Secondary psychosis induced by metabolic disorders
Identifieur interne : 000407 ( Pmc/Curation ); précédent : 000406; suivant : 000408Secondary psychosis induced by metabolic disorders
Auteurs : Olivier Bonnot [France] ; Paula M. Herrera [France, Colombie] ; Sylvie Tordjman [France] ; Mark Walterfang [Australie]Source :
- Frontiers in Neuroscience [ 1662-4548 ] ; 2015.
Abstract
Metabolic disorders are not well-recognized by psychiatrists as a possible source of secondary psychoses. Inborn errors of metabolism (IEMs) are not frequent. Although their prompt diagnosis may lead to suitable treatments. IEMs are well-known to pediatricians, in particular for their most serious forms, having an early expression most of the time. Recent years discoveries have unveiled later expression forms, and sometimes very discreet first physical signs. There is a growing body of evidence that supports the hypothesis that IEMs can manifest as atypical psychiatric symptoms, even in the absence of clear neurological symptoms. In the present review, we propose a detailed overview at schizophrenia-like and autism-like symptoms that can lead practitioners to bear in mind an IEM. Other psychiatric manifestations are also found, as behavioral, cognitive, learning, and mood disorders. However, they are less frequent. Ensuring an accurate IEM diagnosis, in front of these psychiatric symptoms should be a priority, in order to grant suitable and valuable treatment for these pathologies.
Url:
DOI: 10.3389/fnins.2015.00177
PubMed: 26074754
PubMed Central: 4436816
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Herrera</name><affiliation wicri:level="1"><nlm:aff id="aff1"><institution>Psychology Laboratory of Pays de la Loire (LPPL), U2PEA Department of Child and Adolescent Psychiatry, Centre Hospitalier Universitaire de Nantes, University of Angers</institution><country>Nantes, France</country></nlm:aff><country xml:lang="fr">France</country><wicri:regionArea>Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda</wicri:regionArea></affiliation><affiliation wicri:level="1"><nlm:aff id="aff2"><institution>Grupo de Investigación en Neurociencias NeURos, Universidad del Rosario</institution><country>Bogota, Colombia</country></nlm:aff><country xml:lang="fr">Colombie</country><wicri:regionArea>Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda</wicri:regionArea></affiliation></author><author><name sortKey="Tordjman, Sylvie" sort="Tordjman, Sylvie" uniqKey="Tordjman S" first="Sylvie" last="Tordjman">Sylvie Tordjman</name><affiliation wicri:level="1"><nlm:aff id="aff3"><institution>Department of Child an Adolescent Psychiatry, Centre Hospitalier Guillaume Regnier, University of Rennes</institution><country>Rennes, France</country></nlm:aff><country xml:lang="fr">France</country><wicri:regionArea>Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda</wicri:regionArea></affiliation></author><author><name sortKey="Walterfang, Mark" sort="Walterfang, Mark" uniqKey="Walterfang M" first="Mark" last="Walterfang">Mark Walterfang</name><affiliation wicri:level="1"><nlm:aff id="aff4"><institution>Neuropsychiatry Unit, Royal Melbourne Hospital</institution><country>Melbourne, VIC, Australia</country></nlm:aff><country xml:lang="fr">Australie</country><wicri:regionArea>Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda</wicri:regionArea></affiliation><affiliation wicri:level="1"><nlm:aff id="aff5"><institution>Melbourne Neuropsychiatry Centre, University of Melbourne</institution><country>Melbourne, VIC, Australia</country></nlm:aff><country xml:lang="fr">Australie</country><wicri:regionArea>Inflammatory Disease Section, National Human Genome Research Institute, National Institutes of Health, Bethesda</wicri:regionArea></affiliation></author></analytic><series><title level="j">Frontiers in Neuroscience</title><idno type="ISSN">1662-4548</idno><idno type="eISSN">1662-453X</idno><imprint><date when="2015">2015</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Metabolic disorders are not well-recognized by psychiatrists as a possible source of secondary psychoses. Inborn errors of metabolism (IEMs) are not frequent. Although their prompt diagnosis may lead to suitable treatments. IEMs are well-known to pediatricians, in particular for their most serious forms, having an early expression most of the time. Recent years discoveries have unveiled later expression forms, and sometimes very discreet first physical signs. There is a growing body of evidence that supports the hypothesis that IEMs can manifest as atypical psychiatric symptoms, even in the absence of clear neurological symptoms. In the present review, we propose a detailed overview at schizophrenia-like and autism-like symptoms that can lead practitioners to bear in mind an IEM. Other psychiatric manifestations are also found, as behavioral, cognitive, learning, and mood disorders. However, they are less frequent. Ensuring an accurate IEM diagnosis, in front of these psychiatric symptoms should be a priority, in order to grant suitable and valuable treatment for these pathologies.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Abbott, M H" uniqKey="Abbott M">M. H. Abbott</name></author><author><name sortKey="Folstein, S E" uniqKey="Folstein S">S. E. Folstein</name></author><author><name sortKey="Abbey, H" uniqKey="Abbey H">H. Abbey</name></author><author><name sortKey="Pyeritz, R E" uniqKey="Pyeritz R">R. E. Pyeritz</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Akil, M" uniqKey="Akil M">M. Akil</name></author><author><name sortKey="Brewer, G J" uniqKey="Brewer G">G. J. Brewer</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Akil, M" uniqKey="Akil M">M. Akil</name></author><author><name sortKey="Schwartz, J A" uniqKey="Schwartz J">J. A. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Front Neurosci</journal-id><journal-id journal-id-type="iso-abbrev">Front Neurosci</journal-id><journal-id journal-id-type="publisher-id">Front. Neurosci.</journal-id><journal-title-group><journal-title>Frontiers in Neuroscience</journal-title></journal-title-group><issn pub-type="ppub">1662-4548</issn><issn pub-type="epub">1662-453X</issn><publisher><publisher-name>Frontiers Media S.A.</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">26074754</article-id><article-id pub-id-type="pmc">4436816</article-id><article-id pub-id-type="doi">10.3389/fnins.2015.00177</article-id><article-categories><subj-group subj-group-type="heading"><subject>Pharmacology</subject><subj-group><subject>Review</subject></subj-group></subj-group></article-categories><title-group><article-title>Secondary psychosis induced by metabolic disorders</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Bonnot</surname><given-names>Olivier</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="author-notes" rid="fn001"><sup>*</sup></xref><uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/231289"></uri></contrib><contrib contrib-type="author"><name><surname>Herrera</surname><given-names>Paula M.</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/123503"></uri></contrib><contrib contrib-type="author"><name><surname>Tordjman</surname><given-names>Sylvie</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref><uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/83064"></uri></contrib><contrib contrib-type="author"><name><surname>Walterfang</surname><given-names>Mark</given-names></name><xref ref-type="aff" rid="aff4"><sup>4</sup></xref><xref ref-type="aff" rid="aff5"><sup>5</sup></xref><uri xlink:type="simple" xlink:href="http://community.frontiersin.org/people/u/39892"></uri></contrib></contrib-group><aff id="aff1"><sup>1</sup><institution>Psychology Laboratory of Pays de la Loire (LPPL), U2PEA Department of Child and Adolescent Psychiatry, Centre Hospitalier Universitaire de Nantes, University of Angers</institution><country>Nantes, France</country></aff><aff id="aff2"><sup>2</sup><institution>Grupo de Investigación en Neurociencias NeURos, Universidad del Rosario</institution><country>Bogota, Colombia</country></aff><aff id="aff3"><sup>3</sup><institution>Department of Child an Adolescent Psychiatry, Centre Hospitalier Guillaume Regnier, University of Rennes</institution><country>Rennes, France</country></aff><aff id="aff4"><sup>4</sup><institution>Neuropsychiatry Unit, Royal Melbourne Hospital</institution><country>Melbourne, VIC, Australia</country></aff><aff id="aff5"><sup>5</sup><institution>Melbourne Neuropsychiatry Centre, University of Melbourne</institution><country>Melbourne, VIC, Australia</country></aff><author-notes><fn fn-type="edited-by"><p>Edited by: Tommaso Cassano, University of Foggia, Italy; Luca Steardo, Sapienza University of Rome, Italy</p></fn><fn fn-type="edited-by"><p>Reviewed by: Drozdstoy Stoyanov Stoyanov, Medical University, Bulgaria; Alfonso Tortorella, University of Naples, Italy</p></fn><corresp id="fn001">*Correspondence: Olivier Bonnot, Department of Child and Adolescent Psychiatry, Centre Hospitalier Universitaire de Nantes, Hôpital Mère-Enfant, 7 quai Moncousu, 44000 Nantes, France, <email xlink:type="simple">olivier.bonnot@chu-nantes.fr</email></corresp><fn fn-type="other" id="fn002"><p>This article was submitted to Neuropharmacology, a section of the journal Frontiers in Neuroscience</p></fn></author-notes><pub-date pub-type="epub"><day>19</day><month>5</month><year>2015</year></pub-date><pub-date pub-type="collection"><year>2015</year></pub-date><volume>9</volume><elocation-id>177</elocation-id><history><date date-type="received"><day>08</day><month>3</month><year>2015</year></date><date date-type="accepted"><day>30</day><month>4</month><year>2015</year></date></history><permissions><copyright-statement>Copyright © 2015 Bonnot, Herrera, Tordjman and Walterfang.</copyright-statement><copyright-year>2015</copyright-year><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</license-p></license></permissions><abstract><p>Metabolic disorders are not well-recognized by psychiatrists as a possible source of secondary psychoses. Inborn errors of metabolism (IEMs) are not frequent. Although their prompt diagnosis may lead to suitable treatments. IEMs are well-known to pediatricians, in particular for their most serious forms, having an early expression most of the time. Recent years discoveries have unveiled later expression forms, and sometimes very discreet first physical signs. There is a growing body of evidence that supports the hypothesis that IEMs can manifest as atypical psychiatric symptoms, even in the absence of clear neurological symptoms. In the present review, we propose a detailed overview at schizophrenia-like and autism-like symptoms that can lead practitioners to bear in mind an IEM. Other psychiatric manifestations are also found, as behavioral, cognitive, learning, and mood disorders. However, they are less frequent. Ensuring an accurate IEM diagnosis, in front of these psychiatric symptoms should be a priority, in order to grant suitable and valuable treatment for these pathologies.</p></abstract><kwd-group><kwd>IEMs</kwd><kwd>neurometabolic disorders</kwd><kwd>homocysteine</kwd><kwd>urea</kwd><kwd>organic psychosis</kwd><kwd>schizophrenia-like</kwd><kwd>atypicalness</kwd></kwd-group><counts><fig-count count="0"></fig-count><table-count count="1"></table-count><equation-count count="0"></equation-count><ref-count count="68"></ref-count><page-count count="8"></page-count><word-count count="6335"></word-count></counts></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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