Movement Disorders (revue)

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Abnormal response to cortical activation in early stages of Huntington disease.

Identifieur interne : 000F59 ( PubMed/Checkpoint ); précédent : 000F58; suivant : 000F60

Abnormal response to cortical activation in early stages of Huntington disease.

Auteurs : Fanny Mochel [France] ; Tra-My N'Guyen ; Dinesh Deelchand ; Daisy Rinaldi ; Romain Valabregue ; Claire Wary ; Pierre G. Carlier ; Alexandra Durr ; Pierre-Gilles Henry

Source :

RBID : pubmed:22517114

English descriptors

Abstract

We wished to identify noninvasive in vivo biomarkers of brain energy deficit in Huntington disease.

DOI: 10.1002/mds.25009
PubMed: 22517114


Affiliations:


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pubmed:22517114

Le document en format XML

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<title xml:lang="en">Abnormal response to cortical activation in early stages of Huntington disease.</title>
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<name sortKey="Mochel, Fanny" sort="Mochel, Fanny" uniqKey="Mochel F" first="Fanny" last="Mochel">Fanny Mochel</name>
<affiliation wicri:level="1">
<nlm:affiliation>INSERM UMR S975, Institut du Cerveau et de la Moelle, Hôpital La Salpêtrière, Paris, France. fanny.mochel@upmc.fr</nlm:affiliation>
<country xml:lang="fr">France</country>
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<name sortKey="N Guyen, Tra My" sort="N Guyen, Tra My" uniqKey="N Guyen T" first="Tra-My" last="N'Guyen">Tra-My N'Guyen</name>
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<name sortKey="Deelchand, Dinesh" sort="Deelchand, Dinesh" uniqKey="Deelchand D" first="Dinesh" last="Deelchand">Dinesh Deelchand</name>
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<name sortKey="Valabregue, Romain" sort="Valabregue, Romain" uniqKey="Valabregue R" first="Romain" last="Valabregue">Romain Valabregue</name>
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<name sortKey="Wary, Claire" sort="Wary, Claire" uniqKey="Wary C" first="Claire" last="Wary">Claire Wary</name>
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<name sortKey="Carlier, Pierre G" sort="Carlier, Pierre G" uniqKey="Carlier P" first="Pierre G" last="Carlier">Pierre G. Carlier</name>
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<name sortKey="Durr, Alexandra" sort="Durr, Alexandra" uniqKey="Durr A" first="Alexandra" last="Durr">Alexandra Durr</name>
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<name sortKey="Henry, Pierre Gilles" sort="Henry, Pierre Gilles" uniqKey="Henry P" first="Pierre-Gilles" last="Henry">Pierre-Gilles Henry</name>
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<name sortKey="Rinaldi, Daisy" sort="Rinaldi, Daisy" uniqKey="Rinaldi D" first="Daisy" last="Rinaldi">Daisy Rinaldi</name>
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<name sortKey="Valabregue, Romain" sort="Valabregue, Romain" uniqKey="Valabregue R" first="Romain" last="Valabregue">Romain Valabregue</name>
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<name sortKey="Wary, Claire" sort="Wary, Claire" uniqKey="Wary C" first="Claire" last="Wary">Claire Wary</name>
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<name sortKey="Carlier, Pierre G" sort="Carlier, Pierre G" uniqKey="Carlier P" first="Pierre G" last="Carlier">Pierre G. Carlier</name>
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<name sortKey="Durr, Alexandra" sort="Durr, Alexandra" uniqKey="Durr A" first="Alexandra" last="Durr">Alexandra Durr</name>
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<name sortKey="Henry, Pierre Gilles" sort="Henry, Pierre Gilles" uniqKey="Henry P" first="Pierre-Gilles" last="Henry">Pierre-Gilles Henry</name>
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<title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
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<date when="2012" type="published">2012</date>
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<term>Adenosine Triphosphate (metabolism)</term>
<term>Case-Control Studies</term>
<term>Cerebral Cortex (metabolism)</term>
<term>Cerebral Cortex (physiopathology)</term>
<term>Cerebral Cortex (radionuclide imaging)</term>
<term>Female</term>
<term>Humans</term>
<term>Huntington Disease (pathology)</term>
<term>Huntington Disease (radionuclide imaging)</term>
<term>Linear Models</term>
<term>Magnetic Resonance Spectroscopy</term>
<term>Male</term>
<term>Phosphates (metabolism)</term>
<term>Phosphocreatine (metabolism)</term>
<term>Phosphorus Isotopes (metabolism)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Adenosine Triphosphate</term>
<term>Phosphates</term>
<term>Phosphocreatine</term>
<term>Phosphorus Isotopes</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Cerebral Cortex</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Huntington Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="physiopathology" xml:lang="en">
<term>Cerebral Cortex</term>
</keywords>
<keywords scheme="MESH" qualifier="radionuclide imaging" xml:lang="en">
<term>Cerebral Cortex</term>
<term>Huntington Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Case-Control Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Linear Models</term>
<term>Magnetic Resonance Spectroscopy</term>
<term>Male</term>
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<div type="abstract" xml:lang="en">We wished to identify noninvasive in vivo biomarkers of brain energy deficit in Huntington disease.</div>
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<DateCreated>
<Year>2012</Year>
<Month>06</Month>
<Day>25</Day>
</DateCreated>
<DateCompleted>
<Year>2012</Year>
<Month>11</Month>
<Day>13</Day>
</DateCompleted>
<DateRevised>
<Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
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<ISSN IssnType="Electronic">1531-8257</ISSN>
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<Volume>27</Volume>
<Issue>7</Issue>
<PubDate>
<Year>2012</Year>
<Month>Jun</Month>
</PubDate>
</JournalIssue>
<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
</Journal>
<ArticleTitle>Abnormal response to cortical activation in early stages of Huntington disease.</ArticleTitle>
<Pagination>
<MedlinePgn>907-10</MedlinePgn>
</Pagination>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">We wished to identify noninvasive in vivo biomarkers of brain energy deficit in Huntington disease.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">We studied 15 early affected patients (mean motor United Huntington Disease Rating Scale, 18 ± 9) and 15 age- and sex-matched controls. We coupled (31)phosphorus nuclear magnetic resonance spectroscopy with activation of the occipital cortex in order to measure the relative concentrations of adenosine triphosphate, phosphocreatine, and inorganic phosphate before, during, and after visual stimulation.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">In controls, we observed an 11% increase in the inorganic phosphate/phosphocreatine ratio (P = .024) and a 13% increase in the inorganic phosphate/adenosine triphosphate ratio (P = .016) during brain activation, reflecting increased adenosine diphosphate concentrations. Subsequently, controls had a return to baseline levels during recovery (P = .012 and .022, respectively). In contrast, both ratios were unchanged in patients during and after visual stimulation.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">(31)Phosphorus nuclear magnetic resonance spectroscopy could provide functional biomarkers of brain energy deficit to monitor therapeutic efficacy in Huntington disease.</AbstractText>
<CopyrightInformation>Copyright © 2012 Movement Disorder Society.</CopyrightInformation>
</Abstract>
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<LastName>Mochel</LastName>
<ForeName>Fanny</ForeName>
<Initials>F</Initials>
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<ForeName>Pierre-Gilles</ForeName>
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<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>P41 RR 08079</GrantID>
<Acronym>RR</Acronym>
<Agency>NCRR NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>R01 NS 38672</GrantID>
<Acronym>NS</Acronym>
<Agency>NINDS NIH HHS</Agency>
<Country>United States</Country>
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<Chemical>
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<NameOfSubstance UI="D010759">Phosphorus Isotopes</NameOfSubstance>
</Chemical>
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<NameOfSubstance UI="D010725">Phosphocreatine</NameOfSubstance>
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<Chemical>
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