Relationship of Mediterranean diet and caloric intake to phenoconversion in Huntington disease.
Identifieur interne : 000C85 ( Main/Exploration ); précédent : 000C84; suivant : 000C86Relationship of Mediterranean diet and caloric intake to phenoconversion in Huntington disease.
Auteurs : Karen Marder [États-Unis] ; Yian Gu ; Shirley Eberly ; Caroline M. Tanner ; Nikolaos Scarmeas ; David Oakes ; Ira ShoulsonSource :
- JAMA neurology [ 2168-6157 ] ; 2013.
Descripteurs français
- Wicri :
- geographic : Canada, États-Unis.
English descriptors
- KwdEn :
- Adult, Body Mass Index, Canada, Diet, Mediterranean, Disease Progression, Energy Intake (physiology), Female, Humans, Huntington Disease (complications), Huntington Disease (genetics), Huntington Disease (prevention & control), Male, Medication Adherence, Middle Aged, Observation, Phenotype, Predictive Value of Tests, Proportional Hazards Models, Prospective Studies, Retrospective Studies, Severity of Illness Index, Surveys and Questionnaires, Time Factors, Trinucleotide Repeat Expansion (genetics), United States.
- MESH :
- geographic : Canada, United States.
- complications : Huntington Disease.
- genetics : Huntington Disease, Trinucleotide Repeat Expansion.
- physiology : Energy Intake.
- prevention & control : Huntington Disease.
- Adult, Body Mass Index, Diet, Mediterranean, Disease Progression, Female, Humans, Male, Medication Adherence, Middle Aged, Observation, Phenotype, Predictive Value of Tests, Proportional Hazards Models, Prospective Studies, Retrospective Studies, Severity of Illness Index, Surveys and Questionnaires, Time Factors.
Abstract
Adherence to Mediterranean-type diet (MeDi) may delay onset of Alzheimer and Parkinson diseases. Whether adherence to MeDi affects time to phenoconversion in Huntington disease (HD), a highly penetrant, single-gene disorder, is unknown.
DOI: 10.1001/jamaneurol.2013.3487
PubMed: 24000094
Affiliations:
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Le document en format XML
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Tanner</name></author><author><name sortKey="Scarmeas, Nikolaos" sort="Scarmeas, Nikolaos" uniqKey="Scarmeas N" first="Nikolaos" last="Scarmeas">Nikolaos Scarmeas</name></author><author><name sortKey="Oakes, David" sort="Oakes, David" uniqKey="Oakes D" first="David" last="Oakes">David Oakes</name></author><author><name sortKey="Shoulson, Ira" sort="Shoulson, Ira" uniqKey="Shoulson I" first="Ira" last="Shoulson">Ira Shoulson</name></author></analytic><series><title level="j">JAMA neurology</title><idno type="eISSN">2168-6157</idno><imprint><date when="2013" type="published">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Body Mass Index</term><term>Canada</term><term>Diet, Mediterranean</term><term>Disease Progression</term><term>Energy Intake (physiology)</term><term>Female</term><term>Humans</term><term>Huntington Disease (complications)</term><term>Huntington Disease (genetics)</term><term>Huntington Disease (prevention & control)</term><term>Male</term><term>Medication Adherence</term><term>Middle Aged</term><term>Observation</term><term>Phenotype</term><term>Predictive Value of Tests</term><term>Proportional Hazards Models</term><term>Prospective Studies</term><term>Retrospective Studies</term><term>Severity of Illness Index</term><term>Surveys and Questionnaires</term><term>Time Factors</term><term>Trinucleotide Repeat Expansion (genetics)</term><term>United States</term></keywords><keywords scheme="MESH" type="geographic" xml:lang="en"><term>Canada</term><term>United States</term></keywords><keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Huntington Disease</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Huntington Disease</term><term>Trinucleotide Repeat Expansion</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Energy Intake</term></keywords><keywords scheme="MESH" qualifier="prevention & control" xml:lang="en"><term>Huntington Disease</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Body Mass Index</term><term>Diet, Mediterranean</term><term>Disease Progression</term><term>Female</term><term>Humans</term><term>Male</term><term>Medication Adherence</term><term>Middle Aged</term><term>Observation</term><term>Phenotype</term><term>Predictive Value of Tests</term><term>Proportional Hazards Models</term><term>Prospective Studies</term><term>Retrospective Studies</term><term>Severity of Illness Index</term><term>Surveys and Questionnaires</term><term>Time Factors</term></keywords><keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Canada</term><term>États-Unis</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Adherence to Mediterranean-type diet (MeDi) may delay onset of Alzheimer and Parkinson diseases. Whether adherence to MeDi affects time to phenoconversion in Huntington disease (HD), a highly penetrant, single-gene disorder, is unknown.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>État de New York</li></region></list><tree><noCountry><name sortKey="Eberly, Shirley" sort="Eberly, Shirley" uniqKey="Eberly S" first="Shirley" last="Eberly">Shirley Eberly</name><name sortKey="Gu, Yian" sort="Gu, Yian" uniqKey="Gu Y" first="Yian" last="Gu">Yian Gu</name><name sortKey="Oakes, David" sort="Oakes, David" uniqKey="Oakes D" first="David" last="Oakes">David Oakes</name><name sortKey="Scarmeas, Nikolaos" sort="Scarmeas, Nikolaos" uniqKey="Scarmeas N" first="Nikolaos" last="Scarmeas">Nikolaos Scarmeas</name><name sortKey="Shoulson, Ira" sort="Shoulson, Ira" uniqKey="Shoulson I" first="Ira" last="Shoulson">Ira Shoulson</name><name sortKey="Tanner, Caroline M" sort="Tanner, Caroline M" uniqKey="Tanner C" first="Caroline M" last="Tanner">Caroline M. 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