Reliability of reported age at onset for Parkinson's disease
Identifieur interne : 003F63 ( Main/Exploration ); précédent : 003F62; suivant : 003F64Reliability of reported age at onset for Parkinson's disease
Auteurs : Carson R. Reider [États-Unis] ; Cheryl A. Halter [États-Unis] ; Peter F. Castelluccio [États-Unis] ; David Oakes [États-Unis] ; William C. Nichols [États-Unis] ; Tatiana Foroud [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2003-03.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Homme.
English descriptors
- KwdEn :
- Adult, Age of Onset, Age of onset, Aged, Aged, 80 and over, Clinical interview, Data Collection, Diagnosis, Female, Human, Humans, Intertrial interval, Male, Medical record, Middle Aged, Parkinson Disease (diagnosis), Parkinson Disease (epidemiology), Parkinson Disease (genetics), Parkinson disease, Parkinson's disease onset, Questionnaire, Questionnaires, Reproducibility of Results, Sampling Studies, Siblings, test–retest reliability.
- MESH :
- diagnosis : Parkinson Disease.
- epidemiology : Parkinson Disease.
- genetics : Parkinson Disease.
- Adult, Age of Onset, Aged, Aged, 80 and over, Data Collection, Female, Humans, Male, Middle Aged, Questionnaires, Reproducibility of Results, Sampling Studies, Siblings.
Abstract
An individual's age at onset of Parkinson disease (PD) can be collected through a variety of sources, including medical records, family report, and clinical observation. The most common source of PD age at onset information in the research setting is family‐report, which is then typically used to classify a subject as juvenile, young, or late age at onset. The reliability of the family‐reported age at onset of PD has not been rigorously examined. The present study used data from individuals diagnosed with PD to evaluate the reliability of age at onset information by comparing data obtained from three sources: 1) the subject's medical records, 2) a Family History Questionnaire, and 3) a Subject History Questionnaire. Among the 149 subjects with data for all three age at onset sources, the estimated reliability was R = 0.94. Similar reliability was observed when the sample was stratified based on gender, age at examination, disease duration, first symptom of PD, and years of education. The three measures of age at onset of PD show excellent agreement, strengthening confidence in the reliability of the reported age of clinical onset for PD. © 2002 Movement Disorder Society
Url:
DOI: 10.1002/mds.10391
Affiliations:
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Le document en format XML
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Reider</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Neurology, The Ohio State University, Columbus, Ohio</wicri:regionArea><placeName><region type="state">Ohio</region></placeName></affiliation></author><author><name sortKey="Halter, Cheryl A" sort="Halter, Cheryl A" uniqKey="Halter C" first="Cheryl A." last="Halter">Cheryl A. Halter</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana</wicri:regionArea><placeName><region type="state">Indiana</region></placeName></affiliation></author><author><name sortKey="Castelluccio, Peter F" sort="Castelluccio, Peter F" uniqKey="Castelluccio P" first="Peter F." last="Castelluccio">Peter F. Castelluccio</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana</wicri:regionArea><placeName><region type="state">Indiana</region></placeName></affiliation></author><author><name sortKey="Oakes, David" sort="Oakes, David" uniqKey="Oakes D" first="David" last="Oakes">David Oakes</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Biostatistics, University of Rochester, Rochester, New York</wicri:regionArea><placeName><region type="state">État de New York</region></placeName></affiliation></author><author><name sortKey="Nichols, William C" sort="Nichols, William C" uniqKey="Nichols W" first="William C." last="Nichols">William C. Nichols</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Division of Human Genetics, Children's Hospital Medical Center, Cincinnati, Ohio</wicri:regionArea><placeName><region type="state">Ohio</region></placeName></affiliation></author><author><name sortKey="Foroud, Tatiana" sort="Foroud, Tatiana" uniqKey="Foroud T" first="Tatiana" last="Foroud">Tatiana Foroud</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana</wicri:regionArea><placeName><region type="state">Indiana</region></placeName></affiliation></author></analytic><monogr></monogr><series><title level="j">Movement Disorders</title><title level="j" type="abbrev">Mov. Disord.</title><idno type="ISSN">0885-3185</idno><idno type="eISSN">1531-8257</idno><imprint><publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher><pubPlace>New York</pubPlace><date type="published" when="2003-03">2003-03</date><biblScope unit="vol">18</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="275">275</biblScope><biblScope unit="page" to="279">279</biblScope></imprint><idno type="ISSN">0885-3185</idno></series><idno type="istex">84D46327B3146DB17965534D156D83B08C6D4221</idno><idno type="DOI">10.1002/mds.10391</idno><idno type="ArticleID">MDS10391</idno></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0885-3185</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Age of Onset</term><term>Age of onset</term><term>Aged</term><term>Aged, 80 and over</term><term>Clinical interview</term><term>Data Collection</term><term>Diagnosis</term><term>Female</term><term>Human</term><term>Humans</term><term>Intertrial interval</term><term>Male</term><term>Medical record</term><term>Middle Aged</term><term>Parkinson Disease (diagnosis)</term><term>Parkinson Disease (epidemiology)</term><term>Parkinson Disease (genetics)</term><term>Parkinson disease</term><term>Parkinson's disease onset</term><term>Questionnaire</term><term>Questionnaires</term><term>Reproducibility of Results</term><term>Sampling Studies</term><term>Siblings</term><term>test–retest reliability</term></keywords><keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Parkinson Disease</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Age of Onset</term><term>Aged</term><term>Aged, 80 and over</term><term>Data Collection</term><term>Female</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Questionnaires</term><term>Reproducibility of Results</term><term>Sampling Studies</term><term>Siblings</term></keywords><keywords scheme="Pascal" xml:lang="fr"><term>Age apparition</term><term>Diagnostic</term><term>Dossier médical</term><term>Entretien clinique</term><term>Homme</term><term>Intervalle test retest</term><term>Parkinson maladie</term><term>Questionnaire</term></keywords><keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Homme</term></keywords></textClass><langUsage><language ident="en">en</language></langUsage></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">An individual's age at onset of Parkinson disease (PD) can be collected through a variety of sources, including medical records, family report, and clinical observation. The most common source of PD age at onset information in the research setting is family‐report, which is then typically used to classify a subject as juvenile, young, or late age at onset. The reliability of the family‐reported age at onset of PD has not been rigorously examined. The present study used data from individuals diagnosed with PD to evaluate the reliability of age at onset information by comparing data obtained from three sources: 1) the subject's medical records, 2) a Family History Questionnaire, and 3) a Subject History Questionnaire. Among the 149 subjects with data for all three age at onset sources, the estimated reliability was R = 0.94. Similar reliability was observed when the sample was stratified based on gender, age at examination, disease duration, first symptom of PD, and years of education. The three measures of age at onset of PD show excellent agreement, strengthening confidence in the reliability of the reported age of clinical onset for PD. © 2002 Movement Disorder Society</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Indiana</li><li>Ohio</li><li>État de New York</li></region></list><tree><country name="États-Unis"><region name="Ohio"><name sortKey="Reider, Carson R" sort="Reider, Carson R" uniqKey="Reider C" first="Carson R." last="Reider">Carson R. Reider</name></region><name sortKey="Castelluccio, Peter F" sort="Castelluccio, Peter F" uniqKey="Castelluccio P" first="Peter F." last="Castelluccio">Peter F. Castelluccio</name><name sortKey="Foroud, Tatiana" sort="Foroud, Tatiana" uniqKey="Foroud T" first="Tatiana" last="Foroud">Tatiana Foroud</name><name sortKey="Halter, Cheryl A" sort="Halter, Cheryl A" uniqKey="Halter C" first="Cheryl A." last="Halter">Cheryl A. Halter</name><name sortKey="Nichols, William C" sort="Nichols, William C" uniqKey="Nichols W" first="William C." last="Nichols">William C. Nichols</name><name sortKey="Oakes, David" sort="Oakes, David" uniqKey="Oakes D" first="David" last="Oakes">David Oakes</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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