Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
Identifieur interne : 000865 ( PubMed/Corpus ); précédent : 000864; suivant : 000866Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
Auteurs : Wilhelmina G. Leen ; Leena Mewasingh ; Marcel M. Verbeek ; Erik-Jan Kamsteeg ; Bart P. Van De Warrenburg ; Michel A. WillemsenSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.
English descriptors
- KwdEn :
- Adolescent, Adult, Ataxia (diet therapy), Ataxia (etiology), Carbohydrate Metabolism, Inborn Errors (diet therapy), Carbohydrate Metabolism, Inborn Errors (genetics), Cognition Disorders (diet therapy), Cognition Disorders (etiology), Cognition Disorders (psychology), Diet, Carbohydrate-Restricted (adverse effects), Female, Humans, Ketosis (diet therapy), Ketosis (etiology), Male, Monosaccharide Transport Proteins (deficiency), Monosaccharide Transport Proteins (genetics), Movement Disorders (diet therapy), Movement Disorders (genetics), Myoclonus (diet therapy), Myoclonus (etiology), Patient Compliance, Seizures (etiology), Treatment Outcome, Young Adult.
- MESH :
- chemical , deficiency : Monosaccharide Transport Proteins.
- adverse effects : Diet, Carbohydrate-Restricted.
- diet therapy : Ataxia, Carbohydrate Metabolism, Inborn Errors, Cognition Disorders, Ketosis, Movement Disorders, Myoclonus.
- etiology : Ataxia, Cognition Disorders, Ketosis, Myoclonus, Seizures.
- genetics : Carbohydrate Metabolism, Inborn Errors, Monosaccharide Transport Proteins, Movement Disorders.
- psychology : Cognition Disorders.
- Adolescent, Adult, Female, Humans, Male, Patient Compliance, Treatment Outcome, Young Adult.
Abstract
Movement disorders are a prominent feature of glucose transporter-1 (GLUT1) deficiency syndrome (GLUT1DS). First-choice treatment is a ketogenic diet, but compliance is poor. We have investigated the effect of the modified Atkins diet as an alternative treatment for movement disorders in GLUT1DS.
DOI: 10.1002/mds.25515
PubMed: 23801573
Links to Exploration step
pubmed:23801573Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.</title><author><name sortKey="Leen, Wilhelmina G" sort="Leen, Wilhelmina G" uniqKey="Leen W" first="Wilhelmina G" last="Leen">Wilhelmina G. Leen</name><affiliation><nlm:affiliation>Department of Neurology, Radboud University Medical Centre, Donders Institute for Brain, Cognition, and Behaviour, Nijmegen, the Netherlands.</nlm:affiliation></affiliation></author><author><name sortKey="Mewasingh, Leena" sort="Mewasingh, Leena" uniqKey="Mewasingh L" first="Leena" last="Mewasingh">Leena Mewasingh</name></author><author><name sortKey="Verbeek, Marcel M" sort="Verbeek, Marcel M" uniqKey="Verbeek M" first="Marcel M" last="Verbeek">Marcel M. Verbeek</name></author><author><name sortKey="Kamsteeg, Erik Jan" sort="Kamsteeg, Erik Jan" uniqKey="Kamsteeg E" first="Erik-Jan" last="Kamsteeg">Erik-Jan Kamsteeg</name></author><author><name sortKey="Van De Warrenburg, Bart P" sort="Van De Warrenburg, Bart P" uniqKey="Van De Warrenburg B" first="Bart P" last="Van De Warrenburg">Bart P. Van De Warrenburg</name></author><author><name sortKey="Willemsen, Michel A" sort="Willemsen, Michel A" uniqKey="Willemsen M" first="Michel A" last="Willemsen">Michel A. Willemsen</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2013">2013</date><idno type="RBID">pubmed:23801573</idno><idno type="pmid">23801573</idno><idno type="doi">10.1002/mds.25515</idno><idno type="wicri:Area/PubMed/Corpus">000865</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.</title><author><name sortKey="Leen, Wilhelmina G" sort="Leen, Wilhelmina G" uniqKey="Leen W" first="Wilhelmina G" last="Leen">Wilhelmina G. Leen</name><affiliation><nlm:affiliation>Department of Neurology, Radboud University Medical Centre, Donders Institute for Brain, Cognition, and Behaviour, Nijmegen, the Netherlands.</nlm:affiliation></affiliation></author><author><name sortKey="Mewasingh, Leena" sort="Mewasingh, Leena" uniqKey="Mewasingh L" first="Leena" last="Mewasingh">Leena Mewasingh</name></author><author><name sortKey="Verbeek, Marcel M" sort="Verbeek, Marcel M" uniqKey="Verbeek M" first="Marcel M" last="Verbeek">Marcel M. Verbeek</name></author><author><name sortKey="Kamsteeg, Erik Jan" sort="Kamsteeg, Erik Jan" uniqKey="Kamsteeg E" first="Erik-Jan" last="Kamsteeg">Erik-Jan Kamsteeg</name></author><author><name sortKey="Van De Warrenburg, Bart P" sort="Van De Warrenburg, Bart P" uniqKey="Van De Warrenburg B" first="Bart P" last="Van De Warrenburg">Bart P. Van De Warrenburg</name></author><author><name sortKey="Willemsen, Michel A" sort="Willemsen, Michel A" uniqKey="Willemsen M" first="Michel A" last="Willemsen">Michel A. Willemsen</name></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="eISSN">1531-8257</idno><imprint><date when="2013" type="published">2013</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Ataxia (diet therapy)</term><term>Ataxia (etiology)</term><term>Carbohydrate Metabolism, Inborn Errors (diet therapy)</term><term>Carbohydrate Metabolism, Inborn Errors (genetics)</term><term>Cognition Disorders (diet therapy)</term><term>Cognition Disorders (etiology)</term><term>Cognition Disorders (psychology)</term><term>Diet, Carbohydrate-Restricted (adverse effects)</term><term>Female</term><term>Humans</term><term>Ketosis (diet therapy)</term><term>Ketosis (etiology)</term><term>Male</term><term>Monosaccharide Transport Proteins (deficiency)</term><term>Monosaccharide Transport Proteins (genetics)</term><term>Movement Disorders (diet therapy)</term><term>Movement Disorders (genetics)</term><term>Myoclonus (diet therapy)</term><term>Myoclonus (etiology)</term><term>Patient Compliance</term><term>Seizures (etiology)</term><term>Treatment Outcome</term><term>Young Adult</term></keywords><keywords scheme="MESH" type="chemical" qualifier="deficiency" xml:lang="en"><term>Monosaccharide Transport Proteins</term></keywords><keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Diet, Carbohydrate-Restricted</term></keywords><keywords scheme="MESH" qualifier="diet therapy" xml:lang="en"><term>Ataxia</term><term>Carbohydrate Metabolism, Inborn Errors</term><term>Cognition Disorders</term><term>Ketosis</term><term>Movement Disorders</term><term>Myoclonus</term></keywords><keywords scheme="MESH" qualifier="etiology" xml:lang="en"><term>Ataxia</term><term>Cognition Disorders</term><term>Ketosis</term><term>Myoclonus</term><term>Seizures</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Carbohydrate Metabolism, Inborn Errors</term><term>Monosaccharide Transport Proteins</term><term>Movement Disorders</term></keywords><keywords scheme="MESH" qualifier="psychology" xml:lang="en"><term>Cognition Disorders</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adolescent</term><term>Adult</term><term>Female</term><term>Humans</term><term>Male</term><term>Patient Compliance</term><term>Treatment Outcome</term><term>Young Adult</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Movement disorders are a prominent feature of glucose transporter-1 (GLUT1) deficiency syndrome (GLUT1DS). First-choice treatment is a ketogenic diet, but compliance is poor. We have investigated the effect of the modified Atkins diet as an alternative treatment for movement disorders in GLUT1DS.</div></front></TEI><pubmed><MedlineCitation Owner="NLM" Status="MEDLINE"><PMID Version="1">23801573</PMID><DateCreated><Year>2013</Year><Month>09</Month><Day>30</Day></DateCreated><DateCompleted><Year>2014</Year><Month>05</Month><Day>09</Day></DateCompleted><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1531-8257</ISSN><JournalIssue CitedMedium="Internet"><Volume>28</Volume><Issue>10</Issue><PubDate><Year>2013</Year><Month>Sep</Month></PubDate></JournalIssue><Title>Movement disorders : official journal of the Movement Disorder Society</Title><ISOAbbreviation>Mov. Disord.</ISOAbbreviation></Journal><ArticleTitle>Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.</ArticleTitle><Pagination><MedlinePgn>1439-42</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1002/mds.25515</ELocationID><Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Movement disorders are a prominent feature of glucose transporter-1 (GLUT1) deficiency syndrome (GLUT1DS). First-choice treatment is a ketogenic diet, but compliance is poor. We have investigated the effect of the modified Atkins diet as an alternative treatment for movement disorders in GLUT1DS.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">Four patients with GLUT1DS ages 15 to 30 years who had movement disorders as the most prominent feature were prospectively evaluated after initiation of the modified Atkins diet. Movement disorders included dystonia, ataxia, myoclonus, and spasticity, either continuous or paroxysmal, triggered by action or exercise. Duration of treatment ranged from 3 months to 16 months.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">All patients reached mild to moderate ketosis and experienced remarkable improvement in the frequency and severity of paroxysmal movement disorders. Cognitive function also improved subjectively.</AbstractText><AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The modified Atkins diet is an effective and feasible alternative to the ketogenic diet for the treatment of GLUT1DS-related paroxysmal movement disorders in adolescence and adulthood.</AbstractText><CopyrightInformation>© 2013 International Parkinson and Movement Disorder Society.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Leen</LastName><ForeName>Wilhelmina G</ForeName><Initials>WG</Initials><AffiliationInfo><Affiliation>Department of Neurology, Radboud University Medical Centre, Donders Institute for Brain, Cognition, and Behaviour, Nijmegen, the Netherlands.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mewasingh</LastName><ForeName>Leena</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Verbeek</LastName><ForeName>Marcel M</ForeName><Initials>MM</Initials></Author><Author ValidYN="Y"><LastName>Kamsteeg</LastName><ForeName>Erik-Jan</ForeName><Initials>EJ</Initials></Author><Author ValidYN="Y"><LastName>van de Warrenburg</LastName><ForeName>Bart P</ForeName><Initials>BP</Initials></Author><Author ValidYN="Y"><LastName>Willemsen</LastName><ForeName>Michel A</ForeName><Initials>MA</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2013</Year><Month>06</Month><Day>25</Day></ArticleDate></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Mov Disord</MedlineTA><NlmUniqueID>8610688</NlmUniqueID><ISSNLinking>0885-3185</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D009004">Monosaccharide Transport Proteins</NameOfSubstance></Chemical></ChemicalList><SupplMeshList><SupplMeshName Type="Disease" UI="C536830">De Vivo disease</SupplMeshName></SupplMeshList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000293">Adolescent</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D000328">Adult</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D001259">Ataxia</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000178">diet therapy</QualifierName><QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D002239">Carbohydrate Metabolism, Inborn Errors</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000178">diet therapy</QualifierName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D003072">Cognition Disorders</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000178">diet therapy</QualifierName><QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName><QualifierName MajorTopicYN="N" UI="Q000523">psychology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="Y" UI="D050528">Diet, Carbohydrate-Restricted</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000009">adverse effects</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D005260">Female</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D007662">Ketosis</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000178">diet therapy</QualifierName><QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D009004">Monosaccharide Transport Proteins</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000172">deficiency</QualifierName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D009069">Movement Disorders</DescriptorName><QualifierName MajorTopicYN="Y" UI="Q000178">diet therapy</QualifierName><QualifierName MajorTopicYN="N" UI="Q000235">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D009207">Myoclonus</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000178">diet therapy</QualifierName><QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D010349">Patient Compliance</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D012640">Seizures</DescriptorName><QualifierName MajorTopicYN="N" UI="Q000209">etiology</QualifierName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D016896">Treatment Outcome</DescriptorName></MeshHeading><MeshHeading><DescriptorName MajorTopicYN="N" UI="D055815">Young Adult</DescriptorName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">GLUT1 deficiency syndrome</Keyword><Keyword MajorTopicYN="N">ataxia</Keyword><Keyword MajorTopicYN="N">modified Atkins diet</Keyword><Keyword MajorTopicYN="N">myoclonus</Keyword><Keyword MajorTopicYN="N">paroxysmal exercise induced dyskinesia</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="received"><Year>2013</Year><Month>2</Month><Day>12</Day></PubMedPubDate><PubMedPubDate PubStatus="revised"><Year>2013</Year><Month>4</Month><Day>15</Day></PubMedPubDate><PubMedPubDate 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