Group COHORT Investigators</CollectiveName>
</Author>
</AuthorList>
<Language>eng</Language>
<DataBankList CompleteYN="Y"><DataBank><DataBankName>ClinicalTrials.gov</DataBankName>
<AccessionNumberList><AccessionNumber>NCT00313495</AccessionNumber>
</AccessionNumberList>
</DataBank>
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<PublicationType UI="D016448">Multicenter Study</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
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</Article>
<MedlineJournalInfo><Country>United States</Country>
<MedlineTA>JAMA Neurol</MedlineTA>
<NlmUniqueID>101589536</NlmUniqueID>
<ISSNLinking>2168-6149</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C086055">HTT protein, human</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D009419">Nerve Tissue Proteins</NameOfSubstance>
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<CitationSubset>AIM</CitationSubset>
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<CommentsCorrectionsList><CommentsCorrections RefType="CommentIn"><RefSource>Nat Rev Neurol. 2014 Jan;10(1):12-3</RefSource>
<PMID Version="1">24323048</PMID>
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</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D009419">Nerve Tissue Proteins</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D012189">Retrospective Studies</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D012720">Severity of Illness Index</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D018911">Trinucleotide Repeats</DescriptorName>
<QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" Type="Geographic" UI="D014481">United States</DescriptorName>
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<Investigator ValidYN="Y"><LastName>Louis</LastName>
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<Investigator ValidYN="Y"><LastName>Harrison</LastName>
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